- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07598110
FLUDARABINE-TREOSULFAN REDUCED INTENSITY CONDITIONING REGIMEN PRIOR HAPLOIDENTICAL STEM CELL TRANSPLANTATION WITH POST TRANSPLANTATION CYCLOPHOSPHAMIDE FOR OLDER AND/OR FRAIL PATIENTS WITH AML (FT-RIC-HAPLO)
FLUDARABINE-TREOSULFAN REDUCED INTENSITY CONDITIONING REGIMEN PRIOR HAPLOIDENTICAL STEM CELL TRANSPLANTATION WITH POST TRANSPLANTATION CYCLOPHOSPHAMIDE FOR OLDER AND/OR FRAIL PATIENTS WITH AML: FT-RIC-HAPLO-IPC 2025-016
Acute myeloid leukemia (AML) and high-risk myelodysplastic syndromes (MDS) predominantly affect older adults, and their incidence continues to rise with advanced age. For many patients, allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains the only curative option capable of providing long-term disease control through the graft-versus-leukemia (GVL) effect. Historically, however, allo-HSCT was rarely offered to patients older than 50 years because of the high morbidity and mortality associated with myeloablative conditioning regimens and limited supportive care strategies. Over the past two decades, advances in reduced-intensity conditioning (RIC), infection prophylaxis, and donor availability have profoundly transformed the landscape, allowing increasing numbers of older patients to access transplantation.
Multiple studies have demonstrated that allo-HSCT confers a survival benefit in older AML patients in complete remission compared with consolidation chemotherapy alone.
The intensity of conditioning profoundly influences both relapse risk and non-relapse mortality (NRM). myeloablative conditioning (NMAC) regimens are attractive for older adults due to their low toxicity but rely solely on the immunologic GVL effect and thus carry a higher relapse risk. Reduced-intensity conditioning (RIC) regimens, incorporating intermediate-dose alkylating agents such as busulfan, melphalan, or thiotepa, offer stronger anti-leukemic effect but at the cost of greater toxicity.
These observations underscore the central question: can a conditioning regimen combine strong anti-leukemic potency with the low toxicity required for older patients undergoing Haplo-SCT? The main objective is to evaluate the efficacy of FT-RIC regimen before Haplo-SCT for older and/or frail patients diagnosed with AML, who are not eligible for a myeloablative conditioning (MAC) regimen.
To achieve this objective, the investigators will assess Progression Free Survival (PFS) defined as the time from allo-HSCT to AML relapse or death.
This is a Multicenter trial, single arm prospective of phase II. Once the conditioning has been administered and the transplant performed, the patient will receive standard routine follow-up care, with the addition of questionnaires, and for patients followed at the Institut Paoli Calmettes only, blood samples will be collected.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: PAKRADOUNI Jihane
- Numero di telefono: 0491223824
- Email: pakradounij@ipc.unicancer.fr
Backup dei contatti dello studio
- Nome: ARTHUR Allison
- Numero di telefono: 0491223448
- Email: arthura@ipc.unicancer.fr
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
Inclusion Criteria:
- Patient with age between 60 and 75 years old ; or aged 18-59 years if considered by the investigator for any reason as ineligible for MAC regimen (as defined by the EBMT criteria17), notably in case of HCT-CI ≥ 3 (patients planned by the investigators to receive a RIC regimen in clinical routine practice);
- Patients with AML according to the ELN2022 classification criteria requiring allo-HSCT including the MDS/AML sub category);
- Less than 5% bone marrow blast at the time of inclusion (i.e. CR, CRi, CRh, or MLFS after prior treatment, according to ELN 2022);
- Allo-HSCT planed with a haploidentical donor;
- Covered by a Healthcare System;
- Signed informed consent obtained prior to initiation of any study-specific procedures and treatment as confirmation of the patient's awareness and willingness to comply with the study requirements.
Exclusion Criteria:
- Left ventricular function < 40% ;
- Renal clearance < 50 mL/min ;
- Any severe uncontrolled medical condition considered by the investigator as a contraindication for using treosulfan;
- Pregnant women or those who may become pregnant (without effective contraception) or breastfeeding;
- Adults under legal protection (guardianship, curatorship, or judicial protection);
- Inability to comply with the medical follow-up of the trial for geographical, social, or psychological reasons.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: fludarabine and treosulfan
After screening and inclusion, patients will be given a RIC regimen based on the market-approved association of fludarabine and treosulfan (FT-RIC):
|
As per standard practices, patients will be hospitalized during the treatment period.
The treatment is administered by the nurses of the department under the responsibility of the investigator.Fludarabine (30 mg/m²/day from day-6 to day-2), iv andTreosulfan (10 g/m²/day from day-4 to day-2), iv
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
The main objective is to evaluate the efficacy of FT-RIC regimen before Haplo-SCT for older and/or frail patients diagnosed with AML, who are not eligible for a MAC regimen.
