ORIGINAL RESEARCH article
Combining a Universal Telomerase Based Cancer Vaccine With Ipilimumab in Patients With Metastatic Melanoma - Five-Year Follow Up of a Phase I/IIa Trial
- 1Department of Oncology, Oslo University Hospital, Oslo, Norway
- 2Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway
- 3Department of Oncology, Akershus University Hospital, Lørenskog, Norway
- 4Department of Cellular Therapy, Oslo University Hospital, Oslo, Norway
- 5Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway
- 6Ultimovacs Allmennaksjeselskap (ASA), Oslo, Norway
- 7Centre for Cancer Cell Reprogramming, Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway
- 8Center for Bioinformatics, Department of Informatics, University of Oslo, Oslo, Norway
Background: Ipilimumab improves survival for patients with metastatic malignant melanoma. Combining a therapeutic cancer vaccine with ipilimumab may increase efficacy by providing enhanced anti-tumor immune responses. UV1 consists of three synthetic long peptides from human telomerase reverse transcriptase (hTERT). These peptides comprise epitopes recognized by T cells from cancer patients experiencing long-term survival following treatment with a first-generation hTERT vaccine, and generate long-lasting immune responses in cancer patients when used as monotherapy. The objective of this trial was to investigate the safety and efficacy of combining UV1 with ipilimumab in metastatic melanoma.
Patients and Methods: In this phase I/IIa, single center trial [NCT02275416], patients with metastatic melanoma received repeated UV1 vaccinations, with GM-CSF as an adjuvant, in combination with ipilimumab. Patients were evaluated for safety, efficacy and immune response. Immune responses against vaccine peptides were monitored in peripheral blood by measuring antigen-specific proliferation and IFN-γ production.
Results: Twelve patients were recruited. Adverse events were mainly diarrhea, injection site reaction, pruritus, rash, nausea and fatigue. Ten patients showed a Th1 immune response to UV1 peptides, occurring early and after few vaccinations. Three patients obtained a partial response and one patient a complete response. Overall survival was 50% at 5 years.
Conclusion: Treatment was well tolerated. The rapid expansion of UV1-specific Th1 cells in the majority of patients indicates synergy between UV1 vaccine and CTLA-4 blockade. This may have translated into clinical benefit, encouraging the combination of UV1 vaccination with standard of care treatment regimes containing ipilimumab/CTLA-4 blocking antibodies.
Ipilimumab is a monoclonal antibody that inhibits CTLA-4, permitting rapid expansion of T cells primed by antigen presenting cells (1) and was the first treatment to show a survival benefit in metastatic melanoma (2). The effect depends on a pre-existing immune response recognizing the tumor (1). Clinical benefit from ipilimumab is associated with high tumor mutational burden (3) (TMB) and a high number of predicted neoantigens (4, 5). Hence, priming anti-tumor immune responses by therapeutic cancer vaccines with tumor-related antigens before or during treatment may improve outcomes with checkpoint inhibitors (6).
However, a landmark study found no clinical benefit of combining ipilimumab with a cancer vaccine targeting gp100 in melanoma patients (2), discouraging further clinical trials of such combinations. As the gp100 vaccine was composed of a short synthetic peptide designed to elicit CD8 T cell responses, and ipilimumab primarily affects the expansion of CD4 Th cell responses (7), we decided to test the effect of ipilimumab in the context of a peptide vaccine comprising long peptides with CD4 epitopes. Furthermore, the gp100 vaccine regimen differed from the UV1 vaccination in the use of adjuvant. In the landmark study, Incomplete Freund’s Adjuvant (IFA) was used, whereby an antigen depot is created at the site of vaccination, resulting in trapping of vaccine-specific T cells at the injection site as shown in an animal model (8). In the current trial, we used GM-CSF as an adjuvant and compensated for the lack of depot effect by more frequent vaccinations.
