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Impact of in vitro chemosensitivity test-guided platinum-based adjuvant chemotherapy on the surgical outcomes of patients with p-stage IIIA non-small cell lung cancer that underwent complete resection

机译:体外化学敏感性试验指导的铂类辅助化疗对接受完全切除的p期IIIA期非小细胞肺癌患者手术结局的影响

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摘要

The impact of in vitro chemosensitivity test-guided platinum-based adjuvant chemotherapy on the surgical outcomes of patients undergoing complete resection for locally advanced non-small cell lung cancer (NSCLC) has yet to be elucidated. In the present study, the utility of adjuvant chemotherapy based on the collagen gel droplet embedded culture drug sensitivity test (CD-DST) in patients with p (pathology)-stage IIIA NSCLC was retrospectively analyzed. A series of 39 patients that had received platinum-based adjuvant chemotherapy following complete resection between 2007 and 2012 were enrolled. Their surgical specimens were subjected to the CD-DST. The patients were subsequently classified into two groups on the basis of in vitro anti-cancer drug sensitivity data obtained using the CD-DST: The sensitive group (25 patients) were treated with regimens including one or two of the anti-cancer drug(s) that were indicated to be effective by the CD-DST, whereas the non-sensitive group (14 patients) were treated with chemotherapy regimens that did not include any CD-DST-selected anti-cancer drugs. There were no significant differences in the background characteristics of the two groups [including in respect of the pathological TN (tumor-lymph node) stage, tumor histology, epidermal growth factor receptor mutation status, the frequency of each chemotherapy regimen, and the number of administered cycles]. The 5-year disease-free survival (DFS) rate of the sensitive group was 32.3%, whereas that of the non-sensitive group was 14.3% (P=0.037). In contrast, no difference in overall survival (OS) was observed (P=0.76). Multivariate analysis revealed that adjuvant chemotherapy based on the CD-DST had a significant favorable effect on the DFS (P=0.01). Therefore, the present study has demonstrated that CD-DST data obtained from surgical specimens aid the selection of effective platinum-based adjuvant chemotherapy regimens for patients undergoing complete resection for p-stage IIIA NSCLC. The use of CD-DST-guided platinum-based regimens may have a beneficial impact on the DFS of such patients.
机译:尚需阐明体外化学敏感性试验指导的铂类辅助化疗对局部切除的局部晚期非小细胞肺癌(NSCLC)患者手术结局的影响。在本研究中,回顾性分析了基于胶原凝胶小滴包埋培养药物敏感性试验(CD-DST)的辅助化疗在p(病理)IIIA期NSCLC患者中的效用。纳入了39例2007年至2012年完全切除后接受铂类辅助化疗的患者。他们的手术标本接受了CD-DST。随后根据使用CD-DST获得的体外抗癌药敏感性数据将患者分为两组:敏感组(25例患者)接受了包括一种或两种抗癌药的治疗方案)被CD-DST证明是有效的,而非敏感组(14例患者)接受了不包含任何CD-DST选择的抗癌药物的化疗方案。两组的背景特征[包括在病理性TN(肿瘤-淋巴结)分期,肿瘤组织学,表皮生长因子受体突变状态,每种化疗方案的频率以及管理周期]。敏感组的5年无病生存率(DFS)为32.3%,而非敏感组的5年无病生存率为14.3%(P = 0.037)。相反,未观察到总生存期(OS)的差异(P = 0.76)。多因素分析显示,基于CD-DST的辅助化疗对DFS有显着的有利影响(P = 0.01)。因此,本研究表明,从外科手术标本中获得的CD-DST数据有助于为接受p期IIIA期NSCLC完全切除的患者选择有效的铂类辅助化疗方案。 CD-DST指导的铂基治疗方案的使用可能会对此类患者的DFS产生有益的影响。

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