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).
Anlotinib 8mg qd po for 6months if no progression in 4weeks or reach PR in 3months
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5
anlotinib 8mg qd po
Hematology Department
Shanghai, Shanghai Municipality, China
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.
Time frame: 1year
Duration of Response (DOR)
DOR is defined as the duration of time from the date of initial response
Time frame: 1year
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