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首页> 外文期刊>The American journal of Chinese medicine >The efficacy and safety of standardized allergen-removed Rhus verniciflua extract as maintenance therapy after first-line chemotherapy in patients with advanced non-small cell lung cancer
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The efficacy and safety of standardized allergen-removed Rhus verniciflua extract as maintenance therapy after first-line chemotherapy in patients with advanced non-small cell lung cancer

机译:标准化的去除过敏原的鼠李糖提取物作为一线化疗后维持疗法对晚期非小细胞肺癌患者的疗效和安全性

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摘要

Chemotherapy improves the survival of patients with advanced non-small cell lung cancer (NSCLC), but tumor progression is often inevitable. Strategies are needed to improve the therapeutic efficacy of chemotherapy. Over recent years, there has been increasing interest in the role of maintenance therapy after first-line chemotherapy. We investigated the efficacy and safety of standardized allergen-removed Rhus verniciflua Stokes extract (aRVS) as maintenance therapy in patients with non-progressive disease following first-line chemotherapy. We reviewed the medical records of 33 patients with advanced NSCLC, who started treatment with aRVS in a state of tumor regression or stable disease after completion of four or six cycles of induction chemotherapy at the Integrative Cancer Center, Kyung Hee University Hospital at Gangdong from June 2006 to April 2012. The primary objective of this study was progression-free survival (PFS) of aRVS as maintenance therapy. Secondary objectives included assessments of disease control rate (DCR), overall survival (OS), and the safety of aRVS treatment. The median PFS was 5.2 months with a 6- and 12-month PFS rate of 40.6% and 12.9%, respectively. The DCR was 93.9% and the median OS was 34.8 months. The overall survival rates at 12, 24, and 36 months were 84.2%, 76.7% and 49.9%, respectively. We observed no hematologic toxicity, nephrotoxicity, or hepatotoxicity during aRVS treatment. In conclusion, maintenance therapy with aRVS for patients with advanced NSCLC is well-tolerated and offers encouraging improved PFS and OS compared with historical controls. Our data provide further evidence that aRVS may be used beyond disease progression in this clinical setting.
机译:化学疗法可改善晚期非小细胞肺癌(NSCLC)患者的生存率,但肿瘤进展通常是不可避免的。需要改善化疗疗效的策略。近年来,人们对一线化疗后维持治疗的作用越来越感兴趣。我们研究了一线化疗后标准化去除变应原的红景天Stokes提取物(aRVS)作为非进展性疾病患者维持治疗的功效和安全性。我们回顾了33例晚期NSCLC患者的病历,他们于6月在江东庆熙大学附属医院综合癌症中心完成了4到6个周期的诱导化疗后,开始以aRVS治疗,处于肿瘤消退或疾病稳定的状态。 2006年至2012年4月。这项研究的主要目的是作为维持疗法的aRVS的无进展生存期(PFS)。次要目标包括评估疾病控制率(DCR),总体生存率(OS)和aRVS治疗的安全性。中位PFS为5.2个月,其中6个月和12个月PFS分别为40.6%和12.9%。 DCR为93.9%,中位OS​​为34.8个月。在12、24和36个月时的总生存率分别为84.2%,76.7%和49.9%。我们在aRVS治疗期间未观察到血液学毒性,肾毒性或肝毒性。总之,对于晚期NSCLC患者,用aRVS进行维持治疗的耐受性良好,与历史对照相比,可以改善PFS和OS。我们的数据提供了进一步的证据,表明在这种临床情况下,aRVS可以用于疾病进展以外的其他领域。

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