Novakovic Barbara Jezersek, Novakovic Srdjan, Frkovic-Grazio Snezana
Department of Medical Oncology, Institute of Oncology Ljubljana, 1000 Ljubljana, Slovenia.
Oncol Rep. 2006 Jul;16(1):191-5.
Intestinal T cell lymphomas are rare, but highly aggressive in their clinical course. Generally diagnosed in advanced stages and presenting as surgical emergencies, they also respond poorly to standard anti-lymphoma therapies. Since these lymphomas are still not well characterized, we aimed our retrospective research at the evaluation of clinical features and treatment response in patients with intestinal T cell lymphomas diagnosed between February 1996 and November 2004. Fifteen patients were identified from the Department of Pathology database at the Institute of Oncology Ljubljana. Details of history, physical examination, staging investigation, treatment and outcome were taken from patient records. Ten (67%) patients had enteropathy-associated T cell lymphoma (EATL) and 5 (33%) had peripheral T cell lymphoma (PTCL). Surgery was performed on 11 patients with 8 cases on an emergency basis; all visible disease was resected in only 3 patients. In the continuation of treatment, all 15 patients received chemotherapy (predominantly CHOP). Six patients were treated with field radiotherapy as a part of the first treatment. In total, complete response was achieved in 6 patients (40%) with a median duration of 5.3 months (range, 2 to 12 months), stable disease in 3 patients (20%), and progressive disease in 6 patients (40%). Results were better in patients with limited disease. The most frequent treatment complications were small bowel perforation, obstruction, gastrointestinal bleeding, and infection. Even though some patients underwent second- and third-line treatment, 13 (87%) of the total 15 patients died from progressive disease or complications of treatment. The actuarial 1- and 5-year survival rates were 33% and 9%, respectively. The prognosis and standard treatment of patients with intestinal T cell lymphomas are unsatisfactory with only a few long-term survivors. Therefore, earlier diagnosis and the development of more effective treatments are urgently required to improve the prospects of these patients.
肠道T细胞淋巴瘤较为罕见,但其临床病程进展迅速。通常在晚期才得以诊断,多表现为外科急症,对标准抗淋巴瘤治疗的反应也较差。由于这些淋巴瘤的特征仍未完全明确,我们开展了一项回顾性研究,旨在评估1996年2月至2004年11月期间确诊的肠道T细胞淋巴瘤患者的临床特征及治疗反应。从卢布尔雅那肿瘤研究所病理数据库中识别出15例患者。病史、体格检查、分期检查、治疗及预后的详细信息均来自患者病历。10例(67%)患者患有肠病相关T细胞淋巴瘤(EATL),5例(33%)患有外周T细胞淋巴瘤(PTCL)。11例患者接受了手术治疗,其中8例为急诊手术;仅3例患者的所有可见病灶均被切除。在后续治疗中,所有15例患者均接受了化疗(主要为CHOP方案)。6例患者在首次治疗时接受了局部放疗。总体而言,6例患者(40%)达到完全缓解,中位缓解持续时间为5.3个月(范围为2至12个月),3例患者(20%)病情稳定,6例患者(40%)病情进展。疾病局限的患者治疗效果更佳。最常见的治疗并发症为小肠穿孔、梗阻、胃肠道出血及感染。尽管部分患者接受了二线和三线治疗,但15例患者中有13例(87%)死于疾病进展或治疗并发症。1年和5年的精算生存率分别为33%和9%。肠道T细胞淋巴瘤患者的预后及标准治疗效果均不尽人意,长期存活者寥寥无几。因此,迫切需要更早的诊断以及更有效的治疗方法来改善这些患者的预后。