Detail Article

Informations générales (source: ClinicalTrials.gov)

Numéro NCT

NCT04307576 En recrutement IDF

Titre

ALLTogether1 - A Treatment Study Protocol of the ALLTogether Consortium for Children and Young Adults (0-45 Years of Age) With Newly Diagnosed Acute Lymphoblastic Leukaemia (ALL)

Type

Interventional

Pathologie

Leucémies
Leucémie lymphoïde
Leucémie-lymphome lymphoblastique à précurseurs B et T

Phase

Phase 3

Promoteur

Mats Heyman (Voir sur ClinicalTrials)

Date de début

juillet 2020

Date de fin

juin 2032

Dernière mise à jour

13 juillet 2024

Résumé

ALLTogether collects the experience of previously successful treatment of infants, children and young adults, with ALL from a number of well-renowned study groups into a new master protocol, which is both a comprehensive system for stratification and treatment of ALL in this age-group as well as the basis for several randomised and interventional trials included in the study-design.

Détail

Voir le détail ALLTogether is a European clinical treatment study for acute lymphoblastic leukaemia (ALL) in infants, children and young adults. The aims are to improve survival and quality of survival. In young people, ALL has excellent outcome with an overall survival of about 92% in children and 75% in young adults. Infants with BCP-ALL and KMT2A-rearrangements have a worse outcome and are treated according to separate protocols, but infants with KMT2A-germline and T-cell ALL have acceptable outcome on standard ALL therapy. However, patients still die of disease - from relapse because of under-treatment and a large fraction of patients are also over-treated: All patients risk treatment-related death and some suffer long-term side-effects or secondary cancer. To show improvement with such good survival, large populations are needed. Study groups from Sweden, Norway, Iceland, Denmark, Finland, Estonia and Lithuania (NOPHO), the UK (UKALL), the Netherlands (DCOG), Germany (COALL), Belgium (BSPHO), Portugal (SHOP), Ireland (PHOAI), and France (SFCE), have designed a common treatment protocol. The study has a complex clinical trial design with sub-protocols (the randomisations / intervention) connected to a master protocol. The master protocol consists of well established therapy-elements and in its design typical for current ALL therapy. The master protocol therapy is in the study design considered as standard of care (SOC) therapy for infants, children and young adults with ALL. The study structure is defined by a master protocol onto which randomised and interventional sub-protocols as well as sub-studies may be added, run and stop in a modular fashion. The randomisations / intervention may identify therapy that is less toxic, but equally efficacious for sub-groups of patients and innovative therapy that may reduce relapses and death from ALL. In the master protocol, improved risk-stratification is likely to increase survival and reduce unnecessary toxicity and the introduction of therapeutic drug monitoring (TDM) of Asparaginase activity will make the use of Asparaginase more rational and efficient and may thus improve overall outcomes. The investigators hypothesise that patients stratified to the standard-risk group are over-treated. Therefore, it will be tested if the treatment can be safely reduced. In the R1 randomisation, patients will be randomised to receiving the Delayed Intensification (DI) phase of therapy with or without the anthracycline Doxorubicin. A similar hypothesis of over-treatment will also be tested in patients stratified to the intermediate risk-low group. In the R2 randomisation patients will be randomly assigned to either removal of Doxorubicin during the DI phase or removal of Vincristine and Dexamethasone pulses during the maintenance phase or to the control group, which will be treated with Doxorubicin in DI as well as Vincristine and Dexamethasone pulses during maintenance. Patients will only be randomised once. Randomisation R1 and R2 are only considered for children since adults have worse outcome and very poor survival after relapse, but the risk-stratification is likely to reduce the number of high-risk cases also in the adult-group. Patients stratified as intermediate risk-high (IR-high) are identified as having an increased risk of relapse and thus a less favourable prognosis than the standard- and intermediate risk-low groups, but a more favourable prognosis than the high risk patients. The majority of all relapses in childhood ALL is expected to occur in the IR-high group. Following a relapse, only approximately 40% of the children can be successfully treated again and for adults the corresponding figure is less than 20 %, so preventing relapses is very important. New treatment options that improves the antileukaemic efficacy and which have an improved safety profile are urgently needed. For IR-high patients Randomisation 3 (R3) is available. In R3 patients will be randomised to receive either: 1. the addition of two cycles of Inotuzumab ozogamicin (InO) - Besponsa®, before start of the maintenance phase. After these cycles, the patients randomised to the InO arm will receive maintenance for the same duration as in the control arm. 2. the addition of low dose 6-tioguanine (6TG) as an addition to the standard maintenance therapy. 