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Predictive and prognostic significance of liquid biopsy based molecular responce in advanced cholangiocarcinoma

Predictive and prognostic significance of liquid-biopsy-based molecular responce in advanced cholangiocarcinoma

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000035845
Enrollment
Unknown
Registered
2020-08-18
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-08-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cholangiocarcinoma

Interventions

all:systemic therapy for unresectable advanced cholangiocarcinoma

Sponsors

Renji Hospital, School of Medicine, Shanghai Jiao Tong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 120 Years

Inclusion criteria

Inclusion criteria: 1. the patient voluntarily signs the informed consent form; 2. Aged >=18 years old; 3. histologically or cytologically confirmed advanced intra- or extra-hepatic cholangiocarcinoma which is unresectable 4. measurable leisons >=1 (based on RECIST 1.1); 5. the estimated survival time >=3 months; 6. Well compliance and to be able to follow-up; 7. the patient is with the desire of ctDNA test before and after therapy.

Exclusion criteria

Exclusion criteria: 1. pregnant or lactational woman; 2. the baseline hCG test was postive or female patient of reproductive age did not receive hCG test; 3. fertile patients who refused to contraception; 4. patient with attack of other malignancy in 5 years(exculde cured basal cell carcinoma and cervical carcinoma in situ); 5. patient with central nerve system disease; 6. recent cardiovascular disease, include cerebrovascular accient within 6 months, heart infraction with in 6 months, unstable angina, congestive heart failure grade II or above(NYHA classification),severe arrhythmia and uncontroled hypertension; 7. uncontroled severe infection; 8. severe liver or renal disfunction.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate, ORR;Progression-Free-Survival, PFS;

Secondary

MeasureTime frame
overall survival, OS;

Countries

China

Contacts

Public ContactWang Xuan

Renji Hospital, School of Medicine, Shanghai Jiao Tong University

doctor.wxa@163.com+86 15216680015

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026