Childhood Acute Lymphoblastic LeukemiaALL-MB 2015NCT03390387
Childhood Acute Lymphoblastic Leukemia Treatment Protocol Moscow-Berlin 2015 (ALL-MB 2015)
A study testing Dexamethasone continuous, Dexamethasone intermittent and Dexamethasone in people with Childhood Acute Lymphoblastic Leukemia, run by Federal Research Institute of Pediatric Hematology, Oncology and Immunology at 58 sites in 5 countries.
Trial summary
QUESTIONS AND OBJECTIVES OF ALL-MB 2015 STUDY 1. Will the new risk group stratification (especially of T-ALL) to improve overall and event-free survival? 2. Will the new protocol is effective and feasible in patients older than 15 years, and especially in young adults? 3. Read more about this study
- Who is it for?
- Ages 1 year to 50 years
- Conditions the study is for
- Childhood Acute Lymphoblastic Leukemia
- What is being tested?
- Dexamethasone continuous, Dexamethasone intermittent and Dexamethasone
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 4,000 participants
- Where
- 58 sitesin 5 countries
- Study dates
- Nov 2015to Nov 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 1 year to 50 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- Age at diagnosis at 1 to 50 years.
- The start of induction therapy within a time interval of study recruitment phase.
- The diagnosis of ALL is to be proved by the morphological, cytochemical, and immunological analysis of tumor cells in bone marrow (see "Diagnostics"). Patients with B-cell (Burkitt) ALL are excluded.
- Informed consent of the patient parents (guardians) to be treated in one of the clinics included in this multicenter study.
Who cannot join
- ALL is a second malignancies;
- The disease is a relapse of previously misdiagnosed and, therefore, inadequately treated ALL;
- There is severe concomitant disease, which significantly impedes chemotherapy protocol (such as multiple malformations, heart diseases, metabolic disorders, etc.);
- There is a lack of important data needed for the exact adherence to the cytostatic therapy according to a specific chemotherapy protocol (differential diagnosis of ALL-AML (acute myeloid leukemia) is not possible, stratification according to therapeutic group is not possible);
- The patient was treated before for a long time with cytotoxic drugs;
- There were treatment deviations not covered by the protocol and/or not due to side effects of treatment and/or complications of the disease
Trial locations and contacts
58 sites in 5 countries.
58 sites in 5 countries
Russia52 sites, 51 recruiting
- Recruiting
Arkhangelsk Regional Clinical Children's Hospital
Arkhangelsk
- Recruiting
Regional Clinical Children's Hospital
Astrakhan
- Recruiting
Altay Regional Clinical Children's Hospital
Barnaul
- Recruiting
Amur Regional Clinical Children's Hospital
Blagoveshchensk
- Recruiting
Bryansk Regional Children's Hospital
Bryansk
- Recruiting
Chelyabinsk Regional Clinical Children's Hospital
Chelyabinsk
- Recruiting
Transbaikal Regional Oncology Dispensary
Chita
- Recruiting
Irkutsk Regional Children Clinical Hospital
Irkutsk
- Recruiting
Ivanovo Regional Clinical Hospital
Ivanovo
- Recruiting
Republic Clinical Children's Hospital
Izhevsk
- Recruiting
Regional Clinical Children's Hospital
Khabarovsk
- Recruiting
Kirov Research Institute of Hematology and Blood Transfusion
Kirov
- Recruiting
Regional Clinical Children's Hospital
Krasnodar
- Recruiting
Krasnoyarsk Territorial Clinical Children's Hospital
Krasnoyarsk
- Recruiting
Kurgan Regional Clinical Children's Hospital
Kurgan
- Recruiting
