About this trial
A total of 66 patients were enrolled in this exploratory study and randomly assigned to cohort 1 and cohort 2, with 33 patients in each group. Cohort 1: Neoadjuvant therapy (benmelstobart combined with chemotherapy and anlotinib, 3 cycles, every 21 days is a cycle). Surgery was performed 4-6 weeks after the final administration of benmelstobart as assessed by the investigator. Adjuvant therapy was evaluated by the investigator 4-6 weeks after surgery. Patients who achieved R0 resection received adjuvant therapy (benmelstobart combined with anlotinib, 12 cycles, every 21 days is a cycle). Cohort 2: Neoadjuvant therapy (benmelstobart combined with chemotherapy, 3 cycles, every 21 days is a cycle). Surgery was performed 4-6 weeks after the final administration of benmelstobart as assessed by the investigator. Adjuvant therapy was evaluated by the investigator 4-6 weeks after surgery. Patients who achieved R0 resection received adjuvant therapy (benmelstobart, every 21 days is a cycle) .
Eligibility criteria
Qualifiers
Patients voluntarily participate in this study, sign the informed consent form, demonstrate good compliance, and cooperate with follow-up.
Aged 18 to 75 years (inclusive) at the time of signing informed consent, regardless of gender.
Histologically confirmed small cell lung cancer (SCLC).
Confirmed as stage I-IIIB SCLC (T1-3N0-2M0) per AJCC 9th Edition.
Disqualifiers
Histologically confirmed mixed-type SCLC.
Extensive-stage SCLC.
ECOG PS >1.
Active or untreated CNS metastases confirmed by CT/MRI during screening/prior imaging.
Trial design
Treatments tested in this trial
- benmelstobart combined with chemotherapy and anlotinib
- benmelstobart combined with chemotherapy
Treatment groups
Locations
Sponsors and collaborators
Tang-Du Hospital
Lead sponsor