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Conditional immune toxicity rate in patients with metastatic renal and urothelial cancer treated with immune checkpoint inhibitors
  1. Pier Vitale Nuzzo1,
  2. Gregory R Pond2,
  3. Sarah Abou Alaiwi1,
  4. Amin H Nassar1,3,
  5. Ronan Flippot1,
  6. Catherine Curran1,
  7. Kerry L Kilbridge1,
  8. Xiao X Wei1,
  9. Bradley A McGregor1,
  10. Toni Choueiri1,
  11. Lauren C Harshman1 and
  12. Guru Sonpavde1
  1. 1Department of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA
  2. 2Department of Oncology, McMaster University, Hamilton, Ontario, Canada
  3. 3Department of Medicine, Brigham and Women’s Hospital, Boston, Massachusetts, USA
  1. Correspondence to Dr Guru Sonpavde; gurup_sonpavde{at}dfci.harvard.edu

Abstract

Background Immune checkpoint inhibitors (ICIs) are associated with immune-related adverse events (irAEs). Although the incidence and prevalence of irAEs have been well characterized in the literature, less is known about the cumulative incidence rate of irAEs. We studied the cumulative incidence of irAEs, defined as the probability of irAE occurrence over time and the risk factors for irAE development in metastatic urothelial carcinoma (mUC) and renal cell carcinoma (mRCC) patients treated with ICIs.

Methods We identified a cohort of patients who received ICIs for mUC and mRCC. irAEs were classified using Common Terminology Criteria for Adverse Event (CTCAE) V.5.0 guidelines. The monthly incidence of irAEs over time was reported after landmark duration of therapy. Cumulative incidence of irAEs was calculated to evaluate the time to the first occurrence of an irAE accounting for the competing risk of death. Prognostic factors for irAE were assessed using the Fine and Gray method.

Results A total of 470 patients were treated with ICIs between July 2013 and October 2018 (mUC: 199 (42.3%); mRCC: 271 (57.7%)). 341 (72.6%) patients received monotherapy, 86 (18.3%) received ICIs in combination with targeted therapies, and 43 (9.2%) received dual ICI therapy. Overall, 186 patients (39.5%) experienced an irAE at any time point. Common irAEs included hypothyroidism (n=42, 22.6%), rush and pruritus (n=36, 19.4%), diarrhea/colitis (n=35, 18.8%), transaminitis (n=32, 17.2%), and pneumonitis (n=14, 7.5%). Monthly incidence rates decreased over time; however, 17 of 109 (15.6%, 95% CI: 9.4% to 23.8%) experienced their first irAE at least 1 year after treatment initiation. No differences in cumulative incidence were observed based on cancer type, agent, or irAE grade. On multivariable analysis, combined ICI therapy with another ICI or with targeted therapy (p<0.001), first-line ICI therapy (p=0.011), and PD-1 inhibitor therapy (p=0.007) were all significantly associated with irAE development.

Conclusions This study quantitates the incidence of developing irAEs due to ICI conditioned on time elapsed without irAE development. Although the monthly incidence of irAEs decreased over time on therapy, patients can still develop delayed irAEs beyond ICI discontinuation, and thus, continuous vigilant monitoring is warranted.

  • oncology
  • immunology
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Introduction

Treatment with immune checkpoint inhibitors (ICIs) has transformed the field of oncology, improving long-term survival in patients across several types of cancer.1 2 The most commonly used ICIs target cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), programmed cell death protein 1 (PD-1), and PD-ligand 1 (PD-L1).3–5 However, these agents are associated with a distinct spectrum of side effects resulting from activation of the immune system, termed immune-related adverse events (irAEs).6–8

irAEs can potentially affect any organ system, but most commonly involve the skin, gastrointestinal tract, lungs, liver, and endocrine glands.7–9 The incidence of irAEs has been well characterized in the literature with the median time to onset of 2–3 months after initiation.10 11 Nonetheless, delayed or latent irAEs have been reported months or even years after initiating therapy with onset extending beyond treatment discontinuation.12 In clinical trials, the analysis of ICI safety in terms of irAEs is generally reported as incidence proportions. Incidence proportion is typically calculated by crude rates, that is, the ratio of the number of patients who developed the specific adverse event at any point in time to the total number of patients in the cohort. A simple descriptive listing of irAEs in clinical trials is inadequate for modern immunotherapy treatments because this method does not account for the toxicity profile of ICIs conditioned over time. To date, there are limited studies that investigate and quantify the risk of irAEs over time in patients with cancer treated with ICIs.10 13 Accurate estimates of this risk will guide oncologists and patients to make decisions regarding treatment strategy and monitoring.