Regional Clinical Children's Hospital
Kursk
- Recruiting
Regional Children's Hospital
Lipetsk
- Recruiting
Republic Children's Clinical Hospital
Makhachkala
- Recruiting
Morozov Children's Municipal Clinical Hospital
Moscow
- Recruiting
Research Institute of Pediatric Hematology, Oncology and Immunology named after Dmitry Rogachev
Moscow
- Recruiting
Russian Children's Clinical Hospital
Moscow
- Recruiting
Murmansk Clinical Children's Hospital
Murmansk
- Recruiting
Republic Clinical Children's Hospital
Nal'chik
- Recruiting
Nizhnevartovsk Regional Clinical Children's Hospital
Nizhnevartovsk
- Recruiting
Regional Clinical Children's Hospital
Nizhny Novgorod
- Recruiting
Novokuznetsk Municipal Clinical Children's Hospital N4
Novokuznetsk
- Recruiting
Novosibirsk Central District Clinical Hospital
Novosibirsk
- Recruiting
Orenburg Regional Clinical Oncology Dispensary
Orenburg
- Recruiting
Regional Clinical Children's Hospital
Oryol
- Recruiting
Perm Territorial Clinical Children's Hospital
Perm
- Recruiting
Regional Clinical Children's Hospital
Rostov-on-Don
- Recruiting
Rostov Research Institute of Oncology
Rostov-on-Don
- Recruiting
N. Dmitrieva Ryazan Regional Clinical Children's Hospital
Ryazan
- Recruiting
Almazov National Medical Research Center
Saint Petersburg
- Recruiting
Children's Municipal Hospital N1
Saint Petersburg
- Recruiting
Municipal Clinical Hospital N31
Saint Petersburg
- Recruiting
N.N.Petrov National Medical Research Oncology Center
Saint Petersburg
- Recruiting
R. Gorbacheva Research Institute of Pediatric Hematology and Transfusiology; Pavlov First Saint-Petersburg State Medical University
Saint Petersburg
- Recruiting
Municipal Clinical Children's Hospital N1
Samara
- Recruiting
Regional Children's Clinical Hospital
Stavropol
- Completed
Surgut Regional Clinical Hospital
Surgut
- Recruiting
Republic Clinical Children's Hospital
Syktyvkar
- Recruiting
Tomsk Regional Clinical Hospital
Tomsk
- Recruiting
Tula Regional Clinical Children's Hospital
Tula
- Recruiting
Republic Clinical Children's Hospital
Ulan-Ude
- Recruiting
Ulyanovsk Regional Children's Clinical Hospital
Ulyanovsk
- Recruiting
Regional Children's Clinical Hospital N1, Territorial Children's Hematological Center
Vladivostok
- Recruiting
Vologda Regional Clinical Children's Hospital
Vologda
- Recruiting
Voronezh Regional Clinical Children's Hospital N1
Voronezh
- Recruiting
Republic Hospital N1 - National Medicine Centre
Yakutsk
- Recruiting
Regional Clinical Children's Hospital
Yaroslavl
- Recruiting
Regional Clinical Children's Hospital N1; Children Oncology and hematology Center
Yekaterinburg
Belarus3 sites, 3 recruiting
- Recruiting
Republican Research and Practical Center of Radiation Medicine and Human Ecology
Homyel
- Recruiting
Republic Research and Practical Center of Pediatric Oncology, Hematology and Immunology
Minsk
- Recruiting
Mogilev Regional Children's Hospital
Mogilev
Kyrgyzstan1 site
- Completed
National Oncology and Hematology Center, Ministry of Health of the Kyrgyz Republic
Bishkek
Uzbekistan1 site, 1 recruiting
- Recruiting
Research Institute of Hematology and Blood Transfusion
Tashkent
About this study
Official title: Moscow-Berlin 2015 Multicenter Randomized Study for Treatment of Acute Lymphoblastic Leukemia in Children, Adolescents and Young Adults
QUESTIONS AND OBJECTIVES OF ALL-MB 2015 STUDY
- Will the new risk group stratification (especially of T-ALL) to improve overall and event-free survival?
- Will the new protocol is effective and feasible in patients older than 15 years, and especially in young adults?
