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标准化去除过敏原漆树提取物对 Vater 壶腹高级腺癌的影响:病例系列。

Impact of Standardized Allergen-Removed Rhus verniciflua Stokes Extract on Advanced Adenocarcinoma of the Ampulla of Vater: A Case Series.

机构信息

Department of Medical Consilence, Graduate School, Jukjeon Campus, Dankook University, 152 Jukjeon-ro, Suji-gu, Yongin-si 448-701, Republic of Korea.

出版信息

Evid Based Complement Alternat Med. 2013;2013:203168. doi: 10.1155/2013/203168. Epub 2013 Apr 22.

DOI:10.1155/2013/203168
PMID:23710214
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3654714/
Abstract

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.

摘要

背景

Vater 壶腹腺癌(AAV)是一种罕见的恶性肿瘤,其预后优于其他壶腹周围癌症。然而,复发或转移性 AAV 患者的标准治疗尚未建立。我们研究了标准化变应原去除的漆树(aRVS)提取物治疗晚期或转移性 AAV 的临床可行性。

患者和方法

从 2006 年 7 月至 2011 年 4 月,我们回顾性分析了所有单独使用 aRVS 提取物治疗的晚期 AAV 患者。在应用纳入/排除标准后,12 例患者符合最终分析标准。我们评估了这些患者在随访期间的无进展生存期(PFS)和总生存期(OS)。

结果

aRVS 给药的中位时间为 147.0 天(范围:72-601 天)。根据实体瘤反应评价标准,最佳肿瘤反应如下:完全缓解 2 例,稳定疾病 2 例,进展性疾病 8 例。中位 OS 为 15.1 个月(范围:4.9-25.1 个月),中位 PFS 为 3.0 个月(范围:1.6-11.4 个月)。aRVS 治疗的不良反应大多为轻度和自限性。

结论

在标准化 aRVS 提取物治疗下,晚期 AAV 患者的生存期延长,且无明显不良反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe10/3654714/2456c168a58b/ECAM2013-203168.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe10/3654714/a7ed6ad23a0f/ECAM2013-203168.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe10/3654714/198fa7213cf7/ECAM2013-203168.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe10/3654714/2456c168a58b/ECAM2013-203168.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe10/3654714/a7ed6ad23a0f/ECAM2013-203168.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe10/3654714/198fa7213cf7/ECAM2013-203168.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe10/3654714/2456c168a58b/ECAM2013-203168.003.jpg

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