中国生化药物杂志
中國生化藥物雜誌
중국생화약물잡지
CHINESE JOURNAL OF BIOCHEMICAL PHARMACEUTICS
2014年
3期
116-118
,共3页
多西紫杉醇%替吉奥%蒽环类耐药%三阴性乳腺癌
多西紫杉醇%替吉奧%蒽環類耐藥%三陰性乳腺癌
다서자삼순%체길오%은배류내약%삼음성유선암
Docetaxel%S-1%anthracycline-resistant%triple negative breast cancer
目的:观察分析多西紫杉醇联合替吉奥在治疗蒽环类耐药三阴性乳腺癌(triple-negtive breast cancer,TNBC)中的临床疗效。方法选择2009年6月~2011年6月绍兴市人民医院肿瘤放疗科收治的64例三阴性乳腺癌患者,回顾性分析上述病例的临床资料,所有患者使用蒽环类药物治疗无效或复发,继而选择联合多西紫杉醇、替吉奥治疗,观察分析此种方案的临床疗效和不良反应情况。结果64例患者的治疗后有效率为54.69%,病情控制率为79.69%,治疗过程中未见死亡病例,主要不良反应为胃肠道反应和骨髓抑制,但患者对此均可耐受;随访结果显示中位疾病进展时间为10.5个月,2年后无疾病进展生存率为0。结论联合多西紫杉醇、替吉奥治疗蒽环类耐药三阴性乳腺癌的临床效果良好,不良反应相对较轻,是较为理想的辅助化疗方案。
目的:觀察分析多西紫杉醇聯閤替吉奧在治療蒽環類耐藥三陰性乳腺癌(triple-negtive breast cancer,TNBC)中的臨床療效。方法選擇2009年6月~2011年6月紹興市人民醫院腫瘤放療科收治的64例三陰性乳腺癌患者,迴顧性分析上述病例的臨床資料,所有患者使用蒽環類藥物治療無效或複髮,繼而選擇聯閤多西紫杉醇、替吉奧治療,觀察分析此種方案的臨床療效和不良反應情況。結果64例患者的治療後有效率為54.69%,病情控製率為79.69%,治療過程中未見死亡病例,主要不良反應為胃腸道反應和骨髓抑製,但患者對此均可耐受;隨訪結果顯示中位疾病進展時間為10.5箇月,2年後無疾病進展生存率為0。結論聯閤多西紫杉醇、替吉奧治療蒽環類耐藥三陰性乳腺癌的臨床效果良好,不良反應相對較輕,是較為理想的輔助化療方案。
목적:관찰분석다서자삼순연합체길오재치료은배류내약삼음성유선암(triple-negtive breast cancer,TNBC)중적림상료효。방법선택2009년6월~2011년6월소흥시인민의원종류방료과수치적64례삼음성유선암환자,회고성분석상술병례적림상자료,소유환자사용은배류약물치료무효혹복발,계이선택연합다서자삼순、체길오치료,관찰분석차충방안적림상료효화불량반응정황。결과64례환자적치료후유효솔위54.69%,병정공제솔위79.69%,치료과정중미견사망병례,주요불량반응위위장도반응화골수억제,단환자대차균가내수;수방결과현시중위질병진전시간위10.5개월,2년후무질병진전생존솔위0。결론연합다서자삼순、체길오치료은배류내약삼음성유선암적림상효과량호,불량반응상대교경,시교위이상적보조화료방안。
Objective To observe and analyze the clinical efficacy of docetaxel and S-1 in treatment of anthracycline-resistant triple-negtive breast cancer(TNBC).Methods 64 cases with TNBC admitted in People' Hospital of Shaoxing City from June 2009 to June 2011were selected as research object.The clinical data of these cases were analyzed retrospectively.Anthracycline had been used to treat the cases, but with no effect or recurrence.Then docetaxel combined with S-1 was applied to the cases.Clinical efficacy and adverse reactions of the chemotherapy were observed and analyzed. Results After treatment,the efficiency of 64 cases was 54.69%,and the disease control rate was 79.69%.During the treatment,the main adverse reactions were gastrointestinal reactions and bone marrow suppression,without death,and patients could tolerate the adverse event.Follow-up results showed that the median time of progression was 10.5 months.After two years,progression-free survival rate was 0.Conclusion Docetaxel combined with S-1 has good clinical efficacy for anthracycline-resistant triple-negtive breast cancer,with relatively mild side effects,which may be an ideal adjuvant chemotherapy method.