A Multicenter, Phase Ii Trial Of Preoperative Gemcitabine And Nab-Paclitaxel For Resectable Pancreas Cancer: The Agitg Gap Study.

JOURNAL OF CLINICAL ONCOLOGY(2015)

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摘要
4115 Background: Recent pancreatic cancer (PC) series show 41% (95%CI 40-43%) of patients (pts) achieve an R0 resection (margin clearance ≥ 1mm). In neoadjuvant chemotherapy trials for resectable PC, only 54-89% undergo pancreatic resection with R0 rates of 74-80%. Nab-paclitaxel(nab-pacli) and gemcitabine(GEM) chemotherapy(CX) is an active regimen in metastatic disease. We aimed to determine feasibility and R0 resection rate of 85% with peri-operative nab-pacli and GEM for resectable PC. Methods: Pts with operable PC received 2 cycles of neo-adjuvant nab-pacli 125mg/m2 followed by GEM 1000mg/m2CX on days(D) 1, 8 and 15(28D cycle) followed by resection and then post-operative CX(4 cycles). Results: Forty-one pts were enrolled (2012-14). Median age = 65 (range 43-79), 41% male. Thirty-six (88%) pts underwent surgery, while five (12%) did not (2 disease progression, 2 refused surgery, 1 cholangitis). Only 4/36 (10%) had grade ¾ septic events, no grade ¾ pancreatic leak, and no treatment related deaths. Thirty pts had pancreatic resection (73%; 29 had evaluable cancer and 15/29 (52%) had grade 0-2 tumour regression; one did not have cancer on central pathology review). Six (15%) pts had unresectable disease at surgery. Pre-operative nab-pacli and GEM produced an R0 rate of 52% (15/29; 95%CI 34-69%) with a minimum 1mm margin and an R0 rate of 86% (25/29; 95%CI 68-96%) with a 0mm margin. 39/41 (95%) completed planned induction CX (although dose modifications/omission were required - mostly omission of D15). Post-operatively, eighteen pts (18/30, 60%) commenced CX, with 14/18 (78%) completing all 4 cycles of planned CX; whilst four pts commenced chemoradiation, but 2 withdrew due to disease progression. Conclusions: Pre-operative nab-pacli and GEM was delivered safely and achieved an R0 resection rate clinically significantly higher than the mean of surgical series using similar pathology criteria. Our pre-operative regimen was delivered to 95% of patients, but in contrast post-operative CX was less achievable with only 60% commencing treatment. Neoadjuvant nab-pacli and GEM is an encouraging strategy to improve outcomes in resectable PC and merits testing in a randomised setting. Clinical trial information: ACTRN12611000848909.
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关键词
resectable pancreas cancer,preoperative gemcitabine,agitg gap study,nab-paclitaxel
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