Here, we performed a retrospective study that evaluated, for the first time, the cumulative incidence of irAEs in patients with metastatic urothelial carcinoma (mUC) and metastatic renal cell carcinoma (mRCC) treated with ICIs. Additionally, we investigated the concept of conditional toxicity, how the incidence of irAE occurrence may be dynamic and may change over time, as well as the risk factors associated with the development of irAEs.

Methods

Data Collection

We conducted a retrospective medical record review of patients with mUC and mRCC who received ICI-based therapy at the Dana Farber Cancer Institute (DFCI) between July 2013 and October 2018. All patients had a histologically confirmed UC or RCC. Patients treated with a CTLA-4 inhibitor and/or PD-1/PD-L1 inhibitor were eligible. Data regarding clinicopathological features and treatment history were extracted. irAEs were defined as adverse events with a potential immunological basis that medical oncologists could recognize objectively. The patients were divided into two groups based on the presence or absence of irAEs within 1 month of each dose of ICI.

Toxicities were graded using the Common Terminology Criteria for Adverse Events (CTCAE) V.5.0. We noted the irAEs and grade reported by the medical professional who encountered a patient experiencing acute irAE. If the grade was not reported, we assigned it based on a thorough review of the medical record describing the events.

Statistical analysis

Descriptive statistics were used to summarize patient characteristics and outcomes. Time to irAE was defined as the amount of time elapsed from the date of ICI initiation to the development of irAE. The monthly incidence of irAEs was calculated for each 30-day period and was defined as the ratio of the number of patients with an irAE to the number of patients alive without irAE at the start of each month. Similarly, the incidence of irAEs at landmark times was defined as the ratio of the number of patients with an irAE at any time following the landmark time to the number of patients alive at each landmark date who had not experienced a prior irAE. Cumulative incidence was calculated to evaluate the time to the first occurrence of an irAE accounting for the competing risk of death. We used the Fine and Gray method to identify variables associated with irAE development: age at the start of ICI, sex (female vs male), cancer type (mUC vs mRCC), ECOG PS (0 vs ≥1), lung metastases (yes vs no), lymph node metastases (yes vs no), bone metastases (yes vs no), liver metastases (yes vs no), brain metastases (yes vs no), other metastases (yes vs no), ICI type (ICI monotherapy vs dual ICI regimens vs ICI plus another class of agents), line of ICI (first line vs second or more), and type of ICI (PD-L1 inhibitors vs PD-1 inhibitors). A multivariable model was constructed using forward stepwise selection. All tests were two-sided and a p-value of <0.05 was considered statistically significant. Statistical analyzes were performed using SAS V.9.2 or R V.3.50 (www.r-project.org).

Results

Patient characteristics

A total of 470 patients received ICIs between July 2013 and October 2018: 271 mRCC (57.7%) and 199 mUC (42.3%). Baseline patient characteristics are reported in table 1. The median follow-up was 11.9 months (maximum=8.8 years). The cohort comprised 342 (72.8%) men and 128 (27.2%) women, with a median age of 65 years (range: 22–91). Overall, 341 (72.5%) patients received ICI monotherapy, 86 (18.3%) patients received ICI plus another class of agents (including investigational immunotherapy), and 43 (9.2%) patients received a dual ICI regimen. Most (n=312, 660.2%) were treated with anti-PD1-based therapy, whereas a third (n=159,330.8%) received an anti-PD-L1- based regimen. The median duration of therapy was 4.0 (95% CI: 3.6 to 5.0) months. Two hundred and seven (44%) patients received ICI as first-line therapy and 263 (56%) received as second or later line therapy. Three hundred and fifty patients (74.5%) discontinued ICI due to radiological progression (n=226, 64.6%), clinical and radiological progression (n=43, 12.3%), toxicity (n=55, 15.7%), clinician preference (n=19, 5.4%), patient preference (n=3, 0.9%), or unknown reasons (n=4, 1.1%).

