首页> 外文期刊>Radiotherapy and oncology: Journal of the European Society for Therapeutic Radiology and Oncology >Systematic overview of preoperative (neoadjuvant) chemoradiotherapy trials in oesophageal cancer: evidence of a radiation and chemotherapy dose response.
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Systematic overview of preoperative (neoadjuvant) chemoradiotherapy trials in oesophageal cancer: evidence of a radiation and chemotherapy dose response.

机译:食管癌术前(新辅助)放化疗试验系统综述:放疗和化疗剂量反应的证据。

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BACKGROUND AND PURPOSE: Numerous trials have shown that pathological complete response (pCR) following preoperative chemoradiotherapy (CRT) and surgery for oesophageal cancer is associated with improved survival. However, different radiotherapy doses and fractionations and chemotherapy drugs, doses and scheduling were used, which may account for the differences in observed pCR and survival rates. A dose-response relationship may exist between radiotherapy and chemotherapy dose and pCR. PATIENTS AND METHODS: Trials using a single radiotherapy and chemotherapy regimen (5FU, cisplatin or mitomycin C-based) and providing information on patient numbers, age, resection and pCR rates were eligible. The endpoint used was pCR and the covariates analysed were prescribed radiotherapy dose, radiotherapy dosexdose per fraction, radiotherapy treatment time, prescribed chemotherapy (5FU, cisplatin and mitomycin C) dose and median age of patients within the trial. The model used was a multivariate logistic regression. RESULTS: Twenty-six trials were included (1335 patients) in which 311 patients (24%) achieved pCR. The probability of pCR improved with increasing dose of radiotherapy (P=0.006), 5FU (P=0.003) and cisplatin (P=0.018). Increasing radiotherapy treatment time (P=0.035) and increasing median age (P=0.019) reduced the probability of pCR. The estimated alpha/beta ratio of oesophageal cancer was 4.9 Gy (95% confidence interval (CI) 1.5-17 Gy) and the estimated radiotherapy dose lost per day was 0.59 Gy (95% CI 0.18-0.99 Gy). One gram per square metre of 5FU was estimated to be equivalent to 1.9 Gy (95% CI 0.8-5.2 Gy) of radiation and 100mg/m2 of cisplatin was estimated to be equivalent to 7.2 Gy (95% CI 2.1-28 Gy). Mitomycin C dose did not appear to influence pCR rates (P=0.60). CONCLUSIONS: There was evidence of a dose-response relationship between increasing protocol prescribed radiotherapy, 5FU and cisplatin dose and pCR. Additional significant factors were radiotherapy treatment time and median age of patients within the trial.
机译:背景与目的:大量试验表明,食管癌术前放化疗(CRT)和手术后的病理完全缓解(pCR)与存活率提高有关。但是,使用了不同的放疗剂量和分级以及化疗药物,剂量和时间表,这可能解释了观察到的pCR和存活率的差异。放疗与化疗剂量和pCR之间可能存在剂量反应关系。患者和方法:采用单一放疗和化疗方案(基于5FU,顺铂或丝裂霉素C的试验)并提供有关患者人数,年龄,切除和pCR率的信息的试验是合格的。使用的终点是pCR,所分析的协变量是处方放射治疗剂量,放射治疗剂量x剂量/剂量,放射治疗时间,处方化学疗法(5FU,顺铂和丝裂霉素C)剂量以及试验中患者的中位年龄。使用的模型是多元逻辑回归。结果:共纳入26项试验(1335例患者),其中311例患者(24%)达到了pCR。随着放疗剂量(P = 0.006),5FU(P = 0.003)和顺铂(P = 0.018)剂量的增加,pCR的可能性会提高。放射治疗时间的增加(P = 0.035)和中位年龄的增加(P = 0.019)降低了pCR的可能性。食道癌的估计alpha / beta比为4.9 Gy(95%置信区间(CI)1.5-17 Gy),估计每天损失的放射治疗剂量为0.59 Gy(95%CI 0.18-0.99 Gy)。每平方米1克5FU估计相当于1.9 Gy(95%CI 0.8-5.2 Gy)辐射,而100mg / m2的顺铂估计相当于7.2 Gy(95%CI 2.1-28 Gy)。丝裂霉素C剂量似乎不影响pCR率(P = 0.60)。结论:有证据表明,增加方案规定的放射治疗,5FU,顺铂剂量和pCR之间存在剂量反应关系。其他重要因素是试验中放疗的治疗时间和患者的中位年龄。

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