摘要
目的:探讨血管免疫母T细胞性淋巴瘤(angioimmunoblastic T-cell lymphoma,AITL)的病理、临床特点和CHOP方案的近期疗效。方法:同时采用常规组织病理学、免疫组织化学、细胞遗传学对15例淋巴瘤患者淋巴结的手术活检标本进行研究,并以CHOP方案作为初始治疗,复发后以MINE+P方案解救。结果:15例患者均表达T细胞抗原CD45RB、CD3和CD45RO,10例(10/15)表达CD10,10例(10/15)表达CD21,4例(4/14)染色体异常。全组15例均能评价疗效,15例CHOP方案初治有效率100%均有效,(CR 7例,PR 8例)。复发8例,MINE+P方案解救有效6例(CR 3例,PR 3例),有效率75%。毒副反应以粒细胞计数下降和血小板下降为常见,但均可耐受。结论:常规组织学、免疫组化检查、细胞遗传学是确诊AITL的重要手段,CHOP方案初治有效率高,但易复发,MINE+P方案解救有效率较高,毒副反应可以耐受。
Objective:To study the clinical and pathological characteristics of the patients with angioimmunoblastic T-cell lymphoma and the short-term effects of CHOP regimen. Methods: The histological, immunohistochemical, and cytogenetic examination were performed on the biopsy specimens of superficial lymph nodes from 15 patients with angioimmunoblastic T-cell lymphoma. All of the patients received the CHOP regimen as the first-line chemotherapy and MINE+P regimen as the secondline chemotherapy after relapse. Results:T cell antigen CD45RB, CD3, and CD45RO were expressed in superficial lymph nodes of all the 15 patients. Expression of CD10 was detected in 10 out of 15 patients (66.7%)and CD21 expression was also detected in 66.7% patients (10/15). Four patients(4/14, 26.7%)showed chromosomal abnormality. All the 15 patients were evaluable. The response rate to CHOP regimen as the first line chemotherapy is 100 % (7 cases achieved complete response and 8 cases had partial response). Six patlens had the response to MINE+P salvage regimen (3 cases had CR and 3 cases had PR). The main toxicities including neutropenia and thrombocytopenia were tolerable. Conclusion: Routine histological, immunohistochemical, cytogenetic examinations play significant roles in final diagnosis of angioimmunoblastic T-cell lymphoma. The first-line CHOP regimen has high efficacy but tumor is easy to relapse. The MINE+P regimen is an effective salvage regimen with tolerable toxicities.
出处
《肿瘤》
CAS
CSCD
北大核心
2007年第3期231-233,248,共4页
Tumor
关键词
淋巴瘤
非霍奇金
病理
细胞遗传学
抗肿瘤联合化疗方案
Lymphoma,Non-Hodgkin
Pathology
Cytogenetics
Antineoplastic combined chemotherapy protocols