Müller Christian, Omari Jazan, Mohnike Konrad, Bär Caroline, Pech Maciej, Keitel Verena, Venerito Marino
Department of Gastroenterology, Hepatology and Infectious Diseases, Otto-von-Guericke University Hospital, 39120 Magdeburg, Germany.
Department of Radiology and Nuclear Medicine, Otto-von-Guericke University Hospital, 39120 Magdeburg, Germany.
Cancers (Basel). 2023 May 3;15(9):2598. doi: 10.3390/cancers15092598.
Patients with unresectable biliary tract cancer (uBTC) who progress despite first-line gemcitabine plus cisplatin (GC) treatment have limited systemic options with a modest survival benefit. Data are lacking on the clinical effectiveness and safety of personalized treatment based on multidisciplinary discussion for patients with progressing uBTC.
This retrospective single-center study included patients with progressive uBTC who received either best supportive care or personalized treatment based on multidisciplinary discussion, including minimally invasive, image-guided procedures (MIT); FOLFIRI; or both (MIT and FOLFIRI), between 2011 and 2021.
Ninety-seven patients with progressive uBTC were identified. Patients received best supportive care ( = 50, 52%), MIT ( = 14, 14%), FOLFIRI ( = 19, 20%), or both ( = 14, 14%). Survival after disease progression was better in patients who received MIT (8.8 months; 95% CI: 2.60-15.08), FOLFIRI (6 months; 95% CI: 3.30-8.72), or both (15.1 months; 95% CI: 3.66-26.50) than in patients receiving BSC (0.36 months; 95% CI: 0.00-1.24, < 0.001). The most common (>10%) grade 3-5 adverse events were anemia (25%) and thrombocytopenia (11%).
Multidisciplinary discussion is critical for identifying patients with progressive uBTC who might benefit the most from MIT, FOLFIRI, or both. The safety profile was consistent with previous reports.
一线吉西他滨联合顺铂(GC)治疗后病情进展的不可切除胆管癌(uBTC)患者,其全身治疗选择有限,生存获益不大。目前缺乏关于进展期uBTC患者基于多学科讨论的个性化治疗的临床有效性和安全性的数据。
这项回顾性单中心研究纳入了2011年至2021年间病情进展的uBTC患者,这些患者接受了最佳支持治疗或基于多学科讨论的个性化治疗,包括微创影像引导手术(MIT)、FOLFIRI方案,或两者联合(MIT和FOLFIRI)。
共确定了97例病情进展的uBTC患者。患者接受了最佳支持治疗(n = 50,52%)、MIT(n = 14,14%)、FOLFIRI(n = 19,20%)或两者联合(n = 14,14%)。疾病进展后,接受MIT(8.8个月;95%CI:2.60 - 15.08)、FOLFIRI(6个月;95%CI:3.30 - 8.72)或两者联合(15.1个月;95%CI:3.66 - 26.50)的患者的生存期优于接受最佳支持治疗的患者(0.36个月;95%CI:0.oo - 1.24,P < 0.001)。最常见的(>10%)3 - 5级不良事件是贫血(25%)和血小板减少症(11%)。
多学科讨论对于确定进展期uBTC患者中可能从MIT、FOLFIRI或两者联合中获益最大的患者至关重要。安全性与既往报告一致。