Bernabé-Caro Reyes, Chen Yuanbin, Dowlati Afshin, Eason Paula
Hospital Universitario Virgen del Rocío, Seville, Spain.
Cancer & Hematology Centers of Western Michigan, Grand Rapids, MI.
Clin Lung Cancer. 2023 May;24(3):185-208. doi: 10.1016/j.cllc.2023.01.012. Epub 2023 Feb 8.
Second-line treatment options are limited for patients with small-cell lung cancer (SCLC). We conducted a PRISMA-standard systematic literature review to evaluate the treatment landscape for patients with relapsed SCLC (PROSPERO number: CRD42022299759). Systematic searches of MEDLINE, Embase, and Cochrane Library were performed (October 2022) to identify publications (prior 5 years) from prospective studies of therapies for relapsed SCLC. Publications were screened against predetermined eligibility criteria; data were extracted to standardized fields. Publication quality was assessed using GRADE. The data were analyzed descriptively, grouped by drug class. Overall, 77 publications involving 6349 patients were included. Studies of tyrosine kinase inhibitors (TKIs) with established cancer indications accounted for 24 publications; topoisomerase I inhibitors for 15; checkpoint inhibitors (CPIs) for 11, and alkylating agents for 9 publications. The remaining 18 publications featured chemotherapies, small-molecule inhibitors, investigational TKIs and monoclonal antibodies, and a cancer vaccine. According to GRADE assessment, 69% of the publications reported low-/very-low-quality evidence; quality limitations included lack of randomization and small sample sizes. Only 6 publications/6 trials reported phase 3 data; 5 publications/2 trials reported phase 2/3 results. Overall, the clinical potential of alkylating agents and CPIs remained unclear; investigations of combination approaches and biomarker-directed usage are warranted. Phase 2 data from TKI trials were consistently promising; no phase 3 data were available. Phase 2 data for a liposomal formulation of irinotecan were promising. We confirmed an absence of promising investigational drug/regimens in late-stage development; thus, relapsed SCLC remains an area of high unmet need.
小细胞肺癌(SCLC)患者的二线治疗选择有限。我们进行了一项遵循PRISMA标准的系统文献综述,以评估复发SCLC患者的治疗格局(PROSPERO编号:CRD42022299759)。于2022年10月对MEDLINE、Embase和Cochrane图书馆进行了系统检索,以确定复发SCLC治疗前瞻性研究(过去5年)的出版物。根据预先确定的纳入标准对出版物进行筛选;数据被提取到标准化字段。使用GRADE评估出版物质量。数据按药物类别进行描述性分析。总体而言,纳入了77篇涉及6349名患者的出版物。具有既定癌症适应症的酪氨酸激酶抑制剂(TKIs)研究占24篇;拓扑异构酶I抑制剂占15篇;检查点抑制剂(CPIs)占11篇,烷化剂占9篇。其余18篇出版物的特色是化疗、小分子抑制剂、研究性TKIs和单克隆抗体,以及一种癌症疫苗。根据GRADE评估,69%的出版物报告的证据质量为低/极低;质量限制包括缺乏随机化和样本量小。只有6篇出版物/6项试验报告了3期数据;5篇出版物/2项试验报告了2/3期结果。总体而言,烷化剂和CPIs的临床潜力仍不明确;有必要对联合治疗方法和生物标志物导向的使用进行研究。TKI试验的2期数据一直很有前景;尚无3期数据。伊立替康脂质体制剂的2期数据很有前景。我们证实后期开发中没有有前景的研究性药物/方案;因此,复发SCLC仍然是一个未满足需求很高的领域。