首页> 外文OA文献 >Pulmonary toxicity in Stage III non-small cell lung cancer patients treated with high-dose (74 Gy) 3-dimensional conformal thoracic radiotherapy and concurrent chemotherapy following induction chemotherapy: a secondary analysis of Cancer and Leukemia Group B (CALGB) trial 30105
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Pulmonary toxicity in Stage III non-small cell lung cancer patients treated with high-dose (74 Gy) 3-dimensional conformal thoracic radiotherapy and concurrent chemotherapy following induction chemotherapy: a secondary analysis of Cancer and Leukemia Group B (CALGB) trial 30105

机译:III期非小细胞肺癌患者接受高剂量(74 Gy)三维适形胸部放疗和诱导化疗后同步化疗的肺毒性:癌症和白血病B组(CaLGB)试验的二级分析30105

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摘要

PURPOSE: Cancer and Leukemia Group B (CALGB) 30105 tested two different concurrent chemoradiotherapy platforms with high-dose (74 Gy) three-dimensional conformal radiotherapy (3D-CRT) after two cycles of induction chemotherapy for Stage IIIA/IIIB non-small cell lung cancer (NSCLC) patients to determine if either could achieve a primary endpoint of \u3e18-month median survival. Final results of 30105 demonstrated that induction carboplatin and gemcitabine and concurrent gemcitabine 3D-CRT was not feasible because of treatment-related toxicity. However, induction and concurrent carboplatin/paclitaxel with 74 Gy 3D-CRT had a median survival of 24 months, and is the basis for the experimental arm in CALGB 30610/RTOG 0617/N0628. We conducted a secondary analysis of all patients to determine predictors of treatment-related pulmonary toxicity.METHODS AND MATERIALS: Patient, tumor, and treatment-related variables were analyzed to determine their relation with treatment-related pulmonary toxicity.RESULTS: Older age, higher N stage, larger planning target volume (PTV)1, smaller total lung volume/PTV1 ratio, larger V20, and larger mean lung dose were associated with increasing pulmonary toxicity on univariate analysis. Multivariate analysis confirmed that V20 and nodal stage as well as treatment with concurrent gemcitabine were associated with treatment-related toxicity. A high-risk group comprising patients with N3 disease and V20 \u3e38% was associated with 80% of Grades 3-5 pulmonary toxicity cases.CONCLUSIONS: Elevated V20 and N3 disease status are important predictors of treatment related pulmonary toxicity in patients treated with high-dose 3D-CRT and concurrent chemotherapy. Further studies may use these metrics in considering patients for these treatments.
机译:目的:癌症和白血病B组(CALGB)30105在对IIIA / IIIB期非小细胞进行了诱导化疗的两个周期后,采用高剂量(74 Gy)三维保形放射疗法(3D-CRT)测试了两种不同的同时放化疗平台肺癌(NSCLC)患者,以确定其中任一者是否可以达到18个月中位生存期的主要终点。 30105的最终结果表明,由于与治疗相关的毒性,诱导卡铂和吉西他滨以及同时进行的吉西他滨3D-CRT是不可行的。然而,诱导和并发卡铂/紫杉醇联合74 Gy 3D-CRT的中位生存期为24个月,并且是CALGB 30610 / RTOG 0617 / N0628中进行实验的基础。我们对所有患者进行了二级分析,以确定治疗相关的肺毒性的预测因子。方法和材料:分析了患者,肿瘤和治疗相关的变量,以确定它们与治疗相关的肺毒性的关系。结果:年龄较大,年龄较高在单因素分析中,N期,较大的计划目标体积(PTV)1,较小的总肺体积/ PTV1比,较大的V20和较大的平均肺剂量与肺毒性增加相关。多变量分析证实,V20和淋巴结分期以及并发吉西他滨的治疗与治疗相关的毒性有关。由N3病和V20 \ u3e38%的患者组成的高风险组与3-5级肺毒性病例中的80%相关。结论:V20和N3疾病状态升高是接受高剂量治疗的患者与治疗相关的肺毒性的重要预测指标剂量的3D-CRT和同步化疗。进一步的研究可以使用这些指标来考虑患者接受这些治疗。

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