Division of Hematology and Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
BMC Cancer. 2011 Jul 29;11:321. doi: 10.1186/1471-2407-11-321.
Primary intestinal non-Hodgkin lymphoma (NHL) is a heterogeneous disease with regard to anatomic and histologic distribution. Thus, analyses focusing on primary intestinal NHL with large number of patients are warranted.
We retrospectively analyzed 581 patients from 16 hospitals in Korea for primary intestinal NHL in this retrospective analysis. We compared clinical features and treatment outcomes according to the anatomic site of involvement and histologic subtypes.
B-cell lymphoma (n = 504, 86.7%) was more frequent than T-cell lymphoma (n = 77, 13.3%). Diffuse large B-cell lymphoma (DLBCL) was the most common subtype (n = 386, 66.4%), and extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT) was the second most common subtype (n = 61, 10.5%). B-cell lymphoma mainly presented as localized disease (Lugano stage I/II) while T-cell lymphomas involved multiple intestinal sites. Thus, T-cell lymphoma had more unfavourable characteristics such as advanced stage at diagnosis, and the 5-year overall survival (OS) rate was significantly lower than B-cell lymphoma (28% versus 71%, P < 0.001). B symptoms were relatively uncommon (20.7%), and bone marrow invasion was a rare event (7.4%). The ileocecal region was the most commonly involved site (39.8%), followed by the small (27.9%) and large intestines (21.5%). Patients underwent surgery showed better OS than patients did not (5-year OS rate 77% versus 57%, P < 0.001). However, this beneficial effect of surgery was only statistically significant in patients with B-cell lymphomas (P < 0.001) not in T-cell lymphomas (P = 0.460). The comparison of survival based on the anatomic site of involvement showed that ileocecal regions had a better 5-year overall survival rate (72%) than other sites in consistent with that ileocecal region had higher proportion of patients with DLBCL who underwent surgery. Age > 60 years, performance status ≥ 2, elevated serum lactate dehydrogenase, Lugano stage IV, presence of B symptoms, and T-cell phenotype were independent prognostic factors for survival.
The survival of patients with ileocecal region involvement was better than that of patients with involvement at other sites, which might be related to histologic distribution, the proportion of tumor stage, and need for surgical resection.
原发性肠道非霍奇金淋巴瘤(NHL)在解剖和组织学分布方面具有异质性。因此,有必要对涉及大量患者的原发性肠道 NHL 进行分析。
本回顾性分析纳入了韩国 16 家医院的 581 例原发性肠道 NHL 患者。我们比较了根据受累解剖部位和组织学亚型的临床特征和治疗结果。
B 细胞淋巴瘤(n=504,86.7%)比 T 细胞淋巴瘤(n=77,13.3%)更为常见。弥漫性大 B 细胞淋巴瘤(DLBCL)是最常见的亚型(n=386,66.4%),黏膜相关淋巴组织(MALT)结外边缘区 B 细胞淋巴瘤是第二常见的亚型(n=61,10.5%)。B 细胞淋巴瘤主要表现为局限性疾病(Lugano 分期 I/II),而 T 细胞淋巴瘤累及多个肠道部位。因此,T 细胞淋巴瘤具有更差的特征,如诊断时的晚期阶段,并且 5 年总生存率(OS)明显低于 B 细胞淋巴瘤(28%比 71%,P<0.001)。B 症状相对少见(20.7%),骨髓侵犯罕见(7.4%)。回盲部是最常见的受累部位(39.8%),其次是小肠(27.9%)和大肠(21.5%)。接受手术的患者比未接受手术的患者的 OS 更好(5 年 OS 率为 77%比 57%,P<0.001)。然而,这种手术的有益效果仅在 B 细胞淋巴瘤患者中具有统计学意义(P<0.001),而在 T 细胞淋巴瘤患者中没有(P=0.460)。根据受累解剖部位的生存比较显示,回盲部的 5 年总生存率(72%)优于其他部位,这与回盲部有更高比例的接受手术的 DLBCL 患者相一致。年龄>60 岁、体能状态≥2、血清乳酸脱氢酶升高、Lugano 分期 IV、存在 B 症状和 T 细胞表型是生存的独立预后因素。
回盲部受累患者的生存情况优于其他部位受累患者,这可能与组织学分布、肿瘤分期比例和手术切除需求有关。