Adaptive immunity

The efficacy of the T-cell response relies on the presence of multiple major histocompatibility complex (MHC) alleles that can present a large pool of peptides for potential T-cell recognition.7 Humans have three MHC class I loci: human lymphocyte antigens (HLA) A, B, and C; and three MHC class II loci: HLA-DP, DQ, and DR and each locus can encode multiple alleles.8 Diversity within the human MHC loci is based on amino acid differences as well as the inheritance of specific sets of HLA molecules from each parent with little crossover. Rhesus macaques have two MHC class I loci: Mamu-A and Mamu-B whereas an HLA-C orthologue is missing,9 and three MHC class II loci: DP, DQ, and DR.10 Unlike humans, rhesus macaques can have several MHC class I alleles on each chromosome and significant crossover can occur which results in an increased haplotype diversity.

Human and NHP CD4 and CD8 T cells can be divided into naïve, central memory (CM) and effector memory (EM) types11 and similarly delineated using CD28 and CD95 as the primary cell surface markers.12 In both species, naïve cells are defined as CD95^negCD28^pos, CM cells are defined as CD95^posCD28^pos, and EM cells are defined as CD95^posCD28^neg.

Similar to humans, NHP B cells can be identified based on the CD20 and MHC class II expression. Furthermore, rhesus macaque and human B cells can be divided into naïve (IgD⁺CD27^–), unswitched memory (IgD⁺CD27⁺), and switched memory (IgD^–CD27⁺) B-cell subsets13 and exhibit an upregulation of CD80, CD86, and CD40 on activation.14

Innate immunity

Several immune cell subsets play a critical role in mediating innate immune responses including dendritic cells (DCs), natural killer (NK) cells, neutrophils and macrophages.

Human DCs can be divided into two distinct populations: (a) myeloid, or conventional, DC (MDC) characterized as CD11c^posCD123^dim and (b) plasmacytoid DC (PDC) characterized as CD11c^negCD123^bright.15 MDC mainly functions to process and present antigens to naïve T cells and produce interleukin (IL)-12 on activation, whereas, PDC produces interferon (IFN)-α in response to viral infection. These two major DC subsets can be identified in rhesus macaques, using the same surface markers as for human DCs. Moreover, NHP PDC exhibits a similar cytokine and functional response as human PDC, including upregulated IFN-α, tumor necrosis factor (TNF)-α, macrophage inflammatory protein (MIP)-1β, and CXCL10 expression on stimulation with herpes simplex virus. Patterns of Toll-like receptor (TLR) expression in macaque and human DCs are similar, but differ substantially from murine DCs.16 PDC from rhesus and humans express TLR7 and TLR9 but not TLR3, TLR4, and TLR8; both respond to TLR stimulation by upregulation of CD86. Rhesus and human MDC express TLR3, TLR4, TLR7, and TLR8 but not TLR9 and respond to TLR agonists by upregulation of CD40 and CD86. In contrast, murine MDC and PCD both express TLR3, TLR4, TLR7, TLR8, and TLR9.

Human NK cells are identified as CD3^negCD56^pos cells and can be further stratified based on the expression of CD16 and CD56. The majority of blood and spleen resident NK cells are CD16^posCD56^dim, and are primarily cytotoxic. The remaining NK cells are CD16^negCD56^bright, and are less focused on directly killing target cells but rather secrete large amounts of inflammatory cytokines.17 Similarly, NK cells in rhesus macaques are CD3^neg and can be divided into a major CD16^highCD56^neg cytolytic population and a minor CD16^lowCD56^pos cytokine-producing population.18 Similar to human NK cells, all rhesus NK cell subsets express CD2, CD11a, and NKG2A.

NK cells recognize missing and altered self through inhibitory and activating receptors. In humans, recognition of MHC molecules is mediated by the killer inhibitory receptor, a CD94/NKG2 complex. Homologues of the human CD94/NKG2 family members have been identified in rhesus macaques, and have similar stimulatory and inhibitory functions as their human counterparts.19

Considerable discrepancies exist in the phenotypic characterization of macrophages across species, anatomic sites, and disease models, and there are conflicting reports regarding the delineation of myeloid cell subsets.20 Characterization of NHP macrophages, defined as HLA-DR⁺CD11b⁺CD68⁺ leukocytes, has been limited by the availability of cross-reactive reagents and the autofluorescence inherent to macrophages. Macrophages vary widely in phenotype and pro-inflammatory capacity by anatomic location.21 This heterogeneity likely reflects responses to the microenvironments encountered by macrophages in each tissue.