UV1 is a therapeutic cancer vaccine, consisting of three synthetically produced long peptides, primarily inducing CD4+ T helper type 1 (Th1) cells, targeting human telomerase reverse transcriptase (hTERT). Telomerase is expressed in cancer cells at every stage of tumor evolution, from the cancer stem cell to circulating tumor cells and implicated in human cell immortalization and cancer cell pathogenesis (9), proposing a unique cancer antigen as a basis for immunotherapy (10, 11). Based on data from long-term cancer survivors treated with an unrelated first-generation hTERT vaccine, three novel long hTERT peptides were selected for the next generation vaccine, UV1. Immune responses to these peptides were associated with clinical benefit and strong Th1 responses (i.e. secretion of interferon-γ, tumor necrosis factor-α, and IL-2) (12, 13). The UV1 peptides are predicted to contain multiple HLA epitopes (12, 13), providing a potential universal vaccine independent of prior selection based on HLA-typing. UV1 has been investigated in clinical phase I trials in metastatic prostate cancer (14) and NSCLC (15). The scientific rationale for combining UV1 with ipilimumab is based on the potential of the vaccine to generate de novo immune responses in cancer patients, thus, broadening the anti-tumor repertoire in patients. Secondly, eliminating the negative effect CTLA-4 has on vaccine-induced T cells, ipilimumab may unleash the true clinical potential of a vaccine (16). Furthermore, ipilimumab reduces immunosuppression in the tumor microenvironment by blocking CTLA-4 on T regulatory cells (1). This phase I/IIa trial explores the potential synergistic effect of CTLA-4 blockade and hTERT vaccination, allowing for unchecked expansion of hTERT-specific T cell clones, in HLA-unselected patients with metastatic malignant melanoma.
Patients and Methods
Patients aged ≥ 18 years with a histologically confirmed diagnosis of unresectable stage III/IV cutaneous malignant melanoma, Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, and adequate renal, hepatic and hematological function were eligible for inclusion. Any previous treatment was accepted. Exclusion criteria included active brain metastases, history of autoimmune disease, splenic surgery or irradiation, allogeneic stem cell transplantation, known hypersensitivity to investigational products, positive serologic tests for HIV, syphilis, hepatitis B, or hepatitis C, uncontrolled infectious disease, pregnancy and breastfeeding. All patients have provided written informed consent. Recruitment was planned for 20 participants. The trial was conducted in accordance with the ethical principles of the Declaration of Helsinki and the International Conference on Harmonization of Good Clinical Practice and approved by an independent ethics committee and the appropriate national and institutional review boards.
This was an open-label, single-armed, single-center phase I/IIa clinical trial [NCT02275416]. The primary objective was to investigate the safety of combining UV1 with ipilimumab in patients with unresectable metastatic melanoma. Secondary objectives were to assess immune responses to UV1 peptides, overall response rate (ORR), and overall survival (OS) and progression free survival (PFS).
UV1 (Ultimovacs ASA, Oslo, Norway) consists of three peptides, one 30-mer (p719-20) and two 15-mers (p725 and p728) in equimolar amounts. UV1 was produced as a sterile aqueous solution of drug substances, stored (lyophilized) at minus 20°C (+/- 5°C) and reconstituted in water for injection and stored at 2-8°C for use within 6 hours.
UV1 vaccines of 300 µg doses were administered as intradermal abdominal injections before and between treatments of ipilimumab, and thereafter every fourth week up to 28 weeks, and at week 36 and 48 (Supplementary Figure S1) unless clinical deterioration or unacceptable toxicity was encountered. Adjuvant GM-CSF (sargramostim 75 µg) in the form of preservative-free powder (lyophilized Leukine, Sanofi Aventis, Bridgewater, NJ, US) was reconstituted with water and injected intradermally at the same site 10-15 minutes prior to UV1. Ipilimumab (3 mg/kg) was administered every 3 weeks for a total of 4 doses as labeled. Trial drugs were handled by the hospital pharmacy according to standard procedures.
Safety was evaluated by physical examination and blood sampling at each treatment visit and 30 days after administration of the last dose of UV1. Adverse events (AEs) were assessed according to the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) version 4.0.
Computed tomography (CT) was conducted at baseline, week 12, 16, and 24 after the first dose of ipilimumab, and then every 3 months until disease progression. Tumor response was evaluated using RECIST v1.1 (17). OS was defined as the time from treatment initiation to death, and PFS as the time from treatment initiation to objective tumor progression or death. Survival was censored on December 1, 2020.
Peripheral blood mononuclear cells (PBMCs, 50 mL in acid citrate dextrose tubes) were obtained from peripheral blood derived at baseline, 2, 6, and 10 weeks after the first vaccine, and then, every 4 weeks. The UV1-specific proliferative response was determined using two vials of thawed PBMCs per time point as described previously (14). PBMCs were stimulated with UV1 vaccine peptides 725 (hTERT 691-705), 719-20 (hTERT 660-689), and 728 (hTERT 651-665) (Bachem AG, Switzerland) at a concentration 10 µM for each peptide. On day 12, cells were re-stimulated with peptide and tested for proliferation by 3H-thymidine incorporation assays as described previously (14). The stimulation index (SI) was calculated using mean counts of wells containing T cells and irradiated antigen presenting cells (APCs) loaded with UV1 peptide divided by mean counts of wells without peptide. An SI ≥ 3 was considered as a positive response. Blood was analyzed for the presence of IgE specific for GM-CSF and the UV1 peptides using an enzyme-linked immunosorbent assay (ELISA)-based in-house method described in Supplementary Figure S2. If cell numbers were sufficient, IFN-γ ELISPOT assays were performed with pre-stimulated PBMCs from the cultures set up for proliferation as previously described (14).
HLA genotyping was performed retrospectively for each patient by Prolmmune Ltd Tissue Typing Service, using Tier 1 Typing by PCR-sequence specific oligonucleotides (PCR-SSOP) to resolve major allele groups to 4 digits with some degeneracy (e.g. HLA-A*23:01/03/05/06).
Estimation of Tumor Mutational Burden (TMB)
Biopsies were harvested at baseline and week 12. 20 mg of the biopsy was disrupted on a TissueLyser LT followed by DNA extraction using AllPrep DNA/RNA/miRNA Universal kit on the Qiacube (Qiagen). Whole-exome sequencing was performed on all available biopsies and analyzed for TMB.
Exome library preparation was conducted with 1 ug DNA as starting material and using the Agilent AllExome v5 kit, according to the vendor´s protocol. Libraries were sequenced paired-end (2x150 bp), generating approximately 90 M PE reads per tumor and 40 M PE reads per normal, using SBS chemistry on a HiSeq4000 system. Variant calling was performed essentially as described previously (18) (Supplementary Methods). TMB was considered low at (1-5 mutations/Mb), intermediate at (6-19 mutations/Mb) and high at (≥20 mutations/Mb).
Patient Characteristics and Treatment
Patients were recruited between January and October 2015. Inclusion was terminated after twelve of the planned 20 patients were enrolled, as PD-1 inhibitors replaced ipilimumab as standard first-line treatment for metastatic melanoma (November 2015). Patient baseline characteristics are described in Table 1. The median age was 57 (44-74) years. All, but one patient, were ECOG 0. Five were female (42%) and seven male (58%). Three patients (25%) were M1a, two M1b (17%), six M1c (50%) and one M1d (8%) according to AJCC 8th Ed. Six patients (50%) had elevated LDH. Three patients (25%) were BRAF V600E mutation positive and nine (75%) mutation negative. Eight patients were treatment naïve and four patients had received one previous line of treatment, including two patients who received vemurafenib and two patients who received dacarbazine. No patients had prior immunotherapy.
A mean of 5.5 UV1 vaccinations (3-9) and 3.2 (1-4) courses of ipilimumab were administered (Supplementary Table S1). Due to a safety concern in a concurrent UV1 trial in metastatic hormone-naive prostate cancer (14), vaccination was temporarily interrupted in October 2015, but did not affect ipilimumab treatment. As an Independent Data Monitoring Committee deemed further treatment safe, vaccination was continued. However, the Norwegian Medicines Agency required a substantial protocol amendment, and to comply, vaccination was again stopped November 2015. At the time of protocol amendment approval (March 2016), no further vaccinations were scheduled.
Safety was assessed for all patients. Treatment was generally well tolerated, with most AEs being grade 1-2 (Table 2). 95 adverse events were reported, of which 78 were considered related. The most commonly reported treatment-related toxicities were diarrhea, injection site reaction, pruritus, rash, nausea and fatigue. Five patients experienced treatment-related grade 3 toxicity; diarrhea, colitis and rectal hemorrhage, nausea, hypersensitivity, and hypophysitis and dehydration, respectively. No grade 4-5 AEs were reported. Ten serious adverse events (SAEs) were reported in five patients and included hypophysitis, colitis, diarrhea, duodenitis, rectal hemorrhage, dehydration, hypersensitivity, dermatitis, dysarthria, and wound infection. Dysarthria and wound infection were considered unrelated to treatment, whereas the remaining were considered related. Duodenitis, wound infection and dermatitis were classified as grade 2; otherwise, SAEs were classified as grade 3.
One patient experienced a hypersensitivity reaction following the ninth vaccination and completion of four courses of ipilimumab. Symptoms resolved with dexchlorpheniramine 5 mg IV, hydrocortisone 100 mg IV, and salbutamol 2.5 mg inhaled. Further UV1 vaccination in the patient was withdrawn. However, retrospective analyses of blood from this patient revealed increased levels of GM-CSF-specific IgE, but not IgE specific for UV1 peptides (Supplementary Figure S2). Ipilimumab was withdrawn due to toxicity in three patients experiencing hypophysitis (one) and colitis (two). One patient skipped the second course of ipilimumab due to dysarthria considered unrelated to treatment. Otherwise, toxicity did not cause treatment interruption in patients.
Nine patients were evaluable for tumor response according to RECIST 1.1. As best overall response (BOR), one patient achieved a complete response (CR), three a partial response (PR), two stable disease (SD), and three progressive disease (PD) as illustrated in Figure 1. Patients, who were not evaluable according to RECIST 1.1, progressed clinically. Thus, the ORR was 33%. Five patients stopped treatment due to PD. One patient has an ongoing CR as of December 1, 2020 (Figure 2). All patients evaluable for tumor response were immune responders.
Figure 1 Tumor growth by subject. Spider plot illustrating changes in target lesions from baseline in patients evaluable by RECIST v.1.1 (N=9). *Patient N03 was non-evaluable at 12 weeks PR, partial response; PD, progressive disease.
Figure 2 Efficacy assessment by subject censored on December 1 2020. Swimmers plot depicting individual patients as lines, illustrating duration of overall survival in months. Blue and grey colors indicate alive and deceased patients, respectively (N=12). Responses and new systemic treatment are indicated by designated symbols. Patient N06 received locoregional chemotherapy and surgery, but no further systemic treatment.
Median follow-up was 61.0 months. Three patients died within one year of study entry. No deaths were attributed to study treatment. Median OS was not reached. OS was 75% at 1 and 2 years, 67% at 3 years and 50% at 5 years. Median PFS was 6.7 months. PFS was 33% at 1 year and 25% at 2 years.
Eleven patients were evaluable for immune response. One patient was judged non-evaluable due to the lack of post-vaccination samples. UV1-specific T cell responses were recorded in ten out of eleven evaluable patients (91%) (Figure 3A and Supplementary Figure S3). The patient who did not demonstrate an immune response had only one post-vaccination sample at four weeks. All immune responders demonstrated an immune response to the UV1 peptide mix, with a median SI of 23.8 (7.8-60). Two patients exhibited spontaneous, pre-vaccine responses to UV1 peptides and developed a more pronounced and/or broader immune response during treatment, while the remaining developed de-novo responses elicited by vaccination. Six patients exhibited UV1-specific immune responses after four weeks and ten after twelve weeks (Figure 3B). When analyzing immune responses to individual peptides, different patterns were seen, exemplified by proliferation responses in four patients (Figure 4). In the same patients, cell numbers were also sufficient to perform IFN-γ ELISPOT assays at certain time points, largely demonstrating a correlation between the UV1-specific proliferative response and IFN- γ production (Supplementary Figure S4). Unfortunately, there was insufficient patient material to separate CD4 and CD8 T cells for assessment by proliferation and ELISPOT assays. However, T cell cloning of responding cells from one patient (results not shown) and intracellular cytokine staining assessed by flow cytometry in the lung cancer UV1 vaccine study (15) confirmed that the majority of responding T cells were CD4+.
