Clinical outcomes and safety of continuous immunotherapy beyond progression in patients with extensive-stage small cell lung cancer: a retrospective real-world study

广泛期小细胞肺癌患者疾病进展后持续免疫治疗的临床疗效和安全性:一项回顾性真实世界研究

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Abstract

BACKGROUND: Immunochemotherapy has been approved as first-line treatment for extensive-stage small cell lung cancer. However, second-line treatment options and whether continuous immunotherapy will improve clinical outcome are still controversial. This multi-center retrospective study aimed to investigate the efficacy of continuous immunotherapy for the patients who suffered progression from first-line immunochemotherapy. METHODS: We retrospectively reviewed the medical records of patients with extensive-stage small cell lung cancer treated with first-line immunochemotherapy in three major medical centers in Shandong Province. The patients enrolled achieved disease control during first-line immunochemotherapy but subsequently suffered disease progression. RESULTS: From January 2020 to December 2024, a total of 354 patients treated with first-line immunochemotherapy were enrolled. The first-line progression free survival was 6.60 (95%CI: 6.28-6.92) months. A total of 206 patients were enrolled to compare the efficacy of second-line therapies, including chemotherapy alone (C, 40 cases), chemotherapy + anti-angiogenic therapy (C+A, 17 cases), immunochemotherapy (I+C, 122 cases), immunotherapy + anti-angiogenic therapy (I+A, 11 cases) and immunochemotherapy + anti-angiogenic therapy (I+C+A, 16 cases). Therein, I+C+A group obtained the longest second-line progression free survival of 4.60 (95%CI: 2.71-6.50) months. The second-line progression free survival of I+C group was also longer than that of the C group (3.50, 95%CI: 3.07-3.93 vs 2.33, 95%CI: 1.66-3.01). Regarding overall survival, I+A group achieved the longest overall survival of 22.00 (95%CI: 11.39-32.61) months compared with 19.53 (95%CI: 16.81-22.26) months for I+C group. However, there were no statistical differences in second-line progression free survival and overall survival among the groups. In terms of safety, the rates of adverse events in the I+C and C groups were not statistically significant. CONCLUSIONS: Continuous immunotherapy beyond progression in extensive-stage small cell lung cancer shows the trend of prolonging second-line progression free survival, but does not improve the overall survival. Additionally, in the second-line treatment, chemotherapy remains an important cornerstone therapy and anti-angiogenic agent containing strategy may potentially improve survival.

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