Literature DB >> 3115783

Blood clonal B cell excess (CBE) at diagnosis in patients with non-Hodgkin lymphoma (NHL). Relation to clinical stage, histopathology and response to treatment.

C Lindemalm1, H Mellstedt, B Nilsson, P Biberfeld, M Björkholm, B Christensson, G Holm, B Johansson.   

Abstract

Untreated non-leukemic (lymphocytes less than or equal to 4.0 X 10(9)/l) patients with non-Hodgkin lymphoma (NHL) of B cell type often show an excess of B cells in peripheral blood bearing the same light chain isotype as the lymph node tumor cells which may indicate a leukemic spread of the disease. The ratio between kappa- and lambda-bearing lymphocytes (normal range 1.0-3.3) was studied to evaluate the prognostic significance of clonal B cell excess (CBE) at diagnosis in 110 NHL patients. In total 43% had a CBE in peripheral blood. Fifty-two per cent of the patients in clinically advanced stages had CBE and 30% of the patients in stages I and II. CBE was detected in 49% of all patients with low-grade malignant lymphoma and in 32% with high-grade malignancy. Patients with a normal kappa:lambda ratio at diagnosis entered complete remission more often than those with CBE (P less than 0.01). In patients with high-grade but not with low-grade malignant lymphomas remission duration was longer for those with normal kappa:lambda distribution than for the patients with an abnormal ratio (P less than 0.01). Survival was not statistically significantly influenced.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3115783     DOI: 10.1016/0277-5379(87)90273-2

Source DB:  PubMed          Journal:  Eur J Cancer Clin Oncol        ISSN: 0277-5379


  2 in total

1.  Prognostic significance of immunoglobulin isotype expression in B-cell non-Hodgkin's lymphoma.

Authors:  C Lindemalm; B Christensson; G Biberfeld; P Biberfeld; M Björkholm; B Johansson; E Kimby; H Mellstedt
Journal:  Med Oncol Tumor Pharmacother       Date:  1988

2.  Peripheral blood involvement in non-Hodgkin's lymphoma detected by clonal gene rearrangement as a biological prognostic marker.

Authors:  L R Hiorns; J Nicholls; J P Sloane; A Horwich; S Ashley; M Brada
Journal:  Br J Cancer       Date:  1994-02       Impact factor: 7.640

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.