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

被引:295
作者
Lutz, Eric [1 ,11 ]
Yeo, Charles J. [8 ]
Lillemoe, Keith D. [9 ]
Biedrzycki, Barbara [1 ]
Kobrin, Barry [1 ]
Herman, Joseph [2 ]
Sugar, Elizabeth [6 ,7 ]
Piantadosi, Steven [12 ]
Cameron, John L. [3 ]
Solt, Sara [1 ]
Onners, Beth [1 ]
Tartakovsky, Irena [1 ]
Choi, Miri [1 ]
Sharma, Rajni [4 ,5 ]
Illei, Peter B. [4 ,5 ]
Hruban, Ralph H. [1 ,4 ,5 ]
Abrams, Ross A. [10 ]
Le, Dung [1 ]
Jaffee, Elizabeth [11 ,12 ]
Laheru, Dan [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Oncol, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Mol & Radiat Sci, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Surg, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Sol Goldman Pancreat Canc Ctr, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
[7] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD 21205 USA
[8] Thomas Jefferson Univ, Dept Surg, Philadelphia, PA 19107 USA
[9] Indiana Univ Sch Med, Dept Surg, Indianapolis, IN USA
[10] Rush Univ, Dept Radiat Oncol, Chicago, IL 60612 USA
[11] Johns Hopkins Univ, Sch Med, Program Immunol, Baltimore, MD 21205 USA
[12] Cedars Sinai Med Ctr, Samuel Oschin Comprehens Canc Inst, Los Angeles, CA 90048 USA
关键词
RANDOMIZED CONTROLLED-TRIAL; REGULATORY T-CELLS; CURATIVE RESECTION; CANCER; CHEMOTHERAPY; MESOTHELIN; GEMCITABINE; PREVALENCE; THERAPY;
D O I
10.1097/SLA.0b013e3181fd271c
中图分类号
R61 [外科手术学];
学科分类号
摘要
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 x 10(8) 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 postimmunotherapy 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.
引用
收藏
页码:328 / 335
页数:8
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