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.
調査の概要
研究の種類
入学 (推定)
段階
- フェーズ2
連絡先と場所
研究連絡先
- 名前:PAKRADOUNI Jihane
- 電話番号:0491223824
- メール:pakradounij@ipc.unicancer.fr
研究連絡先のバックアップ
- 名前:ARTHUR Allison
- 電話番号:0491223448
- メール:arthura@ipc.unicancer.fr
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的: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):
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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
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
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.
時間枠: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
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
To evaluate adverse events related to the FT combination according to CTCAE V6.0
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
|
協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- FT-RIC-HAPLO-IPC 2025-016
- 2025-523632-39-00 (Ctis)
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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