Clinical study of a survivin long peptide vaccine (SurVaxM) in patients with recurrent malignant glioma
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- Fenstermaker, R.A., Ciesielski, M.J., Qiu, J. et al. Cancer Immunol Immunother (2016) 65: 1339. doi:10.1007/s00262-016-1890-x
Survivin is an anti-apoptotic protein that is highly expressed in many cancers, including malignant gliomas. Preclinical studies established that the conjugated survivin peptide mimic SurVaxM (SVN53-67/M57-KLH) could stimulate an anti-tumor immune response against murine glioma in vivo, as well as human glioma cells ex vivo. The current clinical study was conducted to test safety, immunogenicity and clinical effects of the vaccine. Recurrent malignant glioma patients whose tumors were survivin-positive, and who had either HLA-A*02 or HLA-A*03 MHC class I allele-positivity, were given subcutaneous injections of SurVaxM (500 μg) in Montanide ISA 51 with sargramostim (100 μg) at 2-week intervals. SurVaxM was well tolerated with mostly grade one adverse events (AE) and no serious adverse events (SAE) attributable to the study drug. Six patients experienced local injection site reactions; three patients reported fatigue (grades 1 and 2), and 2 patients experienced myalgia (grade 1). Six of eight immunologically evaluable patients developed both cellular and humoral immune responses to vaccine. The vaccine also stimulated HLA-A*02, HLA-A*03 and HLA-A*24 restricted T cell responses. Three patients maintained a partial clinical response or stable disease for more than 6 months. Median progression-free survival was 17.6 weeks, and median overall survival was 86.6 weeks from study entry with seven of nine patients surviving more than 12 months.
KeywordsApoptosis Glioma Immunotherapy Peptide Survivin Vaccine
Carboxyfluorescein succinimidyl ester
Common terminology criteria for adverse events
Cytotoxic T lymphocytes
Granulocyte macrophage-colony stimulating factor, sargramostim
Hank’s balanced salt solution
Inhibitor of apoptosis protein
Keyhole limpet hemocyanin
Karnofsky performance status
Progression free survival
Roswell Park Cancer Institute
Serious adverse event
The Cancer Genome Atlas
Survivin (BIRC5) is a member of the inhibitor of apoptosis protein (IAP) family [1, 2]. Survivin expression in tumors is associated with a high rate of disease recurrence and resistance to chemotherapy, and it confers a significant survival advantage to tumor cells . Its presence in gliomas and other tumors is reportedly associated with a poor prognosis . It is expressed in all four subtypes of glioblastoma defined by The Cancer Genome Atlas (TCGA) project, including: classical, mesenchymal, neural and proneural variants .
Although expressed during fetal development , survivin is infrequently detected in the normal tissues of adult organisms . Thus, the molecule represents a potential target for cancer immunotherapy. One immunohistochemical study of gliomas demonstrated that 29 of 29 glioma specimens (WHO grades II-IV), but not normal brain tissue, contain survivin-positive cells . The mean percentage of cells detectable by immunohistochemical methods in each specimen was 70.0 % in grade II (low grade) gliomas, 81.3 % in grade III (anaplastic) gliomas and 85.0 % in grade IV gliomas (glioblastoma). Survivin is also present in association with plasma-derived exosomes of glioma patients in which its action remains to be defined .
As a largely intracellular protein, survivin is degraded by the proteasome and resulting epitopes are presented on the surface of tumor cells by MHC class I molecules. Accordingly, survivin-specific cytotoxic T lymphocytes (CTL) have been identified in some cancer patients [9, 10]. In addition to T cell-mediated immunity, many cancer patients develop humoral immune responses to survivin with anti-survivin antibodies detectable in serum . Therefore, survivin is potentially immunogenic and such responses as these could provide the basis for induction of therapeutic anti-tumor immunity in cancer patients in whom the immune system is already primed to recognize survivin.
SurVaxM (SVN53-67/M57-KLH) contains a synthetic long peptide mimic that spans amino acids 53 through 67 of the human survivin protein sequence . The amino acid alteration in this peptide (M57) leads to enhanced binding of the core survivin epitope to HLA-A*0201 molecules . The peptide is conjugated to keyhole limpet hemocyanin (KLH), which acts as a vaccine adjuvant. The long peptide also contains multiple MHC class I epitopes that are presentable by other HLA molecules. In addition, the long peptide is able to stimulate specific CD4+ cytokine support [11, 12]. The presence of MHC class II-restricted CD4+ T cells that are specific for tumor-associated antigens has been recognized as an important element for providing helper factors essential for eliciting and sustaining cytotoxic CD8+ responses against tumors [13, 14].
