A Study of Neoadjuvant Tislelizumab With SBRT in Patients With Resectable Hepatocellular Carcinoma (Notable-HCC)
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|ClinicalTrials.gov Identifier: NCT05185531|
Recruitment Status : Recruiting
First Posted : January 11, 2022
Last Update Posted : November 21, 2022
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|Condition or disease||Intervention/treatment||Phase|
|Hepatocellular Carcinoma||Combination Product: PD-1 plus stereotactic body radiotherapy||Phase 1|
A baseline core tumor biopsy and peripheral venous blood will be collected from eligible participants at screening, and sample tumor tissue from the surgical specimen and PBMC (peripheral blood mononuclear cell) will be snap-frozen and stored for the future relevant studies.
Eligible patients will receive SBRT (8 Gy × 3 fractions, every other day) on day 1, day 3 and day 5; the first dose of Tislelizumab will be administrated concurrently on day 1, then the second on day 22 (the first day of week 4, ± 3 days). Then on day 50 (the first day of week 8, ± 7 days), curative liver resection of HCC will be scheduled.
Patients will be reviewed following completion of SBRT and tislelizumab treatment (Follow-up visit 1; FU1) prior to surgery.
Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST v1.1) and HCC-Specific mRECIST criteria will be used to determine patient response to treatment, including CR (complete response), PR (partial response) and ORR (objective response rate). PBMC will be collected again and stored.
Hepatic resection will be performed as per standard of care. The safety FU2 will be conducted after the first dose of the post-resection tislelizumab. All AEs that occur prior to the visit will be recorded. Participants with on-going AEs at the visit will be followed up by principal investigator (PI) or delegate until resolution or stabilization of the event. Following FU2, participants will be assessed every 3 months (±7 days) thereafter to collect information regarding disease status and survival. Long-term follow-up will continue, for each patient, for a total of 5 years.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||20 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Phase Ib Study of Neoadjuvant Tislelizumab With Stereotactic Body Radiotherapy in Patients With Resectable Hepatocellular Carcinoma|
|Actual Study Start Date :||March 1, 2022|
|Estimated Primary Completion Date :||October 2023|
|Estimated Study Completion Date :||December 2024|
PD-1(Tislelizumab) plus stereotactic body radiotherapy
Combination Product: PD-1 plus stereotactic body radiotherapy
neoadjuvant PD-1(Tislelizumab) plus stereotactic body radiotherapy (8 Gy × 3 fractions) in resectable HCC
- Delay to surgery [ Time Frame: Up to Day 92 ]number of patients experiencing a surgery delay over 6 weeks or later
- ORR after neoadjuvant SBRT+Tislelizumab [ Time Frame: One day before resection ]ORR on pre-resection imaging according to the RECIST v1.1/ mRECIST criteria
- Pathologic response rate on evaluation of the resected specimen [ Time Frame: One month after resection ]pCR (pathological complete response), pPR (pathological partial response), MPR (major pathologic response)
- Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability] [ Time Frame: 2 months after resection ]Safety and tolerability of the sequential SBRT/tislelizumab based on National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v5.0 criteria, including all grade irAEs (Immune-related adverse events) and irAE of grade 3/4.
- Disease-free survival disease-free survival (DFS) [ Time Frame: From date of resection until the date of first documented progression, assessed up to 3 years ]DFS (disease-free survival) after successful curative resection of tumor
- Overall survival [ Time Frame: From date of resection until the date of death from any cause, assessed up to 5 years ]OS (overall survival) after successful curative resection of tumor
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
|Ages Eligible for Study:||18 Years to 80 Years (Adult, Older Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Written informed consent for the trial.
- Aged ≥18 years
- Willing to provide tissue from an excisional biopsy of a tumor lesion
- Confirmed diagnosis of HCC. The diagnosis can be established radiographically by the criteria of the American Association for the Study of the Liver (AASLD), or by histologic diagnosis from the core biopsy.
- Have measurable disease by Computed Tomography (CT)-scan or Magnetic Resonance Imaging (MRI) defined by RECIST (Response Evaluation Criteria In Solid Tumours) 1.1 criteria and HCC specific mRECIST (modified RECIST).