- Whether the intermittent dexamethasone administration in induction will result in a decrease in toxicity and mortality without loss of efficacy?
- Whether the methylprednisolone administration as basic glucocorticoids during induction, consolidation and maintenance therapy will lead to decrease of severe infections and early mortality rate, improve survival and therapy compliance in adolescents and young adults with B-precursor ALL?
- Whether the administration of Bortezomib in patients with B-precursor ALL with initial WBC≥100,000/µl will improve treatment outcome?
- Whether the administration of Idarubicin instead Daunorubicin in low-risk T-ALL patients and two-phase induction in intermediate-risk T-ALL patients will reduce relapse rate and improve survival?
- Conditions
- Childhood Acute Lymphoblastic Leukemia
- Being tested
- Dexamethasone continuous, Dexamethasone intermittent, Dexamethasone, Methylprednisolone, Daunorubicin
- Keywords
- Acute lymphoblastic leukemia, children, adolescents, treatment
- Medical subject headings
- Precursor Cell Lymphoblastic Leukemia-Lymphoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dexamethasone continuousDrug
6 mg/m2, per os, in two divided doses per day q12 hours. 1-28 day (dose in the first few days is depending on the total tumor mass). From day 29 the dose of dexamethasone is reducing: days 29-31 - 3 mg/m2, days 32-34 - 1.5 mg/m2, days 35-36 - 0.75 mg/m2; then dexamethasone is discontinued completely.
Dexamethasone intermittentDrug
6 mg/m2, per os, in two divided doses per day q12 hours. Days: 1-14 (dose in the first few days is depending on the total tumor mass) and 22-28; days 15-21 - pause. From day 29 the dose of dexamethasone is reducing: days 29-30 - 3 mg/m2, days 31-32 - 1.5 mg/m2, then dexamethasone is discontinued completely.
DexamethasoneDrug
Induction: 6 mg/m2, per os, in two divided doses per day q12 hours. 1-28 day (dose in the first few days is depending on the total tumor mass). From day 29 the dose of dexamethasone is reducing: days 29-31 - 3 mg/m2, days 32-34 - 1.5 mg/m2, days 35-36 - 0.75 mg/m2; then dexamethasone is discontinued completely.
Consolidation: 6 mg/m2 per os, in two divided doses per day q12 hours. Weeks 13-14 (days 85-98), weeks 21-22 (days 141-154), weeks 29-30 (days 197-210), weeks 37-38 (days 253-260), weeks 45-46 (days 309-316), weeks 53-54 (days 365-372).
Maintenance therapy: 6 mg/m2, per os, in two divided doses per day q12 hours, for 10 days followed by quick discontinuation during 3 days. Weeks 61-62, 69-70, 77-78, 85-86, 93-94.
Induction: 60 mg/m2, per os, in two divided doses per day q12 hours. 1-28 day (dose in the first few days is depending on the total tumor mass). From day 29 the dose of dexamethasone is reducing: days 29-31 - 30 mg/m2, days 32-34 - 15 mg/m2, days 35-36 - 8 mg/m2; then methylprednisolone is discontinued completely.
Consolidation: 60 mg/m2 per os, in two divided doses per day q12 hours. Weeks 13-14 (days 85-98), weeks 21-22 (days 141-154), weeks 29-30 (days 197-210), weeks 37-38 (days 253-260), weeks 45-46 (days 309-316), weeks 53-54 (days 365-372).
Maintenance therapy: 60 mg/m2, per os, in two divided doses per day q12 hours, for 10 days followed by quick discontinuation during 3 days. Weeks 61-62, 69-70, 77-78, 85-86, 93-94.
DaunorubicinDrug
Induction: 45 mg/m2, intravenously, for 6 hours on days 8 and 22. Consolidation: 30 mg/m2, intravenously, for 6 hours on days 44, 65 (consolidation S1); 107, 121 (consolidation S2); and 163 (consolidation S3).
