Informations générales (source: ClinicalTrials.gov)
A 3-cohort Randomized Study Evaluating the Role of New Immunotherapeutic Agents and of Allogeneic Hematopoietic Stem Cell Transplantation (HSCT) in Frontline Therapy of Adults With Acute Lymphoblastic Leukemia
Interventional
Phase 2/Phase 3
Assistance Publique - Hôpitaux de Paris (Voir sur ClinicalTrials)
mai 2025
mars 2035
02 mars 2026
Adult acute lymphoblastic leukemia (ALL) includes Ph-positive (Phpos) ALL, Ph-negative
(Phneg) B-cell precursor (BCP) ALL and T-ALL/lymphoblastic lymphoma (LL), accounting for
approximately 25, 50 and 25% of all cases, respectively. In younger adults, the results
associated with standard therapy have markedly improved in these 3 groups, due to
chemotherapy intensification in the BCP and T groups and addition of TKIs in the Phpos
group, respectively. This led to reevaluate the role of allogeneic hematopoietic stem
cell transplantation (HSCT) in first remission, which is generally now indicated only in
higher-risk patients, mostly defined as those with persistent high levels of minimal
residual disease (MRD). Nevertheless, event-free survival (EFS) remains at 60-70% at 3
years, meaning there is still room for further improvements.
Fortunately, new immunotherapies have been approved to treat relapsed/refractory (R/R)
BCP-ALL patients, including the anti-CD19 bispecific T-cell engager blinatumomab (BLINA,
Blincyto®, Amgen). 4 BLINA is also approved for the frontline treatment of patients with
persistent high measurable residual disease (MRD) levels after initial therapy (IG/TR MRD
≥0.1% (≥1.10-3
)). BLINA has been also evaluated frontline in combination with TKI in the Phpos group
leading to promising outcome improvements. Toxicities associated with these combined
treatments seem to be limited and manageable. In the Phpos ALL subset, the
third-generation tyrosine kinase inhibitor ponatinib (PONA, Iclusig®, Incyte) has also
been evaluated frontline with promising results when compared to 1st or even 2nd
generation TKI. In the T-ALL/LL subset, anti-CD38 antibodies, approved to treat patients
with multiple myeloma, are potential drugs of interest. The anti-CD38 antibody isatuximab
(ISA, Sarclisa®, Immunogen, Sanofi-Aventis) is currently approved to treat myeloma
patients in 2nd line. In vitro and in vivo preclinical studies suggest that CD38 is a
relevant target in T-ALL and that isatuximab may be useful to eradicate residual disease
in this subgroup of patients. Incorporation/combination of these new agents into
frontline adult ALL therapy could allow reducing relapse incidence and prolonging
survival in these patients, challenging the indication for HSCT in first complete
remission (CR).
The present GRAALL-2024 study is a prospective multicenter multi-country 3-cohort
randomized clinical trial.
The 3 cohorts are :
GRAALL-2024/B : Phneg BCP-ALL GRAAPH-2024 : Phpos ALL GRAALL-2024/T : T-ALL/LL
Eligible patients will be allocated to one on the 3 study cohorts during a common
treatment prephase. The primary objective of the study is to improve the outcome of
younger adults with ALL through optimal frontline incorporation of new antibody-based
therapies, including BLINA in Phneg/pos BCP-ALL patients and ISA in T-ALL/LL patients,
and to refine indication for allogeneic HSCT in first remission in Phneg/pos BCP-ALL
patients.