- Medically fit to undergo surgery as determined by the treating medical and surgical oncology team
- ECOG (Eastern Cooperative Oncology Group) performance status 0 or 1
- Adequate organ and marrow function as defined below:
1) leukocytes ≥3,000/mcL 2) absolute neutrophil count ≥1,500/mcL 3) platelets ≥100,000/mcL 4) total bilirubin ≤ 2 × institutional upper limit of normal (ULN) 5) AST (aspartate aminotransferase)/ALT(alanine aminotransferase) ≤ 3 × institutional ULN 6) creatinine ≤ 1.5 × institutional ULN OR 7) estimated glomerular filtration rate (GFR) ≥50 mL/min/1.73 m2 (according to the Cockcroft-Gault formula) 9. Overall Child-Pugh class A 10. Documented virology status of hepatitis, as confirmed by screening tests for HBV (hepatitis B virus) and HCV (hepatitis C virus)
- For patients with active HBV: HBV DNA <2000 IU/mL during screening, and have initiated anti-HBV treatment at least 14 days prior to SBRT and willingness to continue anti-HBV treatment during the study (per local standard of care; e.g., entecavir).
- Patients with HCV, either with resolved infection (as evidenced by detectable antibody and negative viral load) or chronic infection (as evidenced by detectable HCV RNA), are eligible.
11. Participants with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.
12. Female patient of childbearing potential should have a negative serum pregnancy test within 24 h of her first dose of IMP (Investigational Medicinal Product) 13. Women of childbearing potential must be willing to use a highly effective method of contraception for the course of the study through 5 months after the last dose of IMP. Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the patient.
14. Sexually active males must agree to use an adequate method of contraception starting with the first dose of IMP through 7 months after the last dose of study therapy. Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the patient.
- Extrahepatic metastasis
- Prior systemic anticancer treatment for HCC, including an anti-PD-1, anti-PD-L1 or anti-CTLA-4 antibody
- Prior orthotopic liver transplantation
- Prior abdominal irradiation
- Any major surgery within the 3 weeks prior to enrolment
- Hepatic encephalopathy
- Ascites that is refractory to diuretic therapy
- Is currently receiving anti-cancer therapy (chemotherapy, radiation therapy, immunotherapy or biologic therapy) or has participated or is participating in a study of an IMP or used an investigational device within 4 weeks of the first dose of IMP
- Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy
- Known history of active Bacillus Tuberculosis (TB)
- History of known hypersensitivity to any monoclonal antibody or any of their excipients
- Known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin that has undergone potentially curative therapy, or in situ cervical cancer
- Active autoimmune disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (eg. thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment
- Active infection requiring systemic therapy, with exceptions relating to Hepatitis B and C virus infection
- History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the patient's participation for the full duration of the trial, or is not in the best interest of the patient to participate, in the opinion of the treating Principal Investigator (PI)
- Known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
- Pregnant or breastfeeding
- Known history of Human Immunodeficiency Virus (HIV; HIV 1/2 antibodies)
- Received a live vaccine within 30 days of first dose of IMP administration.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05185531
|Contact: Lei Zhao, MD||+86 531 firstname.lastname@example.org|
|Contact: Jinbo Yue, MD||+86 531 email@example.com|
|Shandong Cancer Hospital and Institute||Recruiting|
|Jinan, Shandong, China, 250117|
|Contact: Lei Zhao, MD +86 053167626368 firstname.lastname@example.org|
|Principal Investigator:||Lei Zhao||Shandong Cancer Hospital and Institute|
|Responsible Party:||Lei ZHAO, Professor, Shandong Cancer Hospital and Institute|
|Other Study ID Numbers:||
|First Posted:||January 11, 2022 Key Record Dates|
|Last Update Posted:||November 21, 2022|
|Last Verified:||November 2022|
|Individual Participant Data (IPD) Sharing Statement:|
|Plan to Share IPD:||No|
|Studies a U.S. FDA-regulated Drug Product:||No|
|Studies a U.S. FDA-regulated Device Product:||No|
stereotactic body radiotherapy, SBRT
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Digestive System Neoplasms
Neoplasms by Site
Digestive System Diseases