Patients and methods
This clinical study (clinicaltrials.gov identifier NCT01250470) was conducted in patients with HLA-A*02 and HLA-A*03 haplotypes who had histologically confirmed survivin-positive malignant gliomas that had recurred or progressed following standard therapy, including surgery, fractionated radiation therapy and chemotherapy with temozolomide. It was designed to test the toxicity (primary outcome) and immunogenicity (secondary outcome) of SurVaxM in emulsion with Montanide ISA 51 and given subcutaneously with sargramostim (GM-CSF) as a dendritic cell attractant and maturant. This was a nonrandomized, single-institution, clinical trial designed to assess a fixed dose vaccine regimen. Based on pre-clinical toxicity studies, a dose level of 500 μg SurVaxM was selected for testing. A regimen of four prime-boost doses at this level was given without dose escalation. In order to test the response to extended dosing, patients that survived 6 months without disease progression or regimen-limiting toxicity were eligible to receive additional booster doses of vaccine. The use of SVN53-67/M57-KLH in this study is registered with the USFDA under IND #14674 held by Roswell Park Cancer Institute (RPCI). The composition of SVN53-67/M57-KLH (SurVaxM) has been previously described . All investigations were performed under a clinical protocol approved by the institutional review board at RPCI and in accordance with an assurance filed with and approved by the US Department of Health and Human Services. Informed consent was obtained from each subject prior to treatment.
Inclusion criteria were: age ≥18 years, histologic proof of recurrent or progressive glioblastoma, anaplastic astrocytoma, anaplastic oligodendroglioma or anaplastic mixed glioma following failure of standard therapy, Karnofsky performance status (KPS) ≥70, HLA-A*02 or HLA-A*03 haplotype, survivin expression by tumor cells documented by immunohistochemistry, no systemic infection or ongoing antibiotic therapy, white blood cell count ≥3000/mm3, platelets ≥100,000/mm3, hemoglobin ≥10.0 g/dL, AST(SGOT)/ALT(SGPT) <2.5 × ULN, total bilirubin ≤2.0 mg/dL and serum creatinine ≤1.5× ULN. Patients with potential for child-bearing were required to agree to the use of acceptable contraceptive methods during treatment and for 3 months after receiving the last dose of vaccine, patients who had had recent cranial surgery were eligible for inclusion, but the vaccine could not be administered prior to the 14th post-operative day.
Nine patients were treated with SurVaxM (500 μg) in emulsion with Montanide ISA 51 with sargramostim (100 μg) every 2 weeks for a total of four doses per patient (prime-boost phase). All patients in each group were followed for at least 6 weeks before the next group of three patients could begin treatment to limit the total number of individuals exposed to possible toxicity. The dose of vaccine was not escalated in an individual patient or between cohorts. Patients were followed clinically every 2 weeks for the first 8 weeks and then monthly until tumor progression or death. Patients were assessed for regimen-limiting toxicity (RLT) using CTCAEv4.0 criteria (see definition of RLT below). Clinical responses were ascertained by neurologic exams on schedule and from serial MRI brain scans. Patients who survived 6 months without tumor progression, RLT or serious adverse event (SAE) were eligible to receive additional doses of the vaccine every 3 months (booster phase).
Evaluation during study
The primary goal of this study was to assess the safety, tolerability and toxicity of the survivin peptide mimic vaccine regimen. A secondary goal was to measure immune responses to the vaccine, including anti-survivin antibody production, survivin-specific multimer immunoreactivity and IFNγ mRNA production following vaccination. Tertiary goals were to measure tumor progression after vaccination, identify any apparent treatment responses and measure survival. Safety was assessed by physical and neurological examinations and laboratory studies.
MRI brain scans were performed serially, and established criteria were used to determine radiographic response for those with measureable disease. Response categories included: (1) complete response (CR), disappearance of all enhancing tumor on consecutive MRI scans at least 1 month apart, off steroids, and neurologically stable or improved; (2) partial response (PR), 50 % reduction in size of enhancing tumor on consecutive MRI scans at least 1 month apart, steroids stable or reduced, and neurologically stable or improved; (3) progressive disease (PD), >25 % increase in size of enhancing tumor or any new tumor on MRI scans, or neurologically worse, and steroids stable or increased; and (4) stable disease (SD), all other situations. The measure of tumor size is the largest cross-sectional diameter multiplied by the largest diameter perpendicular to it. Progression-free survival (PFS) is defined as the duration of time from study entry to progression on MRI or death.