Interestingly, human and NHP macrophages share a primate specific evolutionary-conserved regulation of cathelicidin antimicrobial peptide (CAMP) gene by vitamin D response elements (VDRE).22 In murine monocytes and macrophages, TLR signaling is principally mediated by nitric oxide.23 In contrast, human macrophages upregulate vitamin D receptor and vitamin D-1-hydroxylase to induce CAMP production on TLR activation. The VDRE in the CAMP promoter region is present in humans and NHP and absent in mice, rats and dogs, and is illustrative of the differences in immune system regulation when comparing mice, NHPs, and humans.22

A brief summary on the similarities and differences of the innate and adaptive immune system and immunoregulatory mechanisms in humans and rhesus macaques can be found in table 1.

Immune competence

The reduced ability to resist infectious disease in the elderly human population is well-known.48 Over 90% of influenza-associated deaths in the USA occur in persons aged 65+ years,49 and the incidence of severe sepsis increases over 100-fold in persons 85+ years old compared with children.50 Over 80% of the COVID-19-associated deaths in Italy, Spain, and Japan occurred in humans 70+ years old.51 This age-related reduction in immune competence in humans52 is similarly found in NHPs as illustrated by a comparable loss of naïve CD4 and CD8 T cells and a concomitant accumulation of memory T cells, limiting the T-cell repertoire.6 53 Elderly NHPs also have a reduced immune response to influenza vaccination54 and a poorer CD8 T cell and B-cell response on vaccination with modified vaccinia strain Ankara.55 Temporally, the increase in tumor frequency coincides with reduced immune competence in aging NHPs, resembling the situation in patients with human cancer.

Viral infection

NHPs are similar to humans in their susceptibility to virus-induced neoplasms. For example, Kaposi’s sarcoma-associated herpesvirus which is common in patients with immune-deprived HIV, also termed HHV8, has a relative in the form of rhesus rhadinovirus (RRV).56 RRV is associated with a mesenchymal malignancy termed retroperitoneal fibromatosis, resembling Kaposi’s sarcoma in SIV-infected rhesus macaques.57

Additionally, oncogenic Epstein-Barr virus (EBV) has an analogous rhesus lymphocryptovirus (rhLCV).56 rhLCV has a high degree of homology with human EBV, encoding for an identical viral gene repertoire, and parallels EBV-associated disease including B-cell lymphomas and hairy leukoplakia in SIV-infected macaques.58 Furthermore, the T-cell specific and humoral response to EBV in human and rhLCV in rhesus macaques share similarities, illustrating the potential for studies on EBV and EBV-associated malignancies in rhesus macaques.

Human papilloma virus (HPV) is a highly relevant risk factor for cervical, anal, vulvar, and head and neck cancer in humans.59 Vaccinating rhesus macaques with a DNA vaccine encoding a fusion protein of HPV18 EV6/EV760 or an inexpensive trivalent HPV16/18/58 vaccine produced in Escherichia coli61 both produced successful immunization as determined by the emergence of neutralizing antibodies. Replication incompetent HPV16 pseudovirions with a red fluorescent protein (RFP) reporter system were successfully used in rhesus macaques for visualization of the traumatic effect of Pap smear collection as an infection enhancing factor as well as iota-carrageenan as a potential HPV microbicide.62 Interestingly, an oncogenic rhesus specific papillomavirus, RhPV-1, was identified in a monkey with penile carcinoma in a breeding colony.63 Seventy-one per cent of his mating partners (22/31) had clinical, histopathological, or molecular evidence of infection. The lesions included warty, dysplastic lesions and/or acetowhitening in 35% (11/31) of his mating partners, and two cervical carcinomas. This finding of sexual transmissibility and the oncogenic potential of RhPV-1 is similar to high-risk HPVs in humans. Corroborating results were generated in cynomolgus macaques where cervical intraepithelial neoplasia was associated with papillomavirus infection.64 Notably, the most prevalent type, RhPV-d, is phylogenetically related to oncogenic HPV16 and was transferred via cervical cytobrush samples, resulting in new infections in 4/12 animals. Moreover, within 18 weeks 1/4 infected animals developed abnormal cytology and histology. In addition to captive colonies, papillomavirus DNA was also found in 75.2% (88/117) of wild rhesus macaques roaming the Kam Shan Country Park in Hong Kong.65 Phylogenetic analysis demonstrated the parallel evolution of papillomaviruses in monkeys and similar disease mechanisms and affected body sites. Cynomolgus macaque-associated MfPV3 degrades host p53 by virally-encoded E6 protein, as does HPV16. Moreover, alpha papillomaviruses detected in the cervicovaginal region of NHPs and humans include α9 (HPV16), α7 (HPV18) and α12 (MfPV3) species,66 demonstrating close evolutionary parallels and providing a promising tool to investigate HPV persistence and carcinogenesis in an animal model.

