SALIRI Based Regimen as First-line Treatment for Advanced Metastatic Colorectal Cancer

NCT ID: NCT05160896

Last Updated: 2023-06-08

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 90 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-11-12
• Study Completion Date: 2023-06-30

Brief Summary

The objective is to investigate the efficacy and safety of raltitrexed combined with Irinotecan (SALIRI) based regimen as first-line treatment for advanced metastatic colorectal cancer(mCRC).

Detailed Description

A number of previous studies show that raltitrexed combined with oxaliplatin/irinotecan as first-line treatment for advanced metastatic colorectal cancer(mCRC) is safe and effective. Chinese registered clinical studies show that raltitrexed combined with oxaliplatin has better safety and overall clinical efficacy than 5-FU combined with oxaliplatin in the treatment of mCRC. However, there is no study data on raltitrexed plus irinotecan (SALIRI) combined with targeted drugs as first-line treatment for mCRC in Chinese patients. This an open-label, multi-center, and prospective phase Ⅱ study enroled mCRC patients treated with first-line raltitrexed plus Irinotecan (SALIRI) based chemotherapy. Plan to to enroll 90 patients. The primary outcome is Overall Response Rate(ORR). The secondary Outcomes are Progression Free Survival (PFS)，Overall Survival (OS)，disease control rate (DCR)，the occurrence of adverse reactions(AEs)，and Quality of Life [WHO-QOL].

Conditions

Advanced Metastatic Colorectal Cancer

Study Design

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

Study Groups

MSS or MSI-L/pMMR, RAS and BRAF are both wild type

the primary lesion is located in the left colorectal:

SALIRI plus cetuximab

One cycle (cycle duration 14 days) consists of:

Raltitrexed 2 mg/m² iv, 15min. day 1 Irinotecan 180 mg/m² iv, 30 - 90 min. day 1 cetuximab 500 mg/ m² , iv, day 1

the primary lesion is located in the right colorectal:

SALIRI plus bevacizumab

One cycle (cycle duration 14 days) consists of:

Raltitrexed 2 mg/m² iv, 15min. day 1 Irinotecan 180 mg/m² iv, 30 - 90 min. day 1 Bevacizumab 5 mg/kg, iv, day 1

Group Type: EXPERIMENTAL

Raltitrexed

Intervention Type: DRUG

Raltitrexed 2 mg/m² iv, 15min. day 1

Irinotecan

Intervention Type: DRUG

Irinotecan 180 mg/m² iv, 30 - 90 min. day 1

Bevacizumab

Intervention Type: DRUG

Bevacizumab 5 mg/kg, iv, day 1

Cetuximab

Intervention Type: DRUG

cetuximab 500 mg/ m² , iv, day 1

Interventions

Raltitrexed

Raltitrexed 2 mg/m² iv, 15min. day 1

Intervention Type: DRUG

Irinotecan

Irinotecan 180 mg/m² iv, 30 - 90 min. day 1

Intervention Type: DRUG

Bevacizumab

Bevacizumab 5 mg/kg, iv, day 1

Intervention Type: DRUG

Cetuximab

cetuximab 500 mg/ m² , iv, day 1

Intervention Type: DRUG

Other Intervention Names

Sai Wei Jian; CPT-11; Avastin; ERBITUX

Eligibility Criteria

Inclusion Criteria

1. 18-75 years old.

2. Life expectancy ≥ 3 months.

3. Patients with unresectable advanced colorectal cancer confirmed by histology or cytology.

4. Patients with initially treated metastatic colorectal cancer who were assessed to be unable to undergo radical surgery，or recurrence and metastasis more than 6 months after receiving radical surgery adjuvant chemotherapy, and the metastases can not be removed.

5. At least one measurable lesion by CT or MRI according to RECIST1.1 criteria.

6. ECOG 0 ~ 1.

7. The major organs were functioning normally, and the laboratory examination results within 1 week met the following conditions before enrollment: ①Absolute neutrophil count (ANC)≥1.5×109/L ②Platelet count（PLT）≥90.0 × 109/L ③Hemoglobin concentration（HB） ≥90g/L④ Total bilirubin（TBI）≤1.5×ULN ⑤ Serum creatinine （Cr）≤l.5×ULN ，Endogenous creatinine clearance >60ml/min（Cockcroft-Gault Formula ）⑥Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), Alkaline phosphatase(AP): ≤2.5 ×ULN (≤5 ×ULN for metastases to liver).

8. Women of child-bearing age must undergo a pregnancy test within 7 days prior to enrollment and have a negative result, and are willing to use an appropriate method of contraception during the trial and within 6 months after the last trial drug is given. For men who agree to use an appropriate method of contraception during the trial and up to six months after the last administration of the trial drug.

9. Sign the informed consent voluntarily.

Exclusion Criteria

1. Allergic to any research drug and its excipients.

2. There is a history of brain metastases, uncontrolled spinal cord compression, or cancerous meningitis, or newly discovered evidence of brain or Pia Mater Disease.

3. History of other malignancies, except cured Basal cell or squamous Cell Carcinoma of the skin and carcinoma in situ of the cervix.

4. Participate in another clinical trial within 30 days prior to admission and receive a research drug and any concomitant therapy containing a research drug.

5. Any of the following events occurred during the first 6 months in Group A: cerebrovascular accident (including stroke or transient ischemic attack) , myocardial infarction, severe/unstable angina, coronary/peripheral artery bypass graft, and congestive heart failure NYHA Grade III or IV, drug-treated or clinically significant Arrhythmia, prolonged Q-T interval of ECG, etc.

6. Bowel obstruction or incomplete bowel obstruction, history of inflammatory bowel disease or extensive Colectomy, 50% or extensive small bowel resection with chronic diarrhea.

7. The presence of an active infection or a concomitant disease that seriously endangers the patient's safety or affects the patient's ability to complete the study.

8. Other conditions that the researchers think should be ruled out.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ying Yuan, Ph.D&MD

Role: PRINCIPAL_INVESTIGATOR

Second Affiliated Hospital, School of Medicine, Zhejiang University

Locations

the Second Affiliated Hospital of Medical College of Zhejiang University

Hangzhou, Zhejiang, China

Site Status: RECRUITING

Countries

China

Central Contacts

Ying Yuan, Ph.D&MD

Role: CONTACT

yuanying1999@zju.edu.cn

13858193601

Facility Contacts

Ying Yuan

Role: primary

yuanying1999@zju.edu.cn

13858193601

Other Identifiers

SALIRI-2021

Identifier Type: -

Identifier Source: org_study_id