3. standard maintenance therapy Patients with ABL-class fusions in their leukaemic clone will, as a non-randomised experimental intervention, be treated with an addition of a tyrosine-kinase inhibitor during the induction phase (for patients <25 years) and from the consolidation phase (patients ≥25 years). This intervention may shift therapy for previously resistant cases to lower intensity treatment with the associated reduced morbidity and may also reduce the number of relapses in analogy with the results in Ph+ ALL. The reason for not performing a randomised comparison is the rarity of the aberration and also the diversity of ABL-class fusions, reducing statistical power for any comparison further. For this reason, the results of this intervention may be pooled with other study-groups trying similar approaches. A new intervention is introduced for Down syndrome patients with CD19 positive ALL: ALLTogether1 DS (NRI2). For Down syndrome-ALL patients who have end of Induction MRD detectable but <25% two conventional chemotherapy consolidation blocks will be replaced with two blocks of Blinatumomab. For high-risk B-lineage patients, CAR-T therapy can be an alternative to high-risk blocks and stem-cell transplant, but in this case the intervention (CAR-T infusion) will be performed outside the ALLTogether1 study. However, the stratification-system in ALLTogether1 will define the population with a potential CAR-T indication. ALLTogether1 also includes five sub-studies: Efficacy and pharmacokinetics of Imatinib in ABL-class fusion positive ALL Target population: All ABL-class patients enrolled in the ALLTogether study. Biomaterials to be collected at diagnosis, during TKI treatment, follow-up and relapse. Aims 1. To determine the efficacy and dosing target of imatinib in the treatment of ABL-class leukemia 2. To find the best discriminative biomarkers for TKI response in ABL-class ALL 3. To determine the frequency of intrinsic (at diagnosis) and acquired TKI resistance (due to treatment), including backtracking of mutations using imatinib PK/PD findings during treatment 4. To find causes of TKI resistance in ABL-class patients 5. To describe the pharmacokinetics of Imatinib in TKI-treated patients Objectives 1. To determine the percent of ABL-class patients who need to switch from IR-high to HR because of high MRD levels 2. To determine the effect of imatinib exposure on clinical outcome, including pharmacokinetic measurements of imatinib 3. To determine the molecular response to imatinib by monitoring fusion gene levels and mutational spectrum at diagnosis and during follow up 4. To determine whether the molecular response parameters reflect the Ig/TCR MRD or flow-MRD response or are a better predictor of therapy failure than Ig/TCR or flow-based MRD monitoring 5. To determine the phosphorylation status of ABL-class proteins and presence of TKI-resistance associated mutations in ABL genes prior to imatinib treatment and the emergence of such mutations during treatment with imatinib 6. To determine the presence of mutations in regulatory /other genes before and during imatinib treatment and functionally address the importance of these mutations in TKI resistance 7. To determine whether the efficacy of TKIs depends on the type of fusion gene 8. To describe inter- and intraindividual variations in imatinib PK (=trough levels) during therapy of ABL-class ALL 9. To describe associations between PK of imatinib and end-of-induction MRD (<25 yrs only) and end-of-consolidation MRD (all patients) 10. To describe associations between imatinib PK and relapse rates (overall, bone-marrow and CNS), event-free survival as well as overall survival; 11. To describe associations between imatinib PK and toxicities (including e.g. height z-scores at diagnosis and end of therapy, pancreatitis, treatment delays) with focus on those toxicities that are routinely monitored in ALLTogether. Biomarkers to Reform Approaches to therapy-Induced Neurotoxicity (BRAIN) Target population: All patients registered on ALLTogether1 aged ≥ 4 years at end of therapy (Arm A) and all patients registered on ALLTogether1 aged 4-21 years at start of therapy (Arm B) and without: 1. Pre-existing neurodevelopmental delay (e.g Trisomy 21) prior to diagnosis of ALL 2. Significant visual or motor impairment preventing use of a touch screen ipad All centres are invited to enrol to arm A (Main BRAIN) of the study. Arm B (Longitudinal BRAIN) will be carried out in selected centres. Aims 1. To implement universal screening of all children for adverse neurocognitive outcomes at the end of treatment using a validated user-friendly computer software programme (CogState) and compare neurocognitive outcomes by treatment allocation (Arm A). 