Inherited genetic mutations

Recent studies demonstrated elevated rates of colorectal cancer (CRC) in related rhesus macaques67 68 resembling the autosomal dominant inheritance of human hereditary non-polyposis colorectal cancer (HNPCC).69 70 These tumors frequently lacked expression of MLH1 or PMS2, two key proteins of DNA mismatch repair (MMR). In addition to a similar histopathology, sequencing revealed deletions in the MLH1 promoter region, de novo stop codons in MLH1, and deleterious missense mutations in MSH6 leading to a microsatellite-instable phenotype, closely resembling human HNPCC. Moreover, these heritable CRC cases could be traced back to three founding males with some exonic non-synonymous single nucleotide polymorphisms (SNPs) resembling those described in patients with human Lynch syndrome.71

There are still a broad variety of human inherited risk factors which are not yet described in NHPs, such as BRCA1/2 mutations. The number of fully sequenced NHPs is still relatively low, and these translationally-relevant mutations may yet emerge in cross-institutional initiatives such as the Macaque Genotype and Phenotype resource (mGAP) developed and maintained at the Oregon National Primate Research Center72 73 which links phenotypes observed in large, pedigreed rhesus colonies by DNA sequencing to detect naturally occurring genetic variations.

Transgenic or gene-edited NHP models have been successfully employed to model neurological disease including Parkinson’s disease, Huntington’s disease, or Rett syndrome.74 Similarly, cancer-promoting genetic variants detected in the NHP population could be intentionally introduced and propagated by selective breeding. Both approaches bear a great potential for research on cancer therapy and particularly cancer prevention but would come with substantial ethical concerns, as well as practical concerns for the long-term commitment to study such animals. Needless to say, a thorough and diligent ethical evaluation including comprehensive ethics boards would need to precede the establishment of such a model for heritable cancer. We consider the induction of cancer in NHPs to be both ethically and practically questionable. However, the treatment of animals with naturally-occurring disease provides a benefit to both the science of cancer treatment, and to the animal.

CRC in NHPs

Typical clinical signs of CRC in rhesus macaques include progressive weight loss, palpable abdominal mass, intermittent diarrhea, hypoproteinemia, fecal occult blood, and microcytic anemia.47 75 77 78 Suspected cases require diagnostic confirmation by ultrasound, CT, positron emission tomography, or laparotomy to exclude other gastrointestinal diseases such as diverticulitis. Histology generally reveals right-sided, mucinous adenocarcinoma, with dense, constrictive stroma. Precancerous lesions and polyps are not a reported feature of CRC in macaques.79 Metastasis to local lymph nodes, cases of miliary peritoneal carcinomatosis, or distant metastasis to spleen, lung, or spine are described in rhesus macaques but liver metastasis are not as frequently observed as in patients with human CRC.86

As mentioned above, Lynch-syndrome-like loss of MLH1 due to germline mutations is described for rhesus macaques and accompanied by an increased incidence of MMR deficient (MMRd) CRC.67 68 These familial cases in NHP demonstrate the role of MMRd and its parallels to human HNPCC cases. In contrast, mice with constitutive knockdown of MLH1 or MSH2 as models for MMRd do not develop CRC, but predominantly develop T-cell lymphomas.87

Moreover, MMRd and microsatellite instability suggest a broad range of tumor mutational burden (TMB) and neoantigens. TMB is an established positive response predictor for immune checkpoint blockade.88 89 Pembrolizumab received Food and Drug Administration-approval in 2020 as first-line and single-agent checkpoint inhibitor against MMRd highly-advanced CRC90 and promising data was recently obtained in a phase II trial assessing dostarlimab in MMRd, locally advanced rectal cancer.91 Similar patterns of MMRd CRC in NHPs might extend our understanding of the underlying processes in CRC, and the basis for observed responses to treatment.

