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Optimization of native E. coli-asparaginase therapy in standard risk-group children with acute lymphoblastic leukemia treated by the ALL-MB 2002 protocol

https://doi.org/10.17650/1818-8346-2008-0-3-25-33

Abstract

The paper presents the results of a multicenter randomized study of two-dose COLI-ASP regimens in therapy of consolidation of standard risk-group (SRG) children and adolescents with acute lymphoblastic leukemia (ALL) treated by the ALL-MB-2002 protocol. The principal aim of the study was to elucidate whether the dose of COLI-ASP might be reduced without losing the efficiency of therapy. The analysis covered primary ALL patients notified at 36 clinics of Russia and Belarus, enrolled for the study in the period of May 1, 2002, to October 10, 2006. Out of 819 patients to be examined, 414 received COLI-ASP in a dose of 10,000 U/m2 (a control group), and 405 children took it in a dose of 5,000 U/m2 (a study group). No statistically significant differences were found between the patients in gender, age, baseline leukocytosis, and spleen size. The study showed no statistically and clinically significant differences in event-free, overall, and relapse-free survival (EFS, OS, and RFS, respectively) and relapse rates with the use of two-dose COLI-ASP regimens. However, in the control group, the death rate in remission was twice greater than that in the study group (p = 0.02). Detailed analysis of the outcomes of therapy in some subgroups revealed no differences between the control and study groups. The Cox multiple regression analysis has indicated that the factors influencing EFS and RFS are the baseline sizes of the spleen, baseline leukocytosis, age, and a response to treatment in the period of induction, rather than the dose of E. coli asparaginase. The authors have also found that among the SRG patients, there is a subgroup of patients without risk factors, in whom the reduction in the COLI-ASP dose may substantially increase survival rates, by lowering toxicity and mortality in remission.

About the Authors

M. Yu. Goroshkova
Clinical Children Hospital №4
Russian Federation

Novokuznetsk



Yu. V. Rumyantseva
Federal Research Centre of Pediatric Hematology, Oncology and Immunology
Russian Federation

Moscow



O. V. Aleinikova
Republic Centre for Paediatric Oncology and Haematology
Belarus

Minsk



S. A. Dudkin
Clinical Children Hospital №4
Russian Federation

Novokuznetsk



L. G. Fechina
Regional Centre for Paediatric Oncology and Haematology
Russian Federation

Yekaterinburg



A. V. Shamardina
Regional Clinical Children Hospital
Russian Federation

N. Novgorod



O. V. Streneva
Regional Centre for Paediatric Oncology and Haematology
Russian Federation

Yekaterinburg



K. L. Kondratchik
Morozov Children Clinical Hospital
Russian Federation

Moscow



L. M. Minkina
Clinical Children Hospital
Russian Federation

Vladivostok



E. S. Lapotentova
Republic Centre for Paediatric Oncology and Haematology
Belarus

Minsk



E. V. Inyushkina
Moscow District Oncology Dispanser
Russian Federation

Balaschicha



O. B. Kozlova
Regional Clinical Hospital
Russian Federation

Ivanovo



E. V. Zhukovskaya
Regional Children Clinical Hospital
Russian Federation

Chelyabinsk



O. P. Khlebnikova
Regional Centre for Paediatric Oncology and Haematology
Russian Federation

Yekaterinburg



E. V. Basharova
Regional Children Clinical Hospital
Russian Federation

Chelyabinsk



V. N. Timofeeva
Regional Children Clinical Hospital
Russian Federation

Ulyanovsk



G. P. Pavlova
Republic Children Clinical Hospital
Russian Federation

Cheboksary



V. D. Zlobina
Regional Clinical Hospital
Russian Federation

Novosibirsk



O. A. Utrobina
Regional Clinical Hospital
Russian Federation

Novosibirsk



E. S. Banshchikova
Republic Hospital №1 — National Medicine Centre
Russian Federation

Yakutsk



K. S. Aslanyan
Regional Children Clinical Hospital
Russian Federation

Rostov-on-Don



E. V. Kondakova
Regional Children Clinical Hospital
Russian Federation

Surgut



E. V. Tselousova
Kirov Research Centre of Hematology and Transfusiology
Russian Federation

Kirov



N. V. Myakova
Federal Research Centre of Pediatric Hematology; Russian Children Clinical Hospital
Russian Federation

Moscow



T. V. Turobova
Regional Children Clinical Hospital
Russian Federation

Archangelsk



O. V. Ryskal
Regional Children Clinical Hospital
Russian Federation

Perm



O. Yu. Fuks
Federal Research Centre of Pediatric Hematology, Oncology and Immunology; Morozov Children Clinical Hospital
Russian Federation

Moscow



V. V. Lebedev
Regional Children Clinical Hospital
Russian Federation

Krasnodar



N. F. Chipsanova
Regional cardiological dispanser
Russian Federation

Syktyvkar



S. R. Varfolomeeva
Federal Research Centre of Pediatric Hematology, Oncology and Immunology
Russian Federation

Moscow



A. I. Karachunsky
Federal Research Centre of Pediatric Hematology, Oncology and Immunology
Russian Federation

Moscow



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For citations:


Goroshkova M.Yu., Rumyantseva Yu.V., Aleinikova O.V., Dudkin S.A., Fechina L.G., Shamardina A.V., Streneva O.V., Kondratchik K.L., Minkina L.M., Lapotentova E.S., Inyushkina E.V., Kozlova O.B., Zhukovskaya E.V., Khlebnikova O.P., Basharova E.V., Timofeeva V.N., Pavlova G.P., Zlobina V.D., Utrobina O.A., Banshchikova E.S., Aslanyan K.S., Kondakova E.V., Tselousova E.V., Myakova N.V., Turobova T.V., Ryskal O.V., Fuks O.Yu., Lebedev V.V., Chipsanova N.F., Varfolomeeva S.R., Karachunsky A.I. Optimization of native E. coli-asparaginase therapy in standard risk-group children with acute lymphoblastic leukemia treated by the ALL-MB 2002 protocol. Oncohematology. 2008;(3):25-33. (In Russ.) https://doi.org/10.17650/1818-8346-2008-0-3-25-33

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ISSN 1818-8346 (Print)
ISSN 2413-4023 (Online)