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If for years the treatment strategy of leukemia and related disorders (LRDs, including acute leukemias and predisposition syndromes) has been based solely on whether the patient could receive or not intensive chemotherapy and transplantation, the advent of new targeted or less targeted drugs has led to the development of a growing number of new therapeutic approaches, very often offered to specific patient/disease subsets, justifying the generic term of 'precision medicine'.
As an international leukemia center of excellence, THEMA, the French National Center for Precision Medicine in Leukemia (selected as IHUB-2 by the French National Agency for Research), is a care, research, transfer and education initiative located at the Saint-Louis Research Institute (IRSL) in Paris and devoted to precision medicine in leukemia in a real-life environment.
The present non-interventional study (eTHEMA) is a pillar of the whole THEMA project. As a prerequisite for precision medicine, this program focuses on individual data collection, aiming to collect high-quality data not only in patients treated into prospective clinical trials, but in every THEMA patient with a special interest in outpatients' care and research.
The primary objective of this non-interventional study is to describe the baseline characteristics planned treatments and outcomes of patients newly diagnosed with acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), high-risk myelodysplastic syndrome (MDS), or myeloproliferative neoplasm (MPN)-related myelofibrosis, when managed and treated according to standard diagnosis and care practices.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Acute myeloid Leukemia (AML) | Standard and routine care. For storage,limited volumes of blood or bone marrow aspirate will be added to usual sampling and stored. |
| |
| Acute lymphoblastic leukemia (ALL) | Standard and routine care. For storage,limited volumes of blood or bone marrow aspirate will be added to usual sampling and stored. |
| |
| High-risk myelodysplastic syndrome (MDS) | Standard and routine care. For storage,limited volumes of blood or bone marrow aspirate will be added to usual sampling and stored. |
| |
| Myeloproliferative neoplasm -related myelofibrosis | Standard and routine care. For storage,limited volumes of blood or bone marrow aspirate will be added to usual sampling and stored. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Biobanking | Other | For storage,limited volumes of blood or bone marrow aspirate will be added to usual sampling and stored. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Event Free Survival | at 5 years | |
| Relapse Free Survival | at 5 years | |
| Overall Survival | at 5 years |
| Measure | Description | Time Frame |
|---|---|---|
| Standardized evaluation of hematological response | After induction cycle which is between between day 25 and day 42 for patients treated intensively and between Month 1 and Month 6 for patients treated treated with low intensity regimen | |
| Standardized evaluation of hematological response |
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Inclusion Criteria:
Exclusion Criteria:
LRD which is not morphologically proven (patients with granulocytic sarcoma may be included)
Previous treatment for LRD, apart from:
Patient under guardianship / curatorship
Patient under AME
Opposition of the patient to be enrolled in the eTHEMA cohort
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Patients with newly diagnosed acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), high-risk myelodysplastic syndrome (MDS), or myeloproliferative neoplasm (MPN)-related myelofibrosis, when managed and treated according to standard diagnosis and care practices
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Hervé DOMBRET, Pr | Contact | 1 57 27 68 47 | +33 | herve.dombret@aphp.fr |
| Jérôme Lambert, Pr | Contact | 142499742 | +33 | jerome.lambert@u-paris.fr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hôpital Avicenne | Recruiting | Bobigny | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 40249917 | Derived | Zhao LP, Dumas-Rivero T, Barette L, Aguinaga L, Cheffai A, Chauvel C, Dal Bello R, Raffoux E, Clappier E, Duchmann M, Fenaux P, Lemaire P, Mathis S, Sebert M, Ades L, Itzykson R. Prognostic significance of monocytic-like phenotype in patients with AML treated with venetoclax and azacytidine. Blood Adv. 2025 Jul 22;9(14):3556-3565. doi: 10.1182/bloodadvances.2024015734. |
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| After first consolidation cycle which is between 1 and 2 months |
| Standardized evaluation of hematological response | After last consolidation cycle which is between 3 and 8 months |
| Standardized evaluation of hematological response | Before HSCT |
| Standardized evaluation of hematological response | at day 100 after HSCT |
| Standardized evaluation of hematological response | at 5 years |
| Minimal measurable residual disease (MRD) response | After induction which is between day 25 and day 42 for patients treated intensively and between month 1 and month 6 for patients with low intensity regimen |
| Minimal measurable residual disease (MRD) response | After first consolidation cycle which is between 1 and 2 months |
| Minimal measurable residual disease (MRD) response | After last consolidation cycle which is between 3 and 8 months |
| Minimal measurable residual disease (MRD) response | Before HSCT |
| Minimal measurable residual disease (MRD) response | at day 100 after HSCT |
| Minimal measurable residual disease (MRD) response | at 5 years |
| Incidence of allogeneic HSCT | at 5 years |
| Modalities of allogeneic HSCT | at 5 years |
| Incidence of hematological relapses | at 5 years |
| Type of hematological relapses | at 5 years |
| Incidence of hematological progressions | at 5 years |
| Type of hematological progressions | at 5 years |
| Incidence of MRD relapses | at 5 years |
| Incidence of MRD progressions | at 5 years |
| Proportions of patients with treatment-related toxicities | Treatment-related toxicities will be Evaluated by the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 | at 5 years |
| Cumulative incidences of relapse | at 5 years |
| Cumulative incidences of non-relapse mortality | at 5 years |
| Quality-of-life assessed using the EORTC-QLQ-C30 v3 questionnaire | Quality of life evaluated using questionnaire "European Organization for Research and Treatment of Cancer Quality of Life Questionnaire" (EORTC QLQ-C30- v3). The QLQ-C30 is composed of both multi-item scales and single-item measures. These include five functional scales, three symptom scales, a global health status / QoL scale, and six single items. Each of the multi-item scales includes a different set of items - no item occurs in more than one scale. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. A high score for a functional scale represents a high/healthy level of functioning. A high score for the global health status/ QoL represents a high QoL and a high score for a symptom scale/item represents a high level of symptomatology/problems. | at inclusion |