BC in NHPs

BC has a predicted lifetime incidence of about 6% in female macaques compared with approximately 13% in American women.76 92 93 NHP are seldom maintained for their entire potential life span, limiting BC detection. Moreover, multiparity, ovariectomy, as well as a generally lower rate of obesity may contribute to lower BC in NHP.80

Humans and macaques share similar mammary gland anatomy, physiology, and comparable patterns of development, regression, and sex steroid receptor expression.94 Sex hormones including estrogen, progesterone, luteinizing hormone, and follicle stimulating hormone exhibit a similar pattern in women as in cynomolgus and rhesus macaques.95

Breast neoplasms diagnosed in macaques resemble those seen in humans, including precursor lesions such as atypical hyperplasia; ductal carcinoma in situ; and invasive ductal carcinomas. Moreover, metastasis of high-grade lesions to the axillary lymph nodes, lung, chest wall, and other sites has been documented.76 Notably, the full range of hormone receptor (progesterone receptor and estrogen receptor) and HER2 receptor positivity is observed in rhesus macaque BCs by immunohistochemistry (IHC)94 resulting in similar molecular subtypes including predominantly Luminal A (HR+/HER2−), lower numbers of Luminal B (HR+/HER2+), HER2 (HR−/HER2+), and a small proportion of triple-negative cancers (HR−/HER2−) as described in patients with human BC.76 94 In addition, TP53 positive BC is reported in rhesus macaques suggesting non-synonymous TP53 mutations as observed in 20–35% of sporadic human BC.92

A typical DNA repair deficiency associated with hereditary BC in humans and putative driver for high TMB is homologous recombination repair deficiency by heterozygous loss-of-function mutations in BRCA1 or BRCA2. While extensive studies were conducted to compare BRCA1 and BRCA2 in primate species and their respective evolution,96 there is no detailed knowledge on their potential involvement in heritable BC in NHPs at present.

A brief summary on the comparative oncology in between rhesus macaques and humans addressing cancers in general and CRC and BC in particular can be found in table 2.

General considerations and benefits

TBMs provide a study population of treatment-naïve patients of a comparable life stage, with naturally-occurring tumors, and an unaltered immune status, fostering and accelerating the application of first-line CIT agents. Translation from preclinical experiments to clinical phase I studies in humans currently relies on recruitment of patients with late-stage cancer who have usually undergone multiple cycles of one or more treatment regimens and/or have recurring treatment-resistant clones. Ethical concerns in human trials influence the study design and require combination studies of the prospective agent with the standard-of-care regimen in cases with good to intermediate clinical prognosis,97 98 limiting single-agent studies to cases with a poor prognosis.99–102

Altruistic participation of patients with cancer is a crucial keystone of clinical research and has fostered a multitude of advancements but may not mimic the clinical situation of untreated patients in which first-line CIT approaches proved beneficial.90 103 104 Certain established and emerging CITs can potentially shift from a late-stage salvage therapy to an approved and promising first-line treatment option, fostered by preceding TBM trials.

Needless to say, NHP trials demand nothing less than the gold standards in care, animal welfare, treatment, and study design to follow the principle of the 3 Rs105 meticulously and cause as little discomfort as necessary to generate as much translational data and benefits from this animal model as feasible.

Ongoing efforts by the Primate Cancer Initiative at Wake Forest University, the only program in the USA particularly dedicated to this field, aim to facilitate this model by broad collaborations to recruit NHPs with suspected cancers for prospective treatment studies. Using this approach, the timing of spontaneous cancer cases, the exact cancer location, or the histologic subtype cannot be controlled as in induced or grafted animal models; rather, a screening and recruitment approach is needed. Another key factor for TBM studies is the requirement for specialized veterinary staff and a close affiliation to core resources providing imaging and established NHP-specific IHC and flow cytometry procedures for follow-up biomarker analysis. In addition to improved clinical imaging, an array of NHP-specific assays has been established to provide the same biomarker and tumor characterization pipelines in TBM trials as in their human counterparts (see figure 2). Moreover, a repository of tissues and body fluids at numerous time points and at necropsy is made available to the scientific community on request.

