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Anti-PD-1 monoclonal antibody MEDI0680 in a phase I study of patients with advanced solid malignancies
  1. Aung Naing1,a,
  2. Jeffrey Infante2,13,
  3. Sanjay Goel3,
  4. Howard Burris2,
  5. Chelsea Black4,14,
  6. Shannon Marshall5,15,
  7. Ikbel Achour4,
  8. Susannah Barbee5,16,
  9. Rena May5,17,
  10. Chris Morehouse4,
  11. Kristen Pollizzi6,
  12. Xuyang Song7,
  13. Keith Steele4,
  14. Nairouz Elgeioushi8,
  15. Farzana Walcott9,
  16. Joyson Karakunnel9,18,
  17. Patricia LoRusso10,19,
  18. Amy Weise10,
  19. Joseph Eder11,
  20. Brendan Curti12 and
  21. Michael Oberst6
  1. Aff1 0000 0001 2291 4776grid.240145.6Department of Investigational Cancer TherapeuticsUniversity of Texas MD Anderson Cancer Center 77030 Houston TX USA
  2. Aff2 0000 0004 0480 9560grid.492963.3Drug Development UnitSarah Cannon Research Institute, Tennessee Oncology Nashville TN USA
  3. Aff3 Department of Medical Oncology, Montefiore Medical Center, Albert Einstein College of Medicine Bronx NY USA
  4. Aff4 grid.418152.bTranslational Medicine, Oncology R&D, AstraZeneca Gaithersburg MD USA
  5. Aff5 grid.417441.3Department of Research, Amplimmune Inc. Gaithersburg MD USA
  6. Aff6 grid.418152.bDiscovery Sciences, Oncology R&D, AstraZeneca Gaithersburg MD USA
  7. Aff7 grid.418152.bClinical Pharmacology & Safety Sciences, BioPharmaceuticals R&D, AstraZeneca Gaithersburg MD USA
  8. Aff8 grid.418152.bOncology Biometrics, Oncology R&D, AstraZeneca Gaithersburg MD USA
  9. Aff9 grid.418152.bEarly Oncology Clinical, Oncology R&D, AstraZeneca Gaithersburg MD USA
  10. Aff10 0000 0001 1456 7807grid.254444.7Department of Hematology & OncologyKarmanos Cancer Institute, Wayne State University Detroit MI USA
  11. Aff11 grid.433818.5Medical Oncology, Yale Cancer Center New Haven CT USA
  12. Aff12 0000 0004 0463 5556grid.415286.cEarle A Chiles Research Institute, Providence Cancer Institute Portland OR USA
  13. Aff13 0000 0004 0389 4927grid.497530.cPresent Address: Department of Oncology, Janssen Raritan NJ USA
  14. Aff14 Present Address: PRA Health Sciences Blue Bell PA USA
  15. Aff15 grid.418152.bPresent Address: Early Oncology Clinical, Oncology R&D, AstraZeneca Gaithersburg MD USA
  16. Aff16 Present Address: Department of Immuno-Oncology Research, FivePrime Therapeutics, Inc. South San Francisco CA USA
  17. Aff17 grid.418152.bPresent Address: Late-stage Development, Oncology R&D, AstraZeneca Gaithersburg MD USA
  18. Aff18 Present Address: Department of Clinical Development, Arcus Biosciences Hayward CA USA
  19. Aff19 grid.433818.5Present Address: Medical Oncology, Yale Cancer Center New Haven CT USA
  1. a +1 713 563 0181 anaing{at}mdanderson.org
  • Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Abstract

Background The safety, efficacy, pharmacokinetics, and pharmacodynamics of the anti-programmed cell death-1 antibody MEDI0680 were evaluated in a phase I, multicenter, dose-escalation study in advanced solid malignancies.

Methods MEDI0680 was administered intravenously once every 2 weeks (Q2W) or once every 3 weeks at 0.1, 0.5, 2.5, 10 or 20 mg/kg. Two cohorts received 20 mg/kg once a week for 2 or 4 weeks, then 20 mg/kg Q2W. All were treated for 12 months or until progression. The primary endpoint was safety. Secondary endpoints were efficacy and pharmacokinetics. Exploratory endpoints included pharmacodynamics.

Results Fifty-eight patients were treated. Median age was 62.5 years and 81% were male. Most had kidney cancer (n = 36) or melanoma (n = 9). There were no dose-limiting toxicities. Treatment-related adverse events occurred in 83% and were grade ≥ 3 in 21%. Objective clinical responses occurred in 8/58 patients (14%): 5 with kidney cancer, including 1 with a complete response, and 3 with melanoma. The relationship between dose and serum levels was predictable and linear, with apparent receptor saturation at 10 mg/kg Q2W and all 20 mg/kg cohorts.

Conclusions MEDI0680 induced peripheral T-cell proliferation and increased plasma IFNγ and associated chemokines regardless of clinical response. CD8+ T-cell tumor infiltration and tumoral gene expression of IFNG, CD8A, CXCL9, and granzyme K (GZMK) were also increased following MEDI0680 administration.

Trial registration NCT02013804; date of registration December 12, 2013.

  • MEDI0680
  • PD-1
  • Immunotherapy
  • Kidney cancer
  • Melanoma

Aung Naing and Jeffrey Infante contributed equally to this work.

