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作 者:时淑珍[1] 付静[1] 赵卫红[1] 徐晓辉[1]
机构地区:[1]大连市第三人民医院肿瘤内科,辽宁大连116033
出 处:《中国肿瘤临床与康复》2009年第1期41-43,共3页Chinese Journal of Clinical Oncology and Rehabilitation
摘 要:目的对比观察单药多西他赛每周方案与每3周方案二线治疗晚期非小细胞肺癌(NSCLC)的临床疗效?毒副反应及生活质量。方法每周方案组(A组):多西他赛35 mg/m^2,静滴,第1、8、15天,每4周重复;三周方案组(B组):多西他赛75 mg/m^2,静滴,第1天,每3~4周重复,治疗2个周期评价疗效,每周期评价毒性。采用欧洲癌症研究和治疗组织(EORTC)简体中文版的生活质量调查核心问卷(QLQ-C30)和肺癌专用问卷(QLQ-LC13)评价患者生活质量,化疗前及治疗2个周期后给予评价生活质量。结果A组32例,B组35例,67例均无完全缓解(CR);部分缓解(PR):A组3例,B组4例;稳定(SD)A组5例,B组6例;有效率(RR):A组9.4%,B组11.4%(P=1.000);临床获益率:A组25.0%,B组28.6%(P=0.742)。中位生存期:A组9.2个月,B组6.3个月(P=0.07)。1年生存率:A组31.3%,B组28.6%(P=0.811)。两组Ⅲ/Ⅳ度粒细胞减少分别为15.6%和48.6%(P=0.004)。化疗后两组患者在气促、咳嗽、咯血、疼痛方面症状明显减轻,A组与B组比较,在疼痛(P=0.040)、咳嗽(P=0.045)两方面分值降低明显,差异有显著性。结论单药多西他赛二线治疗晚期非小细胞肺癌,每周方案与三周方案有效率相似,每周方案血液学毒性明显下降,临床症状明显改善,耐受性更好。Objective To compare the efficacy, toxicity and quality-of-life (QOL) between weekly and 3-weekly docetaxel monotherapy in the second-line chemotherapy of patients with advanced non-small cell lung cancer(NSCLC). Methods Group A: docetaxel 35 mg/m^2 iv d1,d8,d15,q4w; Group B: docetaxel 75 mg,/m^2 iv dl, q3-4w. The clinical response was assessed after two bycles. Toxicity was assessed every cycle. QOL was evaluated with the Chinese version of quality of life questionnaire core-30 ( QLQ - c30) of European Organization for Research and Treatment of Cancer(EORTC) and quality of life questionnaire lung cancer ( QLQ -LC13) at baseline and after two cycles. Results There was no complete remission (CR) in all 67 cases. There were 3 partial response (PR) and 5 stable disease(SD) in group A ; 4 PR and 6 SD in group B. The overall response rates(RR) were 9.4% and 11.4% in groups A and B( P = 1. 000) respectively. The clinical benefit rates were 25.0% and 28. 6% in groups A and B (P = 0. 742) respectively. The median survival time was 9.2 months and 6. 3 months respectively in groups A and B (P =0. 070). In groups A and B the 1-year survival rates were respectively 31.3% and 28. 6% (P =0. 811 ). The grades- Ⅲ/Ⅳnentropenia were lower significantly in group A compared with group B ( 15. 6% vs 48. 6% , P = 0. 004). Symptoms such as dyspnea, cough, hemoptysis and pain were relieved after the chemotherapy in both groups. The mean scores of the symptoms decreased significantly, especially the pain ( P = 0. 04) and cough(P =0. 045) in group A compared with gorup B with statistically significant differences. Conclusion Docetaxel as second -line treatment of advanced NSCLC, the overall response rates were similar between groups A and B. The occurrence of hematologic toxicity was lower, symptoms were palliated significantly and the tolerance was better in weekly regimen.
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