白血病·淋巴瘤
白血病·淋巴瘤
백혈병·림파류
JOURNAL OF LEUKEMIA & LYMPHOMA
2013年
11期
645-649
,共5页
李燕郴%王国蓉%耿传营%王慧娟%杨光忠%高文%冷芸%刘爱军%田颖
李燕郴%王國蓉%耿傳營%王慧娟%楊光忠%高文%冷蕓%劉愛軍%田穎
리연침%왕국용%경전영%왕혜연%양광충%고문%랭예%류애군%전영
多发性骨髓瘤%自体造血干细胞移植%总体生存
多髮性骨髓瘤%自體造血榦細胞移植%總體生存
다발성골수류%자체조혈간세포이식%총체생존
Multiple myeloma%Autologous stem cell transplantation%Overall survival
目的 评价自体造血干细胞移植(ASCT)对初治多发性骨髓瘤(MM)的疗效.方法 选取诱导治疗后获得部分缓解(PR)及以上疗效的42例初治MM患者进行ASCT,中位随访34.2个月后,观察患者的疗效、无进展生存(PFS)和总生存(OS).选择同时期的49例诱导治疗后获得PR及以[上疗效的初治MM患者,进入非移植组(non-ASCT),经巩固维持治疗后观察疗效、PFS和OS,比较两组的差异,分析ASCT在MM中的作用.结果 与non-ASCT组相比,ASCT可明显延长患者的OS(未达到/37.2个月,P=O.000),而且对PFS也有延长趋势(33.9个月/39.8个月,P=0.133).ASCT可明显改善DSⅢ期(P=0.009)和ISSⅢ期(P=0.049)患者PFS,但对DSⅠ /Ⅱ期和ISS Ⅰ/Ⅱ期患者的PFS改善不明显.ASCT可明显改善诱导治疗后获得CR患者的PFS(P=0.016),对非常好的PR (VGPR) /PR患者的PFS改善不明显;不同年龄患者OS均明显改善(≤55岁,P=0.039;> 55岁,P=0.000).ASCT可明显改善不同ISS分期患者的OS(Ⅰ/Ⅱ期,P=0.003;Ⅲ期,P=0.012),对DSⅢ期患者的OS也有明显改善作用(P=0.000),但对DSⅠ/Ⅱ期患者OS的作用不明显(P=0.446).诱导治疗后获得CR和VGPR/PR的患者进行移植后,OS可进一步得到改善(CR,P=0.004; VGPR/PR,P=0.004).结论 ASCT可明显改善初治MM患者的生存,使高龄和分期预后不良的MM患者获益更多.
目的 評價自體造血榦細胞移植(ASCT)對初治多髮性骨髓瘤(MM)的療效.方法 選取誘導治療後穫得部分緩解(PR)及以上療效的42例初治MM患者進行ASCT,中位隨訪34.2箇月後,觀察患者的療效、無進展生存(PFS)和總生存(OS).選擇同時期的49例誘導治療後穫得PR及以[上療效的初治MM患者,進入非移植組(non-ASCT),經鞏固維持治療後觀察療效、PFS和OS,比較兩組的差異,分析ASCT在MM中的作用.結果 與non-ASCT組相比,ASCT可明顯延長患者的OS(未達到/37.2箇月,P=O.000),而且對PFS也有延長趨勢(33.9箇月/39.8箇月,P=0.133).ASCT可明顯改善DSⅢ期(P=0.009)和ISSⅢ期(P=0.049)患者PFS,但對DSⅠ /Ⅱ期和ISS Ⅰ/Ⅱ期患者的PFS改善不明顯.ASCT可明顯改善誘導治療後穫得CR患者的PFS(P=0.016),對非常好的PR (VGPR) /PR患者的PFS改善不明顯;不同年齡患者OS均明顯改善(≤55歲,P=0.039;> 55歲,P=0.000).ASCT可明顯改善不同ISS分期患者的OS(Ⅰ/Ⅱ期,P=0.003;Ⅲ期,P=0.012),對DSⅢ期患者的OS也有明顯改善作用(P=0.000),但對DSⅠ/Ⅱ期患者OS的作用不明顯(P=0.446).誘導治療後穫得CR和VGPR/PR的患者進行移植後,OS可進一步得到改善(CR,P=0.004; VGPR/PR,P=0.004).結論 ASCT可明顯改善初治MM患者的生存,使高齡和分期預後不良的MM患者穫益更多.
