- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07586735
A Novel Conditioning Regimen for Haplo-HSCT in Older Patients With SAA
1. juli 2026 opdateret af: Xiao-Jun Huang, Peking University People's Hospital
A Novel Conditioning Regimen for Haploidentical Hematopoietic Stem Cell Transplant in Patients Aged ≥ 40 Years Old With Severe Aplastic Anemia: a Multicenter, Single-arm, Observational Clinical Trial
The goal of this prospective, multicenter, single arm observational study is to evaluate the efficacy and safety of the BFCA regimen in ≥ 40 years old SAA patients undergoing haplo-HSCT.
Studieoversigt
Status
Rekruttering
Intervention / Behandling
Undersøgelsestype
Observationel
Tilmelding (Anslået)
64
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Tingting Han
- Telefonnummer: 8601088326666
- E-mail: htt1984.love@163.com
Studiesteder
-
-
Beijing Municipality
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Beijing, Beijing Municipality, Kina, 100044
- Rekruttering
- Peking Universtiy Peoples' Hospital
-
Kontakt:
- Tingting Han, Doctor
- Telefonnummer: 86-01088424953
- E-mail: htt1984.love@163.com
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Ingen
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Patients aged 40-60 years old who are diagnosed with severe aplastic anemia according to NCCN guidelines and who will receive haploidentical hematopoietic stem cell transplantation at the centers will be recruited.
Beskrivelse
Inclusion Criteria:
- Severe aplastic anemia;
- Aged 40-60 years old;
- Weight 45Kg-100Kg;
- Eastern Cooperative Oncology Group (ECOG) score ≤3;
- No major organ injury (ECG ejection fraction >45%; bilirubin < 2 times the upper limit of normal value; AST and ALT < 3 times the upper limit of normal value; serum creatinine < 2 times the upper limit of normal value);
- No severe infection;
- Subjects voluntarily participated in this clinical trial and signed the informed consent.
Exclusion Criteria:
- With other hematologic diseases;
- Expected survival of less than 1 month;
- Previous autologous or allogeneic hematopoietic stem cell transplantation;
- Pregnant patients;
- Patients with severe mental or neurological disorders that would affect the ability to provide informed consent and/or to report or observe adverse events;
- Other conditions that the investigator determines to be inappropriate for enrollment.
- Current or recent (<4 weeks prior to screening) clinically serious viral, bacterial, fungal, or parasitic infection
- A history of symptomatic herpes zoster infection within 12 weeks prior to screening
- Active or chronic viral infection from hepatitis B virus (HBV), hepatitis C virus (HCV), or human immunodeficiency virus (HIV)
- Have evidence of active tuberculosis (TB), or have previously had evidence of active TB and did not receive appropriate and documented treatment, or have had household contact with a person with active TB and did not receive appropriate and documented prophylaxis for TB
- Exposure to a live vaccine within 12 weeks prior to enrollment or expected to receive a live vaccine during the study
- Clinically significant thrombotic event within 24 weeks of screening or are on anticoagulants and in the opinion of the investigator are not well controlled
- Myocardial infarction (MI), unstable ischemic heart disease, stroke, or New York Heart Association Stage IV heart failure
- A history or presence of cardiovascular, respiratory, hepatic, gastrointestinal, endocrine, neurological, or neuropsychiatric disorders or any other serious and/or unstable illness that, in the opinion of the investigator, could constitute an unacceptable risk when taking investigational product or interfere with the interpretation of data
Any of the following specific abnormalities on screening laboratory tests:
- ALT or AST >2 x ULN, or total bilirubin ≥1.5 x ULN
- hemoglobin <9 g/dL, or total white blood cell (WBC) count <2,500/µL, or neutropenia (absolute neutrophil count <1,200/µL), or lymphopenia (lymphocyte count <750/µL)
- eGFR <50 mL/min/1.73 m2
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
Det første tilknyttede hospital ved Soochow University
|
busulfan 0.8 mg/kg/6h (days -8 to -7), fludarabine 30mg/m2/day (days -6 to -2), cyclophosphamide 25 mg/kg/day (days -5 to -2) and antithymocyte globulin(ATG) 2.5 mg/kg/day (days -5 to -2).
|
|
Peking unviversity Peoples' Hospital
|
busulfan 0.8 mg/kg/6h (days -8 to -7), fludarabine 30mg/m2/day (days -6 to -2), cyclophosphamide 25 mg/kg/day (days -5 to -2) and antithymocyte globulin(ATG) 2.5 mg/kg/day (days -5 to -2).
|
|
Guangzhou First People's Hospital,
|
busulfan 0.8 mg/kg/6h (days -8 to -7), fludarabine 30mg/m2/day (days -6 to -2), cyclophosphamide 25 mg/kg/day (days -5 to -2) and antithymocyte globulin(ATG) 2.5 mg/kg/day (days -5 to -2).
|
|
The First Affiliated Hospital of USTC
|
busulfan 0.8 mg/kg/6h (days -8 to -7), fludarabine 30mg/m2/day (days -6 to -2), cyclophosphamide 25 mg/kg/day (days -5 to -2) and antithymocyte globulin(ATG) 2.5 mg/kg/day (days -5 to -2).
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Faliure free survival (FFS)
Tidsramme: From enrollment to 2 years post-HSCT
|
survival with a response to therapy after HSCT.
Death, graft faliue and relapse were considered as treatment failure.
|
From enrollment to 2 years post-HSCT
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Forekomsten af blandet kimærisme
Tidsramme: 1 år efter HSCT
|
Den blandede kimærisme blev defineret som tilstedeværelsen af 5%-95% donorhæmatopoietiske celler.
|
1 år efter HSCT
|
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Ordrelateret toksicitet
Tidsramme: 100 dage efter HSCT
|
Den behandlingsrelaterede toksicitet (RTT) blev målt i henhold til Seattle Toxicity Criteria (Bearman et al, 1988).
|
100 dage efter HSCT
|
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Myeloid- og blodpladeindplantning
Tidsramme: 100 dage efter HSCT
|
Myeloid- og blodpladeengraftment blev defineret som internationale kriterier.
|
100 dage efter HSCT
|
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The probability of Overall survival
Tidsramme: From enrollment to 2 years post-HSCT
|
Overall survival was defined as the time from transplantation to death from any cause or to the last follow-up
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From enrollment to 2 years post-HSCT
|
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The incidence of Transplantation related mortality
Tidsramme: 2 years post HSCT
|
Transplantation related mortality was defined as death without disease progression.
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2 years post HSCT
|
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The incidence of graft versus host disease(GVHD)
Tidsramme: 100 days post HSCT for aGvHD and 2 years post HSCT for cGvHD
|
The severity of acute and chronic GVHD was evaluated according to standard criteria.
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100 days post HSCT for aGvHD and 2 years post HSCT for cGvHD
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The incidence of Cytomegalovirus(CMV) and Epstein-Barr virus(EBV) reactivation
Tidsramme: 180 days post HSCT
|
The incidence of CMV and EBV reactivation was defined as CMV and EBV viremia.
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180 days post HSCT
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
1. juni 2026
Primær færdiggørelse (Anslået)
1. december 2027
Studieafslutning (Anslået)
30. december 2029
Datoer for studieregistrering
Først indsendt
8. maj 2026
Først indsendt, der opfyldte QC-kriterier
8. maj 2026
Først opslået (Faktiske)
14. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
6. juli 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
1. juli 2026
Sidst verificeret
1. juni 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- PUPH20260508
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