肠病相关t细胞淋巴瘤的临床诊断与治疗

Y. Miao, Qiaojiajie Zhao
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According to AnnArbor clinical d staging, 9 patients(90%) had stage I+II and 1 patient(10%) had stage III. Gastrointestinal lymphoma AnnArbor clinical staging was the same as lugano clinical staging. 6 patients with B symptoms, 6 with physical status score ≥ 2, 5 with IPI > 2, 6 with PIT > 6; all patients had normal examination regardless of bone marrow examination, β2-microglobulin, or glycoconjugate antigen-125, erythrocyte sedimentation rate. 1 patient with anemia, 6 with decreased albumin, 2 with with elevated lactate dehydrogenase, and 1 case with increased C-reactive protein. According to immunohistochemical hints, 6 cases were CD56 positive and 4 in situ hybridization EBER positive; in the mid-term evaluation of combined patients, the complete remission(CR) rate was 90% in 10 patients; in the DA-EPOCH regimen, the complete remission(CR) rate was 80% in 10 patients. 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摘要

目的探讨肠病相关t细胞淋巴瘤(enteropathy-associated T-cell lymphoma, EATL)的临床特点及治疗策略。方法:从2019年开始。02 - 2022。02、对我院收治的10例肠病相关t细胞淋巴瘤患者的临床资料进行回顾性分析,并提出切实可行的治疗方案。结果:所有患者均无肠道疾病史,均因胃肠道症状就诊。5例患者发生肠穿孔并行夹层,3例患者发生小肠肿块并行手术,2例患者发生t细胞淋巴瘤并行相关治疗。6名患者在小肠有病变,其他患者在直肠有病变。根据AnnArbor临床分期,9例患者(90%)为I+II期,1例患者(10%)为III期。胃肠道淋巴瘤AnnArbor临床分期与lugano临床分期相同。B症状6例,身体状态评分≥2者6例,IPI > 2者5例,PIT > 6者6例;所有患者的骨髓检查、β2-微球蛋白、糖结合抗原-125、红细胞沉降率均正常。贫血1例,白蛋白降低6例,乳酸脱氢酶升高2例,c反应蛋白升高1例。免疫组化提示CD56阳性6例,原位杂交EBER阳性4例;在联合患者中期评价中,10例患者完全缓解(CR)率为90%;在DA-EPOCH方案中,10例患者的完全缓解(CR)率为80%。6个化疗疗程结束时,所有化疗患者均达到完全缓解(CR),但其中3例患者在1年内复发,实施二线方案再化疗无法控制病情。随访1-25个月,截至随访时间,随访率高达100%,死亡6例,总2年生存率为40%。结论:肠病相关t细胞淋巴瘤侵袭性强,化疗后可治疗,但易复发。异体造血干细胞移植(allogeneic hematopoietic stem cell transplantation, ASCT)成为一线巩固治疗,但不能获得长期疗效,有待探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Diagnosis and Treatment of Enteropathy-associated T-cell Lymphoma
To investigate the clinical characteristics of enteropathy-associated T-cell lymphoma(EATL) and to give treatment strategies. METHODS:  From 2019. 02-2022. 02, 10 patients with enteropathy-associated T-cell lymphoma were seen in our hospital, their clinical data were retrospectively analyzed, and practical treatment plans were provided. Results:None of the patients had a history of intestinal disease and all presented to the hospital because of symptoms occurring in the gastrointestinal tract.Five patients had intestinal perforation and underwent dissection, three had small bowel masses and underwent surgery, and two had T-cell lymphoma and underwent related treatment. Six patients had lesions in the small intestine and the others had lesions in the rectum. According to AnnArbor clinical d staging, 9 patients(90%) had stage I+II and 1 patient(10%) had stage III. Gastrointestinal lymphoma AnnArbor clinical staging was the same as lugano clinical staging. 6 patients with B symptoms, 6 with physical status score ≥ 2, 5 with IPI > 2, 6 with PIT > 6; all patients had normal examination regardless of bone marrow examination, β2-microglobulin, or glycoconjugate antigen-125, erythrocyte sedimentation rate. 1 patient with anemia, 6 with decreased albumin, 2 with with elevated lactate dehydrogenase, and 1 case with increased C-reactive protein. According to immunohistochemical hints, 6 cases were CD56 positive and 4 in situ hybridization EBER positive; in the mid-term evaluation of combined patients, the complete remission(CR) rate was 90% in 10 patients; in the DA-EPOCH regimen, the complete remission(CR) rate was 80% in 10 patients. At the completion of 6 chemotherapy courses, all chemotherapy patients were in complete remission(CR) at the end of the period assessment, but 3 of them relapsed within one year, and the disease could not be controlled with the implementation of second-line regimen and chemotherapy again. The follow-up period was 1-25 months, with a high follow-up rate of 100% up to the follow-up time, and 6 patients died, with an overall 2-year survival rate of 40%. Conclusion: Enteropathy-associated T-cell lymphoma is highly aggressive, and after chemotherapy, patients can be treated but are prone to relapse. The use of allogeneic hematopoietic stem cell transplantation(ASCT) becomes the first-line consolidation therapy, which cannot obtain long-term efficacy and needs to be explored.
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