Low-intensity therapy cures over 40 % of children with rapid Flow-MRD responding ALL: the ALL-MB 2008 trial results

Author:

Popov A.1ORCID,Henze G.2,Roumiantseva Yu.1ORCID,Budanov O.3ORCID,Belevtsev M.4,Verzhbitskaya T.5ORCID,Boyakova E.6,Movchan L.4,Tsaur G.5ORCID,Fadeeva M.1,Lagoyko S.1ORCID,Zharikova L.1ORCID,Myakova N.1ORCID,Litvinov D.1ORCID,Khlebnikova O.5,Streneva O.5,Stolyarova E.4,Ponomareva N.7ORCID,Novichkova G.1ORCID,Fechina L.5ORCID,Aleinikova O.4,Karachunskiy A.1ORCID

Affiliation:

1. Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology of Ministry of Healthcare of the Russian Federation

2. Charité – Universitätsmedizin Berlin

3. Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology of Ministry of Healthcare of the Russian Federation; Belarusian Research Center for Pediatric Oncology, Hematology and Immunology

4. Belarusian Research Center for Pediatric Oncology, Hematology and Immunology

5. Regional Children’s Hospital; Research Institute of Medical Cell Technologies

6. Moscow City Blood Center named after O. K. Gavrilov

7. Republican Children’s Hospital

Abstract

   Serious side effects occur during therapy for childhood acute lymphoblastic leukemia (ALL), and survivors can experience long-term consequences. This study aimed at identifying patients who can be successfully treated with low treatment intensity combining clinical parameters and minimal residual disease (MRD) measurements. The study was approved by the Independent Ethics Committee and the Scientific Council of the Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology. ALL-MB studies used reduced-intensity therapy from the beginning, for standard risk (SR) patients no cyclophosphamide, a very low daunorubicin dose, no high dose of methotrexate, no cranial irradiation. In the ALL-MB 2008 study, 1702 children (49.1 % of all patients) were classified as SR due to favorable initial characteristics. These included 295 patients treated in institutions who took part in a pilot study on MRD measurement using flow cytometry on day 15 and/or at the end of induction (EOI). The most suitable time point for MRD measurement was EOI with threshold 0.1% in 90.5 % of the patients with excellent results: event-free survival of 95 % and overall survival of 97 %, that identified the large proportion of patients (more than 40 % of all ALL patients). The outcome of children with slower MRD response was significantly worse. Initial SR characteristics plus one single MRD measurement at EOI identify more than 40 % of all children with ALL who can be successfully treated with low-intensity regimens as used in the MB protocols.

Publisher

Fund Doctors, Innovations, Science for Children

Subject

Oncology,Hematology,Immunology,Immunology and Allergy,Pediatrics, Perinatology and Child Health

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