Turpin Anthony, El Amrani Mehdi, Bachet Jean-Baptiste, Pietrasz Daniel, Schwarz Lilian, Hammel Pascal
UMR9020-UMR-S 1277 Canther-Cancer Heterogeneity, Plasticity and Resistance to Therapies, University of Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, F-59000 Lille, France.
Medical Oncology Department, CHU Lille, University of Lille, F-59000 Lille, France.
Cancers (Basel). 2020 Dec 21;12(12):3866. doi: 10.3390/cancers12123866.
Adjuvant chemotherapy is currently used in all patients with resected pancreatic cancer who are able to begin treatment within 3 months after surgery. Since the recent publication of the PRODIGE 24 trial results, modified FOLFIRINOX has become the standard-of-care in the non-Asian population with localized pancreatic adenocarcinoma following surgery. Nevertheless, there is still a risk of toxicity, and feasibility may be limited in heavily pre-treated patients. In more frail patients, gemcitabine-based chemotherapy remains a suitable option, for example gemcitabine or 5FU in monotherapy. In Asia, although S1-based chemotherapy is the standard of care it is not readily available outside Asia and data are lacking in non-Asiatic patients. In patients in whom resection is not initially possible, intensified schemes such as FOLFIRINOX or gemcitabine-nabpaclitaxel have been confirmed as options to enhance the response rate and resectability, promoting research in adjuvant therapy. In particular, should oncologists prescribe adjuvant treatment after a long sequence of chemotherapy +/- chemoradiotherapy and surgery? Should oncologists consider the response rate, the R0 resection rate alone, or the initial chemotherapy regimen? And finally, should they take into consideration the duration of the entire sequence, or the presence of limited toxicities of induction treatment? The aim of this review is to summarize adjuvant management of resected pancreatic cancer and to raise current and future concerns, especially the need for biomarkers and the best holistic care for patients.
辅助化疗目前用于所有接受了胰腺癌切除术且能在术后3个月内开始治疗的患者。自PRODIGE 24试验结果近期发表以来,改良FOLFIRINOX方案已成为非亚洲人群局部胰腺癌术后的标准治疗方案。然而,毒性风险依然存在,对于预处理严重的患者,可行性可能受限。对于身体状况更差的患者,以吉西他滨为基础的化疗仍是合适的选择,例如吉西他滨或5-氟尿嘧啶单药治疗。在亚洲,虽然以S-1为基础的化疗是标准治疗方案,但在亚洲以外地区不易获得,且缺乏非亚洲患者的数据。对于最初无法进行手术切除的患者,强化方案如FOLFIRINOX或吉西他滨-纳米白蛋白结合型紫杉醇已被确认为提高缓解率和可切除性的选择,这促进了辅助治疗的研究。特别是,肿瘤学家在经过长时间的化疗+/-放化疗及手术之后是否应开具辅助治疗?肿瘤学家应仅考虑缓解率、R0切除率,还是初始化疗方案?最后,他们是否应考虑整个疗程的时长,或诱导治疗的毒性是否有限?本综述的目的是总结已切除胰腺癌的辅助治疗管理,并提出当前和未来的关注点,尤其是对生物标志物的需求以及为患者提供最佳整体护理。