  • Abbreviations:
    Ab
    Antibody
    ADA
    Anti-drug antibody
    AE
    Adverse event
    ALT
    Alanine aminotransferase
    ANOVA
    Analysis of variance
    AUC
    Area under the curve
    BOR
    Best overall response
    CDR
    Complementarity-determining region
    CHO
    Chinese hamster ovary
    CR
    Complete response
    DC
    Disease control
    DCR
    Disease control rate
    DCR24
    Disease control rate ≥ 24 weeks
    DLT
    Dose-limiting toxicity
    DOR
    Duration of response
    E:T
    Effector-to-target
    EBV
    Epstein–Barr virus
    EC50
    Drug concentration giving half-maximal response
    ECACC
    European Collection of Authenticated Cell Cultures
    ECL
    Electrochemiluminescence
    ECOG
    Eastern Cooperative Oncology Group
    EDTA
    Ethylenediaminetetraacetic acid
    ELISA
    Enzyme-linked immunosorbent assay
    Fab
    Fragment antigen-binding
    FC
    Fold change
    Fc
    Fragment crystallizable
    FFPE
    Formaldehyde fixed paraffin-embedded
    FOV
    Fields of view
    FTIH
    First-time-in-human
    GM-CSF
    Granulocyte-macrophage colony-stimulating factor
    HLA
    Human leukocyte antigen
    IC50
    Inhibitor concentration where the response (or binding) is reduced by half
    IFNγ
    Interferon gamma
    IgG
    Immunoglobulin G
    IHC
    Immunohistochemistry
    IL-4
    Interleukin-4
    IP-10
    Interferon gamma-induced protein-10
    I-TAC
    Interferon-inducible T-cell alpha chemoattractant
    KD
    Dissociation rate constant
    mAbs
    Monoclonal antibodies
    MdFI
    Median fluorescence intensity
    MFI
    Mean fluorescence intensity
    MTD
    Maximum tolerated dose
    NK
    Natural killer
    NSCLC
    Non-small cell lung cancer
    OR
    Objective response
    ORR
    Objective response rate
    OS
    Overall survival
    PBMC
    Peripheral blood mononuclear cell
    PCR
    Polymerase chain reaction
    PD-1
    Programmed cell death-1
    PD-L1
    Programmed cell death ligand-1
    PD-L2
    Programmed cell death ligand-2
    PE
    Phycoerythrin
    PFS
    Progression-free survival
    PR
    Partial response
    Q2W
    Every 2 weeks
    Q3W
    Every 3 weeks
    QW
    Every week
    RCC
    Renal cell carcinoma
    RECIST
    Response Evaluation Criteria in Solid Tumors
    SAE
    Serious adverse event
    SD
    Stable disease
    SPR
    Surface plasmon resonance
    TEM
    T effector memory cells
    TIL
    Tumor infiltrating lymphocyte
    ΔΔCt
    Delta-delta cycle thresholds
  • Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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    Aung Naing and Jeffrey Infante contributed equally to this work.

    Introduction

    MEDI0680, previously named AMP-514, is a humanized IgG4κ anti-programmed cell death-1 (PD-1) monoclonal antibody developed to block the immune suppressive PD-1 pathway. The binding of tumoral programmed cell death ligand-1 and -2 (PD-L1 and PD-L2) to the PD-1 receptor on T cells suppresses their ability to launch an antigen-specific antitumor immune response [13]. PD-1 expression increases on T cells when they are activated, and increased PD-1 expression on circulating T cells has been associated with poor clinical outcome [4]. Blockade of this ligand binding permits continued activation of T cells and has been associated with clinical efficacy in cancer patients [5, 6].

    In recent years, antagonistic monoclonal antibodies (mAbs) targeting PD-1 and PD-L1 have demonstrated the ability to restore T-cell effector function and reduce tumor progression [4, 5]. PD-1 targeted immunotherapies nivolumab, pembrolizumab, and cemiplimab have been approved in multiple solid tumor indications [79]. Among these, melanoma and kidney cancer, specifically renal cell carcinoma (RCC), are considered two of the most immunogenic types of cancer. The efficacy of PD-1-directed therapies in melanoma may be linked to the high mutational burden associated with this cancer type [10, 11]. Although kidney cancer has a lower mutational burden than melanoma [11], nivolumab has shown encouraging results in clinical trials and has been approved in the US for RCC [8].

    Despite encouraging clinical activity, many patients do not respond to anti-PD-1 mAb therapy or relapse after an initial response, including some patients with evidence of pretreatment PD-L1 expression, immune-cell infiltration, or intermediate-to-high tumor mutational burden [12]. Combinations of anti-PD-1 agents with other immunotherapy agents may offer an opportunity to overcome some of these barriers to response to anti-PD-1 monotherapy. Several combinations are being investigated in ongoing clinical trials, including nivolumab with BMS-986253 (an anti-interleukin-8 mAb; NCT03400332), ALT-803 (an interleukin-15 superagonist complex; NCT02523469), and interferon-gamma (IFNγ) (NCT02614456) [1315] and pembrolizumab with p53MVA, an antitumor vaccine (NCT03113487, NCT02432963) [16]. Another possible combination is with an anti-PD-L1 mAb. Currently, two clinical trials combining anti-PD-1 with anti-PD-L1 agents are ongoing, including one with MEDI0680 (NCT02936102 and NCT02118337) [17, 18]. The biological rationale for this combination approach is simultaneous blockade of PD-1/PD-L1/PD-L2 and PD-1/PD-L1/CD80 interactions [1921]. The purpose of the current study is to characterize the initial safety and clinical efficacy of this anti-PD-1 mAb, and to confirm its intended pharmacodynamic activity.

    Nivolumab and pembrolizumab have shown different safety and efficacy profiles in varying tumor types, despite sharing the same mechanism of action [2227]. Antagonistic antibodies targeting the same protein may have the same mechanism of action, but differences in immunogenicity, binding affinity, plasma half-life, and tissue penetration could affect clinical efficacy, safety, and pharmacokinetics [2830]. Anti-PD-1 mAbs vary due to the degree of antibody humanization and sequence differences in their complementarity-determining regions (CDRs), which determine the precise epitopes bound on the target [28]. MEDI0680 differs from nivolumab and pembrolizumab in its CDR sequence and affinity, which may impact its safety or clinical activity.

    Here we present the clinical results of the dose-escalation phase of the first-time-in-human (FTIH) phase I study of MEDI0680, including safety, tolerability, and efficacy in patients with solid tumors (NCT02013804). We also describe the preclinical characterization of MEDI0680, as well as its pharmacokinetic and pharmacodynamic profiles in patients.

    Materials and methods

    Patients and study design

    In this open-label, multicenter, dose-escalation and expansion study in checkpoint inhibitor-naïve patients with advanced solid malignancies, MEDI0680 was administered intravenously every 2 weeks (Q2W) or every 3 weeks (Q3W) at doses of 0.1, 0.5, 2.5, 10 or 20 mg/kg as indicated in Table 1. Two cohorts received 20 mg/kg every week (QW) for 2 or 4 weeks followed by 20 mg/kg Q2W. Patients were enrolled using a 3 + 3 study design. One cycle of treatment was defined as 21 days for patients on the Q3W schedule and as 28 days for patients on the Q2W schedule. Key eligibility criteria for the study are shown in Additional file 1: Table S1.