Table 1

Baseline patient characteristics (N=470)

Characteristics and frequency of irAEs

Any grade irAEs occurred in 186 (39.5%) patients (table 2). Most developed the irAE while on treatment (n=163, 87.6%), whereas 16 (8.6%) developed the irAE within 1 month of therapy discontinuation, and 7 (3.8%) developed the irAE >1 month after the discontinuation. Only four patients experienced an irAE >35 days after therapy discontinuation at 1.7, 3.8, 5.3, and 15.4 months, respectively. The most frequently observed irAEs of any grade included hypothyroidism (n=42, 22.6%), dermatological toxicity (n=36, 19.4%), diarrhea/colitis (n=35, 18.8%), transaminitis (n=32, 17.2%), and pneumonitis (n=14, 7.5%). Fewer than 10% (n=40, 8.5%) exhibited grade 3 irAEs and two patients (0.4%) experienced grade 4 events. No treatment-related deaths were reported. The median time to irAE was 21 weeks (range: 0.3–356).

Table 2

irAEs according to category and grade

Cumulative incidence of irAEs

Forty-seven (10.0%) patients experienced an irAE within the first month (table 3) of receiving ICIs. The monthly incidence of irAEs was lower in subsequent months with 4.2%, 5.7%, and 1.4% developing their first irAE in month 4, 7, and 10 from ICI initiation, respectively. When examining irAEs after landmark times, 139 of 415 (33.5%) patients with no irAE within the first 30 days eventually experienced an irAE. The rates of irAE development after months 3, 6, 9, and 12 were 27.6% (n=86/312), 22.3% (n=43/193), 14.4% (n=21/146), and 15.6% (n=17/109), respectively (table 3). The cumulative incidence of irAE was 32.1% (95% CI: 27.7% to 36.5%) at 6 months, 38.8% (95% CI: 34.1% to 43.4%) at 1 year, and 46.3% (95% CI: 40.4% to 52.2%) at 5 years (figure 1A). The cumulative incidence of a grade ≥3 irAE was 7.5% (95% CI: 5.0% to 10.0%) at 6 months, 10.6% (95% CI: 7.6% to 13.6%) at 1 year, and 11.7% (95% CI: 8.3% to 15.0%) at 5 years (online supplementary table 1 and figure 1B). Cumulative incidence of irAEs for mRCC and mUC were similar for all irAEs, irrespective of grade of toxicity (figure 1).

Table 3

Monthly incidence and conditional probability of irAEs

Figure 1

Cumulative incidence irAEs plots for mRCC and mUC: irAEs all grades (A), irAEs grades ≥3 (B). The cumulative incidence of irAEs for mRCC and mUC were similar for all irAEs, irrespective of grade of toxicity. The cumulative incidence of irAE was 32.1% (95% CI: 27.7% to 36.5%) at 6 months, 38.8% (95% CI: 34.1% to 43.4%) at 1 year, and 46.3% (95% CI: 40.4% to 52.2%) at 5 years (A). The cumulative incidence of a grade ≥3 irAE was 7.5% (95% CI: 5.0% to 10.0%) at 6 months, 10.6% (95% CI: 7.6% to 13.6%) at 1 year, and 11.7% (95% CI: 8.3% to 15.0%) at 5 years (B). irAE, immune-related adverseevent; mRCC, metastatic urothelialcarcinoma; mUC, metastatic renal cell carcinoma.

Characteristics of irAEs conditioned as a function of time

The type and severity of irAEs experienced after 12 months from ICI initiation were similar to irAEs experienced at any time point. Seventeen of 109 patients (15.6%) were alive at 12 months after initiating an ICI without irAE and later experienced an irAE beyond 12 months. The most common irAE experienced after 1 year was colitis (n=5), followed by hypothyroidism, rash, pneumonitis, myalgia (n=2 each), joint pain, transaminitis, uveitis, and nephritis (n=1 each). In terms of severity, most were grade 1–2 with one grade 4 colitis and one grade 3 myalgia.

Risk factors associated with irAE development

The risk factors associated with the development of irAEs at any time point are shown in the online supplementary table 2. In multivariable analysis, combined ICI therapy (HR=1.83, 95% CI: 1.15 to 2.91) and combined ICI plus other agents (HR=2.29, 95% CI: 1.55 to 3.39) versus IO monotherapy (p<0.001), first-line versus later-line therapy (HR=1.29, 95% CI: 1.06 to 1.56, p=0.011), and PD-1 versus PD-L1 inhibitor therapy (HR=1.64, 95% CI: 1.15 to 2.36, p=0.007) were all significantly associated with irAE development. Type of cancer, age, sex, and performance status were not associated with a higher risk of irAE development.

