Efficacy and Safety of Vorolanib Monotherapy As Third-line or Later Treatment for Advanced Non-small Cell Lung Cancer Patients: a Single-arm, Prospective, Open-label Phase II Clinical Study

Launched by LI-KUN CHEN · Dec 8, 2024

Keywords

ClinConnect Summary

This clinical trial is studying the effectiveness and safety of a drug called Vorolanib for patients with advanced non-small cell lung cancer (NSCLC) who have already tried at least two other treatments. The goal is to see how well Vorolanib can help control the cancer when used on its own, particularly in patients whose cancer has continued to grow or come back after previous therapies. The study will involve 32 participants, and they will take Vorolanib daily for as long as it helps, or until they experience serious side effects, choose to leave the study, or sadly, if they pass away.

To be eligible for this trial, participants must be adults with a confirmed diagnosis of advanced NSCLC and have measurable cancer lesions. They should have received at least two prior treatments and have a good performance status, meaning they can carry out daily activities with minimal issues. Patients must also have normal organ function and not have certain health complications that could affect their safety during the study. Those who join can expect regular check-ups and monitoring to evaluate how well the treatment is working and to watch for any side effects. This trial aims to gather more information on how Vorolanib works, which could help doctors offer new options for patients with advanced lung cancer in the future.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Sign the informed consent
• • 2. Pathologically or cytologically diagnosed with metastatic/relapsed advanced NSCLC, with measurable lesions (according to RECIST 1.1)
• • 3. Previously received at least two systemic therapies, allowing for third-line or higher chemotherapy or unable to tolerate chemotherapy
• • 4. Patients with negative results for driver gene testing or patients with positive results who have already received relevant targeted drugs or systemic anti-tumor treatments and are either resistant or unable to tolerate them
• • 5. Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2. Expected survival time ≥ 3 months
• • 6. Normal major organ function: renal function with creatinine clearance rate ≥ 60 mL/min; liver function with bilirubin ≤ 1.5× upper limit of normal (ULN), ALT/AST ≤ 2.5× ULN (for patients with documented liver metastasis, AST and ALT levels ≤ 5× ULN)
• • 7. Good hematological function, defined as an absolute neutrophil count (ANC) ≥ 1.5×10\^9/L, platelet count ≥ 100×10\^9/L, hemoglobin ≥ 90g/L (without blood transfusion or erythropoietin \[EPO\] dependency within the last 7 days)
• • 8. Good coagulation function, defined as an international normalized ratio (INR) or prothrombin time (PT) ≤ 1.5× ULN; if the subject is on anticoagulation therapy, PT should be within the intended therapeutic range of the anticoagulant
• • 9. Female patients of childbearing potential must agree to use contraception (e.g., intrauterine device, contraceptives, or condoms) during the study and for 6 months after the study ends; must not be breastfeeding and must have a negative serum or urine pregnancy test within 7 days before enrollment. Male patients must agree to use contraception during the study and for 6 months after the study ends
• • 10. Patients with well-controlled pleural or peritoneal effusions that do not cause grade 2 or higher respiratory syndrome (≥ CTCAE grade 2) can be included
• • 11. Patients without clinical symptoms of intracranial hypertension caused by brain metastases or with brain metastasis symptoms that are stable after prior treatment (radiation therapy or surgery) of brain or meningeal metastasis (usually requiring more than 4 weeks post-radiation therapy)
• Exclusion Criteria:
• • 1. Previously failed treatment with multi-target anti-angiogenic drugs, such as anlotinib, cabozantinib, apatinib, lenvatinib, etc. The use of bevacizumab is allowed, but the last administration must be more than 3 weeks before enrollment
• • 2. Small cell lung cancer (including small cell carcinoma, non-small cell lung cancer mixed with other types of tumors)
• • 3. Testing positive for driver genes but not treated with TKIs
• • 4. Tumor invasion of large blood vessels, central squamous cell carcinoma of the lung with cavitation, or non-small cell lung cancer with hemoptysis (\>5ml/day), or where the tumor is likely to invade important blood vessels and cause fatal bleeding during the subsequent study period
• • 5. Accompanied by other types of malignant tumors within the past 5 years or currently
• • 6. Planning to receive systemic anti-tumor therapy within 4 weeks before enrollment or during the study period, including cytotoxic therapy, signal transduction inhibitors, and immunotherapy (or mitomycin C within 6 weeks before receiving experimental drug therapy); received extended-field radiation therapy (EF-RT) within 4 weeks before enrollment or limited-field radiation therapy within 2 weeks before enrollment with evaluation of lesions recommended
• • 7. Unremitting toxic reactions caused by previous treatment, CTCAE grade \>1, excluding hair loss
• • 8. Various factors affecting oral medication (such as inability to swallow, gastrointestinal resection, chronic diarrhea, bowel obstruction)
• • 9. Pleural effusion or ascites leading to respiratory syndrome (≥CTCAE grade 2)
• • 10. Symptoms of brain metastasis not controlled and treated within 2 months
• • 11. Presence of any severe or uncontrolled disease
• • 12. Major surgery, open biopsy, or significant traumatic injury within 28 days before enrollment
• • 13. Bleeding diathesis or history of significant bleeding, regardless of severity; any wound, ulcer, or fracture that has not healed following a bleeding or bleeding event (≥CTCAE grade 3)
• • 14. Arterial/venous thrombosis within 6 months, such as cerebrovascular accident (including transient ischemic attack), venous thrombosis, pulmonary embolism
• • 15. History of substance abuse that cannot be quit or diagnosed with psychiatric disorders
• • 16. Participated in other clinical trials of anti-tumor drugs within 4 weeks
• • 17. Diagnosed with diseases that severely jeopardize patient safety or affect the completion of this study
• • 18. Known history of human immunodeficiency virus (HIV) infection (i.e., HIV 1/2 antibody positive); untreated active hepatitis B; active HCV infection (HCV antibody positive and HCV-RNA levels above detection limit)