    Baseline patient characteristics

    The study design is shown in Additional file 1: Figure S1a, including dose levels and administration frequency for each dose cohort. Eligible patients had advanced solid malignancies that were refractory to standard therapy or for which no standard therapy existed. They were enrolled if they had ≥1 measurable lesion according to Response Evaluation Criteria in Solid Tumors (RECIST v1.1), had not received previous anti-PD-1/PD-L1 antibodies (expanded in a protocol amendment in May 2014 to exclude any immunotherapy except therapeutic cancer vaccines), had sufficient organ function, and had an Eastern Cooperative Oncology Group (ECOG) performance score of 0 or 1.

    Based on accumulating evidence of response to PD-1 inhibition in kidney cancer and melanoma [3135], the study protocol was amended to enroll only patients with these tumor types in cohorts 5–9. Therefore, the majority of patients had kidney cancer (62%) or melanoma (16%).

    Patients received MEDI0680 for 12 months or until progressive disease; those maintaining disease control were followed for an additional 12 months. All patients were followed long-term for survival. Retreatment was permitted in cases of progression during the 12-month follow-up period.

    Endpoints and assessments

    Primary

    The primary endpoint was safety, assessed by evaluating dose-limiting toxicities (DLTs), adverse events (AEs), serious adverse events (SAEs), laboratory evaluations, vital signs, physical examinations, and electrocardiograms. The National Cancer Institute Common Terminology Criteria for Adverse Events Version 4.03 was used to classify and grade AEs and SAEs. Laboratory abnormalities were monitored from the start of the study until 12 months after the last dose of study drug, or until the patient withdrew from follow-up.

    Adverse events of special interest (AESIs) included AEs of hepatic function abnormality meeting the definition of Hy’s law, Grade ≥ 3 endocrinopathies, Grade ≥ 3 dermatologic AEs, Grade ≥ 3 pneumonitis, and other Grade ≥ 3 immune-related AEs.

    Secondary endpoints

    The secondary endpoints of this study are shown in Additional file 1: Figure S1b and included assessment of the pharmacokinetics and immunogenicity of MEDI0680, as well as its efficacy.

    MEDI0680 concentrations in patient serum

    The serum concentration of MEDI0680 was determined using a validated electrochemiluminescence (ECL) ligand binding assay format. Standards, controls, and test samples were incubated with biotinylated anti-MEDI0680 bound to a streptavidin-coated plate. Following incubation, ruthenylated anti-IgG4 was added to the plate to allow the formation of molecular complexes. Unbound material was removed by washing the plate, adding MSD read buffer, and detecting bound complexes by ECL using a SECTOR 6000 MSD imager (MesoScale Discovery). Data were analyzed by linear regression using Watson LIMS™ software (Thermo Fisher Scientific) and the concentrations of MEDI0680 in serum were interpolated from a standard curve. The assay lower limit of quantitation was determined to be 0.5 μg/mL and the upper limit of quantitation was 100 μg/mL.

    Anti-drug antibody responses

    Anti-drug antibodies (ADAs) in serum samples were assessed using validated bridging format ECL assays. For all assays, the samples were diluted 1:10 in assay diluent and then incubated with biotinylated and ruthenylated MEDI0680 to allow the formation of molecular complexes. The negative control was a human serum pool, and positive control samples were prepared by spiking the negative control serum pool with ADA. The complexed samples were loaded into wells of a blocked, streptavidin-coated MSD plate, washed, and the bound complexes detected by ECL using a SECTOR 6000 MSD imager (MesoScale Discovery). The data were processed using Watson LIMS™ software (Thermo Fisher Scientific) and the presence of ADAs was determined based on an assay-specific cut-point. Samples that screened as ADA-positive were further assessed using confirmatory and titer assays.

    Efficacy

    The clinical efficacy and antitumor activity secondary endpoints included objective response (OR) and disease control (DC) based on RECIST v1.1 guidelines, modified to require confirmation of progressive disease by a repeat, consecutive assessment no less than 4 weeks from the date of first documentation. The rationale for this modification was to discourage premature discontinuation of the investigational agent and provide a more complete evaluation of its antitumor activity than would be seen with conventional RECIST criteria. Additional secondary endpoints assessed were duration of response (DOR), progression-free survival (PFS), and overall survival (OS).

    Exploratory endpoints

    Exploratory endpoints including PD-1 receptor occupancy and the pharmacodynamic profile of MEDI0680 were evaluated to assess the biological activity of the drug in both peripheral blood and tumor biopsy samples (Additional file 1: Figure S1b and Table S2).

    PD-1 receptor occupancy

    Occupancy of the PD-1 receptor by MEDI0680 was determined using a whole blood drug saturation assay. Briefly, potassium EDTA anti-coagulated whole blood samples from study patients were washed and then incubated with formalin buffer or with a saturating dose of MEDI0680 (30 μg/mL) at ambient temperature for 30 min. Bound MEDI0680 was detected using a biotin-labeled anti-human IgG4 antibody followed by Phycoerythrin (PE)-conjugated streptavidin, after washes in between binding steps. Fluorochrome labeled anti-human CD3 and CD45RO antibodies were used to determine PD-1 receptor occupancy on antigen-experienced (CD45RO+) CD3+ T cells. Receptor occupancy was defined as the percentage of CD3+ CD45RO+ cells bound to MEDI0680 after incubation with formulation buffer divided by the percentage of MEDI0680 bound CD3+ CD45RO+ cells after MEDI0680 saturation.

