TP53 is the most frequently mutated gene in cancer, but these mutations remain therapeutically non-actionable. Previous study reported arsenic trioxide could rescue structural p53 mutations, endowing p53 mutations with thermostability and transcriptional activity. Under Vivo and Vitro experiments, arsenic trioxide could reactivate mutated p53 to inhibit tumor. This trial aimed to explore the efficacy and safety of arsenic trioxide in refractory cancer patients with structural p53 mutations.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Refractory cancer patients without standard-of-care harboring TP53 mutation received Arsenic Trioxide Injection (0.16mg/kg,d1-5,ivgtt,28days as a duration)
Department of Medical Oncology, Shanghai Changzheng Hospital
Shanghai, China
RECRUITINGObjective Response Rate
Proportion of patients with reduction in tumor burden of a predefined amount, including complete remission and partial remission
Time frame: Evaluation of tumor burden based on RECIST criteria through study completion, an average of 2 months
Progress Free Survival
Time from treatment beginning until disease progression
Time frame: Evaluation of tumor burden based on RECIST criteria until first documented progress through study completion, an average of 2 months
Overall Survival
Time from treatment beginning until death from any cause
Time frame: From date of treatment beginning until the date of death from any cause, through study completion, an average of 1 months
Adverse Effect
Incidence of Treatment-related adverse Events
Time frame: Through study completion, an average of 1 months
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