Discussion

Conventional safety analyzes describing the absolute percentages of adverse events experienced by patients do not account for how the toxicity profile and risk may evolve over time. In this study, we retrospectively analyzed 470 patients including 271 patients with mRCC and 199 patients with mUC who had received ICI-based therapy at a single academic institution with the objective of characterizing the cumulative incidence of irAEs and assessing how risk may change when conditioned on time elapsed. Our results suggest that the monthly risk of developing an irAE persists but decreases over time, irrespective of the type of cancer, specific ICI class, and known prognostic clinical or demographic variables. Our study highlights that when examining the monthly incidence of irAEs, patients are at the highest risk of developing the irAE in the first month of treatment (10%). Although still at risk for developing irAEs during the remaining months of the first year, there was a trend for decreased monthly incidence with time elapsed. Notably, a substantial proportion (15.6%) of patients experienced delayed irAEs after 1 year of treatment. To our knowledge, this is the first study to underscore the important role of time-to-adverse event analysis in the setting of ICIs, which could inform clinical practice and trial designs.

Few studies have investigated the incidence of irAEs with ICI and how the risk may change over time during treatment.10 12 13 In a safety subanalysis of one prospective study, prolonged treatment with ICIs did not result in an increased cumulative incidence of irAEs.10 The safety report of 107 patients with advanced melanoma treated with nivolumab showed that most irAEs occurred within the first 6 months, and cumulative toxicities were not observed with prolonged drug exposure, although details about the type, grade, and incidence of irAE over time were not reported.10 In a retrospective review including 352 patients enrolled in 21 early phase clinical trials of ICI, 260 (74%) patients experienced irAEs.13 In this case, the risk of developing irAEs was studied using the OR model for irAEs occurrence at various time points.13 The OR for irAEs occurrence within the first month compared with after 1 month was 3.13 (95% CI: 1.95 to 5.02) and decreased over time, being 2.80 (95% CI: 1.76 to 4.44) at 3 months.13

Clinical trials typically include a summary table of adverse events incidence irrespective of when the patient experienced the event. This method of reporting toxicities is suboptimal for capturing the impact of time on therapy free from toxicities, especially when that toxicity can be an important cause of treatment discontinuation in patients receiving ICIs. Quantification of irAE risk over time offers important information for clinical decision making for the patient’s treatment strategy. PD-1/-L1 inhibitors are administered continuously over months to years in patients with the stable or responding disease, rather than given for a predefined number of cycles. In contrast to cytotoxic chemotherapy, where the adverse events typically occur early and accumulate during the treatment course, toxicity with ICI may manifest later and thus, clinicians and patients should continue to be vigilant especially in situations of prolonged therapy. Incorporating the cumulative incidence of irAEs in clinical trials is an opportunity to improve the characterization of toxicities and tailoring of monitoring schedule as well as in counseling of patients in the clinic.

It is recognized that irAEs exhibit a characteristic pattern in timing in their occurrence, with some events, like skin, hepatic, and gastrointestinal toxicities, occurring earlier at approximately 2–6 weeks, and pneumonitis or endocrine events occurring on average 9 weeks after treatment initiation.11 In our dataset, when we examined irAEs that occurred within 1 year vs >1 year, no differences in the irAE class emerged, but our analysis may be underpowered. The precise pathophysiology that explains the relatively high rate of late irAEs occurring after 1 year remains unclear. One hypothesis is that early irAEs occur by the cross-reactivity theory, where the unbalancing of the immune system induced by ICI generates a cross-reactivity between tumor neoantigens and normal tissue antigens.14 15 Another theory postulates that ICIs can modulate B cells over time both directly and indirectly via T-cell mediation, altering the production of autoantibodies that can generate delayed irAEs.16 17 Non-specific increase in endogenous T-cell response mediated by dendritic cell or cytokine stimulation could play a role in this process.16 Furthermore, ICIs have a serum half-life of 12–20 days and therefore they can continue to inhibit immune checkpoint pathways for >8 months after the last dose.18