Etablissements
Critères
Tous
1. Patients aged 18 to 65 years old
2. Newly diagnosed ALL or T-LL according to the WHO criteria
3. Immunophenotypic, cytogenetic and/or FISH and molecular evaluation performed and
allowing classifying the patient in one of the Phpos ALL, Phneg BCP-ALL or T-ALL/LL
cohorts
4. Not previously treated except with corticosteroids and/or intrathecal therapy
(prephase)
5. Eligible for allo-HSCT if Phpos ALL or Phneg BCP-ALL
6. ECOG performance status ≤2
7. Patient willing and able to understand the protocol requirements and comply with the
treatment schedule, scheduled visits, electronic patient outcome reporting, exams
and other requirements of the study
8. Patients has signed written inform consent
9. Willingness of women of child-bearing potential (WOCBP) and male subjects whose
sexual partners are WOCBP to use an effective form of contraception, i.e. methods
with a failure rate of <1% per year when used consistently and correctly, during the
study and at least 6 months thereafter
10. Eligible for National Health Insurance (for French patients)
Exclusion Criteria:
Common exclusion criteria :
1. Patient previously treated with systemic chemotherapy, antibody-based therapy or TKI
2. Patients with a history of another primary malignancy that is currently clinically
significant or currently requires active intervention
3. History or presence of clinically relevant CNS pathology such as epilepsy, childhood
or adult seizure, paresis, aphasia, stroke, severe brain injuries, dementia,
Parkinson's disease, cerebellar disease, organic brain syndrome,
coordination/movement disorder, autoimmune disease with CNS involvement, psychosis
(with the exception of CNS leukemia that is well controlled with intrathecal
therapy)
4. Patients with LVEF<50% or other clinically significant heart disease (e.g. unstable
angina, congestive heart failure, uncontrolled hypertension)
5. Prior documented chronic liver disease. Inadequate hepatic functions defined as AST
or ALT > 5 x the institutional upper limit of normal (ULN), or > 5 x ULN unless if
considered due to leukemia. Total bilirubin > 1.5 x ULN unless if considered due to
leukemia or Gilbert/Meulengracht
6. Estimated glomerular filtration rate (GFR) < 50 mL/mn using the MDRD equation
7. Chronic pancreatitis or acute pancreatitis within 6 months before study start
8. Known diagnosis of human immunodeficiency virus (HIV) infection (HIV testing is not
mandatory) or active infection with Hepatitis B or C.
9. Concurrent severe diseases which exclude the administration of therapy
10. Treatment with any other investigational agent or participating in another trial
within 30 days prior to entering this study
11. Pregnancy and breast feeding
12. Patients unwilling or unable to comply with the protocol
13. Patients under a legal protection regime (guardianship, trusteeship, judicial
safeguard)
14. Chronic or current active uncontrolled infectious disease requiring systemic
antibiotics, antifungal, or antiviral treatment
15. Current use of prohibited medication
16. Known hypersensitivity or severe reaction to ponatinib (GRAAPH), blinatumomab
(GRAAPH and GRAALL-B) , isatuximab (GRAALL-T) or their excipients.
17. Receipt of live (including attenuated) vaccines or anticipation of need for such
vaccines during the study
If patients with Phpos ALL:
1. Complete left bundle branch block, right bundle branch block plus left anterior
hemiblock, bi-fascicular block
2. History of or presence of clinically significant ventricular or atrial
tachyarrhythmias
3. Clinically significant resting bradycardia (< 50 beats per minute)
4. Congenital long QT syndrome or QTcF > 470 msec on screening ECG. If QTc > 470 msec
and electrolytes are not within normal ranges before ponatinib dosing, electrolytes
should be corrected and then the patient rescreened for QTcF criterion
5. Currently taking drug(s) that are known to have a risk of causing prolonged QTc or
TdP unless the drug(s) can be changed to acceptable alternatives (ie, an alternate
class of agents that do not affect the cardiac conduction system), or the
participant can safely discontinue the drug(s)
6. Previous myocardial infarction within the last 12 months
7. Symptomatic peripheral vascular disease
8. History of ischemic stroke or transient ischemic attacks (TIAs) within the last 12
months
9. Significant bleeding disorder or thrombophilia unrelated to the underlying
malignancy indication for study participation
10. Gastrointestinal disorders, such as malabsorption syndrome or any other illness that
could affect oral absorption