IdarubicinDrug
Induction: 10 mg/m2, intravenously, for 6 hours on days 8 and 22. Consolidation: 8 mg/m2, intravenously, for 6 hours on days 44, 65 (consolidation S1); 107, 121 (consolidation S2); and 163 (consolidation S3).
BortezomibDrug
1.3 mg/м2, intravenously, bolus injection. Days 85, 89, 92, 96 (consolidation S1); 141, 145, 148, 152 (consolidation S2) and 197, 201, 204, 208 (consolidation S3).
Second phase of inductionDrug
Cyclophosphamide (1,000 mg/m2, intravenously, for 1 hour - days 43 and 71); Cytarabine (75 mg/m2/day, intravenously, bolus injection. Four blocks of 4 days each, days 46-48, 52-55, 59-62, and 66-69); 6-mercaptopurine (60 mg/m2/day, per os, days 43-71); Triple intrathecal therapy (days 52 and 66)
Standard induction therapyDrug
Dexamethasone (6 mg/m2, p/o; 1-29 days); Daunorubicin (45 mg/m2, i.v.; day 8 and 22); Vincristine (1.5 mg/m2, i.v.; days 8, 15, 22, 29 and 36); Triple intrathecal therapy (Methotrexate/Cytarabine/Prednisone; days 0/1, 8, 15, 22, 29 and 36)
Standard consolidation therapyDrug
Consolidation consists of 3 phases: S1, S2 and S3. Each phase is a 6-week therapy with 6-mercaptopurine (50 mg/m2 per day, daily, orally), methotrexate (30 мг/м2, i.m., weekly) and L-asparaginase (10 000 U/m2, i.m., weekly), followed by 2 weeks of re-induction with Vincristine (1.5 mg/m2, i.v., days 1 and 8 of reinduction) plus Dexamethasone (6 mg/m2, p/o, daily, for 10 days followed by quick discontinuation during 3 days). Daunorubicin (30 mg/м2, i.v., N2 during S1, N2 during S2 and N1 during S3). Triple intrathecal therapy (Methotrexate/Cytarabine/Prednisone) N12 (4 injections per each phase)
| Study group | Role | What they receive |
|---|---|---|
| Dexa intermittent | Experimental | Induction therapy with intermittent Dexamethasone administration (1-15 days - 6 mg/m2, 15-22 day - pause, 22-29 days - 6 mg/m2). Receives: Drug: Dexamethasone intermittent |
| Dexa constant | Active comparator | Induction therapy with continuous Dexamethasone administration (6 mg/m2 1-29 days). Receives: Drug: Dexamethasone continuous |
| Dexa | Active comparator | Therapy with Dexamethasone (6 mg/m2) as basic glucocorticoid preparation. Receives: Drug: Dexamethasone |
| Medrol | Experimental | Therapy with Methylprednisolone (60 mg/m2) as basic glucocorticoid preparation. Receives: Drug: Methylprednisolone |
| IDA | Experimental | Induction and consolidation therapy with Idarubicin Receives: Drug: Idarubicin |
| DNR | Active comparator | Induction and consolidation therapy with Daunorubicin Receives: Drug: Daunorubicin |
| Protocol Ib+ | Experimental | Two-phase induction therapy (additional second phase of induction - protocol Ib) Receives: Drug: Second phase of induction |
| Protocol Ib- | Active comparator | Standard induction therapy (without second phase) Receives: Drug: Standard induction therapy |
| Bortezomib- | Active comparator | Consolidation therapy without Bortezomib Receives: Drug: Standard consolidation therapy |
| Bortezomib+ | Experimental | Consolidation therapy with Bortezomib 1.3 mg/m2 N12 (N4 in each reinduction) Receives: Drug: Bortezomib |
What is being measured
The primary outcome is the main question the study is designed to answer.
