About this trial
To evaluate the efficacy and safety of liposome irinotecan combined with platinum and immune checkpoint inhibitor combined with antirotinib maintenance therapy after first-line induction
Eligibility criteria
Qualifiers
Volunteer to join the study, sign the informed consent and sign the date, have good compliance, and cooperate with follow-up
Age≥18 years
Diagnosis of extensive stage small cell lung cancer (ES-SCLC) confirmed histologically or pathologically (according to American Veterans Lung Cancer Association, VALG staging)
ECOG 0-2
Disqualifiers
Patients with meningeal metastases or symptomatic brain metastases
Previous T cell co-stimulation or immune checkpoint therapy, including but not limited to cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) inhibitors, PD-1 inhibitors, PD-L1/2 inhibitors, CD137 agonists, or other targeting T cell drugs;
Past treatment with anlotinib
Factors affecting oral medication, such as inability to swallow, post-GI resection, chronic diarrhea, intestinal obstruction, etc
Trial design
Treatments tested in this trial
- Liposome Irinotecan
- Platinum
- Tislelizumab
- Anlotinib