中华血液学杂志
中華血液學雜誌
중화혈액학잡지
Chinese Journal of Hematology
2010年
1期
16-20
,共5页
郑积富%仇惠英%潘金兰%岑建农%吴亚芳%张俊%吴德沛%薛永权
鄭積富%仇惠英%潘金蘭%岑建農%吳亞芳%張俊%吳德沛%薛永權
정적부%구혜영%반금란%잠건농%오아방%장준%오덕패%설영권
TCF3-PBX1融合基因%白血病,淋巴细胞急性%原位杂交荧光%预后
TCF3-PBX1融閤基因%白血病,淋巴細胞急性%原位雜交熒光%預後
TCF3-PBX1융합기인%백혈병,림파세포급성%원위잡교형광%예후
TCF3-PBX1 fusion gene%Leukemia,lymphoblastic,acute%Adult%In situ hybridization,fluorescence%Prognosis
目的 探讨TCF3-PBX1融合基因阳性的成人急性淋巴细胞白血病(ALL)的形态学、免疫学、细胞遗传学和临床特点.方法采用R显带技术进行常规核型(CC)分析,间期荧光原位杂交(FISH)技术和RT-PCR技术检测TCF3-PBX1融合基因,流式细胞术(FCM)检测细胞免疫表型;分析19例TCF3-PBX1融合基因阳性成人ALL的临床和实验室特征并进行长期随访.结果本组19例TCF3-PBX1融合基因阳件ALL占同期成人ALL的3.13%;其中L_2 12例,L_2 7例.细胞遗传学检测7例为t(1;19)平衡易位,10例为der(19)t(1;19)不平衡易位,2例为正常核型.9例经RT-PCR检测的病例均有TCF3-PBX1融合基因转录本,17例经间期FISH检测TCF3-PBX1融合基因均为阳性.18例行FCM检测的患者中16例为B淋系抗原表达,2例为T淋系抗原表达.17例患者有不同程度的肝、脾、淋巴结等髓外浸润.本组患者经1个疗程诱导化疗后17例获得完全缓解(CR),CR率为94.7%,中位无复发生存时间为3.2个月,中位总生存期为7.2个月.结论 TCF3-PBX1融合基因阳件成人ALL有着独特的临床和实验室特点;治疗缓解率高,但短期内易复发,总生存期短,应该采取更积极的治疗以改善预后;间期双色FISH联合CC及RT-PCR可以提高TCF3-PBX1融合基因的检出率.
目的 探討TCF3-PBX1融閤基因暘性的成人急性淋巴細胞白血病(ALL)的形態學、免疫學、細胞遺傳學和臨床特點.方法採用R顯帶技術進行常規覈型(CC)分析,間期熒光原位雜交(FISH)技術和RT-PCR技術檢測TCF3-PBX1融閤基因,流式細胞術(FCM)檢測細胞免疫錶型;分析19例TCF3-PBX1融閤基因暘性成人ALL的臨床和實驗室特徵併進行長期隨訪.結果本組19例TCF3-PBX1融閤基因暘件ALL佔同期成人ALL的3.13%;其中L_2 12例,L_2 7例.細胞遺傳學檢測7例為t(1;19)平衡易位,10例為der(19)t(1;19)不平衡易位,2例為正常覈型.9例經RT-PCR檢測的病例均有TCF3-PBX1融閤基因轉錄本,17例經間期FISH檢測TCF3-PBX1融閤基因均為暘性.18例行FCM檢測的患者中16例為B淋繫抗原錶達,2例為T淋繫抗原錶達.17例患者有不同程度的肝、脾、淋巴結等髓外浸潤.本組患者經1箇療程誘導化療後17例穫得完全緩解(CR),CR率為94.7%,中位無複髮生存時間為3.2箇月,中位總生存期為7.2箇月.結論 TCF3-PBX1融閤基因暘件成人ALL有著獨特的臨床和實驗室特點;治療緩解率高,但短期內易複髮,總生存期短,應該採取更積極的治療以改善預後;間期雙色FISH聯閤CC及RT-PCR可以提高TCF3-PBX1融閤基因的檢齣率.
목적 탐토TCF3-PBX1융합기인양성적성인급성림파세포백혈병(ALL)적형태학、면역학、세포유전학화림상특점.방법채용R현대기술진행상규핵형(CC)분석,간기형광원위잡교(FISH)기술화RT-PCR기술검측TCF3-PBX1융합기인,류식세포술(FCM)검측세포면역표형;분석19례TCF3-PBX1융합기인양성성인ALL적림상화실험실특정병진행장기수방.결과본조19례TCF3-PBX1융합기인양건ALL점동기성인ALL적3.13%;기중L_2 12례,L_2 7례.세포유전학검측7례위t(1;19)평형역위,10례위der(19)t(1;19)불평형역위,2례위정상핵형.9례경RT-PCR검측적병례균유TCF3-PBX1융합기인전록본,17례경간기FISH검측TCF3-PBX1융합기인균위양성.18례행FCM검측적환자중16례위B림계항원표체,2례위T림계항원표체.17례환자유불동정도적간、비、림파결등수외침윤.본조환자경1개료정유도화료후17례획득완전완해(CR),CR솔위94.7%,중위무복발생존시간위3.2개월,중위총생존기위7.2개월.결론 TCF3-PBX1융합기인양건성인ALL유착독특적림상화실험실특점;치료완해솔고,단단기내역복발,총생존기단,응해채취경적겁적치료이개선예후;간기쌍색FISH연합CC급RT-PCR가이제고TCF3-PBX1융합기인적검출솔.
Objective To explore the morphology,immunophenotype,cytogenetics and clinical features of TCF3-PBX1 fusion gene positive adult acute lymphoblastic leukemia(ALL).Methods R banding was used to analyze conventional cytogenetics(CC),interphase fluorescence in situ hybridization(iFISH)and RT-PCR to detect the TCF3-PBX1 fusion gene,and flow cytometry to immunophenotype.The clinical and laboratory features and long-term follow-up of the patients were analyzed.Results The incidence of 19 TCF3-PBX1-positive adult ALL was 3.13% of total ALL patients.Of them,12 and 7 cases were diagnosed as L_1 and L_2 morphology respectively;7 cases with balanced translocation of chromosome 1 and 19;10 with der(19)t(1:19)formed from unbalanced translocation and 2 with normal karyotypes.TCF3-PBX1 fusion gene was detected by RT-PCR in 9 cases,and by iFISH in 17.16 cases were B-phenotype and the other 2 T-phenotype;17 cases had lymph node,spleen or liver infiltration.Of 18 patients received chemotherapy,17(94.7%)achieved complete remission(CR);the median relapse-free survival(RFS)and median overall survival was 3.2 months and 7.2 months,respectively.Conclusions TCF3-PBX1-positive adult ALL had unique clinical and pathological features with high remission rate,high relapse rate and short survival time and should be considered to receive intensified treatment strategies.iFISH combined with CC and RT-PCR can increase the detection rate of t(1;19)/TCF3-PBX1 fusion gene.