白血病·淋巴瘤
白血病·淋巴瘤
백혈병·림파류
JOURNAL OF LEUKEMIA & LYMPHOMA
2013年
1期
53-56
,共4页
郭姗琦%智亚芹%晋鑫%于泳%杨洪亮%赵智刚%王晓芳%王亚非%张翼鷟
郭姍琦%智亞芹%晉鑫%于泳%楊洪亮%趙智剛%王曉芳%王亞非%張翼鷟
곽산기%지아근%진흠%우영%양홍량%조지강%왕효방%왕아비%장익작
多发性骨髓瘤%沙利度胺%髓外病变%预后
多髮性骨髓瘤%沙利度胺%髓外病變%預後
다발성골수류%사리도알%수외병변%예후
Multiple myeloma%Thalidomide%Extramedullary disease%Prognosis
目的 分析沙利度胺治疗初诊时伴或不伴髓外病变(EM)的多发性骨髓瘤(MM)患者的疗效及对预后的影响.方法 回顾性分析132例MM患者的临床特点及其预后相关因素,分析沙利度胺对伴或不伴EM的MM患者的疗效及对预后的影响.结果 132例患者中位年龄59岁(28~83岁),其中52例(39.4%)伴EM;80例(60.6%)不伴EM.伴EM患者预计总生存(OS)时间为42.5个月,不伴EM患者为54.3个月,差异有统计学意义(P=0.004).所有患者中,服用沙利度胺的MM患者预计OS较未服用者长(50.7个月比41.2个月),差异有统计学意义(P=0.01);对于EM患者,是否服用沙利度胺对患者预后差异无统计学意义(39.7个月比38.5个月,P=0.491),而对初诊时不伴EM的MM患者,服用沙利度胺的患者预后明显优于未服用者(54.6个月比41.2个月,P=0.027).单因素分析显示初诊时伴EM (P=0.004)、浆细胞比例≥20%(P=0.02)、血红蛋白≤110 g/ L(P=0.041)、β2微球蛋白(β2-MG) ≥5.5 mg/L(P=0.018)及未服用沙利度胺(P=0.01)为预后不良指标;COX多因素分析显示,EM、β2-MG以及浆细胞比例为本组患者的独立预后因素(P<0.05).结论 初诊时伴EM患者较不伴EM者预后差,沙利度胺不能改善伴EM患者的预后,可能需要联合硼替佐米等新药或进行自体造血干细胞移植.
目的 分析沙利度胺治療初診時伴或不伴髓外病變(EM)的多髮性骨髓瘤(MM)患者的療效及對預後的影響.方法 迴顧性分析132例MM患者的臨床特點及其預後相關因素,分析沙利度胺對伴或不伴EM的MM患者的療效及對預後的影響.結果 132例患者中位年齡59歲(28~83歲),其中52例(39.4%)伴EM;80例(60.6%)不伴EM.伴EM患者預計總生存(OS)時間為42.5箇月,不伴EM患者為54.3箇月,差異有統計學意義(P=0.004).所有患者中,服用沙利度胺的MM患者預計OS較未服用者長(50.7箇月比41.2箇月),差異有統計學意義(P=0.01);對于EM患者,是否服用沙利度胺對患者預後差異無統計學意義(39.7箇月比38.5箇月,P=0.491),而對初診時不伴EM的MM患者,服用沙利度胺的患者預後明顯優于未服用者(54.6箇月比41.2箇月,P=0.027).單因素分析顯示初診時伴EM (P=0.004)、漿細胞比例≥20%(P=0.02)、血紅蛋白≤110 g/ L(P=0.041)、β2微毬蛋白(β2-MG) ≥5.5 mg/L(P=0.018)及未服用沙利度胺(P=0.01)為預後不良指標;COX多因素分析顯示,EM、β2-MG以及漿細胞比例為本組患者的獨立預後因素(P<0.05).結論 初診時伴EM患者較不伴EM者預後差,沙利度胺不能改善伴EM患者的預後,可能需要聯閤硼替佐米等新藥或進行自體造血榦細胞移植.
목적 분석사리도알치료초진시반혹불반수외병변(EM)적다발성골수류(MM)환자적료효급대예후적영향.방법 회고성분석132례MM환자적림상특점급기예후상관인소,분석사리도알대반혹불반EM적MM환자적료효급대예후적영향.결과 132례환자중위년령59세(28~83세),기중52례(39.4%)반EM;80례(60.6%)불반EM.반EM환자예계총생존(OS)시간위42.5개월,불반EM환자위54.3개월,차이유통계학의의(P=0.004).소유환자중,복용사리도알적MM환자예계OS교미복용자장(50.7개월비41.2개월),차이유통계학의의(P=0.01);대우EM환자,시부복용사리도알대환자예후차이무통계학의의(39.7개월비38.5개월,P=0.491),이대초진시불반EM적MM환자,복용사리도알적환자예후명현우우미복용자(54.6개월비41.2개월,P=0.027).단인소분석현시초진시반EM (P=0.004)、장세포비례≥20%(P=0.02)、혈홍단백≤110 g/ L(P=0.041)、β2미구단백(β2-MG) ≥5.5 mg/L(P=0.018)급미복용사리도알(P=0.01)위예후불량지표;COX다인소분석현시,EM、β2-MG이급장세포비례위본조환자적독립예후인소(P<0.05).결론 초진시반EM환자교불반EM자예후차,사리도알불능개선반EM환자적예후,가능수요연합붕체좌미등신약혹진행자체조혈간세포이식.
Objective To investigate the clinical efficiency and effects on prognosis of thalidomide for newly diagnosed multiple myeloma (MM) with or without extramedullary disease.Methods The clinical features and prognostic factors were retrospectively analyzed in 132 patients.Analyze the efficiency of thalidomide and its effects on prognosis of MM patients with or without extramedullary disease.Results The median age of 132 patients was 59 years (28-83 years),52 patients (39.4 %) had extramellulary multiple myeloma (EM),other 80 patients (60.6 %) were without EM at diagnosis.The estimate overall survival (OS) of patients with EM was 42.5 months,compared with 54.3 months in those without EM,the difference was statistically significant (P =0.004).Patients accepting thalidomide therapy had a longer estimate OS than those without thalidomide therapy (50.7 months vs 41.2 months,P =0.01).For patients with EM,whether take thalidomide or not have no effect on the prognosis,the difference was not statistically significant (39.7 months vs 38.5 months,P =0.491).While for those without EM,the prognosis for patients who take thalidomide was better than that did not take thalidomide (54.6 months vs 41.2 months,P =0.027).Log-rank univariate analysis showed that accompanied with EM (P =0.004),the proportion of plasma cells≥20 % (P =0.02),Hb≤110 g/L (P =0.041),β2-MG ≥ 5.5 mg/L (P =0.018) and without thalidomide therapy (P =0.01) were poor prognostic factors.Multivariate analysis with COX model showed extramedullary disease,β2-MG and the proportion of plasma cells were statistically significant (P < 0.05).Conclusion Patients with EM showed aggressive and complicated prognosis.Thalidomide does not improve the prognosis of patients with EM and they may need combination therapy such as bortezomib or autologous hemopoietic stem cell transplantation.