Department of Hepato-Gastroenterology and Gastrointestinal Oncology, Université de Paris, Paris Descartes University, Hôpital Européen Georges Pompidou, Paris, France.
Department of Medical and Thoracic Oncology, Université de Paris, Hôpital Européen Georges Pompidou, Paris, France.
Br J Cancer. 2021 Jun;124(12):1941-1948. doi: 10.1038/s41416-021-01341-w. Epub 2021 Mar 26.
FOLFIRINOX has shown promising results in locally advanced (LAPA) or borderline resectable (BRPA) pancreatic adenocarcinoma. We report here a cohort of patients treated with this regimen from the AGEO group.
This is a retrospective multicentre study. We included all consecutive patients with non-pre-treated LAPA or BRPA treated with FOLFIRINOX.
We included 330 patients (57.9% male, 65.4% <65 years, 96.4% PS <2). Disease was classified as BRPA in 31.1% or LAPA in 68.9%. Objective response rate with FOLFIRINOX was 29.5% and stable disease 51%. Subsequent CRT was performed in 46.4% of patients and 23.9% had curative intent surgery. Resection rates were 42.1% for BRPA and 15.5% for LAPA. Main G3/4 toxicities were fatigue (15%), neutropenia (12%) and neuropathy (G2/3 35%). After a median follow-up of 26.7 months, median OS (mOS) and PFS were 21.4 and 12.4 months, respectively. For patients treated by FOLFIRINOX alone, or FOLFIRINOX followed by CRT, or FOLFIRINOX + /- CRT + surgery, mOS was 16.8 months, 21.8 months and not reached, respectively (p < 0.0001).
FOLFIRINOX for LAPA and BRPA seems to be effective with a manageable toxicity profile. These promising results in "real-life" patients now have to be confirmed in a Phase 3 randomised trial.
FOLFIRINOX 方案在局部晚期(LAPA)或边界可切除(BRPA)胰腺腺癌中显示出良好的疗效。在此,我们报告了来自 AGEO 组的一组接受该方案治疗的患者。
这是一项回顾性多中心研究。我们纳入了所有未经治疗的 LAPA 或 BRPA 患者,接受 FOLFIRINOX 治疗。
我们共纳入 330 例患者(男性 57.9%,年龄<65 岁者 65.4%,PS<2 者 96.4%)。BRPA 患者占 31.1%,LAPA 患者占 68.9%。FOLFIRINOX 的客观缓解率为 29.5%,疾病稳定率为 51%。46.4%的患者随后接受了 CRT,23.9%的患者有根治性手术的意愿。BRPA 的切除率为 42.1%,LAPA 的切除率为 15.5%。主要的 3/4 级毒性为疲劳(15%)、中性粒细胞减少(12%)和周围神经病变(G2/3 级 35%)。中位随访 26.7 个月后,中位总生存期(mOS)和无进展生存期(PFS)分别为 21.4 个月和 12.4 个月。对于单独接受 FOLFIRINOX 治疗、FOLFIRINOX 联合 CRT 治疗或 FOLFIRINOX+/-CRT+手术治疗的患者,mOS 分别为 16.8 个月、21.8 个月和未达到(p<0.0001)。
FOLFIRINOX 方案治疗 LAPA 和 BRPA 似乎有效,且毒性可管理。这些在“真实世界”患者中的有前景的结果现在需要在 III 期随机试验中得到证实。