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Br J Haematol ; 112(3): 796-805, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11260086

ABSTRACT

Twenty-seven consecutive Italian patients with Fanconi's anaemia (FA) underwent stem cell transplantation (SCT) from an HLA-matched related donor in 10 Italian centres of the Associazione Italiana Ematologia ed Oncologia Pediatrica (AIEOP), Gruppo Italiano di Trapianto di Midollo Osseo (GITMO). Twenty-two patients (81.5%) were conditioned with low-dose (median 20 mg/kg) cyclophosphamide (Cy) and thoraco-abdominal or total body irradiation (median dose 500 cGy), five patients (18.5%) with high-dose Cy (median 120 mg/kg). Graft-vs.-host disease (GVHD) prophylaxis was carried out with cyclosporin A in 26 cases; methotrexate (MTX) was added in eight cases. One patient received MTX alone. The median follow-up was 36 months. Ninety-two percent of patients (25 out of 27) engrafted, grade II and III acute GVHD occurred in 28% and 8% of patients, respectively, with chronic GVHD in 12.5%. Conditioning-related toxicity was mild: 4% of patients had grade III mucositis, 7.4% had grade II haemorrhagic cystitis, 14.8% had grade III liver toxicity and 11.1% had grade III renal toxicity. Transplant-related mortality at 12 months was 19.2%, survival at 36 months was 81.5%, with a median Karnofsky score of 100%. No late tumours occurred after a mean follow-up of the survivors of 5 years. None of the studied variables significantly affected the survival, including conditioning regimen, acute GVHD and clinical non-haematological phenotype. Among the studied variables, only conditioning regimens containing high-dose Cy and the presence of genital abnormalities were significantly (P < 0.05) associated with an increased rate of acute GVHD. Our study demonstrates that the Italian FA patients undergoing SCT from an HLA-matched related donor have a very good outcome. These patients, when compared with others of different ethnic origin who underwent allogeneic bone marrow transplantation, showed a less severe non-haematological phenotype, raising the possibility that this milder phenotype may have, at least in part, contributed to the outcome. Our data may provide a useful tool for further studies aiming to correlate genotype with phenotype.


Subject(s)
Fanconi Anemia/surgery , Hematopoietic Stem Cell Transplantation/methods , Transplantation Conditioning/methods , Adolescent , Bone Marrow Transplantation , Child , Child, Preschool , Congenital Abnormalities/ethnology , Congenital Abnormalities/surgery , Fanconi Anemia/complications , Fanconi Anemia/ethnology , Female , Genotype , Graft vs Host Disease , Growth Disorders/complications , Growth Disorders/ethnology , Growth Disorders/surgery , Histocompatibility Testing , Humans , Italy/epidemiology , Male , Phenotype , Pigmentation Disorders/complications , Pigmentation Disorders/ethnology , Pigmentation Disorders/surgery , Retrospective Studies , Transplantation, Homologous , Treatment Outcome
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