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Acute Myeloid Leukemias (AML) of the child are a rare disease and its prognosis varies according to the subgroup. Secondary AMLs remain a subgroup of poor prognosis, whose cytogenetic and molecular characteristics and prognostic value differ in part from de novo AMLs. The purpose of this national observatory is to record scientific and medical information on cases of secondary AML that have occurred in France since 2013 in order to improve the treatment of children and adolescents with this disease in the years to come. This national observatory will contribute to better knowledge and progress in research into these diseases.
Therapy-related myeloid neoplasms (t-MNs) are a group of hematologic diseases that arise after chemotherapy and/or radiation therapy for a previous cancer or rarely autoimmune diseases. t-MNs had been included in the group of AMLs and remain as a distinct category also in the recent 2016 revision of the WHO classification of myeloid neoplasm and acute leukemia. The latency between exposition to anticancer drugs and development of t-MN may vary from some months up to 10 years, even considering the age at diagnosis of the primary malignancy, the kind of cytotoxic treatment previously used, and the cumulative dose and dose intensity. The prognosis of s-AML is generally considered to be poorer than that of de novo AML. The disease tends to be refractory to chemotherapy, and patients' tolerance of treatment generally is reduced because of prior therapies. 5-year event-free survival (EFS) and overall survival (OS) rates of pediatric t-AML/t-MDS have been reported to be 14% to 30%. However, the results are conflicting and overall lacking when compared with those in adults. The purpose of this national observatory is to record scientific and medical information on cases of secondary Acute Myeloid Leukemias that have occurred in France since 2013 in order to improve the treatment of children and adolescents with this disease in the years to come. The primary objective is to evaluate the association of potential prognostic factors (including clinical-biological factors) with the overall survival of children and adolescents aged 0-18 years diagnosed with secondary AML. The secondary objectives are to test the feasibility of setting up a French national database of secondary AMLs for children and adolescents as a first step towards European implementation, to assess the association of potential prognostic factors with event free survival and the occurrence of treatment-related toxicities, to characterize the molecular abnormalities associated with secondary AMLs in children and adolescents.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Secondary Acute Myeloid Leukemias (AML) of the child |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| collection of the clinical and biological characteristics of secondary AMLs in children | Other | to record scientific and medical information on cases of secondary Acute Myeloid Leukemias that have occurred in France since 2013 |
| Measure | Description | Time Frame |
|---|---|---|
| potential clinical-biological prognostic factors - patient characterics | patient characteristics are sex, patient's age at the start of treatment for secondary AML, date of birth, personal history of genetic predisposition (including brittle diseases - see below), family history of cancers (1st or 2nd degree) | through study completion, an average of 6 months |
| potential clinical-biological prognostic factors - first cancer characteristics | First cancer characteristics are age of onset, determined from the date of diagnosis, and histology, determined by anatomo-pathological diagnosis. | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors :first cancer treatment : types of treatments received | type of treatment: chemotherapy (Anthracyclines, Alkylating agents) and / or radiotherapy and/or Marrow autograft or allograft | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - first cancer treatments: response to treatment | response measured by bone marrow assessment using morphology and minimal residual disease (MRD) assessment : no response, partial response, complete remission | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - first cancer treatments: Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 | nature, incidence and severity of adverse events (AEs) | through study completion, an average of 6 months after patient inclusion |
| Measure | Description | Time Frame |
|---|---|---|
| feasibility of setting up a French national database of secondary AMLs for children and adolescents - Number of cases included over the period | Number of cases included over the period | at the end of the 2 years of the inclusion period |
| feasibility of setting up a French national database of secondary AMLs for children and adolescents - Missing Data |
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Inclusion Criteria:
Exclusion Criteria: None
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children and adolescents aged 0-18 years diagnosed with secondary AML
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Stéphane S DUCASSOU, MD PhD | Contact | 05 57 82 04 38 | stephane.ducassou@chu-bordeaux.fr | |
| Aurore CAPELLI, PhD | Contact | 05 57 82 08 77 | aurore.capelli@chu-bordeaux.fr |
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| ID | Term |
|---|---|
| D015470 | Leukemia, Myeloid, Acute |
| D009362 | Neoplasm Metastasis |
| ID | Term |
|---|---|
| D007951 | Leukemia, Myeloid |
| D007938 | Leukemia |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
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| potential clinical-biological prognostic factors - first cancer treatments: duration of treatment |
duration of treatment determined from the start and end dates |
| through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - first cancer treatments: cumulative dose received | cumulative dose of each type of treatment received ( chemotherapy (Anthracyclines, Alkylating agents) and / or radiotherapy and/or Marrow autograft or allograft) | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - secondary AML characteristics: date of diagnosis | date of diagnosis | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - secondary AML characteristics: median time of onset compared to the date of end of treatment for the 1st cancer | median time of onset compared to the date of end of treatment for the 1st cancer | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - secondary AML characteristics : hematological data assessed by morphology | Leukocytes at diagnosis of secondary AML (G/L) | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - secondary AML characteristics: cytogenetic data | karyotype, exclusive and cumulative anomalies | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - secondary AML characteristics: molecular data | molecular data assessed by Next-Generation Sequencing panel | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - secondary AML treatment: duration of treatment | duration of treatment determined from the start and end dates | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - secondary AML treatment: type of treatment | chemotherapy received and bone marrow transplantation | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - secondary AML treatment : response to treatment | response measured by bone marrow assessment using morphology and minimal residual disease (MRD) assessment : no response, partial response, complete remission | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - secondary AML treatment: Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 | nature, incidence and severity of adverse events (AEs) | through study completion, an average of 6 months after patient inclusion |
| potential clinical-biological prognostic factors - Overall Survival (OS) | Evaluated as time from diagnostic of the second AML to death from any cause or date last seen for patients who are alive at the end of the trial | at the end of the 2 years of the inclusion period |
Proportion and type of missing data in the database after the base freeze |
| at the end of the 2 years of the inclusion period |
| feasibility of setting up a French national database of secondary AMLs for children and adolescents - Centre participation rates | Centre participation rates | at the end of the 2 years of the inclusion period |
| association of potential prognostic factors with event free survival and the occurrence of treatment-related toxicities- Recurrence of the disease | Recurrence of the disease : Relapse criteria (in a patient who has had complete remission): ≥ 5% blasts in the bone marrow (not attributable to post chemotherapy regeneration) | at the end of the 2 years of the inclusion period |
| association of potential prognostic factors with event free survival and the occurrence of treatment-related toxicities- Treatment-related toxicities | Treatment-related toxicities : Metabolic / endocrine complications in particular: growth retardation, hypothyroidism, gonadal insufficiency; Organic complications, in particular: renal failure, heart failure, respiratory failure ; Graft versus host reaction (GvH) | at the end of the 2 years of the inclusion period |
| D006402 |
| Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D009385 | Neoplastic Processes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |