Total Neoadjuvant Therapy With FOLFIRINOX in Combination With Losartan Followed by Chemoradiotherapy for Locally Advanced Pancreatic Cancer A Phase 2 Clinical Trial

被引:401
|
作者
Murphy, Janet E. [1 ]
Wo, Jennifer Y. [2 ]
Ryan, David P. [1 ]
Clark, Jeffrey W. [1 ]
Jiang, Wenqing [1 ]
Yeap, Beow Y. [1 ]
Drapek, Lorraine C. [2 ]
Ly, Leilana [2 ]
Baglini, Christian, V [2 ]
Blaszkowsky, Lawrence S. [1 ]
Ferrone, Cristina R. [3 ]
Parikh, Aparna R. [1 ]
Weekes, Cohn D. [1 ]
Nipp, Ryan D. [1 ]
Kwak, Eunice L. [1 ]
Allen, Jill N. [1 ]
Corcoran, Ryan B. [1 ]
Ting, David T. [1 ]
Faris, Jason E. [1 ]
Zhu, Andrew X. [1 ]
Goyal, Lipika [1 ]
Berger, David L. [3 ]
Qadan, Motaz [3 ]
Lillemoe, Keith D. [3 ]
Talele, Nilesh [2 ]
Jain, Rakesh K. [2 ]
DeLaney, Thomas F. [2 ]
Duda, Dan G. [2 ]
Boucher, Yves [2 ]
Fernandez-Del Castillo, Carlos [3 ]
Hong, Theodore S. [2 ]
机构
[1] Harvard Med Sch, Div Hematol Oncol, Dept Med, Massachusetts Gen Hosp, 55 Fruit St, Boston, MA 02114 USA
[2] Harvard Med Sch, Dept Radiat Oncol, Massachusetts Gen Hosp, Boston, MA 02114 USA
[3] Harvard Med Sch, Dept Surg, Massachusetts Gen Hosp, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
ANGIOTENSIN SYSTEM; CAPECITABINE; GEMCITABINE; ACTIVATION; SURVIVAL; EFFICACY; IMPROVES;
D O I
10.1001/jamaoncol.2019.0892
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
IMPORTANCE Patients with locally advanced pancreatic cancer have historically poor outcomes. Evaluation of a total neoadjuvant approach is warranted. OBJECTIVE To evaluate the margin-negative (R0) resection rate of neoadjuvant FOLFIRINOX (fluorouracil, leucovorin, oxaliplatin, and irinotecan) and losartan followed by chemoradiotherapy for locally advanced pancreatic cancer. DESIGN, SETTING, AND PARTICIPANTS A single-arm phase 2 clinical trial was conducted at a large academic hospital from August 22, 2013, to May 22, 2018, among 49 patients with previously untreated locally advanced unresectable pancreatic cancer as determined by multidisciplinary review. Patients had Eastern Cooperative Oncology Group performance status 0 or 1 and adequate hematologic, renal, and hepatic function. Median follow-up for the analysis was 17.1 months (range, 5.0-53.7) among 27 patients still alive at study completion. INTERVENTIONS Patients received FOLFIRINOX and losartan for 8 cycles. Patients with radiographically resectable tumor after chemotherapy received short-course chemoradiotherapy (5 GyE x 5 with protons) with capecitabine. Patients with persistent vascular involvement received long-course chemoradiotherapy (50.4 Gy with a vascular boost to 58.8 Gy) with fluorouracil or capecitabine. MAIN OUTCOMES AND MEASURES R0 resection rate. RESULTS Of the 49 patients (26 women and 23 men; median age 63 years [range, 42-78 years]), 39 completed 8 cycles of FOLFIRINOX and losartan; 10 patients had fewer than 8 cycles due to progression (5 patients), losartan intolerance (3 patients), and toxicity (2 patients). Seven patients (16%) had short-course chemoradiotherapy while 38 (84%) had long-course chemoradiotherapy. Forty-two (86%) patients underwent attempted surgery, with R0 resection achieved in 34 of 49 patients (69%; 95% CI, 55%-82%). Overall median progression-free survival was 17.5 months (95% CI: 13.9-22.7) and median overall survival was 31.4 months (95% CI, 18.1-38.5). Among patients who underwent resection, median progression-free survival was 21.3 months (95% CI, 16.6-28.2), and median overall survival was 33.0 months (95% CI, 31.4 to not reached). CONCLUSIONS AND RELEVANCE Total neoadjuvant therapy with FOLFIRINOX, losartan, and chemoradiotherapy provides downstaging of locally advanced pancreatic ductal adenocarcinoma and is associated with an R0 resection rate of 61%.
引用
收藏
页码:1020 / 1027
页数:8
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