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Figure 2

Diagnostics, biomarkers, and assays currently employed in TBMs. A multitude of methods can be used to diagnose cancer in TBM, classify the suspicious lesion, and follow-up treatment response. This includes versatile imaging methods, tumor-specific Immunohistochemistry panels, molecular pathological tests, as well as the follow-up of the immunological response in the tumor bed, lymph nodes, and peripheral blood by flow cytometry (created with BioRender). BC, breast cancer; CRC, colorectal cancer; DNAseq, DNA sequencing; ER, estrogen receptor; FAP, fibroblast activation protein; FDG, fluorodeoxyglucose; FFPE, formalin fixed paraffin embedded; i.v., intravenous; LNs, lymph nodes; mRNA, messenger RNA; PBMCs, peripheral blood mononuclear cells; PD-1, programmed cell death protein-1; PET, positron emission tomography; PR, progesterone receptor; RNAseq, RNA sequencing; RT-qPCR, real time quantitative polymerase chain reaction; TBM, tumor-bearing monkey; WES, whole exome sequencing; WGS, whole genome sequencing.

Previous CIT studies in TBM: drug candidates, imaging, and biomarkers

The earliest studies on CIT in TBM focused on fibroblast activation protein α (FAP) which is a dimeric Type II transmembrane glycoprotein with proteolytic activity.106 FAP is scarce in normal, healthy adult tissues but is highly expressed on the surface of cancer-associated fibroblasts in >90% human epithelial malignancies.107 The high and restricted expression on reactive stroma in the tumor microenvironment makes FAP a promising target for tumor treatment, particularly for FAP-targeted bispecific antibodies.83 84 108

In mouse tumor models, FAP expression does not always reflect the expression pattern observed in human patients. In contrast, FAP expression observed in TBM better mimics the situation in humans and is particularly abundant in CRC. De facto, extensive FAP expression has been observed in TBM in the tumor-adjacent stroma (and to a lesser extent in lymphoid fibroreticular cells within adjacent lymph nodes), but not in tumor cell nests,84 a typical expression pattern observed in human tumors.109 Additionally, in both humanized mice and immune competent mouse models, FAP is expressed by murine (and not human) fibroblasts, which consequently requires the employment of murine surrogate FAP-targeted bispecific antibodies to perform murine in vivo studies. On the other hand, FAP-targeted bispecific antibodies employed in TBMs are the same as the compounds later employed in human patients (eg, FAP-4-1BBL), making the use of murine surrogates unnecessary and clearly indicating that TBMs are an ideal animal model for translational research on FAP-targeted CIT compounds.

So far, three FAP-targeted CIT compounds have been tested in TBMs: FAP-IL2v, FAP-4-1BBL and FAP-TAgo (as illustrated in figure 3A).83–85 Of note, the low number of patients (n=1–4) in each of the TBM studies conducted to date emphasizes the limited, but translational, ‘proof of concept’ nature of the obtained data and observations.

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Figure 3

Preclinical studies on CIT agents performed in TBM. (A) Several novel bispecifics were tested in TBM and confirmed tumor-homing of the CIT agent as shown in (B) for FAP-IL2v (lesions highlighted by arrows) in a BC-bearing rhesus-macaques. (C) tumor-homing was also demonstrated for FAP-4–1-BBL (lesion highlighted by an arrow) in a CRC-bearing rhesus macaque and (D) the tissue distribution over time determined. (E) Diphtheria/pertussis/tetanus vaccination in combination with FAP-TAgo induced an expansion of tumorous CD4⁺ memory T cells in BC-bearing rhesus macaques and a strong expansion of peripheral target-positive (F) CD4⁺ T cells and (G) Ki67⁺CD4⁺ T cells. (H) a strong radiographic response was observed in BC2 with no nodules regrowing >12 months later. BC1 had lung metastases at the time of treatment which responded initially (not shown) but reached her humane endpoint soon after. (Illustrations adapted from83–85). ADA, anti-drug antibody; BC, breast cancer; CIT, cancer immunotherapy; CRC, colorectal cancer; FAP, fibroblast activation protein; FDG, fluorodeoxyglucose; LNs, lymph nodes; PD, pharmacodynamics; PK, pharmacokinetics; RheMac, rhesus macaques; SUV, standardized uptake value; TBM, tumor-bearing monkey; TNBC, triple-negative breast cancer.

