- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 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.
연구 개요
연구 유형
등록 (추정된)
단계
- 2 단계
연락처 및 위치
연구 연락처
- 이름: PAKRADOUNI Jihane
- 전화번호: 0491223824
- 이메일: pakradounij@ipc.unicancer.fr
연구 연락처 백업
- 이름: ARTHUR Allison
- 전화번호: 0491223448
- 이메일: arthura@ipc.unicancer.fr
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
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.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: 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
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
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.
기간: 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
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
To evaluate adverse events related to the FT combination according to CTCAE V6.0
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- FT-RIC-HAPLO-IPC 2025-016
- 2025-523632-39-00 (씨티스)
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
급성 골수성 백혈병에 대한 임상 시험
-
National Medical Research Center for Therapy and...Stupino Clinical Hospital, Moscow Region State Medical Institution완전한
-
yuejun Liu모병T-급성 림프구성 백혈병 | 초기 T 급성 림프구성 백혈병 | 혼합 표현형 급성 백혈병, t/myeloid, nos중국
fludarabine and treosulfan에 대한 임상 시험
-
University of OregonSpecial X Inc.완전한부모-자녀 관계 | 육아 | 아동 행동 | 발달 장애 | 개발 지연 | 발달 장애, 아동미국
-
University Hospitals Cleveland Medical Center알려지지 않은
-
Technische Universität Dresdenmedac GmbH아직 모집하지 않음MDS(골수이형성 증후군) | AML - 급성 골수성 백혈병독일
-
National University of Singapore완전한
-
Academisch Medisch Centrum - Universiteit van Amsterdam...Angiogenesis Analytics아직 모집하지 않음
-
Dalarna UniversityUppsala University; The Swedish Research Council모병백치 | 가벼운 인지 장애 | 치매, 혼합 | 알츠하이머형 치매 | 주관적 인지 장애 | 치매 노인성스웨덴
-
Istituto per la Ricerca e l'Innovazione BiomedicaFondazione di Comunità di Messina onlus모병
-
GenSight Biologics모집하지 않고 적극적으로