2. To identify risk factors for adverse outcomes including whether acute neurotoxic events are associated with poor performance on cognitive tests at end of therapy compared to patients without acute neurotoxicity (Arm A). 3. To examine changes in neurocognitive performance over time and the risk/protective factors associated with differences in outcome, such as demographic, clinical, and physical/psychosocial factors (Arm B). Primary end-point a. Proportion of children with a z-score <1.5 on detection and/or identification CogState tasks in each treatment arm at the end of ALL therapy. A z-score < 1.5 correlates with moderate cognitive impairment at a level that may require additional support. Secondary and exploratory end-points 1. Association between CogState scores at end of treatment and overt neurotoxic episodes as recorded on the trial adverse event database. 2. Association between Cogstate scores and clinical and demographic variables - age, sex, ethnicity, CNS status. 3. Proportion of children with scores <1.5SD for one card learning (learning), one back (working memory) and Groton's maze (executive function) on different treatment arms. 4. Association between CogState scores and patient reported outcome measures/Quality of life measurements collected as part of the main ALLTogether1 trial. 5. Changes in neurocognitive scores over time, including CogState and BRIEF-2/BRIEF-A scores. 6. Association between neurocognitive scores over time and interactions with demographic variables (age, sex), clinical variables (treatment arm, neurotoxicity), social-emotional and physical functioning (SDQ, PedsQL 4.0 Generic; PedsQL 3.0 Fatigue), and family factors (MEES; PedsQL FIM) Association between asparaginase activity levels and outcome Target population: All patients included in the ALLTogether1 protocol are eligible for participation. Primary aim To study the association between asparaginase activity levels and outcome (MRD, relapse, survival) Secondary aims 1. To evaluate the association between asparaginase activity levels and toxicities, such as pancreatitis, infections and deep venous thrombosis (DVT) 2. To evaluate the association between asparaginase activity levels and hepatotoxicity in a subset of patients CSF-Flow Target population: All patients included in the ALLTogether1 protocol are eligible for participation Aims 1. To use cerebrospinal fluid (CSF) flow cytometry (FCM) to improve the accuracy of diagnostic tests for CNS leukaemia compared to conventional CSF cytology. An associated objective will be to develop a recommended protocol for CSF flow cytometry with external quality assessment to ensure uniformity of measurement across the ALLTogether consortium. 2. To investigate whether negative FCM identifies a group of children at very low risk of CNS relapse, suitable for testing de-escalation of CNS-directed therapy in future trials. 3. To investigate whether positive FCM can identify children at increased risk of CNS relapse and whether patients with persistent positivity (FCM positive at day 15 onwards) might benefit from studies testing escalated CNS-directed therapy or a switch to more intensive treatment arms. 4. To collect matching CSF supernatant for studies comparing CSF FCM with soluble biomarkers (e.g. metabolic, cell-free DNA, proteomic and microRNA). Maintenance therapy pharmacokinetics/-dynamics study Target population: All patients included in the ALLTogether1 protocol are eligible for participation. For IR-high patients participating in the randomised InO- and TEAM sub-protocols, the monitoring of 6-mercaptopurine (6MP)/Methotrexate (MTX) metabolites at three months intervals is mandatory. Aims and specific objectives 1. To map pharmacokinetics of 6MP and MTX during maintenance therapy in all patients in the ALLTogether protocol. 2. To associate metabolite profiles with TPMT and NUDT15 variants, as routinely analysed in ALLTogether. 3. To explore the association of event-free survival with DNA-TG and other 6MP/MTX metabolites. 4. To explore the association between risk of second cancers with DNA-TG and other 6MP/MTX metabolites. 5. To explore the association of risk of invasive infections with DNA-TG and other 6MP/MTX metabolites. 6. To explore the association of risk of osteonecrosis with DNA-TG and other 6MP/MTX metabolites. 7. To explore the association of sinusoidal obstruction syndrome with DNA-TG and other 6MP/MTX metabolites. Fermer le détail