| Quality-of-life assessed using the EORTC-QLQ-C30 v3 questionnaire | Quality-of-life will be assessed using the EORTC-QLQ-C30 v3 questionnaire.Quality of life evaluated using questionnaire "European Organization for Research and Treatment of Cancer Quality of Life Questionnaire" (EORTC QLQ-C30- v3). The QLQ-C30 is composed of both multi-item scales and single-item measures. These include five functional scales, three symptom scales, a global health status / QoL scale, and six single items. Each of the multi-item scales includes a different set of items - no item occurs in more than one scale. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. A high score for a functional scale represents a high/healthy level of functioning. A high score for the global health status/ QoL represents a high QoL and a high score for a symptom scale/item represents a high level of symptomatology/problems. | at the end of induction which is between day 25 and day 42 for patients treated intensively and between month 1 and month 6 for patients with low intensity regimen |
| Quality-of-life assessed using the EORTC-QLQ-C30 v3 questionnaire | Quality-of-life will be assessed using the EORTC-QLQ-C30 v3 questionnaire. Quality of life evaluated using questionnaire "European Organization for Research and Treatment of Cancer Quality of Life Questionnaire" (EORTC QLQ-C30- v3). The QLQ-C30 is composed of both multi-item scales and single-item measures. These include five functional scales, three symptom scales, a global health status / QoL scale, and six single items. Each of the multi-item scales includes a different set of items - no item occurs in more than one scale. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. A high score for a functional scale represents a high/healthy level of functioning. A high score for the global health status/ QoL represents a high QoL and a high score for a symptom scale/item represents a high level of symptomatology/problems. | after 2 consolidations courses which is between 3 months and 8 months |
| Quality-of-life assessed using the EORTC-QLQ-C30 v3 questionnaire | Quality-of-life will be assessed using the EORTC-QLQ-C30 v3 questionnaire. Quality of life evaluated using questionnaire "European Organization for Research and Treatment of Cancer Quality of Life Questionnaire" (EORTC QLQ-C30- v3). The QLQ-C30 is composed of both multi-item scales and single-item measures. These include five functional scales, three symptom scales, a global health status / QoL scale, and six single items. Each of the multi-item scales includes a different set of items - no item occurs in more than one scale. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. A high score for a functional scale represents a high/healthy level of functioning. A high score for the global health status/ QoL represents a high QoL and a high score for a symptom scale/item represents a high level of symptomatology/problems. | at 3 months after the end of treatment |
| Quality-of-life assessed using the EORTC-QLQ-C30 v3 questionnaire | Quality-of-life will be assessed using the EORTC-QLQ-C30 v3 questionnaire. Quality of life evaluated using questionnaire "European Organization for Research and Treatment of Cancer Quality of Life Questionnaire" (EORTC QLQ-C30- v3). The QLQ-C30 is composed of both multi-item scales and single-item measures. These include five functional scales, three symptom scales, a global health status / QoL scale, and six single items. Each of the multi-item scales includes a different set of items - no item occurs in more than one scale. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. A high score for a functional scale represents a high/healthy level of functioning. A high score for the global health status/ QoL represents a high QoL and a high score for a symptom scale/item represents a high level of symptomatology/problems. | at 6 months after the end of treatment |
| Quality-of-life assessed using the EORTC-QLQ-C30 v3 questionnaire | Quality-of-life will be assessed using the EORTC-QLQ-C30 v3 questionnaire. Quality of life evaluated using questionnaire "European Organization for Research and Treatment of Cancer Quality of Life Questionnaire" (EORTC QLQ-C30- v3). The QLQ-C30 is composed of both multi-item scales and single-item measures. These include five functional scales, three symptom scales, a global health status / QoL scale, and six single items. Each of the multi-item scales includes a different set of items - no item occurs in more than one scale. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. A high score for a functional scale represents a high/healthy level of functioning. A high score for the global health status/ QoL represents a high QoL and a high score for a symptom scale/item represents a high level of symptomatology/problems. | at 12 months after the end of treatment |
| Quality-of-life assessed using the EORTC-QLQ-C30 v3 questionnaire | Quality-of-life will be assessed using the EORTC-QLQ-C30 v3 questionnaire. Quality of life evaluated using questionnaire "European Organization for Research and Treatment of Cancer Quality of Life Questionnaire" (EORTC QLQ-C30- v3). The QLQ-C30 is composed of both multi-item scales and single-item measures. These include five functional scales, three symptom scales, a global health status / QoL scale, and six single items. Each of the multi-item scales includes a different set of items - no item occurs in more than one scale. All of the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. A high score for a functional scale represents a high/healthy level of functioning. A high score for the global health status/ QoL represents a high QoL and a high score for a symptom scale/item represents a high level of symptomatology/problems. | at day 100 after hematopoietic stem cell transplant |
| Incidence of secondary cancer | at 5 years |
| Incidence of secondary cancer | up to 15 years |
| Hopital Robert Debré | Recruiting | Paris | France |
|
| Hôpital Saint Louis | Recruiting | Paris | France |
|
| ID | Term |
|---|---|
| D015470 | Leukemia, Myeloid, Acute |
| D054198 | Precursor Cell Lymphoblastic Leukemia-Lymphoma |
| D009196 | Myeloproliferative Disorders |
| ID | Term |
|---|---|
| D007951 | Leukemia, Myeloid |
| D007938 | Leukemia |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D007945 | Leukemia, Lymphoid |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
| D001855 | Bone Marrow Diseases |
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