Clinical Trials of Systemic Chemotherapy for Resectable Pancreatic Cancer A Review

被引:37
作者
Mavros, Michail N. [1 ]
Moris, Dimitrios [2 ]
Karanicolas, Paul J. [3 ,4 ,5 ]
Katz, Matthew H. G. [6 ]
O'Reilly, Eileen M. [7 ,8 ]
Pawlik, Timothy M. [9 ]
机构
[1] Univ Arkansas Med Sci, Dept Surg, 4301 W Markham St,Slot 725, Little Rock, AR 72205 USA
[2] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
[3] Univ Toronto, Dept Surg, Toronto, ON, Canada
[4] Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
[5] Sunnybrook Hlth Sci Ctr, Dept Surg, Toronto, ON, Canada
[6] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[7] Mem Sloan Kettering Canc Ctr, Dept Med, Div Gastrointestinal Med Oncol, 1275 York Ave, New York, NY 10021 USA
[8] Weill Cornell Med Coll, Dept Med, New York, NY USA
[9] Ohio State Univ, Dept Surg, Wexner Med Ctr, Columbus, OH 43210 USA
关键词
RANDOMIZED CONTROLLED-TRIALS; PACLITAXEL PLUS GEMCITABINE; ADJUVANT CHEMOTHERAPY; PHASE-II; NEOADJUVANT CHEMOTHERAPY; DUCTAL ADENOCARCINOMA; PRACTICE GUIDELINES; EXTERNAL VALIDITY; OPEN-LABEL; MULTICENTER;
D O I
10.1001/jamasurg.2021.0149
中图分类号
R61 [外科手术学];
学科分类号
摘要
IMPORTANCE Adjuvant chemotherapy is the standard of care for resected pancreatic ductal adenocarcinoma (PDAC) based on level 1 evidence, but some studies suggest that a neoadjuvant approach (which is standard for borderline resectable PDAC) may be preferable for upfront resectable PDAC. An in-depth review was conducted of all randomized clinical trials that investigated neoadjuvant and adjuvant treatment of patients with resectable or resected PDAC, focusing on trial design, characteristics of enrolled population, and long-term outcomes. OBSERVATIONS The existing resectable PDAC trials have good internal validity but variable applicability because of their restrictive eligibility criteria. In these trials, overall survival is the criterion standard end point, but disease-free survival is more feasible, proximate, and specific to the assigned intervention (at the cost of subjective outcome assessment) and thus an acceptable end point in certain contexts. The prolonged survival in the PRODIGE 24 trial highlights both the success of mFOLFIRINOX (modified fluorouracil, leucovorin, irinotecan, and oxaliplatin) and the importance of patient selection. Neoadjuvant and perioperative trials have shown promising preliminary results; however, the number of patients who are not subsequently eligible for surgery reflects the limitations of this approach. Head-to-head comparisons of neoadjuvant and adjuvant treatments are limited to date in Western countries. Precision oncology with genomic and somatic testing for actionable mutations has promising preliminary results and may refine the management of PDAC, although the implications for early-stage disease and neoadjuvant therapy are unknown. CONCLUSIONS AND RELEVANCE This review found that adjuvant chemotherapy with mFOLFIRINOX is currently the standard of care in fit patients with resected PDAC; however, the role of neoadjuvant treatment is expanding. Precision oncology may help individualize the treatment regimen and sequence and improve outcomes. Enrollment of patients with resectable PDAC in clinical trials is strongly encouraged.
引用
收藏
页码:663 / 672
页数:10
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