    T-cell activation and proliferation markers

    Peripheral blood mononuclear cell (PBMC) samples were cryopreserved and subsequently evaluated in batches by flow cytometry (BD LSR Fortessa; BD Biosciences). Monoclonal antibodies and viability dye used for flow cytometry panels included: Anti-CD3 BV605, clone SK7 (BD Biosciences); Anti-CD4 PerCP-eFlour710, clone SK3 (eBioscience); Anti-CD8 FITC, clone SK1 (Biolegend); Anti-CCR7 APC, clone G043H7 (Biolegend); Anti-CD45RA PE-Cy7, clone HIT100 (Biolegend); Anti-CD38 BV421, clone HIT2 (Biolegend); Anti-human leukocyte antigen (HLA)-DR PE antibody, clone L243 (Biolegend); Anti-Ki67 BV421, clone B56 (BD Biosciences); Mouse IgG1 BV421, clone X40 (BD Biosciences); Mouse IgG1 PE, clone MOPC21 (Biolegend); Zombie Near-IR Fixable dye (Biolegend). Surface marker staining was followed by intracellular marker staining after fixation and permeabilization. CD4+ and CD8+ T cells were identified after gating on live (Zombie fixable dye negative) CD3+ cells, and CD4 effector memory (TEM) cells were defined as CD3 and CD4 double positive cells that were CCR7– and CD45RA–. Levels of the activation markers CD38 and HLA-DR, as well as the intracellular proliferation marker Ki67, were determined on CD4+ and CD8+ T-cell subsets using FlowJo® Software (FlowJo LLC) by setting gates based on a mouse IgG1 isotype control panel.

    Circulating cytokines

    Plasma samples were assessed for levels of the cytokine IFNγ and the chemokines CXCL9 (monokine induced by IFNγ, MIG), CXCL10 (IFNγ-induced protein-10, IP-10), and CXCL11 (interferon-inducible T-cell alpha chemoattractant, I-TAC) using a custom human MULTI-SPOT cytokine 4-plex assay kit and an SI6000 MSD reader (MesoScale Discovery). Sample signals were compared to calibration curves to determine the concentration of each analyte in plasma samples.

    PD-L1 and CD8 immunohistochemistry

    Tumor biopsies were collected prior to treatment and during treatment (cycle 2 between day 1 and day 15); in addition, archival biopsies were assessed when available. The PD-L1 status of tumor samples was determined from 22 evaluable pretreatment fresh (n = 21) or archival (n = 1) tumor biopsies formaldehyde fixed paraffin-embedded (FFPE) using the VENTANA PD-L1 (SP263) immunohistochemistry (IHC) assay [7]. Samples were classified as having PD-L1 membrane staining of any intensity in ≥ 25% of tumor cells or < 25% of tumor cells [36]. Immunohistochemical staining for CD8 was performed on 14 evaluable fresh paired pre- and on-treatment tumor biopsies (cycle 2 between day 1 and day 15) using rabbit anti-human CD8 monoclonal antibody clone SP239 (Spring Bioscience). Images of immunostained slides were captured using an Aperio digital pathology slide scanner (Leica Biosystems) and examined at 20× magnification. The numbers of CD8+ lymphocytes per entire tissue field containing tumor were counted manually, with a minimum of 3 and a maximum number of 10 fields of view (FOV) counted per case. Areas of necrosis or tissue artifact were excluded. A 20× Aperio image FOV represents 0.4 mm2; therefore, mean CD8+ tumor infiltrated lymphocyte (TILs) per mm2 were calculated by multiplying the mean number of CD8+ T cells/FOV by 2.5. Non-evaluable specimens were defined as biopsies that did not contain at least 100 tumor cells or specimens that did not maintain adherence to slides during the IHC process.

    Tumor gene expression

    Total RNA was isolated from 11 available and evaluable fresh frozen tumor biopsy samples collected pre- and on-treatment (cycle 2 between day 1 and day 15 in the Q2W or Q3W dosing schedule). The level of RNA transcripts for 171 immune-related genes was measured by TaqMan real-time polymerase chain reaction (Thermo Fisher Scientific) using Fluidigm BioMark 96.96 Dynamic Array chips (Fluidigm Corp). Delta-delta cycle thresholds (ΔΔCt) were calculated for each pre- and on-treatment sample pair and shown as Log2 fold change.

    Statistical analyses

    Maximum tolerated dose (MTD) evaluation was based on the DLT-evaluable population, defined as patients who received the protocol-assigned treatment and completed the DLT evaluation period (≥ 21 days for the Q3W schedule and ≥ 28 days for the other dosing schedules) or experienced a DLT during this period. Non-evaluable patients in the dose-escalation phase could be replaced. Tolerability and clinical activity evaluations were based on the as-treated population (all patients receiving any dose of study drug).

    For clinical activity, OR was defined as confirmed complete response (CR) or partial response (PR), and DC was defined as CR, PR, or stable disease (SD) for ≥ 24 weeks (DCR24). The objective response rate (ORR) and disease control rate (DCR) were calculated as a percentage of the as-treated population.

    Results

    Preclinical characterization of MEDI0680

    MEDI0680 is a humanized mAb of the IgG4 isotype containing a serine-to-proline amino acid replacement in the immunoglobulin fragment crystallizable (Fc) hinge region to stabilize the immunoglobulin and prevent inter-strand fragment antigen-binding (Fab) arm exchange [37]. The mAb bound to PD-1 on activated human T cells with a mean apparent half-maximal (EC50) binding value (reflecting bivalent binding) of 822 ± 220 pM (Additional file 1: Figure S2a). The dissociation rate constant (KD) for binding of the antibody to recombinant human PD-1 (monovalent binding) was measured as 29 nM by surface plasmon resonance (Biacore). This binding was highly specific for PD-1 as MEDI0680 bound poorly to closely related family members (Additional file 1: Figure S2b and Table S3). The antibody blocked the binding of recombinant human PD-L1 and PD-L2 to human PD-1 expressing Chinese hamster ovary (CHO) cells, with half-maximal inhibitory concentration (IC50) values of 2.6 nM and 3.6 nM for PD-L1 and PD-L2, respectively (Additional file 1: Figure S3). Consistent with its PD-1:PD-L1 ligand blocking activity, MEDI0680 enhanced in-vitro IFNγ production in allogeneic dendritic cell / T cell mixed lymphocyte reactions (Additional file 1: Figure S4a) and killing of Epstein–Barr virus (EBV)-expressing esophageal squamous cell carcinoma tumor cells by EBV-reactive primary human T cells (Additional file 1: Figure S4b). The activity of MEDI0680 in these preclinical assays supported testing of the drug in this FTIH phase I clinical trial.

    Patient characteristics

    From December 2013 to August 2015, a total of 58 eligible patients with solid tumors were enrolled and treated. Data were collected through November 7, 2017. Patient baseline characteristics are summarized in Table 1 and patient disposition is shown in Additional file 1: Table S4.

