Implication of HTLV-I infection, strongyloidiasis, and P53 overexpression in the development, response to treatment, and evolution of non-Hodgkin's lymphomas in an endemic area (Martinique, French West Indies)

Citation
P. Agape et al., Implication of HTLV-I infection, strongyloidiasis, and P53 overexpression in the development, response to treatment, and evolution of non-Hodgkin's lymphomas in an endemic area (Martinique, French West Indies), J ACQ IMM D, 20(4), 1999, pp. 394-402
Citations number
68
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY
ISSN journal
15254135 → ACNP
Volume
20
Issue
4
Year of publication
1999
Pages
394 - 402
Database
ISI
SICI code
1525-4135(19990401)20:4<394:IOHISA>2.0.ZU;2-I
Abstract
A clinicopathologic study was conducted to assess the implication of HTLV-I infection, Strongyloides stercoralis (Ss) infection? and P53 overexpressio n in the development, response to treatment, and evolution of non-Hodgkin's lymphoma (NHL) in Martinique, French West Indies. Two groups of patients, with 22 and 41 participants with B-cell and T-cell lymphoma, respectively, were analyzed. HTLV-I antibodies were detected in 24 (59%) patients with T- cell lymphoma of whom 19 (46%) fulfilled diagnostic criteria of adult T-cel l leukemia/lymphoma (ATLL). By comparison with other T-cell lymphomas, pati ents with ATLL were significantly younger (52 versus 63 years; p = .03), ha d a significantly higher incidence of hypercalcemia (60% versus 0%; p = .00 01), a trend for higher incidence of digestive tract localization (21% vers us 4%; p = .1 and significantly shorter median survival (6 versus 17 months ; p = .03). Similar results were observed when all 24 HTLV-I-infected patie nts with T-cell lymphoma were compared with the 17 seronegative patients. S trongyloidiasis was diagnosed in 11 of 33 patients tested for Ss infection. All 4 Ss-infected (Ss-positive) ATLL patients treated with combination che motherapy achieved complete remission (CR) versus only 2 of 7 Ss-negative A TLL patients (p = .04). Ln addition, survival of Ss-positive patients with ATLL was better than that of the uninfected patients: 27 versus 5 months, p = .04, respectively). P53 expression was assessed by immunohistochemistry on lymph node biopsies from 37 patients including Is B-cell lymphomas, 14 A TLL, and 5 other T-cell lymphomas. P53 overexpression (P53-positive) was ob served in 6 samples that corresponded in all 6 patients with ATLL. All P53- positive ATLL patients had stage TV disease with elevated lactate dehydroge nase (LDH) levels. By comparison with other ATLL patients studied for p53 e xpression P53-positive ATLL were characterized by a lower response rate to combination chemotherapy (CR: 0 of 6 versus 4 of 6; p = .04) and a shorter survival (2 versus 9 months, p = .04). Our results suggest that ATLL repres ents almost 50% of T-cell lymphomas in Martinique: Ss infection during ATLL seems to be linked with a high response rate to chemotherapy and prolonged survival; and P53 overexpression is observed in almost 50% of aggressive A TLL from Martinique and, even in advanced clinical subtypes, is associated with resistance to chemotherapy and short-term survival.