Study on the Therapeutic Effect of Irinotecan Liposomes in Small Cell Lung Cancer

Launched by TANG-DU HOSPITAL · Jun 20, 2024

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment approach for small cell lung cancer, specifically looking at the effects of a drug called irinotecan liposomes when combined with other chemotherapy drugs. The trial aims to enroll 24 patients who have experienced cancer progression after at least six months of initial treatment that included platinum-based chemotherapy. Participants will receive this new treatment to see if it can help manage their cancer more effectively.

To be eligible for this trial, patients must be 18 years or older and have been diagnosed with extensive stage small cell lung cancer. They should also have at least one measurable tumor that has shown progression after previous treatments. Participants will undergo regular check-ups, and their overall health will be closely monitored throughout the study. It’s important to note that some patients, such as those with certain heart conditions or other serious health issues, may not be able to join the trial. This study is currently recruiting, so interested individuals should discuss this opportunity with their healthcare provider to see if it may be a good fit for them.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • The patient fully understands this study, voluntarily participates and signs an informed consent form (ICF).
• • Age ≥ 18 years old;
• • Patients with extensive stage small cell lung cancer diagnosed by pathology or histology;
• • According to RECIST 1.1 standard, patients have at least one measurable target lesion; For lesions that have undergone radiation therapy in the past, they can only be included as measurable lesions if there is clear disease progression after radiation therapy;
• • Progression confirmed by imaging examination after 6 months of first-line radiotherapy and chemotherapy containing platinum drugs or platinum regimen radiotherapy and chemotherapy ± immunotherapy;
• • Eastern Cancer Collaborative Group (ECOG) physical fitness score: 0-2 points;
• • Estimated survival time ≥ 3 months;
• • Absolute neutrophil count (ANC) ≥ 1.5 x 10 \^ 9/L, platelet count ≥ 90 x 10 \^ 9/L, and hemoglobin count ≥ 90 g/L (no blood transfusion, blood products, use of granulocyte colony-stimulating factor or other hematopoietic stimulating factor correction within 14 days prior to laboratory examination);
• • Liver and kidney function: serum creatinine ≤ 1.5 times the upper limit of normal value; AST and ALT ≤ 2.5 times the upper limit of normal values (≤ 5 times the upper limit of normal values for patients with liver invasion); Total bilirubin ≤ 1.5 times the upper limit of normal value (≤ 3 times the upper limit of normal value for patients with liver invasion);
• • Women of childbearing age must undergo a pregnancy test (serum) within 7 days before enrollment, and the result is negative. They are willing to use appropriate methods of contraception during the trial period and 6 months after the last administration of the trial drug;
• Exclusion Criteria:
• • Patients with large cell neuroendocrine tumors and mixed small cell carcinoma;
• • Patients with active brain metastasis or central nervous system invasion confirmed by imaging evaluation and/or biopsy (prednisone equivalent dose ≥ 10mg);
• • There is an hypersensitivity reaction to any investigational drug or its components;
• • Severe uncontrolled concurrent infections or other serious uncontrolled concomitant diseases, moderate or severe kidney injury; (such as progressive infection, uncontrollable hypertension, diabetes, etc.);
• * Heart function and disease meet one of the following conditions:
• • 1. Long QTc syndrome or QTc interval\>480 ms;
• • 2. Complete left bundle branch block, II or III degree atrioventricular block;
• • 3. Severe and uncontrolled arrhythmias that require medication treatment;
• • 4. The New York College of Cardiology has a classification of ≥ III;
• • 5. Cardiac ejection fraction (LVEF) below 50%;
• • 6. A history of myocardial infarction, unstable angina, severe unstable ventricular arrhythmias, or any other arrhythmias requiring treatment, a history of clinically severe pericardial disease, or evidence of acute ischemic or active conduction system abnormalities on electrocardiogram within the 6 months prior to recruitment.
• • Active infection of hepatitis B and hepatitis C (hepatitis B B virus surface antigen is positive and hepatitis B B virus DNA exceeds 1x103 copies/mL; hepatitis C virus RNA exceeds 1x103 copies/mL);
• • Human Immunodeficiency Virus (HIV) infection (HIV antibody positive);
• • Has previously or currently suffered from other malignant tumors (except for effectively controlled non melanoma skin basal cell carcinoma, breast/cervical carcinoma in situ, and other malignant tumors that have not been treated and have been effectively controlled within the past five years);
• • Pregnant and lactating women, as well as patients of childbearing age who are unwilling to take contraceptive measures;
• • Patients with other malignant tumors that require treatment; The researchers determined that patients who are not suitable to participate in this study.