Systematic evaluation of the clinical effects of supportive mistletoe treatment within chemo- and/or radiotherapy protocols and long-term mistletoe application in nonmetastatic colorectal carcinoma: multicenter, controlled, observational cohort study.

Walter E Friedel, Harald Matthes, Paul R Bock, Kurt S Zänker
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Abstract

In Europe, patients with colorectal carcinoma (CRC) frequently receive mistletoe extracts to improve quality of life and survival. This study was designed to evaluate supportive treatment with mistletoe extract Iscador (ISC) in nonmetastatic CRC patients under routine clinical conditions and to create well-founded hypotheses for future prospective clinical studies. The design of a multicenter, controlled, retrospective, observational cohort study with parallel groups met the Good Epidemiological Practice rules. Anonymous unselected standardized data from eligible patients with surgically treated stage I-III CRC and adjuvant therapy (AT) or conventional aftercare were included. End points were adjuvant therapy-related adverse reactions (AT-ADRs), symptoms, and disease-free survival (DFS). The results were adjusted for confounder effects. Eight hundred four (429 ISC vs 375 control) CRC patients from 26 centers were observed for a median of 58 versus 51 months; the median ISC therapy lasted 52 months. ISC patients showed fewer AT-ADRs (19% vs 48%, p < .001) and fewer persisting symptoms (p < .001). The DFS hazard ratio of 0.60 (p = .013) suggests a survival benefit in ISC patients versus controls. ISC was well tolerated without life-threatening ADRs, drug interactions, or tumor enhancement. These results suggest a beneficial effect of supportive care ISC therapy within AT protocols and long-term ISC treatment in stage I-III CRC patients, particularly improvement in AT-ADRs and symptoms and possible extension of DFS.

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系统评价槲寄生在化疗和/或放疗方案中的临床效果以及槲寄生在非转移性结直肠癌中的长期应用:多中心、对照、观察性队列研究。
在欧洲,结直肠癌(CRC)患者经常接受槲寄生提取物来改善生活质量和生存率。本研究旨在评估常规临床条件下槲寄生提取物Iscador (ISC)对非转移性结直肠癌患者的支持治疗,并为未来的前瞻性临床研究提供有根据的假设。多中心、对照、回顾性、平行组观察队列研究的设计符合良好流行病学规范规则。来自手术治疗的I-III期结直肠癌患者和辅助治疗(AT)或常规术后护理的匿名未选择的标准化数据被纳入研究。终点是辅助治疗相关不良反应(at - adr)、症状和无病生存期(DFS)。结果根据混杂因素进行了调整。来自26个中心的840名CRC患者(429名ISC组患者对375名对照组患者)的平均观察时间为58个月对51个月;中位ISC治疗持续52个月。ISC患者表现出较少的at - adr (19% vs 48%, p < 0.001)和较少的持续症状(p < 0.001)。DFS风险比为0.60 (p = 0.013),表明ISC患者与对照组相比有生存优势。ISC耐受性良好,无危及生命的不良反应、药物相互作用或肿瘤增强。这些结果表明,在AT方案中支持护理ISC治疗和长期ISC治疗对I-III期CRC患者有益,特别是改善AT- adr和症状,并可能延长DFS。
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