Xia Bing, Hong Ling-Zhi, Cai Xu-Wei, Zhu Zheng-Fei, Liu Qi, Zhao Kuai-Le, Fan Min, Mao Jing-Fang, Yang Huan-Jun, Wu Kai-Liang, Fu Xiao-Long
Department of Radiation Oncology, Shanghai Cancer Center, Fudan University, Shanghai, China; Department of Radiation Oncology, Hangzhou Cancer Hospital, Hangzhou, China.
Department of Oncology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Int J Radiat Oncol Biol Phys. 2015 Mar 1;91(3):517-23. doi: 10.1016/j.ijrobp.2014.09.042. Epub 2014 Dec 3.
To prospectively investigate the efficacy and toxicity of accelerated hypofractionated thoracic radiation therapy (HypoTRT) combined with concurrent chemotherapy in the treatment of limited-stage small-cell lung cancer (LS-SCLC), with the hypothesis that both high radiation dose and short radiation time are important in this setting.
Patients with previously untreated LS-SCLC, Eastern Cooperative Oncology Group performance status of 0 to 2, and adequate organ function were eligible. HypoTRT of 55 Gy at 2.5 Gy per fraction over 30 days was given on the first day of the second or third cycle of chemotherapy. An etoposide/cisplatin regimen was given to 4 to 6 cycles. Patients who had a good response to initial treatment were offered prophylactic cranial irradiation. The primary endpoint was the 2-year progression-free survival rate.
Fifty-nine patients were enrolled from July 2007 through February 2012 (median age, 58 years; 86% male). The 2-year progression-free survival rate was 49.0% (95% confidence interval [CI] 35.3%-62.7%). Median survival time was 28.5 months (95% CI 9.0-48.0 months); the 2-year overall survival rate was 58.2% (95% CI 44.5%-71.9%). The 2-year local control rate was 76.4% (95% CI 63.7%-89.1%). The severe hematologic toxicities (grade 3 or 4) were leukopenia (32%), neutropenia (25%), and thrombocytopenia (15%). Acute esophagitis and pneumonitis of grade ≥3 occurred in 25% and 10% of the patients, respectively. Thirty-eight patients (64%) received prophylactic cranial irradiation.
Our study showed that HypoTRT of 55 Gy at 2.5 Gy per fraction daily concurrently with etoposide/cisplatin chemotherapy has favorable survival and acceptable toxicity. This radiation schedule deserves further investigation in LS-SCLC.
前瞻性研究加速超分割胸部放疗(HypoTRT)联合同步化疗治疗局限期小细胞肺癌(LS-SCLC)的疗效和毒性,基于高辐射剂量和短辐射时间在此情况下均很重要这一假设。
符合条件的患者为既往未接受过治疗的LS-SCLC患者,东部肿瘤协作组体能状态为0至2,且器官功能良好。在化疗的第二个或第三个周期的第一天给予HypoTRT,总剂量55 Gy,每次分割剂量2.5 Gy,共30天。给予依托泊苷/顺铂方案化疗4至6个周期。对初始治疗反应良好的患者接受预防性脑照射。主要终点是2年无进展生存率。
2007年7月至2012年2月共纳入59例患者(中位年龄58岁;86%为男性)。2年无进展生存率为49.0%(95%置信区间[CI] 35.3%-62.7%)。中位生存时间为28.5个月(95% CI 9.0-48.0个月);2年总生存率为58.2%(95% CI 44.5%-71.9%)。2年局部控制率为76.4%(95% CI 63.7%-89.1%)。严重血液学毒性(3级或4级)为白细胞减少(32%)、中性粒细胞减少(25%)和血小板减少(15%)。≥3级急性食管炎和肺炎分别发生在25%和10%的患者中。38例患者(64%)接受了预防性脑照射。
我们的研究表明,每天每次分割剂量2.5 Gy、总剂量55 Gy的HypoTRT与依托泊苷/顺铂化疗同步进行,具有良好的生存率和可接受的毒性。这种放疗方案值得在LS-SCLC中进一步研究。