Patients who received at least one dose of vaccine were considered evaluable for the purpose of determining toxicity. Patients who received ≥2 doses of vaccine were deemed evaluable for immunological response; however, those who did not receive ≥2 doses were not replaced (patient #4). Patients who received ≥3 doses of vaccine and had an MRI scan 8 weeks following initiation of therapy were considered evaluable for clinical response. Patients who were unevaluable for clinical response were not replaced (patient #4).
NCI common terminology criteria for adverse events (CTCAEv4.0) were used to evaluate toxicity. Toxicity was considered to be an adverse event possibly, probably or definitely related to treatment. The maximum grade of toxicity for each category of interest was recorded for each patient, and the summary results were tabulated by category and grade. Regimen-limiting toxicities (RLT) were defined to include: (1) any grade 3 or greater toxicity possibly, probably or definitely related to the vaccine, (2) any grade 2 or greater autoimmune disorder, (3) any grade 2 or greater allergic reaction and (4) any peptide vaccine dosing delay >2 weeks.
All patients were followed to ascertain both progression-free survival (PFS) and median overall survival (OS).
Immunohistochemical detection of survivin was performed using a Dako Omnis autostainer (Dako North America, Inc. Carpinteria, CA) with rabbit monoclonal survivin antibody clone EP119 (Bio SB, Santa Barbara, CA). Additional antibodies included: CD4 (4B12, Dako); CD8 (C8/144B, Dako); CD20 (L26, Dako); PD-L1/CD274 (SP142, Spring Bioscience). Stained specimens were viewed by the neuropathologist, co-investigator (JQ), and survivin expression in the nucleus and cytoplasm was determined to be present or absent.
Serum antibody measurements
Patient serum was collected and stored at −80 °C. Serial dilutions of clarified serum were applied to unconjugated survivin peptide, free KLH and random peptide (20 µg/ml, 1 µg/well) on pre-coated ELISA plates (Flat Bottom, Nunc) in triplicate. Samples were incubated at 4 °C overnight and washed (PBS, 1 % BSA). HRP-conjugated anti-human IgG detection antibody (Bio-Rad) was added for 1 h at 25 °C. Plates were washed four times, and TMB colorimetric solution (Biolegend) was added at room temperature and developed for 15 min and read on a Bio-Rad automated plate reader at 450 nm.
Peripheral blood mononuclear cells were isolated within 3 h from blood samples using Ficoll separation technique. Heparinized blood was diluted (1:1) with Hank’s balanced salt solution (HBSS) (Mediatech, Cat#: 21-023-CV). Blood/HBSS diluent was layered on top of lymphocyte separation medium (LSM; Mediatech, Cat#: 25-072-CV) in 50-ml conical tubes. Tubes were centrifuged at 400×g for 30 min. PBMC layer was centrifuged at 600×g for 10 min. Cell pellets were re-suspended in 5 ml of CTL wash solution (Cat#: CTLW010)/RPMI (Mediatech, Cat#: 10-040-CV) solution. The pooled sample was centrifuged at 500×g for 5 min, and the pellet was re-suspended in freezing media (10 % DMSO/90 % fetal bovine serum) and transferred to liquid nitrogen storage.
Custom-designed multimers included the following: MHC Dextramer-PE (Immudex, Copenhagen, Denmark) to A*0201:QMFFCFKEL; A*0301:AQMFFCFK; A*0301:DLAQMFFCFK; A*0301:LAQMFFCFK; as well as iTag-PE Tetramer (BD Coulter) to A*0201:AQMFFCFKEL; and A*24:DLAQMFFCF. Control represents results with a nonsense Dextramer (Immudex). Patient PBMC were washed in PBS and re-suspended at a concentration of 1 × 106 cells/ml. 50 µl of sample was added to each well of a round bottom 96 well plate (Costar), and 5 µl of FcR Block reagent was incubated with cells at room temperature for 10 min. 10 µl of MHC Dextramer or iTag-PE Tetramer was added. The plate was vortexed and incubated for 20 min at room temperature in the dark. Following incubation, 10 µl anti-CD8-FITC (500 µg/ml clone T8; BD Coulter) was added, mixed and incubated for 30 min at room temperature. Cells were washed and re-suspended in PBS-fluorofix buffer (0.5 % paraformaldehyde). Data acquisition was obtained using a Fortessa flow cytometer running FACSDiva software. Data analysis was performed using FCS Express software. Results are based upon gating of CD8+ T cells and indicate the percent of cells positively labeled with specific tetramer.
