Trifluridine/Tipiracil Combined With Cetuximab in the Treatment of Third-line and Above RAS/BRAF Wild-type mCRC

Colorectal Cancer Metastatic Clinical Trial

Official title:

Trifluridine/Tipiracil Combined With Cetuximab in the Treatment of Third-line and Above RAS/BRAF Wild-type Metastatic Colorectal Cancer: A Single-center, Prospective Phase Ib/II Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06379399
• Other study ID #: IRB-2023-1072
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: April 2024
• Est. completion date: December 2025

Study information

• Verified date: April 2024
• Source: Zhejiang Cancer Hospital
• Contact: Wangxia Lv
• Phone: +86-13757141026
• Email: lvwangxia[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is a single-center, prospective, single-arm exploratory study aimed at evaluating the efficacy and safety of trifluridine/tipiracil in combination with cetuximab in the treatment of third-line and above RAS/BRAF wild-type metastatic colorectal cancer.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 26
• Est. completion date: December 2025
• Est. primary completion date: March 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patient able and willing to provide written informed consent and to comply with the study protocol and follow-up inspection.

2. Histologically or cytologically confirmed metastatic adenocarcinoma of the colon; excluding appendiceal and anal canal cancers.

3. Previously received at least second-line treatment, including two standard treatment regimens (such as fluoropyrimidine, capecitabine, irinotecan, oxaliplatin with or without anti-VEGF or anti-EGFR agents), if previously received first-line anti-EGFR therapy, achieving at least a partial response (PR) or above, with a discontinuation interval of at least one year.

4. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.

5. Measurable disease by computed tomography (CT) or magnetic resonance imaging (MRI) (based on RECIST 1.1 criteria, with the longest diameter of tumor lesions on CT/MRI scan =10mm, and the shortest diameter of lymph node lesions on CT/MRI scan =15mm).

6. Wild-type RAS/BRAF gene detected.

7. Able to take oral medication.

8. Normal organ function, meeting the following criteria within 14 days before treatment initiation:

• Neutrophil count =1.5×10^9/L;

• Platelet count =75×10^9/L;

• Hemoglobin =9.0g/dL;

• Aspartate aminotransferase (AST) =2.5×upper limit of normal (ULN) (or =5×ULN if liver metastases);

• Alanine aminotransferase (ALT) =2.5×ULN (or =5×ULN if liver metastases);

• Total bilirubin =1.5×ULN;

• Creatinine clearance (calculated by Cockcroft and Gault formula) >60mL/min or serum creatinine =1.5×ULN;

9. Expected survival time >3 months (90 days).

10. Women of childbearing potential must have used reliable contraception for 7 days prior to enrollment, have had a negative pregnancy test, and agree to use appropriate contraception methods during the trial and for 6 months after the last dose of investigational drug. Men must agree to use appropriate contraception methods or have undergone surgical sterilization during the trial and for 6 months after the last dose of investigational drug.

Exclusion Criteria:

1. Prior treatment with Trifluridine/Tipiracil;

2. Patients with known dMMR or MSI-H advanced colorectal cancer who have not previously received anti-PD-1 or PD-L1 inhibitors;

3. Participation in another drug clinical trial or receipt of systemic chemotherapy, radiotherapy, or biologic therapy within the past 4 weeks;

4. Known or suspected brain metastases;

5. Synchronous or metachronous cancer with a disease-free survival of =5 years (except for colorectal cancer) excluding cured or curatively treated mucosal cancers (esophageal cancer, gastric cancer, cervical cancer, non-melanoma skin cancer, bladder cancer, etc.);

6. Factors significantly affecting oral drug absorption, such as dysphagia, chronic diarrhea, and gastrointestinal obstruction; uncontrolled Crohn's disease or ulcerative colitis;

7. Symptomatic malignant effusion requiring symptomatic treatment (including pleural effusion, ascites, pericardial effusion);

8. Pregnant or lactating women; patients with reproductive potential unwilling or unable to use effective contraceptive measures;

9. Known allergy to the investigational drug, drug class, or its components;

10. Requirement for systemic corticosteroid therapy (excluding local steroids and cetuximab pre-treatment);

11. History of interstitial lung disease (interstitial pneumonia, pulmonary fibrosis, etc.) or radiographic evidence of interstitial lung disease;

12. Active local or systemic infections requiring treatment;

13. New York Heart Association (NYHA) functional classification =II or severe heart disease;

14. Known human immunodeficiency virus (HIV) infection or acquired immunodeficiency syndrome (AIDS) or history of active hepatitis B or hepatitis C;

15. Unresolved toxicity (CTCAE>Grade 1) or incomplete recovery from previous cancer surgery.

16. Patients deemed unsuitable for the study by the investigator.

Related Conditions & MeSH terms

• Colorectal Cancer Metastatic
• Colorectal Neoplasms

Intervention

Drug:
• Cetuximab
Cetuximab will be administered at a fixed dose of 500 mg/m2 once every 2 weeks;
• Trifluridine/Tipiracil
Phase I: 6 patients (male and female) will be enrolled to evaluate safety. Patients will receive Trifluridine/Tipiracil at a dose of 35mg/m2 (maximum single dose of 80 mg). Patients will be followed up for Dose-Limiting Toxicities (DLTs) (2 Cycles, Day 1-Day 28). If =2 patients experience DLTs (2 Cycles, Day 1-Day 28), the study will proceed to Phase II with a dose of 35mg/m2. If =3 patients experience DLTs (2 Cycles, Day 1-Day 28), the study will proceed to Phase II with a dose of 30mg/m2. Based on the results of the 35mg/m2 dose group, 6 patients (male and female) will be enrolled in the 30mg/m2 dose group to evaluate safety. Patients will be followed up for DLTs (2 Cycles, Day 1-Day 28). If =2 patients experience DLTs (1 Cycle, Day 1-Day 28), the study will proceed with a dose of 30mg/m2 in Phase II. Phase II: Trifluridine/Tipiracil: po, twice daily from Day 1-5, every two weeks, based on the recommended dose from Phase I;

Locations

Country	Name	City	State
China	Zhejiang Cancer Hospital	Hangzhou	Zhejiang

Sponsors (1)

Lead Sponsor	Collaborator
Wangxia LV

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression-free survival (PFS)	Progression-free survival defined as the time elapsed between the randomization and the date of radiologic tumour progression according to RECIST version 1.1 by investigator's judgement or death from any cause, whichever comes first.	Approximately 12 months
Secondary	Overall survival (OS)	Overall survival defined as the observed time elapsed between the date of first treatment and the date of death due to any cause.	Approximately 12 months
Secondary	Overall Response Rate (ORR)	Objective Response Rate defined as the proportion of patients with objective evidence of complete response (CR) or partial response (PR) according to RECIST version 1.1 criteria and using investigator's tumor assessment.	Approximately 12 months
Secondary	Disease Control Rate( DCR)	Disease Control Rate defined as the proportion of patients with objective evidence of CR or PR or stable disease (SD) according to RECIST version 1.1 criteria and using investigator's tumor assessment.	Approximately 12 months
Secondary	Quality of life: EORTC QLQ-C30	Assess patients health and activities using the European Organization for Research and Treatment of Cancer Core Quality of Life (EORTC QLQ-C30) module.	Approximately 12 months
Secondary	Adverse Events(safety)	Adverse events were recorded according to Common Terminology Criteria for Adverse Events (version 5.0) of the National Cancer Institute that participants received at least one dose of protocol treatment after randomization.	Up to 28 days after discontinuation of study drug or start of subsequent therapy.