From the Department of Surgery, Massachusetts General Hospital, Boston, MA (Fong, Verdugo, Fernandez-del Castillo, Ferrone, Qadan).
the Department of Medicine, Massachusetts General Hospital, Boston, MA (Allen, Blaszkowsky, Clark, Parikh, Ryan, Weekes).
J Am Coll Surg. 2023 Jun 1;236(6):1126-1136. doi: 10.1097/XCS.0000000000000499. Epub 2022 Dec 8.
FOLFIRINOX is increasingly used in the management of pancreatic ductal adenocarcinoma (PDAC). However, neoadjuvant therapy is associated with toxicity, possible disease progression, and biopsy-related and biliary complications that may preclude operative exploration. Data on the true attrition rate outside of clinical trials or resected surgical series are lacking.
Patients with nonmetastatic PDAC who initiated FOLFIRINOX from 2015 to 2020 were identified from our institution's pharmacy records. Multivariable regression and Cox proportional hazard models were used for adjusted analyses of categorical and survival outcomes, respectively.
Of 254 patients who initiated first-line neoadjuvant FOLFIRINOX, 199 (78.3%) underwent exploration, and 54 (21.3%) did not complete their chemotherapy cycles due to poor tolerability (46.3%), poor response (31.5%), or disease progression (14.8%), among other causes (7.4%). A total of 109 (42.9%) patients experienced grade 3/4 FOLFIRINOX-related toxicity, of whom 73 (28.7%) and 100 (39.4%) required an emergency department visit or inpatient admission, respectively. Finally, not undergoing surgical exploration was associated with impaired overall survival (hazard ratio 7.0; 95% CI 3.8 to 12.8; p < 0.001). Independent predictors of not undergoing exploration were remote history of chemotherapy receipt (odds ratio [OR] 0.06; p = 0.02), inability to complete FOLFIRINOX cycles (OR 0.2, p = 0.003), increase in ECOG score (OR 0.2, p < 0.001), and being single or divorced (OR 0.3, p = 0.018).
Among 254 patients with nonmetastatic PDAC initiated on FOLFIRINOX, of whom 52% were locally advanced, a total of 199 (78.3%) were explored, 142 (71.4%) underwent successful resection, and 129 (90.8%) were resected with negative margins. Despite 109 (42.9)% of patients experiencing significant toxicity, most patients could be managed through treatment-related complications to complete planned neoadjuvant chemotherapy and undergo planned surgical exploration.
FOLFIRINOX 越来越多地用于治疗胰腺导管腺癌(PDAC)。然而,新辅助治疗与毒性、可能的疾病进展以及活检相关和胆道并发症有关,这些并发症可能会阻碍手术探查。缺乏临床试验或切除手术系列之外的真实淘汰率数据。
从我们机构的药房记录中确定了 2015 年至 2020 年期间接受 FOLFIRINOX 一线新辅助治疗的非转移性 PDAC 患者。使用多变量回归和 Cox 比例风险模型分别对分类和生存结果进行调整分析。
在接受一线新辅助 FOLFIRINOX 治疗的 254 名患者中,有 199 名(78.3%)接受了探查,有 54 名(21.3%)因不耐受(46.3%)、疗效不佳(31.5%)或疾病进展(14.8%)等原因未能完成化疗周期。共有 109 名(42.9%)患者出现 3/4 级 FOLFIRINOX 相关毒性,其中 73 名(28.7%)和 100 名(39.4%)分别需要急诊就诊或住院治疗。最后,未进行手术探查与总生存期受损相关(风险比 7.0;95%CI 3.8 至 12.8;p < 0.001)。未进行探查的独立预测因素包括既往接受化疗史(比值比 [OR] 0.06;p = 0.02)、无法完成 FOLFIRINOX 周期(OR 0.2,p = 0.003)、ECOG 评分升高(OR 0.2,p < 0.001)以及单身或离异(OR 0.3,p = 0.018)。
在接受 FOLFIRINOX 治疗的 254 名非转移性 PDAC 患者中,有 52%为局部晚期患者,其中 199 名(78.3%)接受了探查,142 名(71.4%)成功切除,129 名(90.8%)切除边缘阴性。尽管 109 名(42.9%)患者出现严重毒性,但大多数患者可通过治疗相关并发症进行管理,以完成计划的新辅助化疗并进行计划的手术探查。