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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Impact of Standardized Allergen-Removed Rhus verniciflua Stokes Extract on Advanced Adenocarcinoma of the Ampulla of Vater: A Case Series
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Impact of Standardized Allergen-Removed Rhus verniciflua Stokes Extract on Advanced Adenocarcinoma of the Ampulla of Vater: A Case Series

机译:标准化的去除过敏原的鼠李属红景天斯托克斯提取物对晚期壶腹腺癌的影响:一个病例系列

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摘要

Background. Adenocarcinoma of the ampulla of Vater (AAV) is a rare malignancy that has a better prognosis than other periampullary cancers. However, the standard treatment for patients with relapsed or metastatic AAV has not been established. We investigated the clinical feasibility of standardized allergen-removed Rhus verniciflua stokes (aRVS) extract for advanced or metastatic AAV. Patients and Methods. From July 2006 to April 2011, we retrospectively reviewed all patients with advanced AAV treated with aRVS extract alone. After applying inclusion/exclusion criteria, 12 patients were eligible for the final analysis. We assessed the progression-free survival (PFS) and overall survival (OS) of these patients during the follow-up period. Results. The median aRVS administration period was 147.0 days (range: 72-601 days). The best tumor responses according to Response Evaluation Criteria in Solid Tumors were as follows: two with complete response, two with stable disease, and eight with progressive disease. The median OS was 15.1 months (range: 4.9-25.1 months), and the median PFS was 3.0 months (range: 1.6-11.4 months). Adverse reactions to the aRVS treatment were mostly mild and self-limiting. Conclusions. Prolonged survival was observed in patients with advanced AAV under the treatment of standardized aRVS extract without significant adverse effects.
机译:背景。壶腹壶腹腺癌(AAV)是一种罕见的恶性肿瘤,其预后要优于其他壶腹周围癌。但是,对于复发性或转移性AAV患者的标准治疗方法尚未建立。我们研究了标准化的去除过敏原的Rhuns verniciflua斯托克斯(aRVS)提取物用于晚期或转移性AAV的临床可行性。患者和方法。从2006年7月至2011年4月,我们回顾了所有仅用aRVS提取物治疗的晚期AAV患者。应用纳入/排除标准后,有12名患者符合最终分析的条件。我们评估了这些患者在随访期间的无进展生存期(PFS)和总体生存期(OS)。结果。 aRVS给药中位数为147.0天(范围:72-601天)。根据实体瘤反应评估标准,最佳的肿瘤反应如下:两个反应完全,两个疾病稳定,八个疾病进行。 OS中位数为15.1个月(范围:4.9-25.1个月),PFS中位数为3.0个月(范围:1.6-11.4个月)。对aRVS治疗的不良反应大多是轻度的和自限性的。结论在标准aRVS提取物的治疗下,晚期AAV患者生存期延长,且无明显不良反应。

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