放疗剂量增加同时化疗可改善局部晚期宫颈癌的预后

Hegazy Mw, R. Mahmood, I. Al-Badawi, H. Husaini, B. Moftah
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引用次数: 0

摘要

背景:评价体积调制弧线治疗(VMAT)和影像引导放疗(IGRT)同步化疗治疗局部晚期宫颈癌(LACC)的剂量递增效果,并与常规放疗(CRT)在毒性和临床结果方面进行比较。方法和材料:对所有接受常规放射治疗或剂量递增的体积调节电弧治疗的LACC患者进行数据库回顾,同时每周顺铂40mg /m2,然后进行高剂量率近距离治疗。主要终点和次要终点分别为毒性、无病生存期和总生存期。结果:60例患者中,40例接受CRT, 20例接受VMAT。CRT组中位随访时间为47个月(11-89),VMAT组中位随访时间为35个月(13-47)。血红蛋白毒性(I-II级)分别为97.5%和90% (p=0.03),白细胞减少(I-III级)分别为90%和70% (p=0.02)。没有3级或4级胃肠道或泌尿生殖系统(GI或GU)毒性。36个月时,CRT组的无病生存率为45%,VMAT组为75% (p=0.03), CRT组的总生存率为65%,VMAT组为85% (p=0.8)。结论:VMAT与CRT相比毒性明显降低,临床效果相当甚至更好。进一步的研究需要更大的样本量和更长的随访时间来证明其在常规临床实践中的应用是合理的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Radiotherapy Dose Escalation with Concurrent Chemotherapy ImprovesOutcome in Locally Advanced Cervix Carcinoma
Background: To evaluate radiotherapy dose escalation using volumetric modulated arc therapy (VMAT) and image guided radiotherapy (IGRT) with concurrent chemotherapy in locally advanced cervix cancer (LACC) and compare it with conventional radiation therapy (CRT) in terms of the toxicity and clinical outcomes. Methods and Materials: Data base was reviewed for all LACC patients treated either by conventional radiation therapy or dose escalation volumetric modulated arc therapy, with concurrent weekly Cisplatin 40 mg/m2 followed by high dose rate brachytherapy. The primary and secondary endpoints were toxicity, disease-free survival and overall survival respectively. Results: Of 60 patients, 40 patients received CRT and 20 received VMAT. The median follow-up time in the CRT arm was 47 months (11-89), and 35 months (13-47) in the VMAT arm. Hemoglobin toxicity (Grade I-II) was encountered in 97.5% and 90% (p=0.03) while (Grade I-III) Leukopenia was 90% and 70% (p=0.02), respectively. There was no grade 3 or 4 gastrointestinal or genitourinary (GI or GU) toxicity. At 36 months, disease-free survival was 45% in the CRT group versus 75% in the VMAT group (p=0.03), and overall survival was 65% in the CRT group versus 85% in the VMAT group (p=0.8). Conclusion: VMAT is associated with significantly less toxicity and comparable or even better clinical outcome compared with CRT. Further studies with larger sample sizes and longer follow-up times are warranted to justify its use in routine clinical practice.
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