中国肿瘤临床
中國腫瘤臨床
중국종류림상
CHINESE JOURNAL OF CLINICAL ONCOLOGY
2012年
22期
1835-1838
,共4页
廖智超%王国文%邢汝维%韩秀鑫%赵军
廖智超%王國文%邢汝維%韓秀鑫%趙軍
료지초%왕국문%형여유%한수흠%조군
晚期骨肉瘤%二线化疗%三氧化二砷%吉西他滨%多西他赛
晚期骨肉瘤%二線化療%三氧化二砷%吉西他濱%多西他賽
만기골육류%이선화료%삼양화이신%길서타빈%다서타새
Advanced osteosarcoma%Second-line Chemotherapy%Arsenic trioxide%Gemcitabine%Docetaxel
目的:探讨三氧化二砷(arsenic trioxide,As2O3)联合吉西他滨及多西他赛治疗骨肉瘤肺转移的临床疗效.方法:收集26例对一线化疗药物耐药的骨肉瘤肺转移患者,男性14例,女性12例,年龄11~62岁,平均31.2岁,所有患者均接受过传统规范化疗后出现肺转移.应用As2O3(剂量为10 mg/d,d1~28)联合吉西他滨(剂量为800 mg/m2,d1、d8)及多西他赛(剂量为75 mg/m2, d8)每3周重复给药,每2个化疗疗程复查疗效.结果:接受化疗的患者总体有效率(CR+PR)为34.6%(9/26).中位随访时间28.2(1~48)个月,中位总生存期(OS)为16.7个月(95%CI:7.561~18.058)和中位无进展生存期(PFS)为10.3个月(95%CI:6.541~8.754),1、2和4年生存率分别是61.5%、38.4%和15.4%.治疗后最常见的不良反应为骨髓抑制,而常见的非血液学不良反应包括心脏毒性、消化道反应及肝肾功能异常,对症处理后均明显缓解.结论:As2O3联合吉西他滨及多西他赛作为二线化疗药物治疗骨肉瘤肺转移的近期临床疗效较好,且有较好的耐受性.
目的:探討三氧化二砷(arsenic trioxide,As2O3)聯閤吉西他濱及多西他賽治療骨肉瘤肺轉移的臨床療效.方法:收集26例對一線化療藥物耐藥的骨肉瘤肺轉移患者,男性14例,女性12例,年齡11~62歲,平均31.2歲,所有患者均接受過傳統規範化療後齣現肺轉移.應用As2O3(劑量為10 mg/d,d1~28)聯閤吉西他濱(劑量為800 mg/m2,d1、d8)及多西他賽(劑量為75 mg/m2, d8)每3週重複給藥,每2箇化療療程複查療效.結果:接受化療的患者總體有效率(CR+PR)為34.6%(9/26).中位隨訪時間28.2(1~48)箇月,中位總生存期(OS)為16.7箇月(95%CI:7.561~18.058)和中位無進展生存期(PFS)為10.3箇月(95%CI:6.541~8.754),1、2和4年生存率分彆是61.5%、38.4%和15.4%.治療後最常見的不良反應為骨髓抑製,而常見的非血液學不良反應包括心髒毒性、消化道反應及肝腎功能異常,對癥處理後均明顯緩解.結論:As2O3聯閤吉西他濱及多西他賽作為二線化療藥物治療骨肉瘤肺轉移的近期臨床療效較好,且有較好的耐受性.
목적:탐토삼양화이신(arsenic trioxide,As2O3)연합길서타빈급다서타새치료골육류폐전이적림상료효.방법:수집26례대일선화료약물내약적골육류폐전이환자,남성14례,녀성12례,년령11~62세,평균31.2세,소유환자균접수과전통규범화료후출현폐전이.응용As2O3(제량위10 mg/d,d1~28)연합길서타빈(제량위800 mg/m2,d1、d8)급다서타새(제량위75 mg/m2, d8)매3주중복급약,매2개화료료정복사료효.결과:접수화료적환자총체유효솔(CR+PR)위34.6%(9/26).중위수방시간28.2(1~48)개월,중위총생존기(OS)위16.7개월(95%CI:7.561~18.058)화중위무진전생존기(PFS)위10.3개월(95%CI:6.541~8.754),1、2화4년생존솔분별시61.5%、38.4%화15.4%.치료후최상견적불량반응위골수억제,이상견적비혈액학불량반응포괄심장독성、소화도반응급간신공능이상,대증처리후균명현완해.결론:As2O3연합길서타빈급다서타새작위이선화료약물치료골육류폐전이적근기림상료효교호,차유교호적내수성.
Objective: This study aims to investigate the clinical effects of arsenic trioxide (As2O3) combined with gemcitabine and docetaxel on the treatment of osteosarcoma pulmonary metastasis. Methods: Data on 26 osteosarcoma patients suffering from lung metastasis and exhibiting drug resistance to first-line chemotherapy were collected. The patients consisted of 14 males and 12 females. The ages ranged from 11 years to 62 years, with a mean age of 31.2 years. The patients received As2O3 (dose: 10 mg/d, Day 1 to Day 28) combined with gemcitabine (dose: 675 mg/m2, Days 1 and 8) and docetaxel (dose: 75 mg/m2, Day 8). This therapy was repeated every 3 weeks. Results:Patients who received chemotherapy showed an overall efficiency of 76.9% (complete response + partial response + stable disease). After a median follow-up of 28.2 months (48 months), the median overall survival time was calculated at 16.7 months [95% confidence interval (CI) 7.561 to 18.058], and the median progression-free survival was 10.3 months (95%CI 6.541 to 8.754). The 24- and 48-month survival rates reached 38.4% and 15.4%, respectively. Most commonly observed adverse reactions include myelosuppression, cardiotoxicity, digestive reactions, as well as liver and kidney damage. The patients' conditions were apparently relieved after symptomatic treatments. Conclusion:mhe combination of As2O3 with gemcitabine and docetaxel as second-line chemotherapeutic drugs for osteosarcoma cases with pulmonary metastasis exhibited satisfactory clinical short-term effects. These drugs were well tolerated.