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Study for novel molecular markers for predicting the targeting and immunotherapeutic effects of hepatic carcinoma

Study for novel molecular markers for predicting the targeting and immunotherapeutic effects of hepatic carcinoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900028222
Enrollment
Unknown
Registered
2019-12-15
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

Advanced hepatic carcinoma

Interventions

Group 1:Sorafenib treatment
Group 2:Camrelizumab treatment
Group 3:Sorafenib combined with Camrelizumab treatment

Sponsors

Lanzhou University Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) According to clinical symptoms, signs and related imaging, pathological examination, and positive AFP, patients with a clear diagnosis of HCC (refer to Hepatobiliary Cancers NCCN Clinical Practice Guideline in Oncology, Version 4.2017); (2) Aged 18 to 70 years old, life expectancy >=12 weeks; (3) According to the Solid Tumor Response Assessment Criteria (RECIST), there is at least one tumor lesion (no local treatment), and the target lesion has not received local treatment; (4) The lesion is >5mmx5mmx5mm; (5) those who have received topical treatment, such as surgery, radiofrequency ablation, hepatic artery embolization, chemotherapy, radiotherapy, percutaneous puncture or cryoablation, but the target lesion volume increased by more than 25% and stopped for more than 4 weeks; (6) with or without extrahepatic metastases; (7) The Eastern Cancer Cooperative Group (ECOG) score =60x10^9/L; hemoglobin >=85 g/L; prothrombin time international normalized ratio INR =28g/L; total bilirubin <=51.3umol/L; alanine transferase and aspartate transferase <=5 ULN; (11) Renal function: blood creatinine <=1.5 ULN.

Exclusion criteria

Exclusion criteria: (1) Previous systemic treatment (including novel molecular targeted therapy); (2) There are serious infections in the clinic; (3) Patients suspected of drug allergy and serious adverse reactions; (4) Patients who are concurrently unable to assess the efficacy of other serious disease researchers; (5) Those who are in critical condition and need to live in the ICU; (6) Patients with renal insufficiency, who may have pregnancy in March before and after the study.

Design outcomes

Primary

MeasureTime frame
Disease-free survival;Overall survival;Disease control rate;Objective response rate;

Countries

China

Contacts

Public ContactWang Chen

Lanzhou University Second Hospital

wcdfjack@163.com13909483134

Outcome results

None listed

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