Figure 3 Summary of detected pre- and post-vaccination T cell responses against UV1 peptides. (A) T cell proliferation against UV1 peptides in pre- and post-vaccination blood samples from patients evaluable for immune response, depicting the strongest post-vaccination T cell response detected against the hTERT peptide mix for each patient. (N=11). Proliferation was measured in response to peptide-loaded PBMC by 3H-thymidine incorporation. A stimulation index (SI) of >3 was considered as an immune response. The dotted line indicates SI=3. (B) Cumulative percentage of evaluable patients exhibiting immune responses to UV1 peptides. Immune responses at baseline were detected in two patients.
Figure 4 UV1-specific proliferation by T cells at different time points post-vaccination. UV1 peptide-specific proliferation was measured (counts per minute, cpm) at several sampling time points and representative examples are shown for patient N02 (A), patient N07 (B), patient N09 (C) and patient N11 (D). Proliferation was measured in response to peptide-loaded PBMC by 3H-thymidine incorporation. A 3-fold increase in proliferation compared to non-peptide control (T+ APC) was considered as an immune response. Superantigen SEC-3 stimulation was included as a positive control. Dotted line indicates cut-off for positive response, measurements until last positive time point is shown.
Retrospective analyses showed a wide repertoire of HLA alleles in the study population, and immune responses were seen across different HLA types (Supplementary Table S2).
Biopsies were harvested from nine patients at baseline and from four patients at week 12. Baseline TMB is reported in Table 1. Median TMB was 9 mutations/Mb. Two patients were considered to have a low TMB, three patients intermediate, and four patients high. There was no obvious correlation between baseline TMB and clinical response (TMB high vs. TMB non-high). Of the four patients with matching biopsies, two patients achieved PR and two PD as BOR. The two responders experienced considerable post-treatment reductions in TMB, of 9 to 1 mutations/Mb and 39 to 11 mutations/Mb, respectively, whereas the two patients who progressed demonstrated no considerable change.
Patient baseline characteristics in this trial indicate that the study population is representative and comparable to other reports on ipilimumab in metastatic melanoma (2, 19, 20). This phase II trial demonstrates that combining UV1 and ipilimumab is safe with mainly low-grade toxicity including diarrhea, nausea, injection site reaction, pruritus, rash, and fatigue. With the exception of injection site reaction, these are well-known side effects of ipilimumab (2, 19, 20). Low-grade gastrointestinal and skin toxicities were slightly more frequently encountered than in ipilimumab monotherapy. Injection site reactions in the current trial were more commonly reported than in UV1 monotherapy (14), maybe reflecting enhanced immunity. Otherwise, we found no increased toxicity combining ipilimumab with UV1.
One patient experienced a hypersensitivity reaction with bronchospasm after the ninth UV1 vaccination with an increase in IgE towards GM-CSF, but not against UV1 peptides. Hypersensitivity is a rare, but labeled event for sargramostim, and thus, hypersensitivity experienced by this patient was more likely a reaction to the adjuvant rather than to the vaccine.
As telomerase is expressed in hematopoietic cells, skin, and bowel, on-target, off-tumor reactivity constitutes a theoretical side effect. We found no evidence for a shift in side effect profile by targeting telomerase during ipilimumab treatment in this trial. No grade 3-4 hematological toxicities were observed, in line with findings from a randomized phase III trial combining hTERT GV1001 vaccination with chemotherapy in pancreatic cancer (21).
Immune responses in this trial appeared more frequently and rapidly than in patients with prostate cancer (14) and NSCLC (15) receiving UV1 monotherapy. Two patients had spontaneous pre-vaccine immune responses to UV1 peptides. These patients were alive at the time of data censoring and achieved PR and SD as BOR, respectively, indicating a possible clinical advantage of pre-immunity, as has been described in previous reports on melanoma (22) and NSCLC (23). Due to the restricted number of patients and high proportion of immune responders in this trial, a correlation between clinical response and immune responses to specific UV1 peptides could not be established.
As shown previously UV1, peptides are highly immunogenic across different HLA allele types in a Caucasian population (14). This is probably due to a sufficient number of epitopes, ensuring broad population coverage and efficacy of the UV1 vaccine by allowing APCs to select the optimal epitopes for presentation in individual patients. This observation together with the fact that hTERT is expressed in nearly all cancers, supports the universal potential of UV1.
