Third-generation EGFR-TKI Plus Anlotinib as Maintenance for NSCLC With Small Cell Transformation After EGFR-TKI Resistance

Phase 2

Not yet recruiting

• Conditions: Non-small Cell Lung Cancer
• Interventions: Drug: third-generation EGFR-TKI combined with anlotinib

• Registration Number: NCT06634667
• Lead Sponsor: Hunan Province Tumor Hospital

Brief Summary

This study aimed to evaluate the efficacy and safety of third-generation EGFR-TKI plus anlotinib as maintenance after chemotherapy plus immunotherapy in advanced NSCLC with small cell transformation after EGFR-TKI resistance.

Detailed Description

This prospective interventional clinical study aims to evaluate the efficacy and safety of third-generation EGFR-TKI combined with anlotinib as maintenance therapy following 4-6 cycles of chemotherapy and immunotherapy in patients with advanced NSCLC who developed small cell transformation after EGFR-TKI resistance.Approximately 30 non-small cell lung cancer patients who developed small cell transformation after EGFR-TKI resistance were enrolled and treated with 4-6 cycles of chemotherapy plus immunotherapy followed by maintenance therapy with third-generation EGFR-TKI combined with anlotinib.The study is expected to commence recruitment in mainland China in about November 2024. It is expected that the trial will end in December 2026.

Study Timeline

• Status Verified: 2024-10
• Study First Submitted: 2024-10-06
• Study First Submitted QC: 2024-10-08
• Last Update Submitted: 2024-10-08
• Study First Posted: 2024-10-10
• Last Update Posted: 2024-10-10
• Study Start: 2024-11-30
• Primary Completion: 2026-08-31
• Study Completion: 2027-04-30

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• 1. Understand the requirements and contents of the clinical trial, and provide a signed and dated informed consent form.
• 2. Age ≥ 18 years.
• 3. Histopathology is confirmed non-small cell lung cancer .
• 4.Patients with advanced non-small cell lung cancer (NSCLC) who experienced small cell transformation after EGFR-TKI resistance.
• 5. Predicted survival ≥ 12 weeks. .
• 6. ECOG 0-2.
• 7. Adequate bone marrow hematopoiesis and organ function.

Exclusion Criteria

• 1. History of other malignant tumors within 2 years.
• 2. Adverse events (except alopecia of any degree) of CTCAE > grade 1 due to prior treatment (e.g., adjuvant chemotherapy, radiotherapy, etc.) prior to the first dose.
• 3. History of stroke or intracranial hemorrhage within 6 months prior to the first dose.
• 4. The presence of any severe or poorly controlled systemic disease, including poorly controlled hypertension and active bleeding in the judgment of the investigator.
• 5. Subjects with persistent or active infection, including but not limited to hepatitis B (HBV), hepatitis C (HCV), human immunodeficiency virus (HIV) and COVID-19 infection.
• 6. Heart-related diseases or abnormalities
• 7. Past history of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis requiring steroid therapy or interstitial lung disease with active clinical symptoms, immune pneumonia caused by immunotherapy.
• 8. Refractory nausea and vomiting, chronic gastrointestinal disease, difficulty swallowing drugs, or inability to adequately absorb sunvozertinib or anlotinib due to previous bowel resection.
• 9. Live vaccine was given 2 weeks before the first medication.
• 10. Women who are breastfeeding or pregnant.
• 11. Hypersensitivity to the test drug and the ingredients.
• 12. Other conditions assessed by the investigator to be unsuitable for participation in the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
The experimental cohort	third-generation EGFR-TKI combined with anlotinib	third-generation EGFR-TKI combined with anlotinib

Primary Outcome Measures

Name	Time	Method
progression-free survival (PFS)	Time from standard chemotherapy plus immunotherapy to study completion, or up to 36 month	PFS was defined as the duration from the start of standard chemotherapy plus immunotherapy to disease progression or last follow up

Secondary Outcome Measures

Name	Time	Method
Objective Response Rate (ORR)	Time from standard chemotherapy plus immunotherapy to study completion, or up to 36 month	To assess overall response rate according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 by investigator, define as the proportion of subjects who have a complete response (CR) or a partial response (PR)
Adverse events (AEs) according to CTCAE 5.0	Time from standard chemotherapy plus immunotherapy to study completion, or up to 36 month	Number of participants with adverse events (AEs) according to CTCAE 5.0

Trial Locations

Locations (1)

Yongchang Zhang; 🇨🇳 Changsha, Hunan, China