목적 평개자체조혈간세포이식(ASCT)대초치다발성골수류(MM)적료효.방법 선취유도치료후획득부분완해(PR)급이상료효적42례초치MM환자진행ASCT,중위수방34.2개월후,관찰환자적료효、무진전생존(PFS)화총생존(OS).선택동시기적49례유도치료후획득PR급이[상료효적초치MM환자,진입비이식조(non-ASCT),경공고유지치료후관찰료효、PFS화OS,비교량조적차이,분석ASCT재MM중적작용.결과 여non-ASCT조상비,ASCT가명현연장환자적OS(미체도/37.2개월,P=O.000),이차대PFS야유연장추세(33.9개월/39.8개월,P=0.133).ASCT가명현개선DSⅢ기(P=0.009)화ISSⅢ기(P=0.049)환자PFS,단대DSⅠ /Ⅱ기화ISS Ⅰ/Ⅱ기환자적PFS개선불명현.ASCT가명현개선유도치료후획득CR환자적PFS(P=0.016),대비상호적PR (VGPR) /PR환자적PFS개선불명현;불동년령환자OS균명현개선(≤55세,P=0.039;> 55세,P=0.000).ASCT가명현개선불동ISS분기환자적OS(Ⅰ/Ⅱ기,P=0.003;Ⅲ기,P=0.012),대DSⅢ기환자적OS야유명현개선작용(P=0.000),단대DSⅠ/Ⅱ기환자OS적작용불명현(P=0.446).유도치료후획득CR화VGPR/PR적환자진행이식후,OS가진일보득도개선(CR,P=0.004; VGPR/PR,P=0.004).결론 ASCT가명현개선초치MM환자적생존,사고령화분기예후불량적MM환자획익경다.
Objective To evaluate effects of autologous stem cell transplantation (ASCT) on new diagnosed multiple myeloma (MM) patients.Methods 42 newly diagnosed MM patients who obtained partial remission (PR) or better and received ASCT were selected.With a median 34.2 months follow-up,therapeutic effects,progression-free survival (PFS) and overall survival (OS) of 42 newly diagnosed patients received ASCT were analyzed.49 patients who obtained PR or better after induction therapy but not received ASCT were selected as control.The differences of these two groups were analyzed and effects of ASCT on new diagnosed MM patients were evaluated.Results Compared with non-ASCT patients,patients received ASCT had longer OS (not reached vs 37.2 months,P =0.000).ASCT could also prolonged PFS of MM patients,but there was not significant difference (33.9 months vs 39.8 months,P =0.133).ASCT could significantly improved PFS of MM patients with DS Ⅲ stage (P =0.009) and ISS Ⅲ stage (P =0.049),however,it could improve PFS of DS Ⅰ /Ⅱ stage and ISS Ⅰ/Ⅱ] stage.ASCT could significantly improve PFS of patients obtained complete remission (CR) (P =0.016),however,it had not significant effect on patients obtained very good PR (VGPR) or PR after induction therapy.ASCT could significantly improved OS of patients aged ≤55 years old (P =0.039) and > 55 years old (P =0.000).ASCT could significantly improved OS of MM patients with ISS Ⅰ /Ⅱ stage (P =0.003),ISS Ⅲ stage (P =0.012) and DS Ⅲ stage (P =0.000),however,it had not significant effect on patients with DSⅠ/ Ⅱ] stage (P =0.446).After induction therapy,ASCT could further improved OS of patients obtained CR (P =0.004) or VGPR/PR (P =0.004).Conclusion ASCT could significantly improve OS of new diagnosed MM patients and could make MM patients obtaine more benefits who are at high risk at age and stages.