Etablissements

Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données
AP-HP Assistance publique - Hôpitaux de Paris		En recrutement IDF	13/12/2025 07:36:29	Contacter
	AP-HP - Hôpital Armand Trousseau-La Roche Guyon
	AP-HP - Hôpital Lariboisiere-Fernand Widal
	AP-HP - Hôpital Robert Debré
	AP-HP - Hôpital Saint Louis
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Centre Hospitalier Universitaire Caen - 14033 - Caen Cedex 9 - France		En recrutement		Contact (sur clinicalTrials)
CHRU Besançon - 25030 - Besancon Cedex 03 - France		En recrutement		Contact (sur clinicalTrials)
CHRU Brest - Morvan - 29609 - Brest Cedex - France		En recrutement		Contact (sur clinicalTrials)
CHRU de Lille - Hôpital Jeanne de Flandre - 59037 - Lille Cedex - France		En recrutement		Contact (sur clinicalTrials)
CHRU Tours- Hôpital Clocheville - 37000 - Tours - France		En recrutement		Contact (sur clinicalTrials)
CHU Amiens Groupe Hospitalier Sud - 80054 - Amiens Cedex 1 - France		En recrutement		Contact (sur clinicalTrials)
CHU Angers - 49033 - Angers Cedex 9 - France		En recrutement		Contact (sur clinicalTrials)
CHU Bordeaux - Groupe Hospitalier Pellegrin - 33076 - Bordeaux Cedex - France		En recrutement		Contact (sur clinicalTrials)
CHU Clermont-Ferrand - 63000 - Clermont-ferrand - France		En recrutement		Contact (sur clinicalTrials)
CHU de Grenoble site Nord - Hôpital Albert Michallon - 38043 - Grenoble Cedex 9 - France		En recrutement		Contact (sur clinicalTrials)
CHU De La Réunion - Site Nord (Hôpital Félix GUYON) - 97400 - Saint-Denis - France		En recrutement		Contact (sur clinicalTrials)
CHU de Lyon HCL - GH Est-Institut d'hématologie et d'oncologie pédiatrique IHOP - 69373 - Lyon Cedex 08 - France		En recrutement		Contact (sur clinicalTrials)
CHU de Marseille - Hôpital de la Timone - 13385 - Marseille Cedex 5 - France		En recrutement		Contact (sur clinicalTrials)
CHU de Montpellier - Hôpital Arnaud de Villeneuve - 34295 - Montpellier Cedex 5 - France		En recrutement		Contact (sur clinicalTrials)
CHU de Nancy - Hôpital de Brabois Enfant - 54511 - Vandoeuvre-les-nancy cedex - France		En recrutement		Contact (sur clinicalTrials)
CHU Dijon Hôpital François Mitterrand - 21000 - Dijon - France		En recrutement		Contact (sur clinicalTrials)
CHU Nantes-Hôpital enfant-adolescent - 44093 - Nantes Cedex 01 - France		En recrutement		Contact (sur clinicalTrials)
CHU Nice - Hôpital l'Archet 2 - 6200 - Nice - France		En recrutement		Contact (sur clinicalTrials)
CHU Paris - Hôpital Robert Debré - 75019 - Paris - France		En recrutement		Contact (sur clinicalTrials)
CHU Paris Saint Louis - 75010 - Paris - France		En recrutement		Contact (sur clinicalTrials)
CHU Poitiers - 86021 - Poitiers Cedex 6 - France		En recrutement		Contact (sur clinicalTrials)
CHU Reims-American Hospital - 51100 - Reims - France		En recrutement		Contact (sur clinicalTrials)
CHU Rennes - Hôpital sud - 35203 - Rennes Cedex 2 - France		En recrutement		Contact (sur clinicalTrials)
CHU Rouen - 76031 - Rouen Cedex - France		En recrutement		Contact (sur clinicalTrials)
CHU Saint Etienne Hôpital Nord - 42055 - Saint-Étienne - France		En recrutement		Contact (sur clinicalTrials)
CHU STRASBOURG -Hôpital de Hautepierre - 67098 - Strasbourg Cedex - France		En recrutement		Contact (sur clinicalTrials)
CHU Toulouse - 31059 - TOULOUSE Cedex 9 - France		En recrutement		Contact (sur clinicalTrials)
Hôpital de la mère et de l'enfant - 87042 - Limoges - France		En recrutement		Contact (sur clinicalTrials)