    Five of the 9 patients with melanoma had tumors bearing known mutations (4 with BRAF mutations and 1 with EGFR mutation).

    Safety

    An MTD was not reached, thus the highest protocol-defined dose was 20 mg/kg Q2W. Treatment-related AEs occurred in 48 patients (83%) across all cohorts (Table 2). The most commonly reported (> 10%) treatment-related AEs of any grade in the study were fatigue (21%), nausea (16%), decreased appetite (16%), vomiting (14%), anemia (12%), pyrexia (12%), arthralgia (12%), pruritus (10%), and asthenia (10%) (Table 3). Grade 1 or 2 treatment-related AEs occurred in 36/58 (62%) patients. Grade 3 or 4 treatment-related AEs occurred in 12/58 (21%) patients; the most common were anemia (4 patients [7%]); fatigue and aspartate aminotransferase increase (each in 2 patients [3%]); and abdominal pain, alanine aminotransferase (ALT) increase, arthralgia, asthenia, autoimmune hepatitis, blood alkaline phosphatase increase, blood creatine phosphokinase increase, dehydration, diarrhea, hypercalcemia, hyperkalemia, hypertension, lipase increase, myasthenia gravis, myositis, and urinary tract infection (each in 1 patient [2%]). Four patients (7%) discontinued due to treatment-related AEs: 1 due to grade 2 pyrexia; 1 due to grade 3 elevated ALT; 1 due to grade 1 creatinine increase, grade 1 potassium increase, grade 3 fatigue, and grade 2 myalgia; and 1 due to grade 2 asthenia. No treatment-related deaths were observed.

    Safety summary in the as-treated population

    Any-grade treatment-related AEs occurring in ≥10% of total population and all grade ≥ 3 treatment-related AEs

    AEs of special interest

    Grade 3 treatment-related AESIs occurred in 4/58 patients (7%): ALT and AST increases and autoimmune hepatitis (n = 1, discontinued treatment as described above); lipase increase (n = 1, resolved); AST increase and myasthenia gravis (n = 1, both resolved); and diarrhea (n = 1, resolved; no report of colitis). There were no Grade 4 or 5 treatment-related AESIs. Pneumonitis was not observed.

    Clinical activity

    The best objective responses at each dose level are shown in Table 4. In total, 8/58 patients in the as-treated population (14%) had a confirmed OR: 3 had melanoma (2 with BRAF mutations) and 5 had kidney cancer, including 1 who had a CR. The DCR24 was 17/58 (29%). Tumor size change from baseline (spider plot) is shown in Fig. 1a. The timing and duration of response and onset of progressive disease or new lesions in the responding population (swimmer’s plot) is shown in Fig. 1b. The DOR ranged from 9.1 to 110.7 weeks. Three of the 8 responders discontinued study treatment without completing the protocol-defined 12 months of treatment; all had kidney cancer. Of these, 1 with CR and 1 with PR discontinued treatment due to progressive disease, and 1 with PR discontinued due to new brain metastases.

    Best overall response in the as-treated population

    Fig. 1

    Response to MEDI0680 therapy. a Tumor size change from baseline in the as-treated population. b The timing and duration of response and onset of progressive disease or new lesions in the responding population. Blue bars indicate treatment initiation to censoring date or progression date. One patient with kidney cancer and PR had an ongoing response but did not have a disease assessment at the time of the last dose

    All 8 responders were in the 10 mg/kg or 20 mg/kg dose cohorts, where peripheral PD-1 receptor occupancy and blood drug concentrations reached a plateau (see pharmacokinetic and receptor occupancy results below). In these pooled 10 and 20 mg/kg cohorts, the ORR was 8/45 (18%); all responses were observed in the Q2W and Q3W groups. The DCR24 was 17/45 (37%) in this subset.

    Two patients entered retreatment after the initial 12-month period (1 receiving 10 mg/kg Q3W and the other receiving 20 mg/kg Q2W), but discontinued due to progressive disease.

    MEDI0680 pharmacokinetic and pharmacodynamic profiles

    Pharmacokinetics, ADA responses, and PD-1 receptor occupancy

    A dose-proportional increase in peak serum MEDI0680 concentration was observed (Fig. 2a). The mean terminal half-life was estimated to be 19 days, with a standard deviation of 5.6 days at 20 mg/kg Q2W dosing based on simulations in a MEDI0680 population pharmacokinetics model (n = 1000) [38]. Fifty-four patients were evaluated for the development of post-baseline ADAs and 8 (15%) tested positive post-dose. Based on samples from 40 patients, a dose-dependent saturation of PD-1 was observed on CD3+ T cells, with median PD-1 receptor occupancy ≥70% after 1 cycle of MEDI0680 treatment at 10 or 20 mg/kg; the highest, most consistent occupancy was obtained with initial weekly dosing at 20 mg/kg (Fig. 2b).

    Fig. 2

    Pharmacokinetic and receptor occupancy analysis of MEDI0680. a Pharmacokinetic analysis of MEDI0680 in patient serum. Data represent time points up to 150 days. Abbreviation: LLOQ lower limit of quantitation. b PD-1 receptor occupancy by MEDI0680 on CD45 RO+ CD3 T cells among patients treated at various drug doses and schedules, as indicated. Measurements were done at baseline, during the first cycle of MEDI0680 treatment, and on the first day after the completion of the first cycle

    T-cell activation and proliferation, and cytokine levels in peripheral blood

    Among total CD4+ and CD8+ T cells from patients receiving < 10 mg/kg, 10 mg/kg or 20 mg/kg, at least a 2-fold median increase in the percentage of Ki67+ T cells and activated CD38high/HLA-DRhigh CD4+ TEM cells was observed on day 8 post-treatment during the first cycle (Fig. 3a and Additional file 1: Figure S5). Consistent with MEDI0680-dependent peripheral T-cell activation, plasma levels of IFNγ and CXCL9 (MIG), CXCL10 (IP-10), and CXCL11 (I-TAC) were increased on-treatment with a median 1.5-fold change among patients receiving 10 or 20 mg/kg MEDI0680, with the exception of CXCL11 in patients dosed within the 10 mg/kg cohorts, where no on-treatment median change was observed (Fig. 3b). There was no correlation between increased peripheral biomarkers and clinical response at any MEDI0680 dose level (Additional file 1: Figure S6).

