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Partial Stem Cell Transplant for Sickle Cell Disease From Matched Donors

Matched Related Donor Non-myeloablative Hematopoietic Cell Transplantation With Alemtuzumab, 400 cGy TBI, and Abatacept for Sickle Cell Disease and Beta-Thalassemia

This is a non-ablative (partial) stem cell transplant for patients with severe sickle cell disease or beta-thalassemia requiring red cell transfusions. The intensity of the transplant is slightly increased from our previous transplant regimens. The goal is to aim for higher percentage of donor cells to stably remain in the recipients long term.

調査の概要

詳細な説明

Study Description:

Our prior non-myeloablative conditioning regimen (03H0170) included 1mg/kg of alemtuzumab divided over 5 days, 300 cGy total body irradiation (TBI), and sirolimus for immune suppression. Sickle disease-free survival (DFS) and overall survival (OS) were 85% and 94% respectively, graft failure 15%, no transplant related mortality (TRM), and acute or chronic GVHD <5%. A large proportion of patients achieved robust (>=95%) donor myeloid chimerism at day 30, but this proportion decreased quickly to 67.2% at 1, 64.9% at 2, and 60% at 3, and 56.9% at 4 years post-transplant.

A subsequent protocol (000539H) added briquilimab, an antibody targeting CD117 (c-Kit), to alem-300 cGy TBI regimen, but did not reduce the gradual decline in donor myeloid chimerism as originally hypothesized, leading to protocol closure. Rates of graft failure was 20%, no TRM, acute GVHD was 5%, and no chronic GVHD. We now propose to increase TBI to 400 cGy to further deplete host lymphoid and myeloid cells to achieve a higher percentage of donor leukocyte engraftment without substantially increasing toxicity. Since we will continue to use filgrastim to mobilize and collect donor hematopoietic cells, we also add abatacept to preserve the low rates of GVHD.

Objectives:

Primary Objective:

To reduce the proportion of patients with graft failure or donor myeloid chimerism <95%

Secondary Objectives:

  • To compare CD14/15 and CD3 chimerism to prior MRD HCT protocols (03-H-0170, 14-H-0077, and 000539H)
  • To assess the usual transplant related parameters, such as count recovery, transfusion support, rates of GVHD, viral/bacterial infections, rates of transplant related and overall mortality, and compare to prior MRD HCT protocols

Tertiary Objectives:

  • To compare changes in organ function
  • To examine neuropsychological functioning, wellbeing, and pain before and after HCT
  • To obtain reproductive health related changes before and after HCT

Endpoints:

Primary Endpoint: proportion of participants with graft failure or myeloid chimerism <95% at 1 year post HCT

Secondary Endpoints:

  • Percent myeloid (CD14/15) chimerism at day 30, 60, 100, 1 year, 2 years, and 3 years post HCT
  • Percent T cell (CD3) chimerism at day 30, 60, 100, 1 year, 2 years, and 3 years post HCT
  • Day of neutrophil engraftment per CIBMTR definition
  • Day of platelet engraftment per CIBMTR definition
  • Rates of viral reactivation or infection to day 100 post HCT
  • Rates of acute and chronic GVHD at 1 and 2 years post HCT, respectively
  • Rates of graft failure or myeloid chimerism <95% at 1 year post HCT
  • Transplant related mortality at 1, 2, and 3 years post HCT
  • Non-transplant related mortality at 1, 2 and 3 years post HCT

Exploratory Endpoints:

-Quality of life, neuropsychologic function, reproductive health questionnaires, serial testing or imaging of organ function/status

研究の種類

介入

入学 (推定)

90

段階

  • フェーズ2
  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

    • Maryland
      • Bethesda、Maryland、アメリカ、20892
        • 募集
        • National Institutes of Health Clinical Center
        • コンタクト:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • 電話番号:TTY dial 711 800-411-1222
          • メール:ccopr@nih.gov

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

  • INCLUSION CRITERIA

RECIPIENT:

Participants must fulfill one disease category (1 or 2) and 3

  1. Patients with sickle cell disease at high risk for disease related morbidity or mortality, defined by having an end-organ damage (A, B, C, D, OR E) or complication(s) not ameliorated by sickle cell-specific therapies (F):

    A. Stroke defined as a clinically significant neurologic event that is accompanied by an infarct on cerebral MRI ORb

    B. Abnormal trans-cranial Doppler examination (>=200 cm/s); OR

    C. Silent cerebral infarct defined as an infarct-like lesion based on an MRI signal abnormality at least 3 mm in one dimension and visible in two planes on FLAIR or T2- weighted images (or similar image with 3D imaging) and documented neurological examination performed by a neurologist demonstrating the participant has a normal neurologic examination, or an abnormality on examination that could not be explained by the location of the brain lesion(s); OR

    D. Sickle cell related renal insufficiency defined by a creatinine level >=1.5 times the upper limit of normal and kidney biopsy consistent with sickle cell nephropathy OR nephrotic syndrome OR creatinine clearance <60mL/min/1.73m2 for patients <16 years of age or <50mL/min for patients >16 years of age OR requiring peritoneal or hemodialysis; OR

