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R Fanin

Publications and source records attributed to R Fanin.

129 records · Page 8Linked to original sources

Hepatitis C virus infection among cryoglobulinemic and non-cryoglobulinemic B-cell non-Hodgkin's lymphomas.

BACKGROUND AND OBJECTIVE: Since hepatitis C virus (HCV) infection has been associated with different histotypes of B-cell non-Hodgkin's lymphoma (NHL), with or without concomitant production of cryoglobulins (cryolg), we have investigated the prevalence of the infection among NHL with the aim of defining its relationship with the histotype and with the production of cryolg. METHODS: Four-hundred and seventy unselected, consecutive patients with a diagnosis of B-cell NHL were investigated. Anti-HCV antibodies (Ab) and cryolg were sought in all while HCV RNA and rheumatoid factor were detected on HCV-Ab positive samples. RESULTS: Overall, the prevalence of HCV infection was 8.9% (42/470). It was 95.4% (#21) among the 22 patients with, and 4.6% (#21) among the 448 without production of cryoIg. The most common histotype among the HCV-positive, cryoIg-producing cases, was the immunocytoma (16/21, 76%). Among the HCV-positive, non cryoIg-producing cases, the marginal zone and the follicle center lymphomas were the commonest. INTERPRETATION AND CONCLUSIONS: Close association between HCV infection and cryoIg production, already described in mixed cryoglobulinemia, is confirmed also among B-cell NHL. Nevertheless, 50% of HCV-related lymphomas are non-cryoIg producers. Low-grade lymphomas (in particular the immunocytoma) are the most frequent HCV-related lymphomas. Since new therapeutic strategies might be necessary if the virus is detected, screening for cryoIg and for HCV-Ab among B-cell NHL at diagnosis is mandatory.

Cohort Studies↗

Retrospective analysis of 34 cases of hairy cell leukemia treated with interferon-alpha and/or 2-chlorodeoxyadenosine.

The aim of the present study was to compare the outcome of patients affected by typical hairy cell leukemia (HCL) treated with interferon-alpha (IFN-alpha) and/or 2-chlorodeoxyadenosine (2CdA). Thirty-four consecutive patients were enrolled in the study. IFN was administered in 26 cases as first line therapy at a dose of 3 MU every other day for 12 months. 2CdA was given in 8 cases as first-line and in 14 cases as second-line therapy in patients resistant to (2 cases) or relapsed after (12 cases) IFN. The treatment schedule for 2CdA was 0.1 mg/kg/daily for 7 days for 1 cycle (17 patients) or 2 cycles (5 patients). Complete (CR) and partial remission (PR) were 19% and 58%, respectively, for IFN, 75% and 25% for 2CdA in first-line therapy, 86% and 14% for 2CdA in second-line therapy. Median progression-free survival for IFN patients was 19 months and no statistical advantage was detected for those who achieved a CR vs those in PR. In the group treated with 2CdA, only 1 patient (4%) relapsed after a median follow-up of 14 months. At a median follow-up of 59 months (range 4-134), overall survival of all 34 patients was 97%, with only 1 patient having died of an acute leukemia. Our results confirm the favorable outcome currently expected for HCL and emphasize the therapeutic activity of 2CdA in the treatment of this disease.

Adult↗

Bone marrow transplantation in a patient with chronic myeloid leukemia and achondroplasia.

A 25-year-old female with achondroplastic dwarfism, diagnosed when she was six months old, was diagnosed with chronic myeloid leukemia (CML) in chronic phase with 9;22 translocation, A2B3 gene rearrangement and a Sokal index of 0.5. A recombinant interferon-alpha 2A treatment was started in October '94, which obtained a hematological, but not a karyotypic, response at the 6th and 12th month. In August '94, the patient was submitted to allogeneic bone marrow transplantation (alloBMT) from a 36-year-old matched sibling. The procedure was well tolerated. Disease-free survival (DFS) and overall survival (OS) were 21 and 39 months, respectively. We have not found any reported cases of achondroplastic patients submitted to alloBMT in the literature or in the IBMT Registry.

Achondroplasia↗