中国临床实用医学
中國臨床實用醫學
중국림상실용의학
CHINA CLINICAL PRACTICAL MEDICINE
2014年
4期
3-5
,共3页
祁楠%康欢荣%杜楠%付艳%胡佳%李晓松%赵辉
祁楠%康歡榮%杜楠%付豔%鬍佳%李曉鬆%趙輝
기남%강환영%두남%부염%호가%리효송%조휘
贝伐珠单抗%紫杉醇%非小细胞肺癌%恶性胸腔积液
貝伐珠單抗%紫杉醇%非小細胞肺癌%噁性胸腔積液
패벌주단항%자삼순%비소세포폐암%악성흉강적액
Bevacizumab%Paclitaxel%Non-small cell lung cancer%Malignant pleural effusion
目的:观察胸腔内注射贝伐珠单抗联合紫杉醇治疗非小细胞肺癌伴恶性胸腔积液的疗效和安全性。方法选择2012年9月至2013年9月解放军总医院第一附属医院收治的晚期非小细胞肺癌伴恶性胸腔积液患者45例,所有入组患者均接受静脉紫杉醇和顺铂化疗,将所有患者分为贝伐珠单抗联合紫杉醇组(贝伐组)21例和紫杉醇组(化疗组)24例。胸腔给药,每3周为一周期。贝伐组采用贝伐珠单抗300 mg 联合紫杉醇60 mg 进行治疗;化疗组采用紫杉醇60 mg 进行治疗。根据 RECIST 1.1评价标准和 NCI-CTC-AE 3.0分级标准评估疗效和不良反应。结果两组患者治疗后胸腔积液均呈下降趋势,治疗胸腔积液的总有效率贝伐组为81.0%,化疗组为58.3%,差异有统计学意义(P<0.05)。两组患者治疗过程中均未出现不能耐受的不良反应。结论贝伐珠单抗联合紫杉醇可以更好地控制非小细胞肺癌胸腔积液的增长。
目的:觀察胸腔內註射貝伐珠單抗聯閤紫杉醇治療非小細胞肺癌伴噁性胸腔積液的療效和安全性。方法選擇2012年9月至2013年9月解放軍總醫院第一附屬醫院收治的晚期非小細胞肺癌伴噁性胸腔積液患者45例,所有入組患者均接受靜脈紫杉醇和順鉑化療,將所有患者分為貝伐珠單抗聯閤紫杉醇組(貝伐組)21例和紫杉醇組(化療組)24例。胸腔給藥,每3週為一週期。貝伐組採用貝伐珠單抗300 mg 聯閤紫杉醇60 mg 進行治療;化療組採用紫杉醇60 mg 進行治療。根據 RECIST 1.1評價標準和 NCI-CTC-AE 3.0分級標準評估療效和不良反應。結果兩組患者治療後胸腔積液均呈下降趨勢,治療胸腔積液的總有效率貝伐組為81.0%,化療組為58.3%,差異有統計學意義(P<0.05)。兩組患者治療過程中均未齣現不能耐受的不良反應。結論貝伐珠單抗聯閤紫杉醇可以更好地控製非小細胞肺癌胸腔積液的增長。
목적:관찰흉강내주사패벌주단항연합자삼순치료비소세포폐암반악성흉강적액적료효화안전성。방법선택2012년9월지2013년9월해방군총의원제일부속의원수치적만기비소세포폐암반악성흉강적액환자45례,소유입조환자균접수정맥자삼순화순박화료,장소유환자분위패벌주단항연합자삼순조(패벌조)21례화자삼순조(화료조)24례。흉강급약,매3주위일주기。패벌조채용패벌주단항300 mg 연합자삼순60 mg 진행치료;화료조채용자삼순60 mg 진행치료。근거 RECIST 1.1평개표준화 NCI-CTC-AE 3.0분급표준평고료효화불량반응。결과량조환자치료후흉강적액균정하강추세,치료흉강적액적총유효솔패벌조위81.0%,화료조위58.3%,차이유통계학의의(P<0.05)。량조환자치료과정중균미출현불능내수적불량반응。결론패벌주단항연합자삼순가이경호지공제비소세포폐암흉강적액적증장。
Objective To explore the efficacy and safety of intrathoracic injection of paclitaxel combined with bevacizumab in the treatment of non-small cell lung cancer(NSCLC) and malignant pleural effusion(MPE). Methods From September 2012 to September 2013,all patients in the study population were treated with paclitaxel and cisplatin through intravenous injection in the First Affiliated Hospital of Chinese PLA General Hospital. A total of 45 non-small cell lung cancer patients with MPE were randomly assigned to receive intrathoracic injection of bevacizumab combined with paclitaxel(bevacizumab group, 21 cases, bevacizumab 300 mg and paclitaxel 60 mg) and paclitaxel (chemotherapy group, 24 cases, paclitaxel 60 mg) every three weeks. The efficacy and safety was evaluated according to RECIST 1.1 and NCI-CTC-AE 3.0 version criteria respectively.Results Pleural effusion was reduced in both two groups after treatment. The response rate was 81.0% in bevacizumab group and 58.3% in chemotherapy group, and there were statistically significant differences between the two groups (P<0.05). All procedures were well tolerated with no treatment-related severe side effects. Conclusion Bevacizumab combined with paclitaxel are highly effective in the treatment of MPE in NSCLC patients.