    Fig. 3

    Peripheral and intratumoral measures of MEDI0680 activity. a Peripheral CD4+ and CD8+ T-cell activation and proliferation among treatment groups, as indicated. Shown are the fold changes in the percentages of CD4+ and CD8+ Ki67+ and CD4+ TEM CD38high/HLA-DRhigh cells in whole blood post-treatment. Abbreviation: T EM effector memory T cells. b Change in plasma cytokines among treatment groups, as indicated. Shown are the fold change in the plasma levels of IFNγ, CXCL-9, CXCL-10, and CXCL-11 at day 8 post-treatment with MEDI0680. c Examples of PD-L1+ and CD8+ IHC images (20× magnification) from matched pre- and on-treatment biopsies from an RCC patient. The tumor at screening is characterized by abundant CD8+ TILs and PD-L1 on immune cells but not on tumor cells (* symbols on IHC images). The on-treatment tumor has greater CD8+ T-cell infiltration and PD-L1 immunoreactivity on both immune and tumor cells (*). d Levels of CD8+ TILs in tumor biopsies pre- and on-treatment at various dose levels. Abbreviation: hpf high power field. (e) Log2 fold change in on-treatment versus pretreatment CD8A, IFNG, CXCL9, and GZMK gene expression in RCC and melanoma tumor biopsies. A 1.5-fold change is indicated by the dotted line

    PD-L1 expression and T-cell density and activation in tumor biopsies

    Among 22 evaluable pretreatment tumor biopsies, 2/22 (9.1%) were scored PD-L1 ≥ 25% and 20/22 (91%) were PD-L1 < 25%. None of the responders had evaluable tissue for PD-L1 staining. The PD-L1 ≥ 25% biopsies were from a non-squamous non-small cell lung cancer (NSCLC) patient and a melanoma patient; the former was not evaluable for clinical response and the latter had progressive disease as the best OR. Of the 20 patients with PD-L1 < 25%, 2 were not evaluable for clinical response, 10 had SD, and 8 had progressive disease. CD8+ T-cell density and gene expression were evaluated from 14 paired pre- and on-treatment fresh tumor biopsies to determine MEDI0680 activity. During treatment, 8/14 (57%) samples across all dose cohorts showed a 2-fold or greater increase in intratumoral CD8+ T-cell density as measured by IHC (Fig. 3c and d). This was consistent with an increase in CD8A gene expression and genes associated with T-cell effector function (Fig. 3e). On-treatment, 2-fold or greater increases in gene expression of IFNG, CXCL9 (a T-cell chemoattractant), and GZMK (a marker of cytolytic T-cell activity) were also observed (Fig. 3e). Although association with clinical response could not be determined due to a small sample size of evaluable tumor biopsies, MEDI0680 treatment did elicit T-cell infiltration and/or expansion and showed pharmacodynamic evidence of immune-related antitumor activity.

    Discussion

    In this FTIH phase I study, MEDI0680 had a tolerable safety profile and demonstrated clinical activity. No treatment-related deaths were observed and the majority of treatment-related AEs were mild to moderate (62% grade 1/2 and 21% grade 3/4). Four patients (7%) discontinued MEDI0680 due to treatment-related AEs. An MTD was not reached.

    PD-1 receptor occupancy appeared to reach a peak in the 10 mg/kg Q2W and 20 mg/kg Q3W cohorts. Additional patients were recruited at the 20 mg/kg Q2W dose level, including a cohort with weekly dosing for 2 weeks followed by Q2W dosing (20 mg/kg QWx2) and one with weekly dosing for 4 weeks followed by Q2W dosing (20 mg/kg QWx4) to increase confidence that receptor saturation had peaked. No significant differences in receptor occupancy between these groups at cycle 2, day 1 were observed, although median values were numerically higher for the 20 mg/kg cohorts compared to the 10 mg/kg Q2W group. Likewise, pharmacokinetic profiling showed similar trough serum drug levels between the 10 and 20 mg/kg doses, but with numerically higher values for the latter. Considering peripheral PD-1 receptor occupancy and drug levels together with peripheral pharmacodynamic data showing comparable drug activity and similar tolerability profiles at the 10 mg/kg and 20 mg/kg dose levels, 20 mg/kg Q2W was declared the highest protocol-defined dose. Because circulating drug must penetrate tumors against interstitial fluid pressure gradients and despite endocytic consumption within tumors [39], the 20 mg/kg Q2W dose is expected to provide the optimal PD-1 receptor occupancy within tumor tissues themselves.

    The safety profile observed in this study was consistent with that of other drugs targeting the PD-1 pathway in patients with solid tumors [4043]. For example, in a phase I study of 30 patients (with various advanced solid tumors) treated with pembrolizumab 1–10 mg/kg Q2W or 2–10 mg/kg Q3W, 70% of patients had treatment-related AEs (all grade 1 or 2) [27]. In another phase I study of advanced malignancies that included 107 patients with advanced melanoma, Topalian and colleagues showed an 84% incidence of treatment-related AEs with nivolumab 0.1–10 mg/kg Q2W; the events were grade 3/4 in 22% of patients [31]. In the current study, grade 3 treatment-related AESIs occurred in 7% of patients; no grade 4 or 5 AESIs were observed. There were no reports of pneumonitis.

    In the current study, confirmed objective clinical responses were seen in 8/58 (14%) patients. All responses were in patients with melanoma or kidney cancer, including a single confirmed CR. A response rate of 8/45 (18%) was seen in patients receiving 10–20 mg/kg. Because the trial comprised 11 tumor types and 9 doses, it is not possible to directly compare the response rates seen with MEDI0680 to those of other PD-1 antibodies. However, the 34 patients with kidney cancer and 8 patients with melanoma treated at the 10–20 mg/kg dose levels indicate the response may be similar to other PD-1 antibodies approved for those indications. A 15% (5/34) response rate was seen in kidney cancer patients receiving 10–20 mg/kg doses. Among patients with advanced/metastatic RCC, nivolumab showed response rates of 27% in a phase I study, 9–22% in a phase Ib study, and 20–22% in a phase II study [4345]. Pembrolizumab demonstrated an ORR of 34% in a phase II study as first-line treatment in advanced clear cell RCC [27]; this may be numerically higher than response rates seen for nivolumab as well as MEDI0680 in the current study due to the enrollment of patients that had not received prior systemic therapy. In melanoma patients receiving 10–20 mg/kg in this study, MEDI0680 demonstrated a 38% (3/8) response rate. Pembrolizumab showed response rates of 26% and 38% in advanced melanoma in two phase I studies of 173 and 135 patients, respectively [24, 32]. Response rates with nivolumab in advanced melanoma were 28% in the study of solid tumors described above, and 40% in a large phase III randomized trial [31, 33].

