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Ann Hematol. 2012 May;91(5):715-721. doi: 10.1007/s00277-011-1369-y. Epub 2011 Nov 16.

Identification of patients with indolent B cell lymphoma sensitive to rituximab monotherapy.

Author information

1
EA2216 "Immunology and Pathology" and IFR146 "ScInBios", Université Européenne de Bretagne, Brest, France.
2
Laboratory of Immunology, Brest University Medical School Hospital, BP824, Brest, 29609, France.
3
Department of Clinical Oncology, Brest University Medical School Hospital, Brest, France.
4
Unit of Nuclear Medicine, Brest University Medical School Hospital, Brest, France.
5
EA2216 "Immunology and Pathology" and IFR146 "ScInBios", Université Européenne de Bretagne, Brest, France. youinou@univ-brest.fr.
6
Laboratory of Immunology, Brest University Medical School Hospital, BP824, Brest, 29609, France. youinou@univ-brest.fr.

Abstract

The potential predictive value of tumor bulk, genetic, and immunological variants in patients with low-grade non-Hodgkin's lymphoma to respond to treatment with rituximab (RTX) monotherapy was evaluated. Thus, the value of assessing the effect of 18-fluoro-desoxy-D-glucose (FDG) uptake on PET scan, polymorphisms in Fc gamma receptor (FcγR) IIIa-158, FcγRIIa-131, and C1qA-276 genes in predicting the response to treatment were evaluated in 50 low-grade non-Hodgkin's lymphoma patients. The influence of RTX pharmacokinetics, plasma levels of the B cell-activating factor (BAFF), and human antichimeric antibodies was also investigated. The therapeutic response was evaluated 10 weeks after treatment using revised Cheson's criteria. Lower maximal standardized uptake values (SUV(max)) at baseline were predictive of complete response. FcγRIIIa-158 polymorphism was also associated with complete response to RTX confirming previous findings, whereas polymorphisms in the FcγRIIa-131 and C1qA-276 genes were not. Lower blood levels of RTX were observed in males, but the effectiveness of RTX in males and females was the same. BAFF was not detectable in plasma before or after treatment, and no patients developed human antichimeric antibodies. Low-grade non-Hodgkin's lymphoma patients with a low SUV(max) at baseline and an FcγRIIIa-158 V/V genotype generally had a complete response to RTX.

PMID:
22083514
DOI:
10.1007/s00277-011-1369-y
[Indexed for MEDLINE]

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