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Anlotinib Treatment in Steroid Depenent/Refractory cGVHD

Primary Purpose

Chronic Graft-versus-host-disease

Status
Terminated
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Anlotinib
Sponsored by
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Graft-versus-host-disease

Eligibility Criteria

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

Inclusion Criteria:

  1. Participants must be diagnosed as hematopoiesis disorders and receiving hematopoietic stem cells transplantation.
  2. Steroid dependent or refractory classic chronic GVHD disease defined as modified National Institutes of Health criteria(2014) below at any time post-hematopoietic cell transplant(post-HCT)

    1. Dependent disease, defined as, when glucocorticoid (prednisolone doses greater than or equal to(<=) 0.25mg/kg/day or <=0.5mg/kg every other day(prednisolone doses) due to recurrence or progression of cGVHD manifestations, it is considered as steroid-dependent disease if the lowest tapering dose of the second occasion is equal or higher than the lowest tapering dose of the first occasion
    2. Refractory disease, defined as, when cGVHD manifestations progress despite the use of a regime containing glucocorticoid (prednisolone at >=1mg/kg/day for at least 1 week) or persist without improvement despite continued treatment with glucocorticoid (prednisolone at >=0.5mg/kg/day or 1mg/kg every other day) for at least 4 weeks.
  3. Participants must be receiving baseline systemic glucocorticoid therpy for cGVHD at study entry. The dose of steroids must be stable for 14 days prior to starting anlotinib.
  4. At the time of trial enrollment, participants may be receiving other immunosuppressive therapies in addition to glucocorticoids. Immunosuppressant doses must be stable for 14 days prior to starting anlotinib.
  5. Neutrophil≥1.5×109/L,platelet≥50×109/L
  6. Karnofsky or Lansky performance status>=60
  7. Participants should sign the agreement.

Exclusion Criteria:

  1. Known or suspected active acute GVHD.
  2. Current treatment with a tyrosine kinase inhibitor, purin analogs or other cancer chemotherapy in the 4weeks prior to starting study drug.
  3. Concomitant use of warfarin or other Vitamin K antogonists.
  4. Known bleeding disorders or hemophilia.
  5. Known history of human immunodeficiency virus or active with hepatitis C. virus or hepatitis B virus.
  6. Uncontrolled infections not responsive to antibiotics, antiviral medicines, or antifungal medicine or recent infection requiring systemic treatment .

Sites / Locations

  • Hematology Department

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

therapy

Arm Description

therapy with 1 arm. Anlotinib 8mg qd po。

Outcomes

Primary Outcome Measures

Overall response rate as the percentage of participants with response.
Overall response rate is defined as the proportion of subjects who achieved complete response CR or partial response PR. Response criteria are based on NIH cGVHD Response assessment.

Secondary Outcome Measures

Duration of Response (DOR)
DOR is defined as the duration of time from the date of initial response

Full Information

First Posted
January 15, 2020
Last Updated
March 22, 2021
Sponsor
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT04232397
Brief Title
Anlotinib Treatment in Steroid Depenent/Refractory cGVHD
Official Title
A Phase 2 Study of Anlotinib in Subjects With Steroid Depenent/Refractory Chronic Graft Versus Host Disease(cGVHD)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Terminated
Why Stopped
the efficency is not good enough to enroll more patients
Study Start Date
April 10, 2020 (Actual)
Primary Completion Date
September 15, 2020 (Actual)
Study Completion Date
March 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a single center, single arm, prospective, phase II clinical study. The main purpose of this study is to evaluate the efficacy and safety of anlotinib in the treatment of steroid dependent/refractory chronic graft-versus-host disease (cGVHD) after allogeneic peripheral blood stem cell transplantation (allo HSCT).
Detailed Description
Anlotinib 8mg qd po for 6months if no progression in 4weeks or reach PR in 3months

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Graft-versus-host-disease

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
therapy
Arm Type
Experimental
Arm Description
therapy with 1 arm. Anlotinib 8mg qd po。
Intervention Type
Drug
Intervention Name(s)
Anlotinib
Intervention Description
anlotinib 8mg qd po
Primary Outcome Measure Information:
Title
Overall response rate as the percentage of participants with response.
Description
Overall response rate is defined as the proportion of subjects who achieved complete response CR or partial response PR. Response criteria are based on NIH cGVHD Response assessment.
Time Frame
1year
Secondary Outcome Measure Information:
Title
Duration of Response (DOR)
Description
DOR is defined as the duration of time from the date of initial response
Time Frame
1year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participants must be diagnosed as hematopoiesis disorders and receiving hematopoietic stem cells transplantation. Steroid dependent or refractory classic chronic GVHD disease defined as modified National Institutes of Health criteria(2014) below at any time post-hematopoietic cell transplant(post-HCT) Dependent disease, defined as, when glucocorticoid (prednisolone doses greater than or equal to(<=) 0.25mg/kg/day or <=0.5mg/kg every other day(prednisolone doses) due to recurrence or progression of cGVHD manifestations, it is considered as steroid-dependent disease if the lowest tapering dose of the second occasion is equal or higher than the lowest tapering dose of the first occasion Refractory disease, defined as, when cGVHD manifestations progress despite the use of a regime containing glucocorticoid (prednisolone at >=1mg/kg/day for at least 1 week) or persist without improvement despite continued treatment with glucocorticoid (prednisolone at >=0.5mg/kg/day or 1mg/kg every other day) for at least 4 weeks. Participants must be receiving baseline systemic glucocorticoid therpy for cGVHD at study entry. The dose of steroids must be stable for 14 days prior to starting anlotinib. At the time of trial enrollment, participants may be receiving other immunosuppressive therapies in addition to glucocorticoids. Immunosuppressant doses must be stable for 14 days prior to starting anlotinib. Neutrophil≥1.5×109/L,platelet≥50×109/L Karnofsky or Lansky performance status>=60 Participants should sign the agreement. Exclusion Criteria: Known or suspected active acute GVHD. Current treatment with a tyrosine kinase inhibitor, purin analogs or other cancer chemotherapy in the 4weeks prior to starting study drug. Concomitant use of warfarin or other Vitamin K antogonists. Known bleeding disorders or hemophilia. Known history of human immunodeficiency virus or active with hepatitis C. virus or hepatitis B virus. Uncontrolled infections not responsive to antibiotics, antiviral medicines, or antifungal medicine or recent infection requiring systemic treatment .
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
xianmin song, M.D.
Organizational Affiliation
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hematology Department
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200080
Country
China

12. IPD Sharing Statement

Learn more about this trial

Anlotinib Treatment in Steroid Depenent/Refractory cGVHD

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