Treatment of B-cells non-Hodgkin lymphomas with combined immunochemotherapy: ability to treatment optimization

The results of two consecutive multicenter clinical trials enrolled 241 patient with childhood mature B-cells non-Hodgkin lymphomas/leukemia are presented. Patients received treatment according B-NHL 2004mab protocol (n = 83) and B-NHL 2010M (n = 158) with combined immunochemotherapy (ICT) in Russia...

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Main Authors: N. V. Smirnova, N. V. Myakova, M. B. Belogurova, O. V. Ryskal, O. E. Nikonova, G. R. Sharapova, A. S. Fedorova, N. A. Grigorieva, A. V. Shamardina, N. I. Ponomareva, D. S. Abramov, D. M. Konovalov, M. E. Dubrovina, A. A. Maschan, E. V. Samochatova
Format: Article
Language:Russian
Published: ABV-press 2015-12-01
Series:Онкогематология
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Online Access:https://oncohematology.abvpress.ru/ongm/article/view/163
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author N. V. Smirnova
N. V. Myakova
M. B. Belogurova
O. V. Ryskal
O. E. Nikonova
G. R. Sharapova
A. S. Fedorova
N. A. Grigorieva
A. V. Shamardina
N. I. Ponomareva
D. S. Abramov
D. M. Konovalov
M. E. Dubrovina
A. A. Maschan
E. V. Samochatova
author_facet N. V. Smirnova
N. V. Myakova
M. B. Belogurova
O. V. Ryskal
O. E. Nikonova
G. R. Sharapova
A. S. Fedorova
N. A. Grigorieva
A. V. Shamardina
N. I. Ponomareva
D. S. Abramov
D. M. Konovalov
M. E. Dubrovina
A. A. Maschan
E. V. Samochatova
author_sort N. V. Smirnova
collection DOAJ
description The results of two consecutive multicenter clinical trials enrolled 241 patient with childhood mature B-cells non-Hodgkin lymphomas/leukemia are presented. Patients received treatment according B-NHL 2004mab protocol (n = 83) and B-NHL 2010M (n = 158) with combined immunochemotherapy (ICT) in Russian and Belarus pediatric clinics from 2004 to 2015 years. Primary patients with different mature B-NHL (Burkitt lymphoma/leukemia, diffuse large B-cell lymphoma and primary mediastinal B-cell lymphoma (DLBCL and PMBCL)) aged from 2 to 18 years are included in the studies.Protocol B-NHL 2004mab for treatment of children and adolescents with B-NHL/B-AL, stage III and IV, includes a combination of chemotherapy (PCT) and rituximab – an antibody against the B-cells receptor CD20. PCT courses similar to those in the B-NHL BFM90 protocol (group III) with the exception of methotrexate dose in induction courses, reduced to 1 g/m2 /24 h in order to reduce toxicity. Rituximab (Mabthera, 375 mg/m2 /h) used for the first time in the treatment of children and adolescents with B-NHL. Of the 83 patients included, clinical remission was achieved in 77 (92.8 %). With a median follow time of 51.6 months, remission continued in 23 (85.2 %) patients with B-AL, in 32 (88.9 %) patients with LB and 19 (95.0 %) patients – with DLBCL. With median follow time of 65.2 months, event-free and overall survival was 84 ± 6 and 82 ± 8 %, respectively.Based on previous experience in order to further optimize B-NHL treatment, new protocol B-NHL 2010M with effect-adapted therapy and improvement of stratification risk group criteria was proposed. Overall survival in patients of 1st and 2nd risk groups with full implementation of diagnosis and treatment is approaching 100 %. In interim analysis of 3rd risk group patients, pOS was 88 ± 3 %. The incidence of induction death (infections, metabolic complications) remains within 2.7 % (n = 4); refractory cases (n = 2; 1.3 %) and relapses (n = 4; 2.7 %) developed after 2–4 months of remission, were observed only in patients with Burkitt lymphoma/leukemia. In this cases 2nd line therapy and auto-HSCT is not allowed to achieve remission. All PMBCL and DLBCL patients were achieved remission, but in 50 % of cases only after second line, radio- and cell therapy.The authors conclude that a combined immunochemotherapy of B-NHL in children and adolescents, including the target drug (rituximab) and 5-day courses of cytostatic therapy, highly effective, despite a reduce induction intensity. Therapy for the analyzed protocol requires qualitative dynamic efficacy monitoring and timely correction of therapy. In order to solve a refractory problem and further reduce the toxicity, necessary to continue research using fundamental discoveries in recent years.