    As secondary and exploratory endpoints, the pharmacokinetic and pharmacodynamic profiles of MEDI0680 were explored and examined for association with clinical response. Doses of 10–20 mg/kg showed a maximum PD-1 receptor occupancy ≥70%, comparable to the peak occupancy reported for nivolumab [46]. PD-1 targeting by MEDI0680 showed consistent immunological modulation across dose levels, with a frequent increase of activated CD4+ TEM cells (CD38high/HLA-DRhigh) and enhanced proliferation (Ki67 positivity) of CD4+ and CD8+ T cells. This is consistent with the induction of peripheral T-cell activation and proliferation markers monitored in other anti-PD-1 clinical trials [46, 47]. In plasma, MEDI0680 increased circulating IFNγ and IFNγ-induced cytokines (CXCL9, 10, and 11) as previously reported [48]. Similar to these findings, Das et al. examined gene transcription changes in isolated peripheral blood T cells from melanoma patients treated with nivolumab and found changes indicative of natural killer (NK) cell expansion and cytolytic function that included upregulation of the IFNG transcript [49]. They also found increased serum levels of the IFNγ-inducible cytokine CXCL10; in their study, CXCL9 and CXCL11 were not examined. However, they found neither increased plasma IFNγ cytokine levels nor upregulation of Ki67 transcript or protein in nivolumab-treated patients, as was found in the current study with MEDI0680. This discrepancy could be the result of differences in the time of assessment and/or sensitivity of plasma cytokine assays used. Peripheral biomarker modulation by MEDI0680 was observed in all patients regardless of clinical response, although some had only minimal changes. A lack of correlation between peripheral immune response to PD-1 inhibitors and clinical response has been reported in melanoma patients treated with pembrolizumab [46], although results in NSCLC patients treated with anti-PD-1 therapies suggest that an early versus late induction of immune activation in a specific subpopulation of CD8+ T cells (Ki67+ PD-1+) may enrich for response [47].

    In evaluable tumor biopsies, MEDI0680 showed intratumoral pharmacodynamic activity as evidenced by the induction of CD8+ T-cell infiltration and/or expansion and increases of IFNG and IFNγ-inducible gene expression consistent with the mechanisms of action of anti-PD-1 blocking agents. Increased CD8+ T-cell infiltration/proliferation, PD-1, PD-L1, granzyme B, and phosphorylated STAT1 positive immune cells in melanoma tumors have been observed by IHC or gene expression after treatment with pembrolizumab or nivolumab in other trials [50, 51]. In these studies, pretreatment or on-treatment levels of T cells within the tumor or at the tumor margin demonstrated predictive value for response to anti-PD-1 therapy [50, 51]. Other trials with PD-1 inhibitors have also identified pretreatment and post-treatment immune cell correlates with response to therapy [5262]. For example, Daud et al. showed that patients whose melanoma tumors contained ≥ 20% CD8+ T cells with a CTLA-4 high/PD-1 high phenotype demonstrated a significantly higher ORR to anti-PD-1 blockade compared to those whose tumors contained < 20% of these cells [56]. Inoue et al. described higher pretreatment CD8+/Treg and CD8+/CD4+ expression ratios and higher lytic enzyme (GZMA) and major histocompatibility complex class I (HLA-A) expression correlating with anti-PD-1 mAb response in melanoma [57]. Likewise, others have demonstrated that pretreatment IFNγ-related immune gene signatures predicted response to anti-PD-1 therapy in head and neck squamous cell carcinoma, gastric cancer, and melanoma [48, 49, 51]. Collectively, these findings suggest that upregulation of CD8+ T cells and markers of effector T-cell function are common pharmacodynamic biomarkers of anti-PD-1 blockade, and pre- or post-treatment intratumoral levels in some settings are associated with clinical response.

    In conclusion, this study demonstrated that MEDI0680 is a clinically active anti-PD-1 antibody with a tolerable safety profile. Maximum receptor occupancy was achieved at doses where most patients showed evidence of peripheral and intratumoral immune-cell activation. MEDI0680 is currently undergoing clinical testing in combination with the anti-PD-L1 mAb durvalumab versus nivolumab monotherapy in patients with kidney cancer (NCT02118337).

    Funding

    This study (NCT02013804) was funded by AstraZeneca and Amplimmune (Gaithersburg, MD, USA), the manufacturers of MEDI0680. Medical editing support, which was in accordance with Good Publication Practice (GPP3) guidelines, was provided by Susanne Gilbert, MA, of Cirrus Communications (New York, NY, USA) and was funded by AstraZeneca.

    Acknowledgments

    The authors would like to thank the patients, their families, and the investigational site staff for their participation in the study; Michael Overstreet and Jessica Filderman of Amplimmune for their work on the peripheral flow cytometry data and Catherine Auge of AstraZeneca for her work on the binding specificity and cytokine data; and Tom O’Neill, Karla Maloveste, and Charmin King of Amplimmune and Serguei Soukharev, Philip Brohawn, Steven Eck, Song Ren, and Christine Kiefer of AstraZeneca for their contributions to the study and drug development program.

    Authors’ contributions

    AN, JI, SG, HB, SB, PL, AW, JE, BC: Acquisition of data; analysis and interpretation of data; review and revision of the manuscript. CB, IA, SB, RM, CM, KP, XS, KS, FW, NE: Analysis and interpretation of data; writing, review and/or revision of the manuscript. SM, SB, JK, MO: Conception and design; development of methodology; acquisition of data; analysis and interpretation of data; writing, review and/or revision of the manuscript. All authors read and approved the final manuscript.

