Vitamin E Combined With Fruquintinib and Tislelizumab in Microsatellite Stabilized Metastatic Colorectal Cancer Patients

NCT ID: NCT05771181

Last Updated: 2025-06-12

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 25 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-03-01
• Study Completion Date: 2027-02-28

Brief Summary

The goal of this clinical trial is to learn about efficacy of Vitamin E in combination with Fuquinitinib and Tirelizumab in patients with microsatellite stabilized mCRC who have failed standard therapy. The main question is to explore the survival time, safety and tolerability of the treatment. At the same time, the correlation between biomarkers (including PD-L1 expression, tumor mutation load, lymphocyte subpopulation, cytokines, TCR, intestinal microbes, and others) and the efficacy and drug resistance mechanism will be analyzed, so as to provide reference for the subsequent guidance of the screening of benefit groups.

Detailed Description

Dietary supplements are commonly used during conventional cancer treatment. Vitamin E has a variety of functions, including enhancing immunity, anti-inflammation, and anti-oxidation. Tislelizumab is an anti-PD-1 monoclonal antibody, and furoquininib is a tyrosine kinase inhibitor that inhibits tumor angiogenesis. Studies have shown that immunotherapy combined with furoquininib has initial efficacy in the treatment of colorectal cancer. Whether vitamin E combined with immunotherapy and furoquininib can improve the prognosis of patients with colorectal cancer deserves to be studied. Therefore, the objective of this study is to evaluate the efficacy and safety of Vitamin E in combination with Fuquinitinib and Tirelizumab in patients with microsatellite stabilized mCRC who have failed standard therapy.

Conditions

Colorectal Cancer; Microsatellite Stable Colorectal Carcinoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Vitamin E in combination with Fuquinitinib and Tislelizumab

Patients will be treated with Vitamin E, Fuquinitinib and Tislelizumab.

Group Type: EXPERIMENTAL

Vitamin E

Intervention Type: DRUG

Vitamin E: 400mg (QD), oral, once daily, continued until disease progression or intolerable toxicity.

Fruquintinib

Intervention Type: DRUG

Fuquinitinib: 5mg (QD) orally for 2 weeks, 1 week off, repeated every 3 weeks until disease progression or intolerable toxicity.

Tislelizumab

Intervention Type: DRUG

Tislelizumab: 200mg intravenously every 3 weeks (Q3W), was administered until the occurrence of unacceptable toxic effects, or disease progression, withdrawal of consent, or withdrawal as judged by the investigator.

Interventions

Vitamin E

Vitamin E: 400mg (QD), oral, once daily, continued until disease progression or intolerable toxicity.

Intervention Type: DRUG

Fruquintinib

Fuquinitinib: 5mg (QD) orally for 2 weeks, 1 week off, repeated every 3 weeks until disease progression or intolerable toxicity.

Intervention Type: DRUG

Tislelizumab

Tislelizumab: 200mg intravenously every 3 weeks (Q3W), was administered until the occurrence of unacceptable toxic effects, or disease progression, withdrawal of consent, or withdrawal as judged by the investigator.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age ≥18 years old, both sexes;

2. Patients with histologically or cytologically confirmed unresectable and metastatic CRC;

3. Recist1.1-defined disease progression or intolerance to prior standard therapy during or after standard therapy. Standard therapy was required to include all the following agents: fluorouracilines, chemotherapy agents such as irinotecan, and oxaliplatin, with or without an anti-VEGF monoclonal antibody (e.g., bevacizumab). Left-sided KRAS/NRAS/BRAF wild-type subjects received combined anti-EGFR mAb (cetuximab or panitumumab).

