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Diffuse large B-cell non-Hodgkin lymphomas: the clinical relevance of histological subclassification

机译:弥漫性大B细胞非霍奇金淋巴瘤:组织学亚分类的临床意义

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摘要

In the REAL classification the diffuse large B-cell non-Hodgkin lymphomas (NHL) are grouped together, because subclassifications are considered to lack both reproducibility and clinical significance. Others, however, claim that patients with an immunoblastic NHL have a worse prognosis than patients with other types of diffuse large B-cell NHL. Therefore, we investigated the prognostic and clinical significance of histological subclassification of diffuse large B-cell NHL in a uniformly treated series of patients. For this retrospective study, all patients diagnosed as having an immunoblastic (IB) B-cell NHL by the Lymphoma Review Panel of the Comprehensive Cancer Center Amsterdam (CCCA) between 1984 and 1994, and treated according to the guidelines of the CCCA, were analysed. Patients with a centroblastic polymorphic subtype (CB-Poly) or centroblastic (CB) NHL by the Lymphoma Review Panel who were treated in the Netherlands Cancer Institute during the same period according to CCCA guidelines were used as reference groups. All patients' records were reviewed. Clinical parameters at presentation, kind of therapy and clinical outcome were recorded. All available histological slides were separately reviewed by two haemato-pathologists. One hundred and seventy-seven patients were included in the study: 36 patients (20.3%) with an IB NHL, 69 patients (39%) with a CB-Poly NHL and 72 patients (40.7%) with a CB NHL. The patients with an IB NHL tended to be older and presented more often with stage I or II and one extranodal site than patients with a CB and CB-Poly NHL. None of the subtypes showed a clear preference for localization in a particular site. The patients with IB or CB-Poly NHL showed a significantly worse prognosis than patients with CB NHL, with a 5-year overall survival for patients with CB NHL of 56.3% and for patients with IB or CB-Poly NHL 39.1% and 41.6% respectively. The 5-year disease free survival was 53.2% for the patients with CB, 32% for the patients with CB-Poly and 26.9% for the patients with IB NHL. A multivariate analysis showed that histological subtyping was of prognostic significance independent of the International Prognostic Index. This finding merits further exploration in prospective studies in order to judge the value of subclassification of large B-cell NHL as a guideline in therapy choice. © 1999 Cancer Research Campaign
机译:在REAL分类中,将弥散性大B细胞非霍奇金淋巴瘤(NHL)分组在一起,因为认为亚分类既缺乏可重复性,又缺乏临床意义。然而,其他人则声称,具有免疫原性NHL的患者比其他类型的弥散性大B细胞NHL的患者预后更差。因此,我们调查了一系列接受统一治疗的患者中弥漫性大B细胞NHL的组织学亚分类的预后和临床意义。在这项回顾性研究中,分析了1984年至1994年间由阿姆斯特丹综合癌症中心(CCCA)淋巴瘤审查小组诊断为患有免疫原性(IB)B细胞NHL的所有患者,并按照CCCA的指南进行了治疗。将根据CCCA指南在同一时期在荷兰癌症研究所接受过治疗的淋巴瘤复查小组的具有中心粒多态性亚型(CB-Poly)或中心粒性(CB)NHL的患者作为参考组。回顾所有患者的记录。记录就诊时的临床参数,治疗类型和临床结果。两名血液病理学家分别审查了所有可用的组织切片。该研究共纳入了177名患者:IB NHL 36例(20.3%),CB-Poly NHL 69例(39%)和CB NHL 72例(40.7%)。与具有CB和CB-Poly NHL的患者相比,具有IB NHL的患者往往年龄更大,出现I或II期和一个结外部位的频率更高。没有一个亚型显示出对特定地点本地化的明显偏好。 IB或CB-Poly NHL患者的预后显着低于CB NHL,CB NHL患者的5年总生存率为56.3%,IB或CB-Poly NHL的患者为39.1%和41.6%分别。 CB患者的5年无病生存率为53.2%,CB-Poly患者为32%,IB NHL患者为26.9%。多元分析表明,组织学亚型具有独立于国际预后指数的预后意义。这一发现值得在前瞻性研究中进一步探索,以判断大B细胞NHL亚分类作为治疗选择指南的价值。 ©1999癌症研究运动

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