Division of Biliary Surgery, Department of General Surgery, West China Hospital, Sichuan University, Sichuan, 610041, Chengdu, China.
Research Center for Biliary Diseases, West China Hospital, Sichuan University, Sichuan, 610041, Chengdu, China.
BMC Cancer. 2023 Apr 25;23(1):378. doi: 10.1186/s12885-023-10679-8.
Malignant tumors of the biliary system are characterized by a high degree of malignancy and strong invasiveness, and they are usually diagnosed at late stages with poor prognosis. For patients with advanced biliary tract cancer, chemotherapy and targeted therapy are two of the options available to improve prognosis and delay tumor progression. This study aimed to comprehensively evaluate the safety and effectiveness of various chemotherapy schemes for the treatment of advanced biliary tract cancer in published systematic reviews and meta-analyses (SRoMAs).
An umbrella review method was adopted, which aims to summarize the existing evidence from multiple studies around a research topic. SRoMAs up to April 9, 2022, were identified using PubMed, Web of Science, the Cochrane database, and manual screening. Eligible studies were screened according to inclusion and exclusion criteria. This study had been registered at PROSPERO (CRD42022324548). For each eligible study, we extracted the data of general characteristics and the main findings. The methodological quality of the included studies were assessed by the AMSTAR2 scale, and the quality of evidence was evaluated by the GRADE tools.
A total of 1833 articles were searched; 14 unique articles with 94 outcomes were identified by eligibility criteria. The incidence of skin rash (RR = 18.11, 95% CI 5.13-63.91, GRADE: Moderate) and diarrhea (RR = 2.48, 95% CI 1.2-5.10, GRADE: Moderate) was higher in patients receiving gemcitabine-based chemotherapy plus targeted therapy than in patients receiving gemcitabine monotherapy. The number of patients receiving gemcitabine-based chemotherapy who developed leukopenia (OR = 7.17, 95% CI 1.43-36.08, GRADE: Moderate), anemia (OR = 7.04, 95% CI 2.59-19.12, GRADE: High), thrombocytopenia (RR = 2.45, 95% CI 1.39-4.32, GRADE: Moderate), and neutropenia (RR = 3.30, 95% CI 1.04-10.50, GRADE: Moderate) was significantly higher than that of patients who received gemcitabine-free regimens. In addition, patients receiving S-1 monotherapy had significantly better ORR (RR = 2.46, 95% CI 1.27-4.57, GRADE: Moderate) than patients receiving S-1 + gemcitabine. Patients receiving fluoropyrimidine-based chemotherapy had longer OS (HR = 0.83, 95% CI 0.7-0.99, GRADE: Moderate), higher DCR (0R = 5.18, 95% CI 3.3-10.23, GRADE: Moderate), and higher ORR (0R = 3.24, 95% CI 1.18-8.92, GRADE: Moderate) compared with patients who received 5-FU/LV monotherapy or supportive therapy. Surprisingly, we found evidence that gemcitabine-based chemotherapy did not improve postoperative patients' OS (HR = 0.91, 95% CI 0.74-1.12, GRADE: Moderate) when compared with best supportive care.
This study comprehensively evaluated the safety and efficacy of chemotherapy or targeted therapy regimens for advanced biliary tract cancer and found 11 outcomes with "Moderate" or "High" levels; however, most of the outcomes were still at "low" or "very low" levels. More randomized controlled studies are needed in the future to further summarize high levels of evidence.
胆道系统恶性肿瘤具有高度恶性和侵袭性的特点,通常在晚期诊断,预后较差。对于晚期胆道癌患者,化疗和靶向治疗是改善预后和延缓肿瘤进展的两种选择。本研究旨在通过发表的系统评价和荟萃分析(SRoMAs)全面评估各种化疗方案治疗晚期胆道癌的安全性和有效性。
采用伞式评价方法,旨在围绕研究主题总结来自多个研究的现有证据。截至 2022 年 4 月 9 日,通过 PubMed、Web of Science、Cochrane 数据库和手动筛选来识别 SRoMAs。根据纳入和排除标准筛选合格研究。本研究已在 PROSPERO(CRD42022324548)上注册。对于每个合格的研究,我们提取了一般特征和主要发现的数据。使用 AMSTAR2 量表评估纳入研究的方法学质量,并使用 GRADE 工具评估证据质量。
共搜索到 1833 篇文章,通过资格标准确定了 14 篇具有 94 项结果的独特文章。与吉西他滨单药治疗相比,接受吉西他滨为基础的化疗联合靶向治疗的患者皮疹(RR=18.11,95%CI 5.13-63.91,GRADE:中度)和腹泻(RR=2.48,95%CI 1.2-5.10,GRADE:中度)的发生率更高。接受吉西他滨为基础的化疗的患者发生白细胞减少症(OR=7.17,95%CI 1.43-36.08,GRADE:中度)、贫血(OR=7.04,95%CI 2.59-19.12,GRADE:高)、血小板减少症(RR=2.45,95%CI 1.39-4.32,GRADE:中度)和中性粒细胞减少症(RR=3.30,95%CI 1.04-10.50,GRADE:中度)的患者数量明显高于接受无吉西他滨方案的患者。此外,接受替吉奥单药治疗的患者的客观缓解率(RR=2.46,95%CI 1.27-4.57,GRADE:中度)明显优于接受替吉奥+吉西他滨的患者。接受氟嘧啶类化疗的患者的总生存期(HR=0.83,95%CI 0.7-0.99,GRADE:中度)、疾病控制率(OR=5.18,95%CI 3.3-10.23,GRADE:中度)和客观缓解率(OR=3.24,95%CI 1.18-8.92,GRADE:中度)均高于接受 5-氟尿嘧啶/亚叶酸钙单药或支持治疗的患者。令人惊讶的是,我们发现与最佳支持治疗相比,吉西他滨为基础的化疗并没有改善术后患者的总生存期(HR=0.91,95%CI 0.74-1.12,GRADE:中度)。
本研究全面评估了化疗或靶向治疗方案治疗晚期胆道癌的安全性和有效性,发现 11 项结果为“中度”或“高度”;然而,大多数结果仍处于“低”或“非常低”水平。未来需要更多的随机对照研究来进一步总结高水平的证据。