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使用调强放疗治疗肛管鳞状细胞癌时,根治性同步放化疗期间急性毒性的预测因素。

Predictors of acute toxicities during definitive chemoradiation using intensity-modulated radiotherapy for anal squamous cell carcinoma.

作者信息

Julie Diana A R, Oh Jung Hun, Apte Aditya P, Deasy Joseph O, Tom Ashlyn, Wu Abraham J, Goodman Karyn A

机构信息

a Department of Radiation Oncology , Memorial Sloan-Kettering Cancer Center , New York, New York , USA.

b Department of Medical Physics , Memorial Sloan-Kettering Cancer Center , New York, New York , USA.

出版信息

Acta Oncol. 2016;55(2):208-16. doi: 10.3109/0284186X.2015.1043396. Epub 2015 May 18.

Abstract

PURPOSE

To identify clinical and dosimetric factors associated with acute hematologic and gastrointestinal (GI) toxicities during definitive therapy using intensity-modulated radiotherapy (IMRT) for anal squamous cell carcinoma (ASCC).

MATERIALS AND METHODS

We retrospectively analyzed 108 ASCC patients treated with IMRT. Clinical information included age, gender, stage, concurrent chemotherapy, mitomycin (MMC) chemotherapy and weekly hematologic and GI toxicity during IMRT. From contours of the bony pelvis and bowel, dose-volume parameters were extracted. Logistic regression models were used to test associations between toxicities and clinical or dosimetric predictors.

RESULTS

The median age was 59 years, 81 patients were women and 84 patients received concurrent MMC and 5-fluorouracil (5FU). On multivariate analysis (MVA), the model most predictive of Grade 2 + anemia included the maximum bony pelvis dose (Dmax), female gender, and T stage [p = 0.035, cross validation area under the curve (cvAUC) = 0.66]. The strongest model of Grade 2 + leukopenia included V10 (percentage of pelvic bone volume receiving ≥ 10 Gy) and number of MMC cycles (p = 0.276, cvAUC = 0.57). The model including MMC cycle number and T stage correlated best with Grade 2 + neutropenia (p = 0.306, cvAUC = 0.57). The model predictive of combined Grade 2 + hematologic toxicity (HT) included V10 and T stage (p = 0.016, cvAUC = 0.66). A model including VA45 (absolute bowel volume receiving ≥ 45 Gy) and MOH5 (mean dose to hottest 5% of bowel volume) best predicted diarrhea (p = 0.517, cvAUC = 0.56).

CONCLUSION

Dosimetric constraints to the pelvic bones should be integrated into IMRT planning to reduce toxicity, potentially reducing treatment interruptions and improving disease outcomes in ASCC. Specifically, our results indicate that Dmax should be confined to ≤ 57 Gy to minimize anemia and that V10 should be restricted to ≤ 87% to reduce incidence of all HT.

摘要

目的

确定在采用调强放射治疗(IMRT)治疗肛管鳞状细胞癌(ASCC)的根治性治疗期间,与急性血液学和胃肠道(GI)毒性相关的临床和剂量学因素。

材料与方法

我们回顾性分析了108例接受IMRT治疗的ASCC患者。临床信息包括年龄、性别、分期、同步化疗、丝裂霉素(MMC)化疗以及IMRT期间的每周血液学和胃肠道毒性。从骨盆和肠道轮廓中提取剂量体积参数。使用逻辑回归模型来检验毒性与临床或剂量学预测因素之间的关联。

结果

中位年龄为59岁,81例患者为女性,84例患者接受了同步MMC和5-氟尿嘧啶(5FU)治疗。在多因素分析(MVA)中,对2级及以上贫血预测性最强的模型包括骨盆最大剂量(Dmax)、女性性别和T分期[p = 0.035,曲线下交叉验证面积(cvAUC)= 0.66]。对2级及以上白细胞减少预测性最强的模型包括V10(接受≥10 Gy的骨盆骨体积百分比)和MMC周期数(p = 0.276,cvAUC = 0.57)。包括MMC周期数和T分期的模型与2级及以上中性粒细胞减少相关性最佳(p = 0.306,cvAUC = 0.57)。对2级及以上血液学毒性(HT)联合预测性最强的模型包括V10和T分期(p = 0.016,cvAUC = 0.66)。一个包括VA45(接受≥45 Gy的绝对肠体积)和MOH5(最热的5%肠体积的平均剂量)的模型对腹泻预测性最佳(p = 0.517,cvAUC = 0.56)。

结论

骨盆骨的剂量学限制应纳入IMRT计划以降低毒性,这可能减少治疗中断并改善ASCC的疾病结局。具体而言,我们的结果表明Dmax应限制在≤57 Gy以尽量减少贫血,V10应限制在≤87%以降低所有HT的发生率。

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