T cell proliferation
PBMC were tested for peptide-specific proliferation as previously described . PBMC were labeled with carboxyfluorescein succinimidyl ester (CFSE) and stimulated ex vivo with SVN53-67/M57 or control peptide (100 ng/ml over 48 h). Cells were stained for CD4 or CD8 and data acquired via FACS analysis and FCS Software as described above.
CD4+ and CD8+ separation
SureBeadsTM Protein G Magnetic Beads (Cat. 161-4023, Bio-Rad Laboratories, Inc.) were incubated with either LEAF CD8a (clone RPA-T8, Cat. 301018, BioLegened) or LEAF CD4 (clone OKT4, Cat. 317404, BioLegened). The antibody-bound magnetic beads were then incubated with 1 × 105 PBMC. After bead-based CD4/CD8 separation, fluorochrome-labeled antibodies to CD8 (clone RPA-T8, FITC, Cat. 301050, BioLegend) and CD4 (clone OKT4, PE/Cy5, Cat. 317412, BioLegend) were added to remaining PBMC. The samples were acquired and analyzed by FACS as above. Analysis was based upon isolated gating of lymphocyte populations with specific CD markers as indicated. Sample purity is based upon the percent of specific cells removed from the starting population.
Cytokine mRNA isolation and quantification
Patient samples (1 × 105 PBMC) were incubated with SVN53-67/M57 peptide at several concentrations (160–1600 ng/ml) in OpTmizer CTS complete serum-free media (Gibco) overnight at 37 °C in 96 well plates. After incubation, CD4+ and CD8+ T cells were separated from total PBMC by magnetic beads. Anti-human CD4 antibody (5 µg; clone OKT4) or anti-human CD8 antibody (5 µg; clone RPA-T8) (BioLegend, San Diego, CA) was added to Protein G Magnetic SureBeads (BioRad, San Diego, CA) and incubated for 60 min at room temperature with peptide-stimulated cells. Isolated cells were collected and washed in PBS. Total RNA was isolated from separated human CD4+ and CD8+ cells using the PureLink RNA Mini Kit (Life Technologies) according to manufacturer’s instructions. RNA was reverse transcribed using Superscript Vilo Master Mix (Life Technologies). cDNA concentrations were determined using a Nanodrop 2000 Spectrophotometer (Thermo Scientific). RT-qPCR was performed using a 7900HT Fast Real-Time PCR System (Life Technologies) with Power SYBR Green PCR Master Mix (Life Technologies). Primers for IFNγ had the sequences: 5′-GCATCCAAAAGAGTGTGGAG-3′ and 5′-ATGCTCTTCGACCTCGAAAC-3′. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA was used as an internal control, and GAPDH primers had the following sequences: 5′-GGTGAAGGTCGGAGTCAACGG-3′ and 5′-GAGGTCAATGAAGGGGTCATTG-3′. Reactions containing no cDNA were included in each run. Relative cytokine mRNA expression levels were calculated by the ΔΔCt method using RQ Manager software (Applied Biosystems). All samples were run in triplicate. The level of GAPDH gene expression served as an endogenous control. Data are represented as the ratio of the target gene/GAPDH normalized to unstimulated cells. Total mRNA values were expressed relative to PBMC RNA. An unpaired t test with Welch’s correction was applied to all of the data sets.
Number of recurrences
S, R, T, S
S, R, T, S/C, B, SR
S, R, T, S
S, R, T, SR, S, B, O
S, R, T, B, SR
S, R, T, S
S, R, T
S, R, T, S
S, T, S, R, T, S, SR
Adverse events (AE) and toxicity
All nine patients were evaluable for the purposes of determining toxicity. SurVaxM demonstrated a good tolerability profile with no serious adverse events (SAE) during the prime-boost phase of up to four doses. The majority of AEs were grade one. Six of nine patients experienced at least one injection site reaction (all grade one) with localized erythema likely related to the vaccine components. Three patients reported fatigue (grades 1 or 2). Two patients experienced myalgias, probably related to the study regimen. Grade 1 lymphopenia was seen in three patients and leukopenia in three patients (grades 1 and 2). The only grade 3 AE, a seizure, was not related to the vaccine. During the extended dosing phase, one patient suffered acute renal failure (SAE) due to gabapentin toxicity with complete resolution following intravenous hydration. Renal biopsy showed no inflammatory tubular changes, immune complex deposition, glomerulonephritis or other evidence of immunologic toxicity.
T cell responses
Humoral immune responses
Cytokine production in CD4+ and CD8+ cells
CD4+ and CD8+ IFNγ mRNA levels were measured by qPCR using cells isolated by magnetic bead separation from PBMC obtained at week 12. Depletion of PBMC was confirmed to be 94 % (CD4+), and 98 % (CD8+) complete by FACS analysis (data not shown). Isolated cells were re-stimulated in culture with pooled overlapping survivin peptides. Induction of IFNγ mRNA was detected in CD8+ cells, but not in CD4+ cells (Fig. 3c). In general, IFNγ mRNA levels increased with higher peptide concentrations up to a maximum tested concentration of 1.6 µg/ml.
T cell proliferation
Tumor lymphocyte infiltrates
Radiologic response, tumor progression and survival
The longest surviving patient in this study had a low but detectable titer of anti-survivin IgG in pre-immune serum. In line with this, previous studies have revealed circulating anti-survivin antibodies in patients with colon and lung cancer [9, 16] and in glioma patients as well. Similarly, T cell reactivity against survivin has been detected in cancer patients in the absence of specific vaccination [17, 18, 19]. Therefore, wild-type survivin is at least weakly immunogenic and re-stimulation of pre-existing immunity may be one aspect of the vaccine’s action.
Clearly, pre-existing anti-survivin immune responses do not completely eliminate tumor cells. We have previously demonstrated that immunologic tolerance to survivin antigens may be broken using molecular mimicry [11, 20]. SurVaxM contains a synthetic peptide with an amino acid substitution (SVN53-67/M57) that enhances HLA-A*0201 binding acting as a molecular mimic within this contextual background [11, 15, 21]. As a result, the core epitope induces a more potent immune response in humans than the corresponding wild-type survivin peptide . The enhanced binding of SVN53-67/M57 to MHC-I molecules enables it to activate T cells that can cross-react with the wild-type tumor antigens leading to an anti-tumor response [11, 22]. Antigen modification may also aid directly in overcoming T cell tolerance since patients with non-HLA-A*02 haplotypes (i.e., HLA-A*03, HLA-A*11 and HLA-A*24) also developed CD8+ T cell responses to the vaccine in the current study.
The survivin peptide SVN53-67 contains multiple HLA-A*02 epitopes, as well as antigen-binding motifs for HLA-A*03; HLA-A*11, HLA-A*24, HLA-A*26, HLA-A*68, HLA-B*13, HLA-B*14, HLA-B*15, HLA-B*35, HLA-B*39 and HLA-B*44. We have confirmed in this clinical study that HLA-A*02, HLA-A*03 and HLA-A*24 patients generate survivin-specific humoral and cellular immune responses. In pre-clinical studies, we demonstrate that survivin peptide (SVN53-67/M57) stimulated CTL responses against autologous and allogeneic tumor cells from patients with HLA-A*2901, HLA-A*3002 haplotypes . Moreover, in one patient treated under a compassionate use exemption survivin-specific HLA-A*11-restricted CD8+ T cells were generated in high numbers (data not shown). Consequently, the peptide vaccine is immunogenic in a relatively large segment of the population.
The survivin gene transcript is processed into a number of different mRNA splice variants. All of the various species noted to date retain exon 2, which encodes the region from which the peptide sequence in SurVaxM is derived. In addition to wild-type survivin, the survivin-2B and survivin–ΔEx3 transcripts, which are translated [23, 24], should also be targeted by immune responses generated by SurVaxM.