The fact that the cumulative incidence rates of irAEs were similar in mRCC and mUC should not be surprizing as the pathophysiology of irAEs is anticipated to be driven by host genetics and not tumor biology.19 Interestingly, the rate of grade ≥3 irAEs was only 8.5% despite an overall irAE rate of 39.5%, which suggests that prompt recognition and management of irAEs possible in an academic tertiary care center, may mitigate the risk of severe irAEs. Moreover, we showed that the type of ICI or drug combination did not affect the cumulative incidence, suggesting that the trend for safety over time is independent of the type of ICI. As expected, ICI combination therapy was associated with a higher incidence of irAEs.20–23 PD-1 inhibitors have been previously reported to carry a higher risk of toxicities compared with PD-L1 inhibitors, and our findings are consistent with these data.24 The association of first-line therapy with a higher risk of irAEs compared with later line settings is intriguing and has not been reported before to our knowledge. This result is biologically plausible given a likely more intact host immune system leading to a more robust systemic immune response in treatment-naïve or less advanced disease patients. However, these results require validation and conclusions are limited pending further understanding of host genetic factors or other host or tumor biologic contributors that may increase the risk of irAEs.

Limitations of our study include its retrospective nature. Patients were all treated at a single institution, so it is possible that results may not be completely generalizable to other institutions with different practice patterns or patient populations. Second, we relied on the clinical information reported in the charts for the identification and grading, of irAEs and thus some irAEs may have been misclassified or not reported. However, this risk is lessened by the execution of the study at a major academic institution with investigators who are highly experienced in the recognition and management of irAEs. Third, the frequency and type of irAEs may vary depending on the specific ICI treatment; thus, a different irAE profile may be observed with different ICI regimens. Differences in the cumulative incidence rate may be seen based on specific agents or combinations, but we did not have the power to examine these subsets separately beyond combination versus monotherapy analyzes. We believe the rates of irAEs, in particular serious irAEs, while slightly lower than many trials, are similar and as expected. Moreover, given the greater awareness of irAEs following the publication of multiple trials in different malignancies, toxicities may have been more promptly managed leading to a somewhat lower rate of severe irAEs. We examined only data from metastatic RCC and UC, which was available to us; however, the consistent results of our analysis regardless of malignancy suggests that the type of malignancy does not impact conditional irAE rates.

Conclusions

In conclusion, this is the first retrospective study that quantitates the incidence of developing irAEs with ICI conditioned on time elapsed in a cohort of patients with mRCC and mUC treated with ICIs. Our results highlight that the monthly incidence of irAEs decreases over time on therapy; however, a significant proportion of delayed irAEs occur even ≥1 year after initiating ICIs. Thus, awareness and ongoing vigilant monitoring is required throughout ICI therapy and likely beyond discontinuation. In conjunction with an investigation into clinical and biologic predictors of early and late irAEs, incorporation of conditional irAE rates is warranted in ongoing and future immunotherapy studies to enhance our understanding of ICI toxicity profile and optimize patient care.

Acknowledgments

The auhtors thank the patients for their contributions to research.

References

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Footnotes

  • Twitter @PierVitaleNuzzo, @AminNassarMD, @DrChoueiri, @sonpavde

  • PVN and GRP contributed equally.

  • Presented at Society for Immunotherapy of Cancer (SITC) annual meetting 2019 in National Harbor, Maryland, USA and Merit Award at ASCO Genitourinary Cancers Symposium 2020, San Francisco, CA, USA.

  • Contributors PVN, GRP and GS: conception and design. PVN, GRP, SAA, AHN, RF, KK, XXW, BAM, LH, TKC, and GS:

    development and methodology. PVN, SAA, AHN, RF, KK, XXW, BAM, LH, TKC and CC: collection clinical data. GSP: statistical analysis. PVN, GRP, SAA, AHN, RF, KK, XXW, BAM, LH, TKC and GS: analysis and interpretation of data. PVN and CC: administrative, technical, or material support. GS: study supervision. All authors: writing, review and/or revision of the manuscripts; read and approved the final manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent for publication Written informed consent was obtained from patients to collect clinical information.

  • Ethics approval This study was approved by the Institutional Review Board at Dana Farber Cancer Institute.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement Data are available upon reasonable request. All data relevant to the study are included in the article or uploaded as supplementary information. All data and materials relevant to this article are available to referees at submission and to readers promptly upon request

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