- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07584317
AI-Based Multimodal Integration for Tumor Microenvironment Analysis and Response Prediction in HCC Treated With TACE Plus Immunotherapy and Targeted Therapy (CHANCE2601)
Artificial Intelligence-Based Multimodal Data Integration for Tumor Microenvironment Analysis and Response Prediction in Hepatocellular Carcinoma Patients Undergoing TACE Combined With Immunotherapy and Targeted Therapy
연구 개요
상세 설명
연구 유형
등록 (추정된)
연락처 및 위치
연구 연락처
- 이름: Zhicheng Jin, MD
- 전화번호: +86-025-83272121
- 이메일: jinzhic@foxmail.com
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
Retrospective Study Cohort 1.1 Inclusion Criteria Age ≥18 years; Patients with hepatocellular carcinoma confirmed by histopathology or clinical diagnosis; At least one intrahepatic lesion that is repeatedly measurable according to RECIST v1.1.
1.2 Exclusion Criteria Known sarcomatoid hepatocellular carcinoma or fibrolamellar hepatocellular carcinoma; Presence of other active malignancies within the past 5 years or concurrent active malignancies other than hepatocellular carcinoma; Missing preoperative imaging examinations, including CT or MRI, or poor image quality; Missing key baseline clinical data; Loss to follow-up after treatment.
- Prospective Study Cohort 2.1 Inclusion Criteria Age ≥18 years; Patients with hepatocellular carcinoma confirmed by histopathology or clinical diagnosis; Scheduled to receive first-line TACE combined with immunotherapy and targeted therapy; At least one intrahepatic lesion that is repeatedly measurable according to RECIST v1.1; Expected survival of more than 3 months. 2.2 Exclusion Criteria Known sarcomatoid hepatocellular carcinoma or fibrolamellar hepatocellular carcinoma; Presence of other active malignancies within the past 5 years or concurrent active malignancies other than hepatocellular carcinoma; Other factors that, in the investigator's judgment, make the patient unsuitable for participation in this study; Severe allergy to iodinated contrast agents that preclude imaging examinations or TACE treatment.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
개입 / 치료 |
|---|---|
|
Retrospective cohort
Patients with hepatocellular carcinoma who received TACE combined with immunotherapy and targeted therapy, as well as other treatment modalities, will be retrospectively included.
Multimodal data from this cohort will be used to develop and train the AI-based model.
|
Investigators utilize a AI-based supportive system to predict clinical outcomes for patients with hepatocellular carcinoma who received TACE combined with immunotherapy and targeted therapy
|
|
Prospective cohort
Patients with hepatocellular carcinoma who receive TACE combined with immunotherapy and targeted therapy will be prospectively enrolled.
Multimodal data, including clinical, imaging, and biospecimen-related data when available, will be collected to validate the AI-based multimodal model.
|
Investigators utilize a AI-based supportive system to predict clinical outcomes for patients with hepatocellular carcinoma who received TACE combined with immunotherapy and targeted therapy
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Prediction Performance of the AI Model
기간: From enrollment to approximately 2 years
|
The area under curve (AUC) of Receiver Operating Characteristic (ROC) curves o f the AI model in predicting the clinical outcomes in patients receiving TACE combined with immunotherapy and targeted therapy.
|
From enrollment to approximately 2 years
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
전반적인 생존(OS)
기간: 최대 약 2년
|
OS는 병용 치료를 시작한 시점부터 원인에 관계없이 사망할 때까지의 시간으로 정의됩니다.
|
최대 약 2년
|
|
Objective response rate(ORR)
기간: up to approximately 2 years
|
The ORR is defined as the proportion of patients with a documented complete response(CR) or partial response(PR) per RECIST 1.1 or per mRECIST.
|
up to approximately 2 years
|
|
Progression free survival(PFS)
기간: up to approximately 2 years
|
The PFS is defined as the time from the initiation of any combination treatment to the first documented progressive disease (according to RECIST 1.1 or mRECIST) or death due to any cause, whichever occurs first.
|
up to approximately 2 years
|
|
Other prediction performance of the model
기간: From enrollment to approximately 2 years
|
Evaluation of the accuracy, sensitivity, and specificity of the prediction model in clinical application
|
From enrollment to approximately 2 years
|
공동 작업자 및 조사자
스폰서
간행물 및 유용한 링크
일반 간행물
- Zhong BY, Fan W, Guan JJ, Peng Z, Jia Z, Jin H, Jin ZC, Chen JJ, Zhu HD, Teng GJ. Combination locoregional and systemic therapies in hepatocellular carcinoma. Lancet Gastroenterol Hepatol. 2025 Apr;10(4):369-386. doi: 10.1016/S2468-1253(24)00247-4. Epub 2025 Feb 21.
- Jin ZC, Wei J, Xiao YD, Si A, Chen JJ, Zhu XL, Li JZ, Nie F, Ding R, Zhou HF, Ding W, Zhong BY, Xie Y, Hu HT, Yin GW, Ji JS, Zhang WH, Shi HB, Wu JB, Xu GH, Yuan CW, Yang WZ, Liu RB, Wu YM, Zheng CS, Xu AB, Huang MS, Li JP, Chen L, Wen SW, Wang YQ, Gu SZ, Li D, Wang D, Zhou GH, Wang WD, Peng Z, Wang X, Zhu HD, Tian J, Teng GJ. Decoding tumor heterogeneity with imaging biomarkers predicts response to TACE plus immunotherapy and targeted therapy in HCC (CHANCE2204). Hepatology. 2025 Nov 10. doi: 10.1097/HEP.0000000000001593. Online ahead of print.
- Vithayathil M, Koku D, Campani C, Nault JC, Sutter O, Ganne-Carrie N, Aboagye EO, Sharma R. Machine learning based radiomic models outperform clinical biomarkers in predicting outcomes after immunotherapy for hepatocellular carcinoma. J Hepatol. 2025 Oct;83(4):959-970. doi: 10.1016/j.jhep.2025.04.017. Epub 2025 Apr 17.
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .