Reiter A, Tiemann M, Ludwig W D, Wacker H H, Yakisan E, Schrappe M, Henzler D, Sykora K W, Brandt A, Odenwald E
Abt. Päd. Hämatologie/Onkologie, Med. Hochschule Hannover.
Klin Padiatr. 1994 Jul-Aug;206(4):222-33. doi: 10.1055/s-2008-1046608.
One of the goals of the study NHL-BFM 90 was to investigate the distribution and prognosis of the different subtypes of Non-Hodgkin's Lymphoma (NHL) in children and adolescents according to histological, cytomorphological and immunological characteristics. From 4/1990 to 12/1992, 346 patients (pts) (84 females, 262 males) were enrolled (median age: 9.1 years; range: 0.8-17.9 years). Histology was available from 290 pts (84%), cytomorphology from 155 (44%), and immunophenotyping from 245 (70%). Cases with L1 oder L2 cytomorphology according to the French-American-British Classification were classified as lymphoblastic lymphoma and those with L3 cytomorphology as Burkitt-Type lymphoma or acute B-cell leukemia (B-ALL) if a histological classification was not available. By means of the combined analysis of all three diagnostic criterias the classification of the NHL according to the updated Kiel-classification was possible in 312 cases: 49% were classified as Burkitt-type-lymphoma (incl. B-ALL), 22% als lymphoblastic lymphoma, 10% as large cell anaplastic lymphoma (LCAL), 6% as centroblastic lymphoma, only few cases were classified as NHL of other subtypes, 3 pts (1%) suffered from low grade malignant lymphomas, and in 34 pts (10%) the NHL was not further classified. Patients were stratified according to NHL-subentities in 3 branches (Non-B-NHL, B-NHL, LCAL) of different treatment modalities. The estimated probability of a 3-year event free survival (pEFS) was 88 +/- 2% for the whole group (follow up 7 to 40 months, median 23 months) while pEFS of different subtypes was: lymphoblastic lymphoma: 91 +/- 4%; Burkitt-type-lymphoma/B-ALL: 90 +/- 2%; centroblastic lymphoma: 94 +/- 6%, LCAL: 88 +/- 6%. We conclude that the stratification of treatment modalities in study NHL-BFM 90 according to biological entities provided patients of different NHL-subtypes an equal chance to survive event free. The efficacy of the treatment strategy for rare subtypes, however, is not evaluable yet.
NHL - BFM 90研究的目标之一是根据组织学、细胞形态学和免疫学特征,调查儿童和青少年非霍奇金淋巴瘤(NHL)不同亚型的分布及预后。从1990年4月至1992年12月,共纳入346例患者(pts)(84例女性,262例男性)(中位年龄:9.1岁;范围:0.8 - 17.9岁)。290例患者(84%)有组织学资料,155例(44%)有细胞形态学资料,245例(70%)有免疫表型分析资料。根据法国 - 美国 - 英国分类法,具有L1或L2细胞形态学特征的病例若无法进行组织学分类,则分类为淋巴母细胞淋巴瘤,具有L3细胞形态学特征的病例分类为伯基特型淋巴瘤或急性B淋巴细胞白血病(B - ALL)。通过对所有三项诊断标准的综合分析,312例病例能够按照更新后的基尔分类法对NHL进行分类:49%被分类为伯基特型淋巴瘤(包括B - ALL),22%为淋巴母细胞淋巴瘤,10%为大细胞间变性淋巴瘤(LCAL),6%为中心母细胞淋巴瘤,只有少数病例被分类为其他亚型的NHL,3例患者(1%)患有低级别恶性淋巴瘤,34例患者(10%)的NHL未进一步分类。患者根据NHL亚实体被分为不同治疗方式的3组(非B - NHL、B - NHL、LCAL)。整个组的3年无事件生存率(pEFS)估计为88±2%(随访7至40个月,中位时间23个月),不同亚型的pEFS为:淋巴母细胞淋巴瘤:91±4%;伯基特型淋巴瘤/B - ALL:90±2%;中心母细胞淋巴瘤:94±6%,LCAL:88±6%。我们得出结论,NHL - BFM 90研究中根据生物学实体对治疗方式进行分层,为不同NHL亚型的患者提供了同等的无事件生存机会。然而,罕见亚型治疗策略的疗效尚未可评估。