广泛期小细胞肺癌患者一线化疗免疫治疗后胸部巩固放疗的疗效和安全性:一项回顾性队列研究

IF 4 2区 医学 Q2 ONCOLOGY Translational lung cancer research Pub Date : 2024-12-31 Epub Date: 2024-12-27 DOI:10.21037/tlcr-2024-1182
Lin Zheng, Yang Yang, Fan Bu, Ruizhi Ye, Fengming Zhang, Zhixiang Ji, Xirong Zhu, Hong Chen, Rongjun Shao, Lidan Liu, Xixi Ying, Lingying Zhu, Enyu Wang, Jifeng Feng, Zhiyong Shi, Jun Fang, Yuezhen Wang, Zhirui Zhou, Guangxian You
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引用次数: 0

摘要

背景:胸部放疗(TRT)在改善化疗反应性小细胞肺癌(SCLC)病例的局部控制和总生存(OS)方面显示出潜在的益处。然而,它在化学免疫治疗时代的作用仍未得到充分探索。在当前的免疫治疗时代,本研究评估了巩固性TRT (cTRT)在大分期SCLC (ES-SCLC)患者中的疗效和安全性,并评估了其对OS的影响。此外,还探讨了最佳放疗剂量和分割方案。方法:回顾性队列研究将2019年1月至2023年11月在泰州市肿瘤医院确诊的124例ES-SCLC患者分为cTRT组和非cTRT组。我们比较了两组患者的基线特征、治疗过程和生存结果。形成不同放疗剂量和分级方案的cTRT亚组,比较基线特征、放疗疗效和安全性、放疗后复发模式和生存结局。选择OS作为主要观察终点。使用log-rank检验分析两组间OS的差异。通过单变量和多变量Cox回归分析确定与总患者队列中OS相关的因素。结果:两组(cTRT和非cTRT)的基线特征大致相当,具有以下显著差异:cTRT组女性比例较低(1.7% vs. 15.2%, P=0.02),神经元特异性烯醇化酶水平较低(NSE,中位数:15.87 vs. 32.00 ng/mL, P=0.009),钠浓度较高(中位数:140.50 vs. 138.25 mmol/L, P=0.01)。此外,cTRT组接受了更多的一线治疗周期(中位数:4.00 vs. 3.00, P=0.001)。与非cTRT组相比,cTRT组的OS更长[中位生存期15.5个月对10.5个月;风险比(HR) =2.0497;95%置信区间(CI): 1.3548-3.1010;结论:cTRT改善了ES-SCLC患者的OS,并表现出可控的相关毒性。放疗剂量和分割方案的选择对治疗结果的影响有待进一步研究。
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Efficacy and safety of consolidative thoracic radiotherapy after first-line chemoimmunotherapy in patients with extensive-stage small-cell lung cancer: a retrospective cohort study.

Background: Thoracic radiotherapy (TRT) has shown potential benefits in improving local control and overall survival (OS) in chemotherapy-responsive small-cell lung cancer (SCLC) cases. However, its role in the era of chemoimmunotherapy remains underexplored. In the current era of immunotherapy, this study evaluated the efficacy and safety of consolidative TRT (cTRT) in patients with extensive-stage SCLC (ES-SCLC) and assessed its impact on OS. Additionally, the optimal radiotherapy dose and fractionation schemes were also explored.

Methods: In this retrospective cohort study, 124 patients with ES-SCLC diagnosed at Taizhou Cancer Hospital between January 2019 and November 2023 were categorized into cTRT and non-cTRT groups. We compared the baseline characteristics, treatment processes, and survival outcomes between the two groups. Moreover, cTRT subgroups of different radiotherapy doses and fractionation schemes were formed and compared in terms of baseline characteristics, radiotherapy efficacy and safety, patterns of recurrence after radiotherapy, and survival outcomes. OS was selected as the primary endpoint for observation. Differences in OS between the groups were analyzed using log-rank tests. Univariable and multivariable Cox regression analyses were performed to identify factors correlated with OS in the overall patient cohort.

Results: The baseline characteristics between the two groups (cTRT and non-cTRT) were generally comparable, with the following significant differences: the cTRT group had a lower proportion of females (1.7% vs. 15.2%, P=0.02), lower levels of neuron-specific enolase (NSE, median: 15.87 vs. 32.00 ng/mL, P=0.009), and higher sodium concentrations (median: 140.50 vs. 138.25 mmol/L, P=0.01). Additionally, the cTRT group underwent more first-line treatment cycles (median: 4.00 vs. 3.00, P=0.001). Compared with the non-cTRT group, the cTRT group had a longer OS [median survival 15.5 vs. 10.5 months; hazard ratio (HR) =2.0497; 95% confidence interval (CI): 1.3548-3.1010; P<0.001]. There were no significant differences in survival outcomes associated with the different radiotherapy dosage or fractionation schedules. The most common adverse event was neutropenia, but no severe treatment-related deaths occurred. Multivariable Cox analysis revealed that the sodium concentration (HR =0.8751; 95% CI: 0.7944-0.9642; P=0.007), initial treatment response (HR =0.7022; 95% CI: 0.4949-0.9964; P=0.048), total number of systemic treatment cycles (HR =0.5501; 95% CI: 0.3618-0.8364; P=0.005), and whether to receive cTRT (HR =1.7484; 95% CI: 1.1033-2.7708; P=0.02) were independent prognostic factors for OS.

Conclusions: cTRT improved the OS of patients with ES-SCLC and exhibited manageable associated toxicity. Further research is needed to confirm the effect of radiotherapy dose and fractionation scheme selection on treatment outcomes.

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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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