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Clinical use of molecular targeted agents for primary small bowel adenocarcinoma: A multicenter retrospective cohort study by the Osaka Gut Forum

机译:分子靶向药物在原发性小肠腺癌中的临床应用:大阪肠道论坛的多中心回顾性队列研究

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摘要

Primary small bowel adenocarcinoma (SBA) is a rare cancer for which effective treatment strategies have not yet been established. The results of previous retrospective studies suggest that chemotherapy contributes to a longer survival time in patients with SBA. However, there are few case reports about the efficacy of molecular targeted agent-containing chemotherapy for SBA. In the present study, the treatment and follow-up data of patients with SBA who received chemotherapy with or without molecular targeted agents were retrospectively analyzed. Each patient was treated in one of ten hospitals participating in the Osaka Gut Forum between April 2006 and March 2014. The following factors were evaluated: Age, sex, Eastern Cooperative Oncology Group performance status (PS), tumor location, tumor differentiation, chemotherapy regimen, resection of primary tumor, tumor biomarker expression, distant metastasis, best response under chemotherapy, time to disease progression, subsequent treatments, survival status and treatment toxicity. A total of 27 patients (17 males and 10 females; mean age, 63.4 years old; range, 36–83 years old) received chemotherapy due to non-curative tumor resection, unresectable tumor or post-operative recurrence. The median overall survival time was 14.8 months (range, 2–58 months). A univariate analysis revealed a PS of 0 (P=0.0228) and treatment with platinum-based chemotherapy (P=0.0048) were significant factors for an improved prognosis. An age-adjusted multivariate analysis also revealed that a platinum-based regimen was a significant positive prognostic factor (P=0.0373). Molecular targeted agents were administered to 8 patients, for whom it was their first- or second-line therapy. Among the 17 patients who received oxaliplatin-based chemotherapy as a first-line chemotherapy, a PS of 0 (P=0.0255) and treatment with bevacizumab (P=0.0121) were significant positive prognostic factors. Toxicities higher than Grade 3 occurred in 8/27 patients with SBA; however, serious side effects due to the molecular targeted agents were not experienced. The results of the present study indicate that chemotherapy containing molecular targeted agents is a well-tolerated and effective treatment option for SBA.
机译:原发性小肠腺癌(SBA)是一种罕见的癌症,尚未建立有效的治疗策略。先前回顾性研究的结果表明,化学疗法有助于SBA患者更长的生存时间。但是,很少有病例报告涉及含分子靶向药物的化学疗法对SBA的疗效。在本研究中,回顾性分析了接受或不接受分子靶向药物化疗的SBA患者的治疗和随访数据。在2006年4月至2014年3月期间,每位患者在参加大阪肠道论坛的十家医院之一中接受了治疗。评估了以下因素:年龄,性别,东部合作肿瘤小组的工作状态(PS),肿瘤位置,肿瘤分化,化疗方案,原发肿瘤切除,肿瘤生物标志物表达,远处转移,化学疗法最佳反应,疾病进展时间,后续治疗,生存状况和治疗毒性。由于非治愈性肿瘤切除,无法切除的肿瘤或术后复发,共有27例患者(男17例,女10例;平均年龄63.4岁;范围36-83岁)接受了化疗。中位总生存时间为14.8个月(范围2–58个月)。单因素分析显示PS为0(P = 0.0228),铂类化疗(P = 0.0048)是改善预后的重要因素。年龄调整后的多变量分析还显示,铂类方案是显着的阳性预后因素(P = 0.0373)。对8例患者进行了分子靶向药物治疗,这是他们的一线或二线治疗方法。在接受以奥沙利铂为基础的一线化疗的17例患者中,PS为0(P = 0.0255)和贝伐单抗治疗(P = 0.0121)是显着的阳性预后因素。 8/27的SBA患者发生了高于3级的毒性。然而,由于分子靶向剂,没有出现严重的副作用。本研究的结果表明,含分子靶向药物的化疗是SBA的良好耐受和有效治疗选择。

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