Literature DB >> 6574590

Immunological typing of acute lymphoblastic leukaemia.

H J van der Reijden, E R van Wering, J M van de Rijn, C J Melief, M B van 't Veer, H Behrendt, A E von dem Borne.   

Abstract

The blasts of 37 adult and 126 childhood cases of acute lymphoblastic leukaemia (ALL) were characterized with a panel of xeno-antisera and rosette tests. The Orthoclone monoclonal antibodies (OK series) were applied as well. Like other investigators, we were able to distinguish 4 major classes of ALL: T-ALL, common-ALL with the subclass pre-B-ALL, null-ALL, and B-ALL. We did not encounter a common-ALL antigen-positive T-ALL subclass. In both adult and childhood ALL, all classes were present, and in about the same frequency as reported by others. In children, common-ALL was the most frequent (66%); in adults, null-ALL (38%). T-ALL was seen both in adults and in children with about the same frequency (27 and 23%, respectively). We found pre-B-ALL only in children. Patients with B-ALL comprised the smallest group in both adult and children (8 and 1.5%, respectively). The application of the OKT antibodies led to recognition of 3 major subclasses of T-ALL: an immature, a common thymocyte and a mature thymocyte subclass. These antibodies were helpful in defining a better classification of null-ALL. With regard to remission induction and prognosis in adult ALL, complete remissions were always obtained in T-ALL, followed by 70% of complete remissions in common-ALL. The worst prognosis was encountered in null-ALL and B-ALL, with 50 and 0% remission, respectively, and a shorter survival in null-ALL of those patients who achieved complete remission. Thus, in high number of cases of null-ALL in adults partly explains the generally much worse prognosis for adult ALL.

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Year:  1983        PMID: 6574590     DOI: 10.1111/j.1600-0609.1983.tb01507.x

Source DB:  PubMed          Journal:  Scand J Haematol        ISSN: 0036-553X


  3 in total

1.  Acute lymphoblastic leukaemia in adults: immunological subtypes and clinical features at presentation.

Authors:  M B van't Veer; W L van Putten; L F Verdonck; G J Ossenkoppele; B Löwenberg; J C Kluin-Nelemans; P W Wijermans; H C Schouten; W Sizoo; A W Dekker
Journal:  Ann Hematol       Date:  1993-06       Impact factor: 3.673

2.  Electron microscopy: a contribution to further classification of acute unclassifiable childhood leukemia.

Authors:  E R van Wering; P Brederoo; J H van Dijk-de Leeuw; J van der Meulen; M B van 't Veer
Journal:  Blut       Date:  1990-05

3.  Childhood leukaemia in The Netherlands, 1973-1986: temporary variation of the incidence of acute lymphocytic leukaemia in young children.

Authors:  J W Coebergh; A van der Does-van den Berg; E R van Wering; H A van Steensel-Moll; H A Valkenburg; M B van't Veer; P I Schmitz; G E van Zanen
Journal:  Br J Cancer       Date:  1989-01       Impact factor: 7.640

  3 in total

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