食管癌高剂量放疗合并或不合并化疗的临床结果:一项印度东北部的研究

Q3 Pharmacology, Toxicology and Pharmaceutics
Bhaskarjyoti Talukdar
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引用次数: 0

摘要

目的:本研究的目的是评估印度东北部食管癌(EC)患者高剂量放疗63 Gy (Gy)合并或不合并化疗的临床结果。材料和方法:2017-2018年(2年)在印度阿萨姆邦高哈蒂医学院国家癌症研究所(SCI)接受高剂量放疗或不同时化疗的所有报告的EC患者都被纳入研究。本研究为回顾性研究,对两年的回顾性数据进行临床结果分析。数据统计分析采用社会科学统计软件包(SPSS),无病生存率(DFS)采用Kaplan-Meier法计算。结果:同期共治疗105例患者。所有患者接受的总剂量为63 Gy。105例患者中,76例(72.4%)患者同时接受化疗,29例(27.6%)患者仅因合并症而未接受化疗。在这里,首次随访时,89例(84.8%)患者完全缓解,10例(9.5%)患者部分缓解,6例(5.7%)患者病情进展。评估治疗相关的毒性。没有患者出现>级2级毒性。此外,中位无病生存期(DFS)为13个月,估计平均值为16.98个月。标准误差(SE) =1.683,置信区间(CI) =13.682-20.279。结论:高剂量放疗(63 Gy)联合化疗作为顺铂或紫杉醇加卡铂的每周方案是一种有效的I - IVA期EC的最终治疗方法,毒性可接受。无论治疗方式如何,EC的中位DFS都是最小的。在中位生存时间前生存率迅速下降,中位生存时间后生存率保持不变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CLINICAL OUTCOME OF HIGH DOSE RADIOTHERAPY WITH OR WITHOUT CONCURRENT CHEMOTHERAPY IN ESOPHAGEAL CANCER (EC): A STUDY FROM NORTH – EAST INDIA
OBJECTIVE: The objective of this study is to evaluate the clinical outcomes of high dose radiotherapy 63 Gray (Gy) with or without concurrent chemotherapy in Esophageal Cancer (EC) patients of North-East, India. MATERIAL AND METHODS: All reported EC patients belonging to different states of North-East and treated with radical intent with high dose radiotherapy with or without concurrent chemotherapy during the period 2017-2018 (2 years) at State Cancer Institute (SCI),Gauhati Medical College (GMC), Assam, India were included in the study. This study was retrospective in nature and two years retrospective data were analyzed for clinical outcome. Statistical analysis of data was done using Statistical Packages for Social Sciences (SPSS) and Disease Free Survival (DFS) was calculated using Kaplan-Meier method. RESULTS: Total 105 patients were treated during the period. All patients received a total dose of 63 Gy radiation. Out of 105 patients, 76 patients (72.4%) received concurrent chemotherapy and 29 patients (27.6%) not received chemotherapy only due to co-morbidities. Here, at first follow up, 89 (84.8%) patients showed complete response, 10 (9.5%) showed partial response and 6 (5.7%) showed progressive disease. Treatment related toxicities were assessed. None of the patient developed > Grade 2 toxicity. Further, Median Disease Free Survival (DFS) was 13 months with estimated mean was 16.98 months. Also, Standard Error (SE) =1.683, Confidence Interval (CI) =13.682-20.279. CONCLUSION: The high dose radiation (63 Gy) with concurrent chemotherapy as weekly regimen of Cisplatin or Paclitaxel plus Carboplatin is an effective definitive treatment of Stage I – IVA EC with acceptable toxicity. Median DFS is minimal in EC irrespective of the treatment. The rate of survival is decreasing rapidly before the median DFS and the rate of survival is constant after the Median DFS.
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