Trial reportNature communications2026
The combination of a cancer vaccine, pembrolizumab, and stereotactic body radiation in patients with locally advanced pancreatic cancer: a single-arm, phase II study.
Trial report in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02648282 (A Phase II Study of GM-CSF Secreting Allogeneic Pancreatic Cancer Vaccine in Combination With PD-1 Blockade Antibody), which is not on this map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
A Phase II Study of GM-CSF Secreting Allogeneic Pancreatic Cancer Vaccine in Combination With PD-1 Blockade Antibody (Pembrolizumab) and Stereotactic Body Radiation Therapy (SBRT) for the Treatment of Patients With Locally Advanced Adenocarcinoma of the Pancreas
Who cites it
2 citing papers in PubMed.
- Review
- Targeting innate immunity in cancer: mechanistic foundations, therapeutic vaccination, and clinical translation.Frontiers in immunology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
31 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In this Phase II study (NCT02648282) of locally advanced pancreatic cancer (LAPC), 58 patients were enrolled and intended for an immunotherapy including GM-CSF-secreting allogeneic pancreatic cancer vaccine (GVAX) and pembrolizumab and stereotactic body radiation therapy (SBRT) following standard chemotherapy. Fifty-four evaluable patients received two cycles of immunotherapy and SBRT and reassessed for resectability. After resection or biopsy, patients received continued immunotherapy for two years. At a median follow-up of 19.6 months, the median distant metastasis free survival (DMFS), the primary endpoint, for all evaluable patients was 9.8 months. Secondary endpoint analysis shows that, of these, 35 patients (64.8%) were deemed potentially resectable, and 24 underwent R0/R1 resections. Resected patients had a majority of R0 resections (91.7%). The overall resection rate was 44.4%. Patients who underwent resection had a median DMFS of 20.3 months. Median overall survival (OS), a secondary endpoint, for all evaluable patients from the start of the immunotherapy was 21.8 months, with resected patients reaching 29.7 months and unresected patients at 12.1 months. From diagnosis, median OS was 28.2 months, with resected patients achieving 36.7 months, while unresected patients had 19.7 months. In conclusion, the combination of GVAX, pembrolizumab, and SBRT showed promising efficacy in LAPC patients with favorable survival outcomes, especially those who underwent R0/R1 resections. However, patients with unresectable disease still maintained significantly worse DMFS and OS. The regimen demonstrated a manageable safety profile.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.