CD4 T cells have been recognized as crucial for effective immunotherapy (7), mainly due to their capacity to enhance cytotoxic T cell responses and re-program the tumor microenvironment. They are also responsible for generating a broad reactivity to new hTERT epitopes (intramolecular epitope spreading) following telomerase peptide vaccination (13). Moreover, ipilimumab has been shown to induce expansion of Th1-like CD4 effector T cells in addition to its effect on exhausted CD8 T cells (7), proposing a suitable companion for a long peptide vaccine inducing CD4 T cell responses. This is a distinct mechanism of CTLA-4 blockade-induced immune response compared to anti-PD-1, where the expansion of tumor-infiltrating exhausted CD8 T cells is believed to be the main mechanism of action (7).
The early-onset and frequent immune responses observed in this trial suggest an effect of CTLA-4 inhibition on the fast expansion of vaccine-specific T cells. This interpretation is strongly supported by data from an animal model investigating gp100 vaccine combined with CTLA-4 checkpoint blockade (24). This report compares different vaccine formulations and elucidates the mechanisms behind reduced tumor control when IFA was used, involving trapping, functional impairment and subsequent destruction of effector T cells at antigen depots with few T cells reaching the tumor (24). Moreover, IFA appeared to create a T cell graveyard at the injection site, where the T cells actually managing to escape apoptosis rapidly became exhausted and had a poor memory formation (25). Thus, this mechanism has been suggested as a possible explanation for the lack of synergy between gp100 vaccine and ipilimumab in the landmark study by Hodi et al. were IFA was used as an adjuvant (2, 24). Interestingly, Hailemichael et al. demonstrated that non-persistent vaccine formulations can reverse these negative effects of depot formulations and act synergistically with CTLA-4 and PD-L1 blockade (24). Data from the current trial extends these results to the clinical setting and points the way to further clinical trials involving combinations of the UV1 vaccine and immune checkpoint blockade.
The distribution of TMB is representative and consistent with what has previously described in patients with metastatic melanoma (26). Thus, the favorable outcomes reported here, as compared to ipilimumab monotherapy, cannot alone be ascribed to a selected population with higher mutation counts conferring improved responses to ipilimumab. The post-treatment reduction in TMB seen in responders is in line with patients treated with PD-1 inhibitors (27) and may reflect killing of tumor cells expressing mutations by neoantigen-specific T cells. We therefore investigated baseline biopsies for the presence of acquired mutations in 29 genes known to be involved in antigen processing and presentation providing immune evasion and primary checkpoint inhibitor resistance (28). Tumors from both responders and non-responders had single nucleotide variants in these genes, and we found no clear correlation between the number or types of genes mutated and response to therapy (Supplementary Figure S5). Notably, Li et al. recently identified an association between a higher TMB and TERT mutations, conferring an improved prognosis in patients with metastatic melanoma receiving CTLA-4 blockade, and thus, for combined targeting of telomerase and CTLA-4 in these patients (29).
In this trial, we observed an ORR of 33% of patients, favorable to ipilimumab monotherapy (2, 19, 20). Caution must be taken in interpreting these results, as this trial was not designed to assess the potential superiority as compared to ipilimumab monotherapy, and due to limitations in the number of patients included. As illustrated in Figure 1, and previously described for ipilimumab, different patterns of response were observed, including slow onset responses and pseudo-progression. The latter may reflect a slow onset clinical response, reflecting the time it takes for a clinical immune response to evolve, the appearance of a tumor immune infiltrate, edema or an actual increase in tumor burden followed by response (30). One patient who achieved a PR had previously received BRAF-targeted therapy, and one patient, who had previously received dacarbazine, obtained SD, indicating clinical benefits also in second-line treatment.
Median PFS is markedly longer in this trial and the proportion of patients alive at five years substantially higher, than reported previously on ipilimumab monotherapy (2, 19, 20, 31, 32). Although not directly comparable, in an ipilimumab monotherapy phase IV trial at our hospital [NCT02068196], with similar inclusion criteria, 5-year OS was 28% (unpublished). We are aware of the small numbers of patients in the current trial; however, baseline data suggests a representative population.