Event-free survival
Measured: 3 years, 5 years and 10 years after study start
Overall survival
Measured: 3 years, 5 years and 10 years after study start
Cumulative incidence of relapse
Measured: 3 years, 5 years and 10 years after study start
Secondary outcomes (2)
Early death rate
Measured: 3 years, 5 years and 10 years after study start
Remission death rate
Measured: 3 years, 5 years and 10 years after study start
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Jan 2018
- Study startNov 2015
- Primary completionNov 2020 (estimated)
- Study completionNov 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Childhood Acute Lymphoblastic LeukemiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 4,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Federal Research Institute of Pediatric Hematology, Oncology and Immunology
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Karachunskiy Alexander, Federal Research Institute of Pediatric Hematology, Oncology and Immunology
- Investigators
- Alexander I. Karachunskiy, Professor, MD, Principal investigator, Research Institute of Pediatric Hematology, Oncology and Immunology
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03390387
- Sponsor's protocol ID
- ALL-MB 2015
- Acronym
- ALL-MB 2015
- Status last verified
- Feb 2020
- First submitted
- 27 Dec 2017
- Last updated
- 5 Feb 2020
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 5 Feb 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Moscow-Berlin 2015 Multicenter Randomized Study for Treatment of Acute Lymphoblastic Leukemia in Children, Adolescents and Young Adults
- ClinicalTrials.gov ID
- NCT03390387
- Acronym / sponsor ID
- ALL-MB 2015 / ALL-MB 2015
- Conditions
- Childhood Acute Lymphoblastic Leukemia
- Keywords
- Acute lymphoblastic leukemia, children, adolescents, treatment
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 4,000 participants (estimated)
- Lead sponsor
- Federal Research Institute of Pediatric Hematology, Oncology and ImmunologyUniversity, hospital or other
- Study start
- Nov 2015 (actual)
- Primary completion
- Nov 2020 (estimated)
- Study completion
- Nov 2025 (estimated)
- First posted
- 4 Jan 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
QUESTIONS AND OBJECTIVES OF ALL-MB 2015 STUDY
- Will the new risk group stratification (especially of T-ALL) to improve overall and event-free survival?
- Will the new protocol is effective and feasible in patients older than 15 years, and especially in young adults?
- Whether the intermittent dexamethasone administration in induction will result in a decrease in toxicity and mortality without loss of efficacy?
- Whether the methylprednisolone administration as basic glucocorticoids during induction, consolidation and maintenance therapy will lead to decrease of severe infections and early mortality rate, improve survival and therapy compliance in adolescents and young adults with B-precursor ALL?
- Whether the administration of Bortezomib in patients with B-precursor ALL with initial WBC≥100,000/µl will improve treatment outcome?
- Whether the administration of Idarubicin instead Daunorubicin in low-risk T-ALL patients and two-phase induction in intermediate-risk T-ALL patients will reduce relapse rate and improve survival?
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 10
| Arm | Type | Receives |
|---|---|---|
| Dexa intermittent | Experimental | Drug: Dexamethasone intermittentInduction therapy with intermittent Dexamethasone administration (1-15 days - 6 mg/m2, 15-22 day - pause, 22-29 days - 6 mg/m2). |
| Dexa constant | Active comparator | Drug: Dexamethasone continuousInduction therapy with continuous Dexamethasone administration (6 mg/m2 1-29 days). |
| Dexa | Active comparator | Drug: DexamethasoneTherapy with Dexamethasone (6 mg/m2) as basic glucocorticoid preparation. |
| Medrol | Experimental | Drug: MethylprednisoloneTherapy with Methylprednisolone (60 mg/m2) as basic glucocorticoid preparation. |
| IDA | Experimental | Drug: IdarubicinInduction and consolidation therapy with Idarubicin |
| DNR | Active comparator | Drug: DaunorubicinInduction and consolidation therapy with Daunorubicin |
| Protocol Ib+ | Experimental | Drug: Second phase of inductionTwo-phase induction therapy (additional second phase of induction - protocol Ib) |
| Protocol Ib- | Active comparator | Drug: Standard induction therapyStandard induction therapy (without second phase) |
| Bortezomib- | Active comparator | Drug: Standard consolidation therapyConsolidation therapy without Bortezomib |
| Bortezomib+ | Experimental | Drug: BortezomibConsolidation therapy with Bortezomib 1.3 mg/m2 N12 (N4 in each reinduction) |
Who may qualify
- Ages
- 1 year to 50 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (4 listed)
- Age at diagnosis at 1 to 50 years.
