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RIC Regimen for Elderly or High Comorbidity Burden Patients Receiving Haplo-HSCT

Primary Purpose

Acute Leukemia, Myelodysplastic Syndromes

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Cytarabine
Sponsored by
Peking University People's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Leukemia focused on measuring RIC regimen, comorbidity, elderly, haploidentical, transplant-related mortality

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients older than 55 years or those with HCT-CI scores of ≥3, without ISD nor URD, receiving haplo-HSCT

Exclusion Criteria:

  • patients having identical sibling or unrelated donors; patients with active infection; patients having organ failure; patients with poor compliance.

Sites / Locations

  • Peking University, Institute of HematolgoyRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

RIC regimen

Arm Description

Old patients or those have high comorbidity burden without identical sibling donor or unrelated donor would receive RIC haplo-HSCT. RIC preconditioning regimen consisted of cytarabine (2 g/m2/day, days -10 to -9), busulfan (3.2 mg/kg/day on days -8 to -6), cyclophosphamide (1.0 g/m2/day, days -5 to -4), fludarabine (30 mg/m-2/day, days -6 to -2), semustine (250 mg/m-2, day -3), and rabbit antithymocyte globulin (thymoglobulin, 2.5 mg/kg/d, days -5 to -2; Sanofi, France).

Outcomes

Primary Outcome Measures

Transplant-related mortality
Death without disease progression or relapse

Secondary Outcome Measures

Full Information

First Posted
January 21, 2018
Last Updated
September 23, 2020
Sponsor
Peking University People's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03412409
Brief Title
RIC Regimen for Elderly or High Comorbidity Burden Patients Receiving Haplo-HSCT
Official Title
Reduced Intensity Conditioning Regimen for Elderly or High Comorbidity Burden Patients Receiving Haploidentical Hematopoietic Stem Cell Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2018 (Actual)
Primary Completion Date
September 1, 2021 (Anticipated)
Study Completion Date
September 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University People's Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study aimed to evaluate the efficacy of reduced intensity conditioning (RIC) regimen in elderly or high comorbidity burden patients who receive haploidentical hematopoietic stem cell transplantation (haplo-HSCT). Haplo-HSCT is an effective treatment option for patients who did not have identical sibling donor (ISD) or unrelated donor (URD). However, post-transplant transplant-related mortality (TRM) is one of the major causes for transplant failure, and the risk of TRM for old patients or those with high comorbidity burden was higher. RIC regimen may decrease the risk of TRM for haplo-HSCT recipients. The study hypothesis: Using RIC haplo-HSCT regimen in elderly patients or those with high comorbidity burden can reduce TRM and improve survival.
Detailed Description
RIC regimen was given for elderly patients or those with high comorbidity burden who would receive haplo-HSCT. The elderly patients were defined as older than 55 years. The burden of comorbidities in HSCT recipients was assessed based on the hematopoietic cell transplantation-specific comorbidity index (HCT-CI), and patients with score ≥3 were assigned as high burden. The primary end point was transplant-related mortality, and the secondary endpoints included overall survival, disease-free survival, relapse, engraftment, graft-versus-host disease (GVHD), and infections. Following time is 1 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Leukemia, Myelodysplastic Syndromes
Keywords
RIC regimen, comorbidity, elderly, haploidentical, transplant-related mortality

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
RIC regimen
Arm Type
Experimental
Arm Description
Old patients or those have high comorbidity burden without identical sibling donor or unrelated donor would receive RIC haplo-HSCT. RIC preconditioning regimen consisted of cytarabine (2 g/m2/day, days -10 to -9), busulfan (3.2 mg/kg/day on days -8 to -6), cyclophosphamide (1.0 g/m2/day, days -5 to -4), fludarabine (30 mg/m-2/day, days -6 to -2), semustine (250 mg/m-2, day -3), and rabbit antithymocyte globulin (thymoglobulin, 2.5 mg/kg/d, days -5 to -2; Sanofi, France).
Intervention Type
Drug
Intervention Name(s)
Cytarabine
Other Intervention Name(s)
Busulfan, Cyclophosphamide, Fludarabine, Semustine, Antithymocyte globulin
Intervention Description
RIC preconditioning regimen consisted of cytarabine (2 g/m2/day, days -10 to -9), busulfan (3.2 mg/kg/day on days -8 to -6), cyclophosphamide (1.0 g/m2/day, days -5 to -4), fludarabine (30 mg/m-2/day, days -6 to -2), semustine (250 mg/m-2, day -3), and rabbit antithymocyte globulin (thymoglobulin, 2.5 mg/kg/d, days -5 to -2; Sanofi, France).
Primary Outcome Measure Information:
Title
Transplant-related mortality
Description
Death without disease progression or relapse
Time Frame
Participants will be followed for an expected average of 1 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients older than 55 years or those with HCT-CI scores of ≥3, without ISD nor URD, receiving haplo-HSCT Exclusion Criteria: patients having identical sibling or unrelated donors; patients with active infection; patients having organ failure; patients with poor compliance.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiao-Dong Mo, MD
Phone
8610-8832-6001
Email
mxd453@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Xiao-Dong Mo
Phone
8610-8832-4577
Email
mxd453@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiao-Jun Huang
Organizational Affiliation
Institute of Hematology, Peking University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking University, Institute of Hematolgoy
City
Beijing
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiao-Dong Mo

12. IPD Sharing Statement

Citations:
PubMed Identifier
33718234
Citation
Sun YQ, Han TT, Wang Y, Yan CH, Wang FR, Wang ZD, Kong J, Chen YH, Chen H, Han W, Chen Y, Zhang YY, Zhang XH, Xu LP, Liu KY, Huang XJ. Haploidentical Stem Cell Transplantation With a Novel Conditioning Regimen in Older Patients: A Prospective Single-Arm Phase 2 Study. Front Oncol. 2021 Feb 26;11:639502. doi: 10.3389/fonc.2021.639502. eCollection 2021.
Results Reference
derived

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RIC Regimen for Elderly or High Comorbidity Burden Patients Receiving Haplo-HSCT

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