首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Increasing tumor volume is predictive of poor overall and progression-free survival: secondary analysis of the Radiation Therapy Oncology Group 93-11 phase I-II radiation dose-escalation study in patients with inoperable non-small-cell lung cancer.
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Increasing tumor volume is predictive of poor overall and progression-free survival: secondary analysis of the Radiation Therapy Oncology Group 93-11 phase I-II radiation dose-escalation study in patients with inoperable non-small-cell lung cancer.

机译:肿瘤体积的增加预示着不良的总体生存率和无进展生存率:放射治疗肿瘤学小组93-11 I-II期放射线剂量增加研究对不能手术的非小细胞肺癌患者的二次分析。

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PURPOSE: Patients with non-small-cell lung cancer (NSCLC) in the Radiation Therapy Oncology Group (RTOG) 93-11 trial received radiation doses of 70.9, 77.4, 83.8, or 90.3 Gy. The locoregional control and survival rates were similar among the various dose levels. We investigated the effect of the gross tumor volume (GTV) on the outcome. METHODS AND MATERIALS: The GTV was defined as the sum of the volumes of the primary tumor and involved lymph nodes. The tumor response, median survival time (MST), and progression-free survival (PFS) were analyzed separately for smaller (< or =45 cm(3)) vs. larger (>45 cm(3)) tumors. RESULTS: The distribution of the GTV was as follows: < or =45 cm(3) in 79 (49%) and >45 cm(3) in 82 (51%) of 161 patients. The median GTV was 47.3 cm(3). N0 status and female gender were associated with better tumor responses. Patients with smaller (< or =45 cm(3)) tumors achieved a longer MST and better PFS than did patients with larger (>45 cm(3)) tumors (29.7 vs. 13.3 months, p < 0.0001; and 15.8 vs. 8.3 months, p < 0.0001, respectively). Increasing the radiation dose had no effect on the MST or PFS. On multivariate analysis, only a smaller GTV was a significant prognostic factor for improved MST and PFS (hazard ratio [HR], 2.12, p = 0.0002; and HR, 2.0, p = 0.0002, respectively). The GTV as a continuous variable was also significantly associated with the MST and PFS (HR, 1.59, p < 0.0001; and HR, 1.39, p < 0.0001, respectively). CONCLUSIONS: Radiation dose escalation up to 90.3 Gy did not result in improved MST or PFS. The tumor responses were greater in node-negative patients and women. An increasing GTV was strongly associated with decreased MST and PFS. Future radiotherapy trials patients might need to use stratification by tumor volume.
机译:目的:放射治疗肿瘤学组(RTOG)93-11试验中的非小细胞肺癌(NSCLC)患者接受了70.9、77.4、83.8或90.3 Gy的放射剂量。不同剂量水平的局部控制和生存率相似。我们调查了总肿瘤体积(GTV)对预后的影响。方法和材料:GTV定义为原发肿瘤和累及淋巴结体积的总和。对于较小的(<或= 45 cm(3))和较大的(> 45 cm(3))肿瘤,分别分析了肿瘤反应,中位生存时间(MST)和无进展生存期(PFS)。结果:GTV的分布如下:161例患者中,79例(49%)≤45 cm(3),82例(51%)≥45 cm(3)。 GTV中位数为47.3 cm(3)。 N0状态和女性性别与更好的肿瘤反应相关。肿瘤较小(<或= 45 cm(3))的患者比肿瘤较大(> 45 cm(3))的患者获得更长的MST和更好的PFS(29.7 vs. 13.3个月,p <0.0001;和15.8vs。 8.3个月,p <0.0001)。增加放射剂量对MST或PFS没有影响。在多变量分析中,只有较小的GTV是改善MST和PFS的重要预后因素(危险比[HR]为2.12,p = 0.0002; HR为2.0,p = 0.0002)。 GTV作为连续变量也与MST和PFS显着相关(分别为HR,1.59,p <0.0001; HR,1.39,p <0.0001)。结论:辐射剂量增加至90.3 Gy并不能改善MST或PFS。淋巴结阴性患者和女性的肿瘤反应更大。 GTV升高与MST和PFS降低密切相关。未来的放射治疗试验患者可能需要根据肿瘤体积进行分层。

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