白血病·淋巴瘤
白血病·淋巴瘤
백혈병·림파류
JOURNAL OF LEUKEMIA & LYMPHOMA
2012年
1期
42-46
,共5页
郭智%何学鹏%杨凯%刘晓东%陈鹏%刘兵%刘丹%王丙然%陈惠仁
郭智%何學鵬%楊凱%劉曉東%陳鵬%劉兵%劉丹%王丙然%陳惠仁
곽지%하학붕%양개%류효동%진붕%류병%류단%왕병연%진혜인
免疫母细胞淋巴结病%治疗结果%无病生存
免疫母細胞淋巴結病%治療結果%無病生存
면역모세포림파결병%치료결과%무병생존
Immunoblastic lymphadenopathy%Treatment outcome%Disease-free survival
目的 分析血管免疫母细胞性T细胞淋巴瘤( AILT)的临床特点及近期疗效,为提高AILT诊治水平提供借鉴.方法 对2005年1月至2010年1月收治的20例AILT患者的临床资料进行回顾性分析,总结患者的临床及病理特点、治疗和生存情况.结果 20例AILT患者中位年龄55.9岁,均有淋巴结肿大,11例有B组症状,确诊依据淋巴结活组织检查,免疫组织化学均表达T细胞抗原CD3、CD45RO,治疗均采用以CHOP方案为主的化疗,其他治疗包括DICE、ESHAP、Hyper-CVAD方案及自体造血干细胞移植,随访5~ 69个月,全组中位生存期为20.2个月(5~69个月),1、2、3年无病生存率分别为67%、33%、11%,8例处于持续缓解状态,占全组的40%,分别生存63、47、27、24、24、12、5、1个月.结论 AILT患者年龄偏大,化疗过程中并发症较多,虽然早期化疗可使患者症状有不同程度减轻,但停止治疗后容易复发,国际预后指数( IPI)对长期生存的影响非常重要,临床需要更有效的治疗方案来提高AILT的疗效.
目的 分析血管免疫母細胞性T細胞淋巴瘤( AILT)的臨床特點及近期療效,為提高AILT診治水平提供藉鑒.方法 對2005年1月至2010年1月收治的20例AILT患者的臨床資料進行迴顧性分析,總結患者的臨床及病理特點、治療和生存情況.結果 20例AILT患者中位年齡55.9歲,均有淋巴結腫大,11例有B組癥狀,確診依據淋巴結活組織檢查,免疫組織化學均錶達T細胞抗原CD3、CD45RO,治療均採用以CHOP方案為主的化療,其他治療包括DICE、ESHAP、Hyper-CVAD方案及自體造血榦細胞移植,隨訪5~ 69箇月,全組中位生存期為20.2箇月(5~69箇月),1、2、3年無病生存率分彆為67%、33%、11%,8例處于持續緩解狀態,佔全組的40%,分彆生存63、47、27、24、24、12、5、1箇月.結論 AILT患者年齡偏大,化療過程中併髮癥較多,雖然早期化療可使患者癥狀有不同程度減輕,但停止治療後容易複髮,國際預後指數( IPI)對長期生存的影響非常重要,臨床需要更有效的治療方案來提高AILT的療效.
목적 분석혈관면역모세포성T세포림파류( AILT)적림상특점급근기료효,위제고AILT진치수평제공차감.방법 대2005년1월지2010년1월수치적20례AILT환자적림상자료진행회고성분석,총결환자적림상급병리특점、치료화생존정황.결과 20례AILT환자중위년령55.9세,균유림파결종대,11례유B조증상,학진의거림파결활조직검사,면역조직화학균표체T세포항원CD3、CD45RO,치료균채용이CHOP방안위주적화료,기타치료포괄DICE、ESHAP、Hyper-CVAD방안급자체조혈간세포이식,수방5~ 69개월,전조중위생존기위20.2개월(5~69개월),1、2、3년무병생존솔분별위67%、33%、11%,8례처우지속완해상태,점전조적40%,분별생존63、47、27、24、24、12、5、1개월.결론 AILT환자년령편대,화료과정중병발증교다,수연조기화료가사환자증상유불동정도감경,단정지치료후용역복발,국제예후지수( IPI)대장기생존적영향비상중요,림상수요경유효적치료방안래제고AILT적료효.
Objective To improve the diagnosis efficiency of patients with angioimmunoblastic T-cell lymphoma (AILT) by analyzing the clinical characteristics and curative effect of AILT. Methods Retrospective studies were used on clinicopathological features,immunophenotypes,treatment and survival of 20 angioimmunoblastic T-cell lymphoma patients,who were collected between January 2005 and January 2010 of Beijing Military General Hospital. Results In the 20 patients receiving chemotherapy,the median age was 55.9 years old.All of the 20 had lymph nodes and 11 of whom were accompanied with B group of symptoms,which were confirmed by lymph node biopsy and T cell antigen CD3, CD45Ro positive expression in all the patients. ALL of the patients received the CHOP regimen and combining with other treatment such as DICE,ESHAP, Hyper-CVAD or autologous hematopoietic stem cell transplantation. A follow-up by 5 to 69 months showed that median survival was 20.2 (5-69) months and 1,2,and 3-year disease free survival (DFS) were 67 %,33 %,and 11% respectively.8 patients of the group (40 %) with a sustained remission (CCS) respectively survived 63,47,27,24,24,12,5,1 months so far.Conclusion Most patients were older with many complications during chemotherapy, which resulted in easy relapse, and even the symptoms were alleviated at the early stage of the chemotherapy. IPI prognostic index is more important with long-term survival in AITL.Therefore further studies are required to improve the outcome.