Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| PHRC/04-04 | |||
| CIC0203/043 |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Ministry of Health, France | OTHER_GOV |
| Novartis | INDUSTRY |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The purpose of this study is to determine whether Imatinib is safe and effective in association with intensive treatment of Ph+ALL in children.
Recent advances in treatment have increased the cure of childhood ALL to 75% or better. However, attempts to improve results for resistant subtypes of ALL, such as Ph+ ALL, have been largely unsuccessful. Imatinib, an inhibitor of protein-tyrosine kinases, is currently being tested in several phase I, II and III trials covering most Chronic Myeloid Leukemia patient populations and patients with overtly relapsed or refractory Ph+ALL. Pediatric patients with Ph+ALL will receive Imatinib, added to intensive, post-induction BFM-type chemotherapy. The endpoint will be the evaluation on the long-term clinical outcome, in particular on the Disease Free Survival (DFS).
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Good risk Ph+ALL | Other | For protocols which adopt a steroid prephase: patients who are Prednisone-good responder and achieve CR after the induction course. For protocols which do not adopt steroid prephase: patients who have M1/M2 BM at day 15 or M1 BM at day 21 and achieve CR after the induction course. Expected stratification in this group: 70-75%. |
|
| Poor risk Ph+ALL | Other | For protocols which adopt a steroid prephase: patients who are Prednisone poor-responders. For protocol which do not adopt a steroid prephase: patients who have M3 BM at day 15 or M2/M3 BM at day 21. For all protocols: patients who do not achieve CR after the induction course. Expected stratification: 25-30%. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Standard chemotherapy + Imatinib | Drug | Patients receive Imatinib together with the standard chemotherapy regimen of phase IB and after each of three consecutive blocks of the standard chemotherapy in the consolidation phase |
| Measure | Description | Time Frame |
|---|---|---|
| Disease free survival (DFS). DFS will be calculated as the time from inclusion to either one of the following events: relapse, death in CCR, second malignancies. | 2 years |
| Measure | Description | Time Frame |
|---|---|---|
| Compare long term outcome between patients treated by BFM-chemotherapy and patient undergoing more intensive chemotherapy (protocole COGAALL0031 : Children Oncology Group-USA). | 2 years | |
| Long-term clinical outcome : Disease free survival (DFS), Event-Free Survival (EFS) and Overall Survival (OS) in each risk groups. |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Andrea Biondi, MD | Ospedale S. Gerardo - Monza | Study Director |
| Virginie Gandemer, MD | Rennes University Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Service d'hématologie pédiatrique CHRU | Amiens | 80080 | France | |||
| Service hématologie pédiatrique Hôpital Saint-Jacques |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 22898679 | Result | Biondi A, Schrappe M, De Lorenzo P, Castor A, Lucchini G, Gandemer V, Pieters R, Stary J, Escherich G, Campbell M, Li CK, Vora A, Arico M, Rottgers S, Saha V, Valsecchi MG. Imatinib after induction for treatment of children and adolescents with Philadelphia-chromosome-positive acute lymphoblastic leukaemia (EsPhALL): a randomised, open-label, intergroup study. Lancet Oncol. 2012 Sep;13(9):936-45. doi: 10.1016/S1470-2045(12)70377-7. Epub 2012 Aug 14. | |
| 30501871 |
| Label | URL |
|---|---|
| Primary Publication | View source |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
| 2 years |
| Pattern of molecular response (MRD) | 5 time points between S4 and S22 |
| Conversion rate to CR in patients resistant to the first part of the induction phase of chemotherapy included in the Poor-risk group. | 2 years |
| Besançon |
| 25000 |
| France |
| Service d'hémato-oncologie - Hôpital des Enfants Pellegrin | Bordeaux | 33076 | France |
| Hôpital Morvan | Brest | 29200 | France |
| Hématologie oncologie pédiatrique-CHU Caen | Caen | France |
| Hémato-Oncologie et Thérapie Cellulaire Pédiatrique - Hôtel Dieu | Clermont-Ferrand | 63058 | France |
| Hémato-Oncologie Pédiatrique - Hôpital d'Enfants | Dijon | 21034 | France |
| Pédiatrie CHU - Hôpital Nord | Grenoble | 38043 | France |
| Hôpital Jeanne de Flandre | Lille | 59037 | France |
| Limoges University Hospital | Limoges | 87042 | France |
| Hôpital DEBROUSSE Institut d'hématologie et d'oncologie pédiatrique | Lyon | France |
| Hôpital Arnaud de Villeneuve | Montpellier | France |
| Hématologie Pédiatrique - Hôpital Trousseau | Paris | 75571 | France |
| Hémato-immunologie-Robert Debré | Paris | France |
| Hématologie Hôpital Jean Bernard | Poitiers | 86021 | France |
| Hématologie pédiatrique-Hopital américain | Reims | France |
| Service d'hématologie pédiatrique - Hôpital Sud | Rennes | 35033 | France |
| Service d'Immuno Hémato Oncologie Pédiatrique - Hôpital Charles Nicolle | Rouen | 76031 | France |
| Hématologie, Oncologie pédiatrique-CHU Saint Etienne | Saint-Etienne | France |
| Hopital des enfants | Toulouse | France |
| CHU- Centre Gatien de Clocheville | Tours | 37044 | France |
| Hôpital d'enfants | Vandœuvre-lès-Nancy | 54511 | France |
| Result |
| Biondi A, Gandemer V, De Lorenzo P, Cario G, Campbell M, Castor A, Pieters R, Baruchel A, Vora A, Leoni V, Stary J, Escherich G, Li CK, Cazzaniga G, Cave H, Bradtke J, Conter V, Saha V, Schrappe M, Grazia Valsecchi M. Imatinib treatment of paediatric Philadelphia chromosome-positive acute lymphoblastic leukaemia (EsPhALL2010): a prospective, intergroup, open-label, single-arm clinical trial. Lancet Haematol. 2018 Dec;5(12):e641-e652. doi: 10.1016/S2352-3026(18)30173-X. |
| 33242441 | Derived | Tasian SK, Peters C. Targeted therapy or transplantation for paediatric ABL-class Ph-like acute lymphocytic leukaemia? Lancet Haematol. 2020 Dec;7(12):e858-e859. doi: 10.1016/S2352-3026(20)30369-0. No abstract available. |
| ID | Term |
|---|---|
| D054198 | Precursor Cell Lymphoblastic Leukemia-Lymphoma |
| D010677 | Philadelphia Chromosome |
| D007938 | Leukemia |
| ID | Term |
|---|---|
| D007945 | Leukemia, Lymphoid |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
| D014178 | Translocation, Genetic |
| D002869 | Chromosome Aberrations |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
Not provided
Not provided
| ID | Term |
|---|---|
| D000068877 | Imatinib Mesylate |
| ID | Term |
|---|---|
| D001549 | Benzamides |
| D000577 | Amides |
| D009930 | Organic Chemicals |
| D001565 | Benzoates |
| D000146 | Acids, Carbocyclic |
| D002264 | Carboxylic Acids |
| D001555 | Benzene Derivatives |
| D006841 | Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D010879 | Piperazines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D011743 | Pyrimidines |
Not provided
Not provided