Surufatinib Combined With Irinotecan as a Second-line Treatment for Small Cell Lung Cancer

NCT ID: NCT05595889

Last Updated: 2022-11-29

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-12-01
• Study Completion Date: 2025-09-30

Brief Summary

To evaluate the clinical efficacy and safety of surufatinib combined with irinotecan in the second line treatment of small cell lung cancer.

Detailed Description

According to the inclusion and exclusion criteria, 40 patients with small cell lung cancer who failed to receive standard first-line therapy were selected to evaluate the efficacy and safety of surufatinib combined with irinotecan in the second-line treatment of small cell lung cancer.

Conditions

Small Cell Lung Cancer; Angiogenesis; Chemotherapy Effect

Study Design

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

Study Groups

Surufatinib combined with irinotecan

Surufatinib combined with irinotecan as a second-line treatment for small cell lung cancer

Group Type: EXPERIMENTAL

Surufatinib

Intervention Type: DRUG

250 mg/day p.o. QD

Irinotecan

Intervention Type: DRUG

Participants will receive irinotecan，100 mg/m2，Intravenous drip, day 1 and day 8 of every 3 weeks

Interventions

Surufatinib

250 mg/day p.o. QD

Intervention Type: DRUG

Irinotecan

Participants will receive irinotecan，100 mg/m2，Intravenous drip, day 1 and day 8 of every 3 weeks

Intervention Type: DRUG

Other Intervention Names

SULANDA

Eligibility Criteria

Inclusion Criteria

• Age ≥18 years; Volunteer to participate in the trial and sign informed consent;
• Small cell lung cancer diagnosed by histopathology;
• Previous failure to receive first-line standard treatment was defined as intolerable toxic and side effects, disease progression during treatment, or recurrence after treatment; Intolerability was defined as grade IV (thrombocytopenia grade III and above) for hematologic toxicity and grade III or above for nonhematologic toxicity. Note: Each line of drug refers to medication for at least 1 cycle regardless of single drug or multi-drug combination;
• ECOG score: 0-1;
• At least one lesion detectable by CT, according to RECIST 1.1;
• Expected survival ≥12 weeks;
• At least one measurable lesion (RECIST 1.1 criteria, see Appendix 2);
• The functions of major organs and bone marrow are basically normal:
• Blood routine: white blood cell ≥ 4.0 x 109/L, neutrophil ≥ 1.5 x 109/L, platelet ≥ 100 x 109/L, hemoglobin ≥ 90 g/L; A) International normalized ratio (INR) ≤1.5× upper limit of normal (ULN), and activated partial thromboplastin time (APTT) ≤1.5×ULN; B) Liver function: total bilirubin ≤ 1.5 x ULN; In the absence of liver metastasis, ALT/AST /ALP ≤ 2.5 x ULN; ALT/AST /ALP ≤ 5 x ULN in patients with liver metastasis; C) Renal function: serum creatinine ≤ 1.5 x ULN, and creatinine clearance (CCr) 60 mL/min (see Appendix 6); D) Normal cardiac function, left ventricular ejection fraction (LVEF) ≥ 50% by two-dimensional echocardiography.
• Brain metastases must have been asymptomatic or treated and stabilized after discontinuation of steroids and anticonvulsants for at least 1 month prior to study treatment;
• Patients of childbearing age (including female and female partners of male patients) must take effective birth control measures;
• Good compliance is expected, and the efficacy and adverse reactions can be followed up according to the protocol requirements.

Exclusion Criteria

• Small cell lung cancer with other pathological types of tumors;
• Previously received anti-angiogenic drugs, including bevacizumab, sovanitinib, sunitinib, sorafenib, anlotinib, apatinib, etc.
• Receive the following treatments within the first 4 weeks of treatment, including but not limited to surgery, chemotherapy, radical radiotherapy, biotargeted therapy, immunotherapy, and other investigational drugs;
• Pregnant or lactating women;
• With pleural effusion or ascites, respiratory syndrome (≥CTC AE grade 2 dyspnea);
• Symptomatic brain or meningeal metastases (except those who have undergone local radiotherapy or surgery for brain metastases for more than 6 months and have stable disease control);
• Severe infection (e.g., intravenous infusion of antibiotics, antifungals, or antivirals) within 4 weeks prior to treatment, or unexplained fever > 38.5 ° C during screening/initial administration;
• Hypertension that is not well controlled with antihypertensive medication (systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg)
• The urine routine indicated urinary protein ≥2+, and 24-hour urinary protein quantity >1.0g;
• Obvious clinical bleeding symptoms or obvious bleeding tendency within 3 months before treatment (bleeding > 30 mL within 3 months, hematemesis, melanism, blood in stool), hemoptysis (fresh blood > 5 mL within 4 weeks), etc. Or treatment for a venous/venous thrombotic event in the previous 6 months, such as a cerebrovascular accident (including transient ischemic attack, cerebral hemorrhage, cerebral infarction), deep vein thrombosis, and pulmonary embolism; Long-term anticoagulant therapy with warfarin or heparin or long-term antiplatelet therapy (aspirin ≥300 mg/day or clopidogrel ≥75 mg/day) is required;
• Active heart disease, including myocardial infarction and severe/unstable angina, developed 6 months before treatment. Echocardiography showed left ventricular ejection fraction < 50% and poor arrhythmia control (including QTcF interval, > 450 ms in men and > 470 ms in women).
• The patient had had other malignancies (except cured basal cell carcinoma of the skin and carcinoma in situ of the cervix) within the previous 3 years or at the same time.
• Known allergy to the study drug or any of its excipients;
• Active or uncontrolled severe infections;

1. Known human immunodeficiency virus (HIV) infection;

2. A known history of clinically significant liver disease, including viral hepatitis [known hepatitis B virus (HBV) carriers must exclude active HBV infection, i.e., HBV DNA positivity (>1×104 copies /mL or >2000 IU/ mL);

3. Known hepatitis C virus infection (HCV) and HCV RNA positive (>1×103 copies /mL), or other hepatitis, liver cirrhosis];

• Any other disease, with clinical significance of metabolic abnormalities, abnormal physical examination or laboratory abnormalities, according to researchers, there is reason to suspect the patient has not suitable for the use of study drugs of a disease or condition (such as have a seizure and require treatment), or will affect the interpretation of results, or to make patients in high-risk situations;
• Other conditions deemed inappropriate for inclusion by the investigator.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fujian Cancer Hospital

OTHER_GOV

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Zhiyong He

Role: STUDY_CHAIR

Fujian Cancer Hospital

Central Contacts

Zhiyong He

Role: CONTACT

heyong1015@163.com

13805086391

Meifang Li

Role: CONTACT

362952772@qq.com

15985795022

Other Identifiers

HMPL-012-E1-SCLC-001

Identifier Type: -

Identifier Source: org_study_id