Figure 2 summarizes subsequent treatment after progression on study drugs. Notably, seven patients received PD-1 inhibitors after progression. PD-1 checkpoint blockade and BRAF- inhibition have shown OS benefits in metastatic melanoma, and thus, subsequent treatment has influenced patient OS in this trial. However, in a phase II trial reporting on the sequential use of nivolumab after ipilimumab in a similar population, 1-year OS was 54% and the median OS was 16.9 months (33). In comparison, in the current trial, 1-year OS was 75% and the median OS was not reached after 61.0 months follow-up. Moreover, no significant difference in OS was observed in patients with BRAF mutated metastatic melanoma that were randomized between nivolumab and investigator’s choice chemotherapy and had progressed after ipilimumab and BRAF-targeted treatment (34). These reports suggest that sequential checkpoint blockade alone cannot explain OS benefits in this trial. However, the UV1-induced immune responses may persist long after end of treatment, long-term survival may be the result of a secondary effect of UV1-specific T cells being released from the PD-1/PD-L1 checkpoint by PD-1 inhibitors.
In conclusion, safety was established, and thus, the primary endpoint was met. Clinical benefit and immune responses observed in this trial are compatible with the known mechanisms of action of the two drugs, suggesting that UV1 and ipilimumab combine favorably by both enabling the clinical potential of the vaccine and providing a broader anti-tumor immune response for an improved effect of ipilimumab. This provides a rationale for combining UV1 with ipilimumab and nivolumab, a current first-line treatment of advanced melanoma. A phase I multi-center trial investigating UV1 in combination with pembrolizumab [NCT03538314] is now fully recruited, and an international randomized trial [NCT04382664] investigating UV1 and ipilimumab combined with nivolumab, versus ipilimumab combined with nivolumab is ongoing.
Data Availability Statement
The datasets presented in this article are available via the European Genome-Phenome Archive (https://ega-archive.org/) EGA accession number EGAS00001005253. Requests to access the datasets should be directed to firstname.lastname@example.org.
The studies involving human participants were reviewed and approved by Regional Ethical Committee South East. The patients/participants provided their written informed consent to participate in this study.
Conception or design of the work: EMI, SA, TG, GG. Data collection: EA, PB, MN, TG. Data analysis and interpretation: EA, EMI, EE, WR, K-MH, DV, SN, EH, TG, GG. Drafting the article: EA, EMI, EE, WR, TG, GG. All authors contributed to the article and approved the submitted version.
This work was supported by Ultimovacs ASA, the Norwegian Ministry of Health and Care Services, and the Norwegian Cancer Society [grant number 2220815]. Ultimovacs was involved in the study design of the trial.
Conflict of Interest
EMI and GG are inventors of a UV1 vaccine patent. EI, WR, GG and SA are shareholders in Ultimovacs ASA. EE, WR, SA and GG are employees of Ultimovacs ASA. MN has received personal honoraria from BMS for lectures.
The authors declare that this study received funding from Ultimovacs ASA. The funder had the following involvement with the study: study design of the trial.
We thank patients and their families, Ann Helen Torstveit, Ellen Støver, Cathrine Hoelstad and Signe Øien Fretland who were instrumental in conducting this trial, and Grete Berntsen and Hedvig Vidarsdotter Juul for excellent assistance with immunomonitoring.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2021.663865/full#supplementary-material
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Keywords: telomerase (hTERT), peptide vaccine immunotherapy, ipilimumab, melanoma, phase I/IIa studies
Citation: Aamdal E, Inderberg EM, Ellingsen EB, Rasch W, Brunsvig PF, Aamdal S, Heintz K-M, Vodák D, Nakken S, Hovig E, Nyakas M, Guren TK and Gaudernack G (2021) Combining a Universal Telomerase Based Cancer Vaccine With Ipilimumab in Patients With Metastatic Melanoma - Five-Year Follow Up of a Phase I/IIa Trial. Front. Immunol. 12:663865. doi: 10.3389/fimmu.2021.663865
Received: 03 February 2021; Accepted: 30 March 2021;
Published: 11 May 2021.
Edited by:Khashayarsha Khazaie, Mayo Clinic College of Medicine and Science, United States
Reviewed by:Hans-Georg --- Rammensee, University of Tübingen, Germany
Jacques Medioni, Université de Paris, France
Copyright © 2021 Aamdal, Inderberg, Ellingsen, Rasch, Brunsvig, Aamdal, Heintz, Vodák, Nakken, Hovig, Nyakas, Guren and Gaudernack. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Elin Aamdal, email@example.com