We used anti-survivin and anti-KLH IgG levels as a potential biomarker for assessing the immune response to vaccine. Eight patients were evaluable (≥2 priming doses) for immune response. Seven had high antibody titers to the survivin vaccine peptide, and 4 had high titers to KLH. Similarly, T cell responses to survivin were seen in seven patients following vaccination. Generally, patients with minimal disease burden had stronger antibody and T cell responses, although there were too few patients to make a definitive conclusion about the role of bulk disease in systemic immunosuppression. In addition, CD8+, CD4+ and B cell infiltrates were detected in recurrent tumor tissue obtained from patients following progression on-study. In one patient with a germinal center-like structure, PD-L1 was also expressed by adjacent glioma cells, suggesting that PD-1/PD-L1 interaction in the tumor microenvironment could be important for the immune effector response to SurVaxM in some patients .
Vaccination strategies utilizing individual CD8+ T cell epitopes alone do not routinely produce significant clinical responses. It is critical to stimulate CD4+ helper T cells simultaneously to potentiate the CD8+ T cell-driven anti-tumor response [11, 15, 20, 21, 26]. Specific CD4+ T cell stimulation results in the production of IFNγ, IL-2 and IL-4 which lead to more robust and sustained CTL activity [27, 28]. The presence of CD4+ support was detected by survivin peptide-induced CD4+ proliferation and can be inferred by the presence of IgM-to-IgG class switching. Generic peptides, such as tetanus, have been used to boost CD4+ T cell activity systemically. However, CD4+ T cells that are generated through exposure to tumor-associated antigens via antigen presentation on MHC class II are tumor-specific and play a more direct role in the tumor microenvironment [13, 14, 26, 27]. SVN53-67/M57-KLH activates multiple survivin-specific CD8+ T cell clones and stimulates survivin-specific CD4+ T cell proliferation [11, 12, 15, 21, 29]. Thus, in addition to stimulating CD8+ cellular and antibody-mediated immune responses, SurVaxM may provide important tumor-specific CD4+ helper support.
This first-in-human study demonstrated the safety, tolerability and immunogenicity of SurVaxM in patients with recurrent malignant glioma following failure of standard therapy. Progression-free survival was 17.6 weeks, and overall survival was 86.6 weeks. Comparatively, an analysis of eight consecutive phase II chemotherapy trials of patients with recurrent malignant glioma, historical PFS was 10 weeks and historical OS was 30 weeks . Similarly, in a recent phase III clinical trial, which included an arm with physician’s choice chemotherapy in patients with recurrent glioblastoma, median PFS was 9 weeks and median OS was 25.7 weeks in the chemotherapy arm . Currently, a larger multi-institutional, phase II clinical trial of SurVaxM plus standard therapy (Stupp protocol) is being conducted in patients with newly diagnosed glioblastoma.
This project was funded by research grants from: the American Cancer Society RSG-11-153-01-LIB (to M.J. Ciesielski), the American Brain Tumor Association (to N. Yang), the Roswell Park Alliance Foundation, Mr. Philip H. Hubbell and the Linda Scime Endowment. Roswell Park Cancer Institute is supported by National Cancer Institute Cancer Center Support Grant NIH 5P30 CA16056-29.
M.J. Ciesielski and R.A. Fenstermaker were involved in concept and design; M.J. Ciesielski, R.A. Fenstermaker, J. Qiu, N. Yang and A.D. Hutson developed the methodology; M.J. Ciesielski, R.A. Fenstermaker, J. Qiu, L.R. Mechtler and A. Belal acquired the data; M.J. Ciesielski, R.A. Fenstermaker, J. Qiu, A. Belal and A.D. Hutson were involved in the analysis and interpretation of data; R.A. Fenstermaker, M.J. Ciesielski, M. Ahluwalia, K.P. Lee, L.R. Mechtler and J. Qiu wrote, reviewed and/or revised the manuscript; M.J. Ciesielski, R.A. Fenstermaker, C.L. Frank and A.D. Hutson provided administrative, technical or material support (i.e., reporting or organizing data, constructing databases); M.J. Ciesielski, R.A. Fenstermaker and L.R. Mechtler supervised the study.
Compliance with ethical standards
Conflict of interest
R.A. Fenstermaker and M.J. Ciesielski are co-inventors on patents regarding SVN53-67/M57-KLH and are co-founders of MimiVax, LLC, which has licensed such patents from Roswell Park Cancer Institute. No additional potential conflicts of interest were disclosed by the other authors.
|Funder Name||Grant Number||Funding Note|
|American Cancer Society|
|American Brain Tumor Association|
|Roswell Park Alliance Foundation, Roswell Park Cancer Institute|
|Mr. Phillip H. Hubbell|
|Linda Scime Endowment|
|National Cancer Institute|
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