- The start of induction therapy within a time interval of study recruitment phase.
- The diagnosis of ALL is to be proved by the morphological, cytochemical, and immunological analysis of tumor cells in bone marrow (see "Diagnostics"). Patients with B-cell (Burkitt) ALL are excluded.
- Informed consent of the patient parents (guardians) to be treated in one of the clinics included in this multicenter study.
Key exclusion criteria (6 listed)
- ALL is a second malignancies;
- The disease is a relapse of previously misdiagnosed and, therefore, inadequately treated ALL;
- There is severe concomitant disease, which significantly impedes chemotherapy protocol (such as multiple malformations, heart diseases, metabolic disorders, etc.);
- There is a lack of important data needed for the exact adherence to the cytostatic therapy according to a specific chemotherapy protocol (differential diagnosis of ALL-AML (acute myeloid leukemia) is not possible, stratification according to therapeutic group is not possible);
- The patient was treated before for a long time with cytotoxic drugs;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Dexamethasone continuous6 mg/m2, per os, in two divided doses per day q12 hours. 1-28 day (dose in the first few days is depending on the total tumor mass). From day 29 the dose of dexamethasone is reducing: days 29-31 - 3 mg/m2, days 32-34 - 1.5 mg/m2, days 35-36 - 0.75 mg/m2; then dexamethasone is discontinued completely. | Drug | Dexa constant |
| Dexamethasone intermittent6 mg/m2, per os, in two divided doses per day q12 hours. Days: 1-14 (dose in the first few days is depending on the total tumor mass) and 22-28; days 15-21 - pause. From day 29 the dose of dexamethasone is reducing: days 29-30 - 3 mg/m2, days 31-32 - 1.5 mg/m2, then dexamethasone is discontinued completely. | Drug | Dexa intermittent |
| DexamethasoneInduction: 6 mg/m2, per os, in two divided doses per day q12 hours. 1-28 day (dose in the first few days is depending on the total tumor mass). From day 29 the dose of dexamethasone is reducing: days 29-31 - 3 mg/m2, days 32-34 - 1.5 mg/m2, days 35-36 - 0.75 mg/m2; then dexamethasone is discontinued completely. Consolidation: 6 mg/m2 per os, in two divided doses per day q12 hours. Weeks 13-14 (days 85-98), weeks 21-22 (days 141-154), weeks 29-30 (days 197-210), weeks 37-38 (days 253-260), weeks 45-46 (days 309-316), weeks 53-54 (days 365-372). Maintenance therapy: 6 mg/m2, per os, in two divided doses per day q12 hours, for 10 days followed by quick discontinuation during 3 days. Weeks 61-62, 69-70, 77-78, 85-86, 93-94. | Drug | Dexa |
| MethylprednisoloneInduction: 60 mg/m2, per os, in two divided doses per day q12 hours. 1-28 day (dose in the first few days is depending on the total tumor mass). From day 29 the dose of dexamethasone is reducing: days 29-31 - 30 mg/m2, days 32-34 - 15 mg/m2, days 35-36 - 8 mg/m2; then methylprednisolone is discontinued completely. Consolidation: 60 mg/m2 per os, in two divided doses per day q12 hours. Weeks 13-14 (days 85-98), weeks 21-22 (days 141-154), weeks 29-30 (days 197-210), weeks 37-38 (days 253-260), weeks 45-46 (days 309-316), weeks 53-54 (days 365-372). Maintenance therapy: 60 mg/m2, per os, in two divided doses per day q12 hours, for 10 days followed by quick discontinuation during 3 days. Weeks 61-62, 69-70, 77-78, 85-86, 93-94. | Drug | Medrol |
