This is a perspective clinical study to assess the safety and efficacy of PD-1 inhibitors in patients with LT. Eligible patients have recurrent or metastatic cancer after LT, are not amenable to, or refractory after, locoregional therapy or to a curative treatment approach (eg, surgery, or ablation) and have previously been treated with sorafenib or other targeted therapy, either intolerant to this treatment or show radiographic progression after treatment. Biopsy is needed to exclude patients with positive allograft PD-L1 expression.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
240mg I.V. Q3W
Shanghai Zhongshan Hospital
Shanghai, Shanghai Municipality, China
RECRUITINGSerious Adverse Event Rate
the occurrence rate of serious adverse event after PD-1 inhibitor treatment
Time frame: 1.5 years
Acute Graft Rejection Rate
the occurrence rate of acute graft rejection after PD-1 inhibitor treatment
Time frame: 1.5 years
Objective Response Rate
Objective Response Rate after PD-1 inhibitor treatment
Time frame: 3 years
Progression Free Survival Rate
survival time after PD-1 inhibitor treatment till tumor progression
Time frame: 3 years
Over all survival Rate
survival time after PD-1 inhibitor treatment till patient death
Time frame: 3 years
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