Prognostic value of chemotherapy in addition to concurrent chemoradiotherapy in T3-4N0-1 nasopharyngeal carcinoma: a propensity score matching study.

Prognostic value of chemotherapy in addition to concurrent chemoradiotherapy in T3-4N0-1 nasopharyngeal carcinoma: a propensity score matching study.
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T3-4N0-1鼻咽癌化疗加同步放化疗的预后价值:倾向评分匹配研究

DOI:
10.18632/oncotarget.20014
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发表时间:
2017-09-29
期刊:
影响因子:
--
通讯作者:
He X
He X
中科院分区:
其他
文献类型:
--
作者:
Wu LR;Yu HL;Jiang N;Jiang XS;Zong D;Wen J;Huang L;Xie P;Chen W;Wang TT;Gu DY;Yan PW;Yin L;He X

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本研究的目的是评估在调强放疗(IMRT)时代,诱导化疗(IC)或辅助化疗(AC)联合同步放化疗(CCRT)对T3 - 4N0 - 1鼻咽癌(NPC)患者的作用。 我们回顾性分析了685例新诊断为T3 - 4N0 - 1鼻咽癌患者的数据。采用倾向评分匹配(PSM)方法对患者进行匹配。不同组之间的生存结果采用Kaplan - Meier法计算,并使用对数秩检验进行比较。采用Cox比例风险模型确定独立的预后因素。 从原始队列中总共选取了236对患者。单因素分析显示,CCRT联合IC/AC组与单纯CCRT组的3年总生存率(OS)(90.8%对90.3%,P = 0.820)、无远处转移生存率(DFFS)(87.3%对89.4%,P = 0.896)和无局部区域复发生存率(LRFFS)(95.4%对93.0%,P = 0.311)相当。多因素分析发现,治疗组不是OS(风险比,0.964;95%置信区间,0.620 - 1.499;P = 0.869)、DFFS(风险比,1.036;95%置信区间,0.626 - 1.714;P = 0.890)和LRFFS(风险比,0.670;95%置信区间,0.338 - 1.327;P = 0.250)的独立预后因素。根据总分期进一步进行亚组分析也得到了类似的结果。 在IMRT时代,接受CCRT治疗的T3 - 4N0 - 1鼻咽癌患者不能从额外的诱导化疗或辅助化疗中获益。
Purpose The objective of this study is to evaluate the contribution of induction (IC) or adjuvant (AC) chemotherapy additional to concurrent chemoradiotherapy (CCRT) for patients with T3-4N0-1 nasopharyngeal carcinoma (NPC) in the era of intensity-modulate radiotherapy (IMRT). Method and Materials We retrospectively reviewed the data on 685 patients with newly diagnosed T3-4N0-1 NPC. Propensity score matching (PSM) method was used to match patients. Survival outcomes between different groups were calculated by Kaplan-Meier method and compared using log-rank test. Cox proportional hazard model was adopted to establish independent prognostic factors. Results In total, 236 pairs were selected from the primary cohort. Univariate analysis revealed 3-year overall survival (OS) (90.8% vs. 90.3%, P = 0.820), distant failure-free survival (DFFS) (87.3% vs. 89.4%, P = 0.896) and locoregional failure-free survival (LRFFS) (95.4% vs. 93.0%, P = 0.311) rates were comparable between CCRT plus IC/AC and CCRT alone groups. Multivariate analysis found that treatment group was not an independent prognostic factors for OS (HR, 0.964; 95% CI, 0.620-1.499; P = 0.869), DFFS (HR, 1.036; 95% CI, 0.626-1.714; P = 0.890) and LRFFS (HR, 0.670; 95% CI, 0.338-1.327; P = 0.250). Further subgroup analysis according to overall stage also obtained similar results. Conclusion Patients with T3-4N0-1 NPC receiving CCRT could not benefit from additional induction or adjuvant chemotherapy in the era of IMRT.
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