| DaunorubicinInduction: 45 mg/m2, intravenously, for 6 hours on days 8 and 22. Consolidation: 30 mg/m2, intravenously, for 6 hours on days 44, 65 (consolidation S1); 107, 121 (consolidation S2); and 163 (consolidation S3). | Drug | DNR |
| IdarubicinInduction: 10 mg/m2, intravenously, for 6 hours on days 8 and 22. Consolidation: 8 mg/m2, intravenously, for 6 hours on days 44, 65 (consolidation S1); 107, 121 (consolidation S2); and 163 (consolidation S3). | Drug | IDA |
| Bortezomib1.3 mg/м2, intravenously, bolus injection. Days 85, 89, 92, 96 (consolidation S1); 141, 145, 148, 152 (consolidation S2) and 197, 201, 204, 208 (consolidation S3). | Drug | Bortezomib+ |
| Second phase of inductionCyclophosphamide (1,000 mg/m2, intravenously, for 1 hour - days 43 and 71); Cytarabine (75 mg/m2/day, intravenously, bolus injection. Four blocks of 4 days each, days 46-48, 52-55, 59-62, and 66-69); 6-mercaptopurine (60 mg/m2/day, per os, days 43-71); Triple intrathecal therapy (days 52 and 66) | Drug | Protocol Ib+ |
| Standard induction therapyDexamethasone (6 mg/m2, p/o; 1-29 days); Daunorubicin (45 mg/m2, i.v.; day 8 and 22); Vincristine (1.5 mg/m2, i.v.; days 8, 15, 22, 29 and 36); Triple intrathecal therapy (Methotrexate/Cytarabine/Prednisone; days 0/1, 8, 15, 22, 29 and 36) | Drug | Protocol Ib- |
| Standard consolidation therapyConsolidation consists of 3 phases: S1, S2 and S3. Each phase is a 6-week therapy with 6-mercaptopurine (50 mg/m2 per day, daily, orally), methotrexate (30 мг/м2, i.m., weekly) and L-asparaginase (10 000 U/m2, i.m., weekly), followed by 2 weeks of re-induction with Vincristine (1.5 mg/m2, i.v., days 1 and 8 of reinduction) plus Dexamethasone (6 mg/m2, p/o, daily, for 10 days followed by quick discontinuation during 3 days). Daunorubicin (30 mg/м2, i.v., N2 during S1, N2 during S2 and N1 during S3). Triple intrathecal therapy (Methotrexate/Cytarabine/Prednisone) N12 (4 injections per each phase) | Drug | Bortezomib- |
Primary outcome
Event-free survival
Time frame: 3 years, 5 years and 10 years after study start
Overall survival
Time frame: 3 years, 5 years and 10 years after study start
Cumulative incidence of relapse
Time frame: 3 years, 5 years and 10 years after study start
2 secondary outcomes
Early death rate
Time frame: 3 years, 5 years and 10 years after study start
Remission death rate
Time frame: 3 years, 5 years and 10 years after study start
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Feb 2020.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Alexander I. Karachunskiy, Professor, MD principal investigator
Research Institute of Pediatric Hematology, Oncology and Immunology
58 sites in 5 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Dexamethasone continuous, Dexamethasone intermittent and Dexamethasone in people with Childhood Acute Lymphoblastic Leukemia, run by Federal Research Institute of Pediatric Hematology, Oncology and Immunology at 58 sites in 5 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 5 Feb 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 58 sites in Russia, Belarus, Armenia, Kyrgyzstan, Uzbekistan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Alexander I. Karachunskiy, Professor, MD (+7-926-218-84-09, info@mbstudy.net), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Event-free survival (time frame: 3 years, 5 years and 10 years after study start). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Feb 2020.