Prospective, Single-arm, Phase II Clinical Study of Irinotecan Hydrochloride Liposome Injection Combined With Platinum and Immune Checkpoint Inhibitors Combined With Anlotinib for the Maintenance of Extensive Small Cell Lung Cancer After First-line Induction

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorChina Medical University, China

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

Treatment groups

31 Participants
are divided into 1 treatment group