Fruquintinib Plus Irinotecan in the Treatment of Advanced Gastric Cancer

NCT ID: NCT05643677

Last Updated: 2022-12-09

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 47 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-12-31
• Study Completion Date: 2025-11-30

Brief Summary

This study explores the efficacy and safety of fruquintinib combined with irinotecan in the second-line treatment of patients with advanced gastric cancer, aiming to bring more second-line treatment options for patients with advanced gastric cancer.

Detailed Description

This study was a single-arm, open-label, single-center phase II study. A total of 47 patients with advanced gastric cancer who had previously failed standard first-line therapy were recruited to receive combined treatment with fruquintinib and irinotecan. The patients' progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), overall survival (OS) and safety were evaluated.

Conditions

Gastric Cancer

Study Design

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

Study Groups

Fruquintinib combined with irinotecan

Fruquintinib combined with irinotecan as a second-line treatment for advanced gastric cancer

Group Type: EXPERIMENTAL

Fruquintinib

Intervention Type: DRUG

4 mg PO, QD (3 weeks on, 1 week off)

Irinotecan

Intervention Type: DRUG

participants will receive irinotecan, 100 mg/m2, intravenous drip, day1 and day 14 of every 4 weeks

Interventions

Fruquintinib

4 mg PO, QD (3 weeks on, 1 week off)

Intervention Type: DRUG

Irinotecan

participants will receive irinotecan, 100 mg/m2, intravenous drip, day1 and day 14 of every 4 weeks

Intervention Type: DRUG

Other Intervention Names

Elunate

Eligibility Criteria

Inclusion Criteria

1. Have fully understood this study and voluntarily signed informed consent;

2. ≥18 years old;

3. Histologically and/or cytologically confirmed metastatic or locally advanced gastric cancer or gastroesophageal conjunctive adenocarcinoma with at least one previous systemic therapy (note: Previous systemic treatment options approved by this protocol include single-drug or multi-drug combination chemotherapy or chemotherapy combined with immunotherapy, or failure of anti-HER-2 targeted therapy after positive HER-2);

4. At least one extragastric measurable lesion according to RECIST v1.1 criteria;

5. ECOG physical condition 0-1;

6. BMI≥18；

7. The expected survival time ≥12 weeks;

8. The functions of vital organs during the first 14 days of enrollment met the following requirements:

• Neutrophil absolute count ≥1.5×109/L;
• Platelet ≥80×109/L;
• hemoglobin ≥90g/L;
• Total bilirubin < 1.5 ULN;
• ALT and AST < 2.5 ULN (< 5 ULN in patients with liver metastasis);
• Serum creatinine (Cr) ≤1.5×ULN or creatinine clearance (CCr)≥60ml/min;
• endogenous creatinine clearance > 50ml/min;

9. Effective contraceptive measures should be taken by women of childbearing age or by men whose partners wish to have children;

10. Good compliance, cooperate with follow-up.

Exclusion Criteria

1. Prior treatment with VEGF or VEGFR inhibitors;

2. Past treatment with irinotecan (However, patients who had previously received neoadjuvant or failed postoperative adjuvant therapy could be included as first-line therapy）;

3. Had participated in other drug clinical trials and received at least one drug therapy within 4 weeks prior to enrollment or had received other systemic antitumor therapy including chemotherapy, signal transduction inhibitors, immunotherapy, other investigational drugs;

4. Had other malignancies within 5 years prior to inclusion, except basal cell or squamous cell carcinoma of the skin after radical resection, or carcinoma in situ of the cervix;

5. The patient has a current disease or condition that affects drug absorption, or the patient is unable to take fuquinitinib orally;

6. Subjects who are allergic to the study drug or any of its adjuncts;

7. Electrolyte abnormalities identified by the investigator as clinically significant;

8. Hypertension that was not controlled by medication before enrollment was defined as: systolic blood pressure ≥150mmHg and/or diastolic blood pressure ≥100 mmHg;

9. Prior to enrollment, active gastric and duodenal ulcers, ulcerative colitis and other digestive diseases, active bleeding in unresectable tumors, or other conditions that researchers determined may cause gastrointestinal bleeding and perforation;

10. Patients with significant evidence or history of bleeding tendency within 3 months prior to enrollment (bleeding within 3 months>30 mL, hematemesis, black feces, hematochezia), hemoptysis (within 4 weeks>5 mL fresh blood) or a thromboembolic event (including stroke and/or transient ischemic attack) within 12 months;

11. History of severe cardiovascular and cerebrovascular diseases:

• Cerebrovascular accident (excluding lacunar infarction, mild cerebral ischemia or transient ischemic attack), myocardial infarction, unstable angina, and poorly controlled arrhythmia (including QTc interval ≥450ms for male and 470 ms for female) within 6 months before the first administration of the study drug (QTc interval ≥ 490ms for female) Fridericia formula);
• New York Heart Association (NYHA) Cardiac Function Rating &gt; Grade II or left ventricular ejection fraction (LVEF) < 50%;

12. Clinically uncontrolled active infections, such as acute pneumonia, active hepatitis B or C (previous history hepatitis B virus infection regardless of drug control, hepatitis B virus DNA≥1×104 copies /mL or &gt; 2000 IU/ml);

13. Symptomatic brain or meningeal metastases (except those with brain metastases that have undergone local radiotherapy or surgery for more than 6 months and whose disease control is stable);

14. Women who are pregnant (tested positive for pregnancy before medication) or who are breastfeeding;

15. Two consecutive urine routine tests indicated urine protein ≥2+, and the 24-hour urine protein volume was reexamined &gt; 1.0g;

16. Patients with clinical symptoms of ascites or pleural effusion;

17. The patients were not considered suitable for inclusion in this study.

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

Sponsors

Fujian Medical University

OTHER

Sponsor Role: lead

Responsible Party

Xi Shi

archiater

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Xi Shi

Role: PRINCIPAL_INVESTIGATOR

First Affiliated Hospital of Fujian Medical University

Central Contacts

Xi Shi

Role: CONTACT

Phone: 13960769368

Email: ittsxi@163.com

Other Identifiers

HMPL-013-E1-GC001

Identifier Type: -

Identifier Source: org_study_id