Combined chemoimmunotherapy of patients with mature B-cell non-Hodgkin lymphomas age group until 18 years: results of multicenter study NHL 2004 m with rituximab and modified B-NHL BFM 90 protocol applications
- Authors: Samochatova E.V.1, Schelikhova L.N.1,2, Belogurova M.B.3, Schamardina A.V.4, Bascharova E.V.4, Litvinov D.V.2, Myakova N.V.1,2, Fechina L.G.4, Chlebnikova O.P.4, Inuschkina E.V.5, Riskal O.V.4, Schammasov P.Z.6, Yunusova I.M.6, Umnova S.Y.4, Konovalov D.M.1, Talalaev A.G.7, Roumiantseva J.V.8, Maschan A.A.8
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Affiliations:
- Federal Research Center of Pediatric Hematology, Oncology and Immunology
- Russian Children Clinical Hospital
- Municipal Clinical Hospital № 31
- Regional Children Clinical Hospital
- Moscow District Oncology Dispanser
- Republic Children Clinical Hospital
- Pathology Department, Pediatric faculty of the Russian State Medical University
- Research Center of Pediatric Hematology, Oncology and Immunology
- Issue: No 3 (2009)
- Pages: 4-14
- Section: HEMATOLOGIC MALIGNANCIES: TREATMENT, SUPPORTIVE CARE
- Published: 27.08.2009
- URL: https://oncohematology.abvpress.ru/ongm/article/view/766
- DOI: https://doi.org/10.17650/1818-8346-2009-0-3-4-14
- ID: 766
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Abstract
Therapy results of 61 patients (children and adolescents, 2—17 years of age; a median — 8.76 years) with B-cells non-Hodgkin lymphomas III—IV stage and B-cell acute leukemia (B-NHL/B-ALL), treating according to protocol with polichemotherapy and monoclonal antibodies against B-cell receptor CD20 — rituximab (Mabthera, Hoffmann La Roche) applications, are presented. The protocol consist of cytoreductive phase and 6 polychemotherapy courses, similar to original protocol B-NHL-BFM 90, with exception of decreasing methotrexate dosage in 2 first courses from 5 to 1 g/m2/24 hours. Rituximab — 375 mg/m2 IV — in Day 0 first 4 courses was given.
Four patients have died within first 3 weeks of therapy, 2 were primary refractory patients and 55 patients have achieved complete remissions. There was no case of remission death; relapse has developed only at one patient (neuroleukemia in patient with Burkitt lymphoma). 54 patients (88%) are in continuous complete remission. Overall and event-free survival rate were 0,90±0,04 with median follow-up after therapy ending 34 months (12—53 months). Authors discuss tactics of such combined therapy, features of remission registration, considering that at third of patients, residual mass was long-term detected, and for which assessment besides CT/MRT a positron-emission tomography (PET) and/or a repeated biopsy were done. Also it is possible to conclude that with use of target therapy chemotherapy intensity of such tumors can be reduced. Authors concluded that in cases of target therapy efficacy criteria should be modified, and it is necessary to use as much as possible informative technique to remission control (PET, minimal residual disease assessment with use of molecular-genetic methods).
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About the authors
E. V. Samochatova
Federal Research Center of Pediatric Hematology, Oncology and Immunology
Author for correspondence.
Email: samochatova@niidg.ru
Moscow
Russian FederationL. N. Schelikhova
Federal Research Center of Pediatric Hematology, Oncology and Immunology; Russian Children Clinical Hospital
Moscow
Russian FederationM. B. Belogurova
Municipal Clinical Hospital № 31
St-Petersburg
Russian FederationA. V. Schamardina
Regional Children Clinical Hospital
N. Novgorod
Russian FederationE. V. Bascharova
Regional Children Clinical Hospital
Chelyabinsk
Russian FederationD. V. Litvinov
Russian Children Clinical Hospital
Moscow
Russian FederationN. V. Myakova
Federal Research Center of Pediatric Hematology, Oncology and Immunology; Russian Children Clinical Hospital
Moscow
Russian FederationL. G. Fechina
Regional Children Clinical Hospital
Yekaterinburg
Russian FederationO. P. Chlebnikova
Regional Children Clinical Hospital
Yekaterinburg
Russian FederationE. V. Inuschkina
Moscow District Oncology Dispanser
Balashicha
Russian FederationO. V. Riskal
Regional Children Clinical Hospital
Perm
Russian FederationP. Z. Schammasov
Republic Children Clinical Hospital
Kazan
Russian FederationI. M. Yunusova
Republic Children Clinical Hospital
Makhachkala
Russian FederationS. Yu. Umnova
Regional Children Clinical Hospital
Irkutsk
Russian FederationD. M. Konovalov
Federal Research Center of Pediatric Hematology, Oncology and Immunology
Moscow
Russian FederationA. G. Talalaev
Pathology Department, Pediatric faculty of the Russian State Medical University
Moscow
Russian FederationJ. V. Roumiantseva
Research Center of Pediatric Hematology, Oncology and Immunology
Moscow
Russian FederationA. A. Maschan
Research Center of Pediatric Hematology, Oncology and Immunology
Moscow
Russian FederationReferences
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