    Availability of data and materials

    The clinical dataset analyzed during the current study is available at clinicaltrials.gov, https://clinicaltrials.gov/ct2/show/results/NCT02013804. Other datasets used and/or analyzed during the current study are available and may be obtained in accordance with AstraZeneca’s data sharing policy, which is described at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

    Notes

    Ethics approval and consent to participate

    The study was performed in accordance with ethical principles that have their origin in the Declaration of Helsinki and are consistent with the International Conference on Harmonisation/Good Clinical Practice and applicable regulatory requirements. The protocol was approved by Institutional Review Boards (IRBs)/Independent Ethics Committees (IECs) at each center. Patients provided written informed consent to participate.

    Consent for publication

    Not applicable.

    Competing interests

    Aung Naing: Research grants from NCI, EMD Serono, AstraZeneca, Healios Onc., Nutrition, Atterocor, Amplimmune, Karyopharm Therapeutics, Incyte, Regeneron, Merck, BMS, Pfizer, Neon Therapeutics, Calithera BioSciences, and TopAlliance BioSciences; grants and advisory board membership with ARMO BioSciences, Novartis, and CytomX Therapeutics; grants from Immune Deficiency Foundation (spouse).

    Jeffrey Infante: Consultant for Armo Biosciences and Biomed Valley; employee of Janssen Oncology.

    Sanjay Goel: Funding to conduct clinical trial from AstraZeneca.

    Howard Burris: Consultant or advisor to Mersana, AstraZeneca, Bristol-Myers Squibb, FORMA Therapeutics, Janssen, Novartis, Roche/Genentech, and TG Therapeutics; research funding from Roche/Genentech, Bristol-Myers Squibb, Incyte, Tarveda Therapeutics, Mersana, AstraZeneca, Macrogenics, Novartis, Boehringer-Ingelheim, Eli Lilly, Seattle Genetics, AbbVie, Bayer, Celldex, Merck, Celgene, Agios, Jounce Therapeutics, Moderna Therapeutics, CytomX Therapeutics, GlaxoSmithKline, Verastem, Tesaro, Immunocore, Takeda, Millennium, BioMed Valley Discoveries, Pfizer, PTC Therapeutics, TG Therapuetics, Loxo, Vertex, eFFECTOR Therapetics, Janssen, Gilead Sciences, Valent Technologies, BioAtla, CicloMed, Harpoon Therapeutics, Jiangsu Hengrui Medicine, Revolution Medicines, Daiichi Sankyo, H3 Biomedicine, Neon Therapeutics, OncoMed, Regeneron, and Sanofi; expert testimony for Novartis.

    Patricia LoRusso: Advisory boards for Genentech, AstraZeneca, Ipsen, AbbVie, Genmab, Roche, CytomX, and SOTIO; Data Safety Monitoring Boards for Agios, Five Prime, Halozyme, and Tyme.

    Amy Weise: Speakers’ bureau for Array Biopharma.

    Joseph Eder: No conflicts to disclose.

    Brendan Curti: Institution receives research funding from AstraZeneca.

    Chelsea Black, Shannon Marshall, Ikbel Achour, Rena May, Chris Morehouse, Kristen Pollizzi, Xuyang Song, Keith Steele, Nairouz Elgeioushi, Farzana Walcott, Joyson Karakunnel, and Michael Oberst are current or former employees of AstraZeneca and own stocks/shares in AstraZeneca. Susannah Barbee is a former employee of Amplimmune.

    Ab
    Antibody
    ADA
    Anti-drug antibody
    AE
    Adverse event
    ALT
    Alanine aminotransferase
    ANOVA
    Analysis of variance
    AUC
    Area under the curve
    BOR
    Best overall response
    CDR
    Complementarity-determining region
    CHO
    Chinese hamster ovary
    CR
    Complete response
    DC
    Disease control
    DCR
    Disease control rate
    DCR24
    Disease control rate ≥ 24 weeks
    DLT
    Dose-limiting toxicity
    DOR
    Duration of response
    E:T
    Effector-to-target
    EBV
    Epstein–Barr virus
    EC50
    Drug concentration giving half-maximal response
    ECACC
    European Collection of Authenticated Cell Cultures
    ECL
    Electrochemiluminescence
    ECOG
    Eastern Cooperative Oncology Group
    EDTA
    Ethylenediaminetetraacetic acid
    ELISA
    Enzyme-linked immunosorbent assay
    Fab
    Fragment antigen-binding
    FC
    Fold change
    Fc
    Fragment crystallizable
    FFPE
    Formaldehyde fixed paraffin-embedded
    FOV
    Fields of view
    FTIH
    First-time-in-human
    GM-CSF
    Granulocyte-macrophage colony-stimulating factor
    HLA
    Human leukocyte antigen
    IC50
    Inhibitor concentration where the response (or binding) is reduced by half
    IFNγ
    Interferon gamma
    IgG
    Immunoglobulin G
    IHC
    Immunohistochemistry
    IL-4
    Interleukin-4
    IP-10
    Interferon gamma-induced protein-10
    I-TAC
    Interferon-inducible T-cell alpha chemoattractant
    KD
    Dissociation rate constant
    mAbs
    Monoclonal antibodies
    MdFI
    Median fluorescence intensity
    MFI
    Mean fluorescence intensity
    MTD
    Maximum tolerated dose
    NK
    Natural killer
    NSCLC
    Non-small cell lung cancer
    OR
    Objective response
    ORR
    Objective response rate
    OS
    Overall survival
    PBMC
    Peripheral blood mononuclear cell
    PCR
    Polymerase chain reaction
    PD-1
    Programmed cell death-1
    PD-L1
    Programmed cell death ligand-1
    PD-L2
    Programmed cell death ligand-2
    PE
    Phycoerythrin
    PFS
    Progression-free survival
    PR
    Partial response
    Q2W
    Every 2 weeks
    Q3W
    Every 3 weeks
    QW
    Every week
    RCC
    Renal cell carcinoma
    RECIST
    Response Evaluation Criteria in Solid Tumors
    SAE
    Serious adverse event
    SD
    Stable disease
    SPR
    Surface plasmon resonance
    TEM
    T effector memory cells
    TIL
    Tumor infiltrating lymphocyte
    ΔΔCt
    Delta-delta cycle thresholds

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    Footnotes

    • Electronic supplementary material The online version of this article (10.1186/s40425-019-0665-2) contains supplementary material, which is available to authorized users.

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