| Literature DB >> 27392319 |
Marta Pillon1, Lara Mussolin2,3, Elisa Carraro2, Valentino Conter4, Maurizio Aricò5, Luciana Vinti6, Alberto Garaventa7, Matilde Piglione8, Salvatore Buffardi9, Alessandra Sala4, Nicola Santoro10, Luca Lo Nigro11, Rossella Mura12, Annalisa Tondo13, Fiorina Casale14, Piero Farruggia15, Paolo Pierani16, Simone Cesaro17, Emanuele S G d'Amore18, Giuseppe Basso2.
Abstract
Burkitt lymphoma (BL) and Diffuse Large B-Cell Lymphoma (DLBCL) account for most cases of non-Hodgkin lymphoma (NHL) in childhood. We report the clinical characteristics, outcome and prognostic factors in children with BL or DLBCL treated according to the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) LNH-97 protocol. Patients aged up to 18 years that were newly diagnosed with BL/DLBCL were included in the study. Therapy consisted of pre-phase followed by 2-6 high-dose chemotherapy courses tailored according to lactate dehydrogenase (LDH) value and disease stage. A total of 442 patients (379 BL, 63 DLBCL) were enrolled between 1997 and 2014, of whom 18 failed to achieve remission, 6 experienced treatment-related death, 2 developed second malignancy and 20 relapsed. At a median follow-up time of 5 years, overall survival was 93% (±1%) and event-free survival was 90% (±1%). LDH value above the median value had an independently negative prognostic value (P < 0·0001). However, in the subgroup of 128 patients in which minimal disseminated disease (MDD) was analysed, MDD-positivity became the only unfavourable prognostic factor for progression-free survival. Tailored chemotherapy could be extremely effective with limited toxicity. Identification of MDD as a hallmark of a higher risk of treatment failure may provide a target population for treatment intensification by anti-CD20.Entities:
Keywords: Associazione Italiana Ematologia Oncologia Pediatrica LNH-97 protocol; B-cell non-Hodgkin lymphoma; childhood; diffuse large B-cell lymphoma; minimal disseminated disease; prognostic factors
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Year: 2016 PMID: 27392319 DOI: 10.1111/bjh.14240
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998