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Cited by 403

The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.

A Lethally Irradiated Allogeneic Granulocyte-Macrophage Colony Stimulating Factor-Secreting Tumor Vaccine for Pancreatic Adenocarcinoma: A Phase II Trial of Safety, Efficacy, and Immune Activation

Open access
Eric, Lutz, Yeo, Charles J., Lillemoe, Keith D., Biedrzycki, Barbara, Kobrin, Barry, Herman, Joseph, Sugar, Elizabeth, Piantadosi, Steven, Cameron, John L., Solt, Sara, Onners, Beth, Tartakovsky, Irena, Choi, Miri, Sharma, Rajni, Illei, Peter B., Ralph H., Hruban, Abrams, Ross A., Le, Dung, Elizabeth, Jaffee, Laheru, Dan·2011·Annals of Surgery

Abstract

PURPOSE: Surgical resection provides the only possibility of cure for pancreas cancer. A standard adjuvant approach has not been established. We tested the safety and efficacy of a granulocyte-macrophage colony-stimulating factor (GM-CSF)-based immunotherapy administered in patients with resected pancreatic adenocarcinoma. PATIENTS AND METHODS: A single institution phase II study of 60 patients with resected pancreatic adenocarcinoma was performed. Each immunotherapy treatment consisted of a total of 5 × 108 GM-CSF-secreting cells distributed equally among 3 lymph node regions. The first immunotherapy treatment was administered 8 to 10 weeks after surgical resection. Subsequently, patients received 5-FU based chemoradiation. Patients who remained disease-free after completion of chemoradiotherapy received treatments 2 to 4, each 1 month apart. A fifth and final booster was administered 6 months after the fourth immunotherapy. The primary endpoint was disease free survival and secondary endpoints were overall survival and toxicity, and the induction of mesothelin specific T cell responses. RESULTS: The median disease-free survival is 17.3 months (95% CI, 14.6-22.8) with median survival of 24.8 months (95% CI, 21.2-31.6). The administration of immunotherapy was well tolerated. In addition, the post-immunotherapy induction of mesothelin-specific CD8+ T cells in HLA-A1+ and HLA-A2+patients correlates with disease-free survival. CONCLUSIONS: An immunotherapy approach integrated with chemoradiation is safe and demonstrates an overall survival that compares favorably with published data for resected pancreas cancer. These data suggest additional boost immunotherapies given at regular intervals beyond 1 year postsurgery should be tested in future studies, and provide the rationale for conducting a multicenter phase II study.

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Metadata

Authors
Eric, L., Yeo, C. J., Lillemoe, K. D., Biedrzycki, B., Kobrin, B., Herman, J., Sugar, E., Piantadosi, S., Cameron, J. L., Solt, S., Onners, B., Tartakovsky, I., Choi, M., Sharma, R., Illei, P. B., Ralph H., H., Abrams, R. A., Le, D., Elizabeth, J., & Laheru, D.
Venue
Annals of Surgery
Published
2011-02
Volume
253
Issue
2
Pages
328-335
ISSN
0003-4932 (ISSN-L)
OpenAlex
W1988065950
Cited by
403
References
19
FWCI
14.89
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: A Lethally Irradiated Allogeneic Granulocyte-Macrophage Colony Stimulating Factor-Secreting Tumor Vaccine for Pancreatic Adenocarcinoma: A Phase II Trial of Safety, Efficacy, and Immune Activation. https://app.cochat.ai/papers/10.1097/sla.0b013e3181fd271c
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Eric, L., Yeo, C. J., Lillemoe, K. D., Biedrzycki, B., Kobrin, B., Herman, J., Sugar, E., Piantadosi, S., Cameron, J. L., Solt, S., Onners, B., Tartakovsky, I., Choi, M., Sharma, R., Illei, P. B., Ralph H., H., Abrams, R. A., Le, D., Elizabeth, J., & Laheru, D. (2011). A Lethally Irradiated Allogeneic Granulocyte-Macrophage Colony Stimulating Factor-Secreting Tumor Vaccine for Pancreatic Adenocarcinoma: A Phase II Trial of Safety, Efficacy, and Immune Activation. Annals of Surgery. https://doi.org/10.1097/sla.0b013e3181fd271c

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.