FAP-IL2v

Simlukafusp alfa (FAP-IL2v, RO6874281/RG7461) is an immunocytokine targeting FAP and bearing an IL-2 variant with retained affinity for IL-2 Rβγ and abolished binding to IL-2Rα.83 FAP expression in tumor stroma of a HER2⁺ BC-bearing rhesus macaque was confirmed by IHC and 3× fluorodeoxyglucose (FDG)-avid lesions identified by PET scans. Based on postmortem histology, 2/3 FDG-avid lesions were confirmed as tumor nodules while the remaining FDG-avid axillary lymph node was most likely active due to an inflammatory response. The monkey was given 0.5 mg/kg of FAP-IL2v and tracer amounts of 89Zr-labeled FAP-IL2v intravenously with PET demonstrating selective accumulation in all three lesions identified by FDG-PET scans within 67 hours and 154 hours (see figure 3B). Furthermore, an immune cell infiltration was observably induced in tumor biopsies obtained 3 days post FAP-IL2v administration.

FAP-4-1BBL

FAP-4-1BBL is a bispecific antibody-like fusion protein that simultaneously targets FAP and 4-1BB, a member of the tumor necrosis factor receptor super family (TNFRSF) transiently expressed on activated T cells.84 To confirm the intended MoA and elucidate the systemic distribution in a translatable animal model, a rhesus macaque (male, 21 years old, 8.5 kg) with spontaneous CRC at the ileocecal junction was recruited for this study (see figure 3C,D). The monkey was given 0.5 mg/kg FAP-4–1-BBL mixed with tracer amounts of 89Zr-labeled FAP-4–1-BBL (165MBq) intravenously and PET scans recorded after 48 hours and 120 hours. Importantly, persistent tissue accumulation within the rhesus CRC was observed initially at the 48 hours time point and increased towards the 120 hours time point. These NHP results paved the way for a phase I clinical study110 111 and a separate clinical imaging substudy.112 Importantly, the data initially obtained in the TBM, emphasizing tumor-specific uptake and the expected biodistribution pattern of ⁸⁹Zr- FAP-4–1-BBL, could be recapitulated in the human clinical setting.112

FAP-TAgo

Another combined imaging/biomarker study in TBM investigated a second FAP-targeted TNFRSF agonist, termed FAP-TAgo.85 Two BC-bearing rhesus monkeys (1× triple-negative, 1× Luminal A) were first pre-immunized with a diphtheria/pertussis/tetanus vaccine, and then exposed to a single administration of FAP-TAgo (100 mg/kg, intravenous). In both TBMs, we detected the induction of the TNFRSF agonist in the periphery as well as a strong systemic immune activation. This increase in target-positive CD4⁺ and Ki67⁺CD4⁺ T cells was exclusive for TBM and only marginally observed in the healthy control animals (figure 3E–G). Consistently, the induction of CD4⁺ memory T cells was observed in the tumor of both TBMs after FAP-TAgo treatment which most importantly resulted in extensive tumor regression in both TBM (figure 3H). These results are even more impressive, when considering that FAP-TAgo was administered only once. Hence, these observations validated the applied pre-immunization strategy to induce the TNFRSF protein expression in T cells and confirmed the target to be pursued in the clinical setting. The investigation of FAP-TAgo in TBM and the resulting data analysis is currently being finalized with a novel successor trial.

Potential for expansion of TBM studies

The National Institutes of Health (NIH) in 2018 reported that there are over 100,000 nonhuman primates in the USA of which approximately 2/3 are rhesus macaques and 15% are cynomolgus macaques,113 114 and this number has generally increased over time. Within this total there are substantial aging populations, supported by the NIH through the National Primate Research Centers and other funding sources. Existing inter-institutional collaborations115 could provide a blueprint for development of a national Primate Cancer Network. We believe there is the potential nationwide to study over 100 NHPs per year with malignancies, primarily colorectal, breast and cervix, and substantially more if an effort were made to detect precancerous lesions of the cervix and vagina. Optimal development of this underused aspect of naturally-occurring disease in NHPs would require funding for establishment of a collaborative network enabling diagnostic screening, and support for local or referral-based treatment of patients with NHP cancer at academic medical centers or primate research centers with appropriate expertize and facilities in veterinary medicine, pathology, comparative oncology, and imaging.