4. Before enrollment, the tumor tissue was pMMR by immunohistochemistry, or MSS or MSI-L by PCR or NGS;

5. Patients with ECOG score of 0-1 and expected survival time ≥3 months, patients who can cooperate to observe adverse reactions and efficacy;

6. At least one measurable tumor lesion according to RECIST 1.1 criteria;

7. Good organ function:

1. neutrophil ≥1.5*109/L; Platelet ≥100*109/L; Hemoglobin ≥9g/dl; Serum albumin ≥3g/dl;

2. Thyroid stimulating hormone (TSH) ≤ 1 times the upper limit of normal, T3 and T4 in the normal range;

3. bilirubin ≤ 1.5 times the upper limit of normal value; ALT and AST≤ 2 times the upper limit of normal;

4. Serum creatinine ≤ 1.5 times the upper limit of normal, creatinine clearance ≥60ml/min;

5. International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 times the upper limit of the normal range, unless the patient is receiving anticoagulant therapy and the PT value is within the intended range for anticoagulant therapy;

6. Activated partial thromboplastin time (aPTT) ≤ 1.5 times the upper limit of normal;

8. There were no serious concomitant diseases that could make the survival time less than 5 years;

9. Negative pregnancy test in female subjects (for female patients of childbearing potential); Infertile female patients;

10. Male patients of childbearing potential and female patients of childbearing potential and at risk of pregnancy must agree to use adequate contraception for the entire duration of the study and for 12 months after receiving treatment with the protocol;

11. Signed and dated informed consent indicating that the patient has been informed about all relevant aspects of the study;

12. Patients who are willing and able to comply with the visit schedule, treatment plan, laboratory tests, and other study procedures;

13. Willing to comply with the arrangement during the study period can not participate in any other clinical research on drugs and medical devices.

Exclusion Criteria

1. Pathological diagnosis of other intestinal tumors, such as gastrointestinal stromal tumor;

2. Tumor tissues were dMMR detected by immunohistochemistry, or MSI-H detected by PCR or NGS

3. Prior treatment with PD-1 antibody, PD-L1 antibody, or CTLA-4 antibody;

4. Previous or concurrent history of other malignant tumors, excluding adequately treated non-melanoma skin cancer, cervical carcinoma in situ and thyroid papillary carcinoma;

5. Active autoimmune disease, history of autoimmune disease (such as interstitial pneumonia, colitis, hepatitis, hypophysitis, vasculitis, nephritis, hyperthyroidism, hypothyroidism, including but not limited to these diseases or syndromes); It does not include autoimmune-mediated hypothyroidism treated with stable doses of thyroid replacement hormone; Type I diabetes on stable doses of insulin; Vitiligo or cured childhood asthma/allergy without any intervention in adulthood;

6. A history of immunodeficiency, including HIV positive, other acquired or congenital immunodeficiency diseases, or organ transplantation or allogeneic bone marrow transplantation;

7. Contraindications to antiangiogenic drugs (such as active bleeding, gastrointestinal bleeding, hemoptysis, etc.);

8. History of interstitial lung disease (excluding radiation pneumonitis without steroid treatment) and non-infectious pneumonia;

9. Patients with active pulmonary tuberculosis infection detected by medical history or CT examination, or with a history of active pulmonary tuberculosis infection within 1 year before enrollment, or with a history of active pulmonary tuberculosis infection more than 1 year before enrollment but without regular treatment;

10. The subject has active hepatitis B (HBV DNA ≥2000 IU/mL or 104 copies/mL), hepatitis C (hepatitis C antibody positive and HCV-RNA above the detection limit of the assay)

11. Severe cardiopulmonary and renal dysfunction;

12. Have hypertension that is not well controlled with antihypertensive medication (systolic blood pressure ≥140mmHg or diastolic blood pressure ≥90mmHg);

13. A history of psychotropic substance abuse, alcohol or drug abuse;

14. Other factors that may affect subject safety or trial compliance as judged by the investigator. Severe medical conditions requiring concomitant treatment (including mental illness), serious laboratory abnormalities, or other family or social factors.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fudan University

OTHER

Sponsor Role: lead

Responsible Party

Li Dawei

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Dawei Li, PhD

Role: PRINCIPAL_INVESTIGATOR

Fudan University

Locations

270 Dongan Road, Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

Dawei Li, PhD

Role: CONTACT

li_dawei@fudan.edu.cn

+8613774201693

Zhiyu Chen, PhD

Role: CONTACT

chanhj@aliyun.com

+8618721841159

Facility Contacts

Dawei Li, PhD

Role: primary

li_dawei@fudan.edu.cn

+8613774201693

Zhiyu Chen, PhD

Role: backup

chanhj@aliyun.com

+8618721841159

Other Identifiers

VENTIF

Identifier Type: -

Identifier Source: org_study_id