A Meta-Analysis of the Efficacy and Toxicity of Twice-Daily vs. Once-Daily Concurrent Chemoradiotherapy for Limited-Stage Small Cell Lung Cancer Based on Randomized Controlled Trials

التفاصيل البيبلوغرافية
العنوان: A Meta-Analysis of the Efficacy and Toxicity of Twice-Daily vs. Once-Daily Concurrent Chemoradiotherapy for Limited-Stage Small Cell Lung Cancer Based on Randomized Controlled Trials
المؤلفون: Qian Wu, Yiting Xiong, Shujuan Zhang, Xinling Chen, Fengming Yi, Yiping Wei, Wenxiong Zhang
المصدر: Frontiers in Oncology
Frontiers in Oncology, Vol 9 (2020)
بيانات النشر: Frontiers Media S.A., 2020.
سنة النشر: 2020
مصطلحات موضوعية: 0301 basic medicine, Oncology, Cancer Research, medicine.medical_specialty, medicine.medical_treatment, Cochrane Library, once-daily, lcsh:RC254-282, law.invention, concurrent chemoradiotherapy, 03 medical and health sciences, 0302 clinical medicine, Randomized controlled trial, law, Internal medicine, medicine, limited-stage small cell lung cancer, Adverse effect, business.industry, twice-daily, Hazard ratio, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Confidence interval, Radiation therapy, meta-analysis, 030104 developmental biology, 030220 oncology & carcinogenesis, Relative risk, Meta-analysis, Systematic Review, business
الوصف: Background: Currently, the accepted standard management of limited-stage small cell lung cancer (SCLC) is concurrent chemoradiotherapy (CCRT), but the frequency of radiotherapy is controversial. Therefore, this meta-analysis, which compared the efficacy and toxicity between twice-daily (BID) and once-daily (OD) CCRT, was performed to help clinicians make better decisions. Methods: Relevant randomized controlled trials (RCTs) were collected by searching the PubMed, Ovid MEDLINE, Embase, ScienceDirect, Web of Science, the Cochrane Library, Scopus and Google Scholar databases to assess antitumor effects (overall survival, OS; progression-free survival, PFS; overall response rate, ORR) and toxicity (adverse effects, AEs). Results: We screened 1499 articles and included 5 RCTs including 1421 patients. We found that BID CCRT improved OS (hazard ratio, HR = 0.88, 95% confidence interval, CI 0.78-0.99, p = 0.03), the 1-year OS rate (OSR-1y, risk ratio, RR = 1.07, 95%CI 1.01-1.13, p = 0.03), and OSR-4y (RR = 1.22, 95%CI 1.03-1.43, p = 0.02), with better trends in OSR-2y, OSR-3y, and OSR-5y, compared to OD CCRT. In addition, BID CCRT had a higher complete response (CR, RR = 1.31, 95%CI 1.01-1.70, p = 0.04) than OD CCRT. PFS (HR = 0.92, 95%CI 0.79-1.07, p = 0.29), annual PFS rate, ORR (RR = 0.99, 95%CI 0.93-1.05, p = 0.72), and AEs for all grades (RR = 1.00, 95%CI 0.98-1.01, p = 0.57), and grades 3-5 (RR = 1.02, 95%CI 0.95-1.09, p = 0.60) were similar between the two arms. Conclusions: BID CCRT appears to be better than OD CCRT for limited-stage SCLC, with better antitumor effects (OS, OSR, and CR) and similar AEs. However, the high levels of AEs in both arms should be taken as a sign of caution. More large sample and high-quality RCTs need to be conducted to confirm our conclusions.
اللغة: English
تدمد: 2234-943X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::212f3202cec7c9d8338302790a071b48Test
http://europepmc.org/articles/PMC6960125Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....212f3202cec7c9d8338302790a071b48
قاعدة البيانات: OpenAIRE