    Age (Years): <= 5 / Upper limit of normal serum creatinine (mg/dl): 0.8

    Age (Years): 5 < age <= 10 / Upper limit of normal serum creatinine (mg/dl): 1.0

    Age (Years): 10 < age <= 15 / Upper limit of normal serum creatinine (mg/dl): 1.2

    Age (Years): > 15 / Upper limit of normal serum creatinine (mg/dl): 1.3

    E. Tricuspid regurgitant jet velocity (TRV) of >=2.5 m/s in patients at least 3 weeks after a vaso-occlusive crisis; OR

    F. Recurrent severe priapism defined as at least two episodes of an erection lasting >=4 hours requiring medical intervention (e.g. aspiration, injection of vasoconstrictor, prior penile surgery.); OR

    G. Sickle hepatopathy defined as EITHER ferritin >1000mcg/L OR direct bilirubin >0.4 mg/dL at baseline; OR

    H. Vaso-occlusive crises: more than 1 hospital admission per year while on a therapeutic dose of sickle cell treatment /medication; OR

    I. Acute chest syndrome (ACS): any ACS while on sickle cell treatment /medication

  2. Patients with beta-thalassemia who have grade 2 or 3 iron overload, determined by the presence of 2 or more of the following:

    • Portal fibrosis by liver biopsy
    • Inadequate chelation history (defined as failure to maintain adequate compliance with chelation with deferoxamine initiated within 18 months of the first transfusion and administered at least 5 days each week)
    • Hepatomegaly of greater than 2 cm below the costochondral margin or by other imaging scans
  3. Non disease specific

    • Ages >=4 years and less than 65 years old
    • Fully matched human leukocyte antigen (HLA) donors at A, B, C, and DR loci (8 of 8 or 10 of 10)
    • Ability to comprehend and willing to sign an informed consent, assent obtained from minors when applicable. Negative serum or urine beta-HCG, when applicable
    • Agree to use birth control throughout the study and 3 months after abatacept or sirolimus administration.

      • Female subjects must agree to use a medically acceptable method of birth control such as oral contraceptive, intrauterine device, barrier and spermicide, or implant/injection from start of screening until immunosuppression is stopped.
      • Male subjects must agree to use effective contraception (including condoms) from start of screening until immunosuppression is stopped.

DONOR:

  • Fully matched human leukocyte antigen (HLA) donors at A, B, C, and DR loci (8 of 8 or 10 of 10) are intended for this study.
  • Donors age 4 or older and >=15 kg (or weight deemed acceptable by IR for line placement, DTM for apheresis, and pediatric consult service) eligible to donate hematopoietic stem cells, are eligible for this study.
  • Donors will be evaluated in accordance with existing Standard NIH Policies and Procedures for determination of eligibility and suitability for clinical donation. Donors will sign on a separate protocol, 20-H-0099 NHLBI standard of care protocol for the mobilization and collection of HSCs. Note that participation in this study is offered to all eligible donors, but is not required for a donor to make a stem cell donation, so it is possible that not all donors will enroll onto this study.

EXCLUSION CRITERIA

RECIPIENT:

  • Karnofsky or Lanksy performance status of <40
  • Diffusing capacity of carbon monoxide <35% predicted: DLCO corrected for hemoglobin or KCO (corrected for lung volume). This criterion may be omitted in young children (e.g. near age 5) or other individuals who may have difficulty understanding or complying with instructions of testing.
  • Baseline oxygen saturation of <85% or PaO2 <70
  • Left ventricular ejection fraction: <35% estimated by ECHO
  • Transaminases >5x upper limit of normal for age
  • Evidence of uncontrolled bacterial, viral, or fungal infections (currently taking medication and progression of clinical symptoms) within one month prior to starting the conditioning regimen
  • Major anticipated illness or organ failure incompatible with survival from HCT
  • Pregnant or breastfeeding

DONOR:

  • Pregnant or breastfeeding
  • Cognitively impaired subjects

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

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:非ランダム化
  • 介入モデル:順次割り当て
  • 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
他の:Matched related donors
Donors for patients
About 5 tablespoons of blood will be collected from donors for research purposes.
実験的:Transplant recipients
Patients with symptomatic sickle cell disease or beta-thalassemia
About 5 tablespoons of blood will be collected from donors for research purposes.
Total Body Irradiation 400 cGy
1 mg/kg
10 mg/kg x 6

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
Donor myeloid chimerism
時間枠:1 year
percentage of donor myeloid chimerism
1 year

二次結果の測定

結果測定
メジャーの説明
時間枠
Donor CD3 chimerism
時間枠:1 year
percentage of donor myeloid chimerism
1 year
Overall survival
時間枠:1 year
percentage of patients surviving at 1 year
1 year
Acute Graft versus Host Disease
時間枠:1 year
percentage of patients with Grade 2-4 acute GVHD
1 year

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:John F Tisdale, M.D.、National Heart, Lung, and Blood Institute (NHLBI)

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年7月8日

一次修了 (推定)

2032年6月30日

研究の完了 (推定)

2035年6月30日

試験登録日

最初に提出

2026年5月16日

QC基準を満たした最初の提出物

2026年5月16日

最初の投稿 (実際)

2026年5月20日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月4日

QC基準を満たした最後の更新が送信されました

2026年9月3日

最終確認日

2026年9月2日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

We are planning to collect and report data as a group.

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

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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