Department of Oncology, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, No. 23, Back Road of Art Gallery, Dongcheng District, Beijing, 100010, China.
Trials. 2021 Jul 8;22(1):437. doi: 10.1186/s13063-021-05407-1.
Extensive-stage small-cell lung cancer (ES-SCLC) is characterized by extensive metastases, aggressive progression, and poor prognosis. Chemotherapy is applied as a preferred first-line regimen for ES-SCLC, but inadequate for improving its overall survival. Traditional Chinese medicine (TCM) is widely used in the clinical practice of ES-SCLC for its synergy with chemotherapy. However, there is still no substantial evidence to prove that TCM can effectively improve the long-term efficacy of ES-SCLC patients. The study intends to determine whether the TCM with chemotherapy can improve the overall survival (OS) in treating with ES-SCLC when compared with chemotherapy alone.
METHOD/DESIGN: A multicenter, randomized, single-blind, placebo-controlled clinical trial will be conducted to determine whether the TCM granules combined with chemotherapy can improve the OS of ES-SCLC. Two hundred seventy participants will randomly receive 4-6 cycles (21 days per cycle) of chemotherapy plus TCM granules or placebo. The primary outcome measure is OS. The secondary outcome measures includes progression-free survival (PFS), objective response rate (ORR), quality of life (QoL), and tumor markers. Visits will be performed at the end of each cycle during the treatment period and then every 3 months in the follow-up period until the patients' death or study completion.
The study's result will provide a high-level evidence for TCM granules using with chemotherapy on the first-line treatment of ES-SCLC.
Chinese Clinical Trial Registry ChiCTR1900022991 . Registered on 6 May 2019 (prospective registration).
广泛期小细胞肺癌(ES-SCLC)的特征是广泛转移、侵袭性进展和预后不良。化疗是 ES-SCLC 的首选一线治疗方案,但不能改善其总体生存率。中药在 ES-SCLC 的临床实践中被广泛应用,因其与化疗具有协同作用。然而,目前仍没有实质性证据证明中药能有效改善 ES-SCLC 患者的长期疗效。本研究旨在确定与单纯化疗相比,化疗联合中药是否能提高 ES-SCLC 的总生存期(OS)。
方法/设计:将进行一项多中心、随机、单盲、安慰剂对照的临床试验,以确定中药颗粒联合化疗是否能提高 ES-SCLC 的 OS。270 名参与者将随机接受 4-6 个周期(每个周期 21 天)的化疗加中药颗粒或安慰剂。主要结局指标为 OS。次要结局指标包括无进展生存期(PFS)、客观缓解率(ORR)、生活质量(QoL)和肿瘤标志物。在治疗期间,每个周期结束时进行访视,然后在随访期间每 3 个月进行一次访视,直到患者死亡或研究完成。
该研究结果将为中药颗粒联合化疗作为 ES-SCLC 一线治疗提供高级别的证据。
中国临床试验注册中心 ChiCTR1900022991。注册于 2019 年 5 月 6 日(前瞻性注册)。