Phase II Single-arm Clinical Study of PD-1 Antibody and Bevacizumab in the Treatment of Relapsed or Refractory High-risk Gestational Trophoblasitc Neoplasia After Second-line or Above Combined Chemotherapy

Who is this study for? Patients with relapsed or refractory high-risk gestational trophoblasitc neoplasia after second-line or above combined chemotherapy
What treatments are being studied? PD-1 inhibitor+Bevacizumab
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Gestational trophoblastic Neoplasia(GTN) is a kind of malignant tumor in women of childbearing age. It is easy to metastasized through the blood system in the early stage, so it is a relatively malignant tumor. The tumor is highly sensitive to chemotherapy, and low-risk patients have good prognosis, with survival rate and cure rate approaching 100%, but high-risk patients are prone to drug resistance, or relapse after remission. For relapsed, refractory, high-risk GTN, multiple remedies have been reported in the literature, but the remission rate is only 75-80%. For relapsed or refractory high-risk GTN, multiple remedies have been reported in the literature, but the remission rate is only 75-80%. Currently, targeted therapy and immunotherapy are widely used in various refractory solid tumors. For GTN, there are also a number of related studies. In this study, PD-1 inhibitors combined with bevacizumab were used to treat refractory high-risk GTN with relapse or drug resistance after receiving previous second-line or above multidrug combination therapy, to study the efficacy and safety of the treatment regimen.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Signed Informed Consent

• Clinically diagnosed as recurrent or drug-resistant trophoblastic tumor

• After treatment with at least two or more multidrug chemotherapy regimens

• Survival is expected to exceed 3 months

• Age ≥18 years, age ≤75 years

• Karnofsky score ≥60分,ECOG score ≤2分

• No serious complications

• Take effective contraceptives during treatment

• Patients can be followed up as required

⁃ Blood test within 3 days: ANC≥1.5×109/L, PT ≥100×109/L, Hb≥90g/L, BIL ≤ 1.5 times of the high limit of normal value, ALT/ALST ≤ 1.5 times of the high limit of normal value, BUN and Cr≤ normal value

⁃ Coagulation function, thyroid function and myocardial enzyme in the normal range

Locations
Other Locations
China
Women's Hospital School of Medicine Zhejiang University
RECRUITING
Hangzhou
Contact Information
Primary
Xing Xie, phD
panzimin@163.com
+8613606705128
Backup
Zimin Pan, MD
panzimin@zju.edu.cn
+8613758142505
Time Frame
Start Date: 2021-04-15
Estimated Completion Date: 2026-04-15
Participants
Target number of participants: 20
Treatments
Experimental: Double medicine combined
participants received 200mg of PD-1 inhibitors combined 15mg of bevacizumab per square body surface area intravenously every 3 weeks
Related Therapeutic Areas
Sponsors
Leads: Women's Hospital School Of Medicine Zhejiang University

This content was sourced from clinicaltrials.gov

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