Lasso di tempo: through study completion an average of 4 years
|
Progression Free Survival (PFS) defined as the time from allo-HSCT to AML relapse or death
|
through study completion an average of 4 years
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
To evaluate adverse events related to the FT combination according to CTCAE V6.0
Lasso di tempo: through study completion an average of 4 years
|
Conditioning related toxicity according to CTCAE V.6.0
|
through study completion an average of 4 years
|
|
To evaluate engraftment after FT-RIC
Lasso di tempo: through study completion an average of 4 years
|
rate of graft failure
|
through study completion an average of 4 years
|
|
To evaluated hematological recovery after FT-RIC
Lasso di tempo: after hematological recovery
|
Cumulative incidence of neutrophil and platelet recovery
|
after hematological recovery
|
|
to evaluate incidence of both acute and chronic GVHD after FT-RIC
Lasso di tempo: through study completion an average of 4 years
|
Cumulative incidence of acute GVHD and Cumulative incidence of chronic GVHD
|
through study completion an average of 4 years
|
|
To evaluate survival, non-relapse mortality and cause of death after FT-RIC
Lasso di tempo: through study completion an average of 4 years
|
Probability of Overall Survival and Probability of GVHD
|
through study completion an average of 4 years
|
|
To evaluate the immunosuppressive therapy duration after FT-RIC
Lasso di tempo: through study completion an average of 4 years
|
Prevalence of immunosuppressive therapy (IST) and GVHD at 3, 6, 9, 12 months
|
through study completion an average of 4 years
|
Collaboratori e investigatori
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- FT-RIC-HAPLO-IPC 2025-016
- 2025-523632-39-00 (Ctis)
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Leucemia mieloide acuta
-
People's Hospital of Guangxi Zhuang Autonomous...CompletatoLesioni polmonari acute (ALI)Cina
-
Fenerbahce UniversityIscrizione su invitoUstioni acuteTurchia (Türkiye)
-
BioMérieuxReclutamentoInfezioni respiratorie acute (ARI)Stati Uniti
-
Lumos DiagnosticsReclutamento
-
Lohmann & RauscherReclutamentoFerite acute e cronicheGermania
-
MMSx Authority Institute for Movement Mechanics...CompletatoDolore muscoloscheletrico - Condizioni acute e subacuteStati Uniti, India
-
Aswan UniversityIscrizione su invitoDiagnosi precoce di lesioni renali acuteEgitto
-
Antoni RibasNon ancora reclutamentoLa guarigione delle ferite | Ferite Cutanee AcuteStati Uniti
-
Region of Southern DenmarkOdense Municipality, Denmark; Kerteminde Municipality, Denmark; Svendborg Municipality...Completato
-
Peking University Third HospitalShanghai Jiao Tong University School of MedicineAttivo, non reclutante
Prove cliniche su fludarabine and treosulfan
-
Federal Research Institute of Pediatric Hematology...Russian Children's Clinical Hospital of the N.I. Pirogov Russian National Research... e altri collaboratoriNon ancora reclutamentoHSCT | Sindrome da rottura di Nijmegen | Condizionamento a Base di Treosulfano
-
Azienda Socio Sanitaria Territoriale degli Spedali...Attivo, non reclutanteLeucemia mieloide acuta (AML) | Trapianto di cellule staminali emopoietiche (HSCT)Italia
-
Sheba Medical CenterSconosciutoLinfoma di Hodgkin | Linfoma non HodgkinIsraele
-
IRCCS San RaffaeleSconosciutoLeucemia | Mieloma multiplo | Linfoma di Hodgkin | Leucemia linfatica cronica | Leucemia mieloide cronica | Sindrome mielodisplasica | Linfoma diffuso a grandi celluleItalia
-
Hospices Civils de LyonSconosciutoNeoplasie ematologiche | Trapianto allogenicoFrancia
-
IRCCS San RaffaeleTerminatoMieloma multiplo | Malattia del trapianto contro l'ospite | Leucemia, acuta | Neoplasie ematologiche correlate al trapianto | Midollo osseo irradiatoItalia
-
OHSU Knight Cancer InstituteNational Cancer Institute (NCI); medac GmbHCompletato
-
Xuanwu Hospital, BeijingReclutamentoSonno | Epilessia refrattariaCina
-
Center for Clinical Research and PreventionUniversity of Copenhagen; Slagelse SygehusNon ancora reclutamentoDepressione, Ansia | Intervento | Studio controllato randomizzato
-
Dalarna UniversityUppsala University; The Swedish Research CouncilReclutamentoDemenza | Compromissione cognitiva lieve | Demenza, mista | Demenza di tipo Alzheimer | Compromissione cognitiva soggettiva | Demenza senileSvezia