Prinzi Federica Lo, Salani Francesca, Camera Silvia, Rizzato Mario Domenico, Saborowski Anna, Antonuzzo Lorenzo, Rossari Federico, Satake Tomoyuki, Peeters Frederik, Pressiani Tiziana, Lucchetti Jessica, Kim Jin Won, Abidoye Oluseyi, Rapposelli Ilario Giovanni, Gallio Chiara, Tamberi Stefano, Finkelmeier Fabian, Giordano Guido, Chiara Pircher, Chon Hong Jae, Braconi Chiara, Qaisar Aitzaz, Pastorino Alessandro, Castet Florian, Tamburini Emiliano, Yoo Changhoon, Parisi Alessandro, Diana Anna, Scartozzi Mario, Prager Gerald W, Avallone Antonio, Schirripa Marta, Kim Il Hwan, Perkhofer Lukas, Oneda Ester, Verrico Monica, Couto Nuno, Adeva Jorge, Chan Stephen L, Spinelli Gian Paolo, Personeni Nicola, Garajova Ingrid, Rodriquenz Maria Grazia, Leo Silvana, Alvim Cecilia Melo, Roque Ricardo, Polito Mariam Grazia, Di Giacomo Emanuela, Farinea Giovanni, Bartalini Linda, Grelli Giada, De Rosa Antonio, Lavacchi Daniele, Ikeda Masafumi, Dekervel Jeroen, Niger Monica, Balsano Rita, Tonini Giuseppe, Kang Minsu, Tesini Giulia, Boccaccino Alessandra, Himmelsbach Vera, Landriscina Matteo, Djaballah Selma Ahcene, Bekaii-Saab Tanios, Fornaro Lorenzo, Masi Gianluca, Vogel Arndt, Lonardi Sara, Rimini Margherita, Rimassa Lorenza, Casadei-Gardini Andrea
Operative Research Unit of Medical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.
Int J Cancer. 2025 Nov 15;157(10):2092-2102. doi: 10.1002/ijc.70009. Epub 2025 Jul 11.
In recent years, there has been increasing interest in the possible prognostic impact of concomitant medications in patients with cancer treated with immunotherapy combinations. This real-world analysis aims to evaluate the impact of concomitant medications on survival outcomes in patients with advanced biliary tract cancer (BTCs) treated with cisplatin, gemcitabine and durvalumab (CGD) therapy. The study cohort included patients with a diagnosis of advanced BTCs who were taking concomitant medications for their comorbidities before the start of CGD. The primary objectives were overall survival (OS) and progression-free survival (PFS). The initial population consisted of 666 patients, who were retrospectively collected from 41 sites in 12 countries. Data on concomitant medications were available for 493 patients. After a median follow-up of 8.8 months (95% CI: 7.8-9.8), patients who did not take steroids (prednisone >10 mg/day or equivalent) or nonsteroidal anti-inflammatory drugs (NSAIDs) and opioids, before the start of CGD, had longer OS and PFS in univariate analysis. The multivariate analysis confirmed longer OS for patients who did not take steroids. Patients who did not take steroids had an OS of 14.8 months (95% CI: 13.1-29.1) versus 5.0 months (95% CI: 2.14-11.32) of patients who took prednisone >10 mg/day or equivalent. No differences were reported in terms of overall response rate (ORR), disease control rate (DCR) (p = 1.0 and p = .16, respectively), and safety profile between the two groups. Our analysis suggests that patients who did not receive steroids before the start of GCD had longer survival and highlighted the relevance of balancing concomitant medications and chemoimmunotherapy.
近年来,免疫疗法联合治疗的癌症患者中,同时使用的药物对预后的潜在影响越来越受到关注。这项真实世界分析旨在评估同时使用的药物对接受顺铂、吉西他滨和度伐利尤单抗(CGD)治疗的晚期胆管癌(BTC)患者生存结局的影响。研究队列包括在开始CGD治疗前因合并症而同时使用药物的晚期BTC患者。主要目标是总生存期(OS)和无进展生存期(PFS)。初始队列由666例患者组成,这些患者是从12个国家的41个地点回顾性收集的。493例患者有同时使用药物的数据。在中位随访8.8个月(95%CI:7.8 - 9.8)后,在单因素分析中,在开始CGD治疗前未服用类固醇(泼尼松>10mg/天或等效药物)、非甾体抗炎药(NSAIDs)和阿片类药物的患者有更长的OS和PFS。多因素分析证实未服用类固醇的患者OS更长。未服用类固醇的患者OS为14.8个月(95%CI:13.1 - 29.1),而服用泼尼松>10mg/天或等效药物的患者OS为5.0个月(95%CI:2.14 - 11.32)。两组之间在总缓解率(ORR)、疾病控制率(DCR)(分别为p = 1.0和p = 0.16)和安全性方面未报告差异。我们的分析表明,在开始GCD治疗前未接受类固醇治疗的患者生存期更长,并强调了平衡同时使用的药物和化学免疫治疗的相关性。