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spelling doaj-art-469abc7ec64f446c93dbb0d22210eeb62025-08-20T03:01:29ZrusABV-pressОнкогематология1818-83462413-40232015-12-01104152410.17650/1818-8346-2015-10-4-15-24175Treatment of B-cells non-Hodgkin lymphomas with combined immunochemotherapy: ability to treatment optimizationN. V. Smirnova0N. V. Myakova1M. B. Belogurova2O. V. Ryskal3O. E. Nikonova4G. R. Sharapova5A. S. Fedorova6N. A. Grigorieva7A. V. Shamardina8N. I. Ponomareva9D. S. Abramov10D. M. Konovalov11M. E. Dubrovina12A. A. Maschan13E. V. Samochatova14Federal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitriy Rogachev, Ministry of Health of RussiaFederal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitriy Rogachev, Ministry of Health of RussiaMunicipal Clinical Hospital No 31Perm, Regional Children Clinical HospitalPerm, Regional Children Clinical HospitalNizhnevartovsk Regional Children HospitalRepublician Center for Pediatric Oncology, Hematology and Immunology, Ministry of Health of Republic of BelarusP.G. Vyzhletsov Archangelsk Regional Children Clinical HospitalN. Novgorod Regional Children Clinical HospitalRussian Children Clinical Hospital, Ministry of Health of RussiaFederal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitriy Rogachev, Ministry of Health of RussiaFederal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitriy Rogachev, Ministry of Health of RussiaFederal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitriy Rogachev, Ministry of Health of RussiaFederal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitriy Rogachev, Ministry of Health of RussiaFederal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitriy Rogachev, Ministry of Health of RussiaThe results of two consecutive multicenter clinical trials enrolled 241 patient with childhood mature B-cells non-Hodgkin lymphomas/leukemia are presented. Patients received treatment according B-NHL 2004mab protocol (n = 83) and B-NHL 2010M (n = 158) with combined immunochemotherapy (ICT) in Russian and Belarus pediatric clinics from 2004 to 2015 years. Primary patients with different mature B-NHL (Burkitt lymphoma/leukemia, diffuse large B-cell lymphoma and primary mediastinal B-cell lymphoma (DLBCL and PMBCL)) aged from 2 to 18 years are included in the studies.Protocol B-NHL 2004mab for treatment of children and adolescents with B-NHL/B-AL, stage III and IV, includes a combination of chemotherapy (PCT) and rituximab – an antibody against the B-cells receptor CD20. PCT courses similar to those in the B-NHL BFM90 protocol (group III) with the exception of methotrexate dose in induction courses, reduced to 1 g/m2 /24 h in order to reduce toxicity. Rituximab (Mabthera, 375 mg/m2 /h) used for the first time in the treatment of children and adolescents with B-NHL. Of the 83 patients included, clinical remission was achieved in 77 (92.8 %). With a median follow time of 51.6 months, remission continued in 23 (85.2 %) patients with B-AL, in 32 (88.9 %) patients with LB and 19 (95.0 %) patients – with DLBCL. With median follow time of 65.2 months, event-free and overall survival was 84 ± 6 and 82 ± 8 %, respectively.Based on previous experience in order to further optimize B-NHL treatment, new protocol B-NHL 2010M with effect-adapted therapy and improvement of stratification risk group criteria was proposed. Overall survival in patients of 1st and 2nd risk groups with full implementation of diagnosis and treatment is approaching 100 %. In interim analysis of 3rd risk group patients, pOS was 88 ± 3 %. The incidence of induction death (infections, metabolic complications) remains within 2.7 % (n = 4); refractory cases (n = 2; 1.3 %) and relapses (n = 4; 2.7 %) developed after 2–4 months of remission, were observed only in patients with Burkitt lymphoma/leukemia. In this cases 2nd line therapy and auto-HSCT is not allowed to achieve remission. All PMBCL and DLBCL patients were achieved remission, but in 50 % of cases only after second line, radio- and cell therapy.The authors conclude that a combined immunochemotherapy of B-NHL in children and adolescents, including the target drug (rituximab) and 5-day courses of cytostatic therapy, highly effective, despite a reduce induction intensity. Therapy for the analyzed protocol requires qualitative dynamic efficacy monitoring and timely correction of therapy. In order to solve a refractory problem and further reduce the toxicity, necessary to continue research using fundamental discoveries in recent years.https://oncohematology.abvpress.ru/ongm/article/view/163non-hodgkins lymphomachildren and adolescentstargeted therapyrituximab (mabthera)
spellingShingle N. V. Smirnova
N. V. Myakova
M. B. Belogurova
O. V. Ryskal
O. E. Nikonova
G. R. Sharapova
A. S. Fedorova
N. A. Grigorieva
A. V. Shamardina
N. I. Ponomareva
D. S. Abramov
D. M. Konovalov
M. E. Dubrovina
A. A. Maschan
E. V. Samochatova
Treatment of B-cells non-Hodgkin lymphomas with combined immunochemotherapy: ability to treatment optimization
Онкогематология
non-hodgkin
s lymphoma
children and adolescents
targeted therapy
rituximab (mabthera)
title Treatment of B-cells non-Hodgkin lymphomas with combined immunochemotherapy: ability to treatment optimization
title_full Treatment of B-cells non-Hodgkin lymphomas with combined immunochemotherapy: ability to treatment optimization
title_fullStr Treatment of B-cells non-Hodgkin lymphomas with combined immunochemotherapy: ability to treatment optimization
title_full_unstemmed Treatment of B-cells non-Hodgkin lymphomas with combined immunochemotherapy: ability to treatment optimization
title_short Treatment of B-cells non-Hodgkin lymphomas with combined immunochemotherapy: ability to treatment optimization
title_sort treatment of b cells non hodgkin lymphomas with combined immunochemotherapy ability to treatment optimization
topic non-hodgkin
s lymphoma
children and adolescents
targeted therapy
rituximab (mabthera)
url https://oncohematology.abvpress.ru/ongm/article/view/163
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