Teng-Fei Chen,1 Zhan-Jiang Li,2 Hua-Si Zhao,1 Rui Yang2 1Department of Respiratory Medicine Ward 2, The First Affiliated Hospital of Zhengzh
Teng-Fei Chen,1 Zhan-Jiang Li,2 Hua-Si Zhao,1 Rui Yang2 1Department of Respiratory Medicine Ward 2, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, People’s Republic of China; 2Department of Respiratory Medicine Ward 1, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, People’s Republic of ChinaCorrespondence: Rui Yang, Department of Respiratory Medicine Ward 1, The First Affiliated Hospital of Zhengzhou University, No. 1 East Jian-She Road, Erqi District, Zhengzhou, 450052, People’s Republic of China, Tel +86- 13592645178, Email yrain2012@126.comObjective: This study aims to evaluate the efficacy and safety of anlotinib combined with immune checkpoint inhibitors (ICIs) in patients with previously immunotherapy-treated extensive-stage small cell lung cancer (ES-SCLC).Methods: This retrospective study screened ES-SCLC patients who experienced failure after prior ICIs-based treatment and received anlotinib combined with ICIs therapy clinically. Anlotinib was administered at a standard dosage, ICIs regimens included PD-1 inhibitors (Tislelizumab, 200 mg; serplulimab, 4.5 mg/kg) and PD-L1 inhibitors. Efficacy and safety data during treatment were retrospectively collected, and patients were followed up regularly to obtain long-term survival data. Subgroup analysis was conducted to identify the differences in treatment outcomes in various baseline characteristics.Results: Of the 68 ES-SCLC patients included, no complete response, 22 patients achieved partial response, 28 had stable disease, 14 experienced disease progression and 4 patients were not available for efficacy. Objective response rate (ORR) was 32.4% (95% CI: 21.5– 44.8%), and disease control rate (DCR) was 73.5% (95% CI: 61.4– 83.5%). The median progression-free survival (PFS) was 5.6 months (95% CI: 3.87– 7.33), the median duration of response (DoR) was 6.8 months (95% CI: 0.80– 12.83). At the data cutoff date, the median follow-up duration was 12.5 months (range: 1.1– 31.5 months), yielding a median overall survival (OS) of 13.2 months (95% CI: 7.09– 19.31). Subgroup analysis highlighted that patients who were previously intolerant to immunotherapy had a longer OS (median OS: 15.5 vs 10.9 months, P = 0.031). Safety analysis showed that 61 patients (89.7%) experienced treatment-related adverse events (TRAEs) of varying severity with 37 patients (54.4%) developing grade 3 or higher. The most common TRAEs included fatigue, nausea and vomiting, hypertension, hematologic toxicity, and liver function abnormalities.Conclusion: Anlotinib combined with ICIs demonstrated that immunotherapy rechallenge in previously ICIs-treated ES-SCLC was feasible and of clinical significance preliminarily. However, larger-scale clinical studies were required to validate these findings subsequently.Keywords: previously immunotherapy-treated, extensive-stage SCLC, anlotinib, immune checkpoint inhibitors, immune rechallenge, efficacy, safety