Critères

Genre

Tous

Nombre d'inclusion

Critère d'inclusion

Inclusion Criteria:

- Patients newly diagnosed with T-lymphoblastic (T-cell) or B-lymphoblastic precursor
(BCP) leukaemia (ALL) according to the WHO-classification of Tumours of
Haematopoetic and Lymphoid Tissues (Revised 4th edition 2017) and with a diagnosis
confirmed by an accredited laboratory at a participating paediatric oncology or
adult haematology centre.

- Age 0 - < 46 years (one day before 46th birthday) at the time of diagnosis with the
exception of infants with KMT2A-rearranged (KMT2A-r) BCP ALL.

- Patients with surface immunoglobulin negative (sIG-) BCP-ALL and an IG::MYC
rearrangement, unless they have a concurrent BCL2/6 rearrangement. T-ALL patients
with MYC translocations.

- Informed consent signed by the patient and/or parents/legal guardians according to
country-specific age-related guidelines.

- The ALL diagnosis should be confirmed by an accredited laboratory at a participating
paediatric oncology or adult haematology centre.

- The patient should be diagnosed and treated at a participating paediatric oncology
or adult haematology centre in the participating countries.

- The patient should be a resident in one of the participating countries on a
permanent basis or should intend to settle in a participating country, for instance
by an application for asylum. Patients who are visiting the country as tourists
should not be included. However, returning expatriots with primary diagnosis abroad
may be included if no treatment has been administered and the diagnostic procedures
are repeated at a participating centre.

- All women of childbearing potential (WOCBP) have to have a negative pregnancy test
within 2 weeks prior to the start of treatment.

- For each intervention/randomisation an additional set of inclusion-criteria is
provided.

Critère de non inclusion

- Age < 365 days and KMT2A-rearranged (KMT2A-r) BCP-ALL (documented presence of a
KMT2A-split by FISH and/or a KMT2A fusion transcript).

- Age >45 years at diagnosis.

- Patients with a previous malignant diagnosis (ALL as a second malignant neoplasm -
SMN).

- Relapse of ALL.

- Patients with mature B-ALL (as defined by surface IG positivity) or any patients
with IG::MYC and a concurrent BCL2/6 rearrangement.

- Patients with Ph-positive ALL (documented presence of t(9;22)(q34;q11) and/or of the
BCR::ABL fusion transcript). These patients will be transferred to an appropriate
trial for t(9;22) if available.

- Previously known ALL prone syndromes (e.g. Li-Fraumeni syndrome, germline ETV6
mutation), except for Down syndrome. Exploration for such ALL prone syndromes is not
mandatory and patients in whom genetic work-up reveals a new germ-line mutation
(index-cases) will remain in the study.

- Treatment with systemic corticosteroids (>10mg/m2/day) for more than one week and/or
other chemotherapeutic agents in a 4-week interval prior to diagnosis
(pre-treatment).

- Pre-existing contraindications to any treatment according to the ALLTogether
protocol (constitutional or acquired disease prior to the diagnosis of ALL
preventing adequate treatment).

- Any other disease or condition, as determined by the investigator, which could
interfere with the participation in the study according to the study protocol, or
with the ability of the patients to cooperate and comply with the study procedures.

- Women of childbearing potential who are pregnant at the time of diagnosis.

- Women of childbearing potential and fertile men who are sexually active and are
unwilling to use adequate contraception during therapy. Efficient birth control is
required.

- Female patients, who are breast-feeding.

- Essential data missing from the registration of characteristics at diagnosis (in
consultation with the protocol chair).

- For each intervention/randomisation an additional set of exclusion-criteria is
provided.

NCT04307576 - ALLTogether1 - A Treatment Study Protocol of the ALLTogether Consortium for Children and Young Adults (0-45 Years of Age) With Newly Diagnosed Acute Lymphoblastic Leukaemia (ALL)

Informations générales
Etablissements
Critères
Accès à la fiche NCT

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