阿特珠单抗与依托泊苷和卡铂联合治疗晚期小细胞肺癌患者的免疫化疗效果预测因素

A. E. Kuzminov, T. D. Barbolina, E. Reutova, D. Yudin, V. V. Breder, K. Laktionov
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引用次数: 0

摘要

导言。肺癌仍然是全球癌症相关死亡的主要原因。30 年来,采用免疫化疗的随机临床研究首次显示,晚期小细胞肺癌患者的中位总生存期显著延长。然而,免疫化疗疗效的重要预测因素尚未发现。通过寻找免疫化疗有效性的预测因素,改善晚期小细胞肺癌患者的长期治疗效果。共有35名晚期小细胞肺癌患者(11名女性和24名男性)接受了阿特珠单抗联合依托泊苷和卡铂的免疫化疗作为一线治疗。患者的平均年龄为61岁。在免疫化疗基线期,10名患者为IVA期,24名患者为IVB期,1名患者为IIIB期。我们回顾性评估了白细胞增多症、血小板增多症、乳酸脱氢酶水平、中性粒细胞与淋巴细胞比率、纤维蛋白原水平、血型等因素对中位无进展生存期和总生存期的预后影响。无进展生存期中位数为6.2个月(95% CI为4.6-7.8个月),总生存期中位数为16.0个月(95% CI为9.4-22.6个月)。中位无进展生存期呈上升趋势,但治疗开始时白细胞增多、血小板增多、纤维蛋白原水平升高和乳酸脱氢酶水平正常的差异无统计学意义。治疗开始时的中性粒细胞与淋巴细胞比率对中位无进展生存期有显著影响。当中性粒细胞与淋巴细胞比值小于3时,中位无进展生存期从4.5个月(95% CI 3.9-5.1)增至6.9个月(95% CI 5.6-8.2),差异有统计学意义。血型为 B(III)的患者的中位无进展生存期为 5.0(95% CI 3.5-6.5)个月,而血型不同的患者的中位无进展生存期为 6.2(95% CI 4.7-7.7)个月(P = 0.047)。白细胞增多症、血小板增多症、纤维蛋白原水平、乳酸脱氢酶水平和中性粒细胞与淋巴细胞比率等因素对总生存期没有显著影响。B(III)血型患者的生存率明显较低:B(III)血型患者的中位总生存期为 12.1 个月(95% CI 9.3-14.9 个月),而其他血型患者的中位总生存期为 12.1 个月(95% CI 9.3-14.9 个月)(P = 0.017)。晚期小细胞肺癌患者免疫化疗疗效预测因素的重要性应通过更大的样本量和多变量分析加以证实。该研究仍在继续招募患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictors of the immunochemotherapy effectiveness of atezolizumab in combination with etoposide and carboplatin in patients with advanced small cell lung cancer
Introduction. Lung cancer remains the leading cause of cancer-related deaths worldwide. For the first time in 30 years, the randomized clinical studies employing immunochemotherapy showed a significant increase in median overall survival for patients with advanced small cell lung cancer. However, no significant predictors of the immunochemotherapy effectiveness were identified.Aim. To improve long-term outcomes of treatment of patients with advanced small cell lung cancer through search for predictors of the immunochemotherapy effectiveness.Materials and methods. A total of 35 patients (11 women and 24 men) with advanced small cell lung cancer who received immunochemotherapy with atezolizumab combined with etoposide and carboplatin as first-line treatment were included in the analysis. The average age for patients was 61 years. At the immunochemotherapy baseline, 10 patients had stage IVA disease, 24 patients had stage IVB disease, and one patient had stage IIIB disease. We retrospectively assessed the prognostic impact on the median progression-free survival and overall survival of such factors as leukocytosis, thrombocytosis, lactate dehydrogenase level, neutrophil to lymphocyte ratio, fibrinogen level, blood type.Results. Median progression-free survival was 6.2 (95% CI 4.6–7.8) months, median overall survival was 16.0 (95% CI 9.4– 22.6) months. There was an increasing trend in median progression-free survival, but without statistically significant differences in leukocytosis, thrombocytosis, elevated fibrinogen levels and normal lactate dehydrogenase levels at the beginning of therapy. The neutrophil to lymphocyte ratio at the beginning of therapy had a significant impact on median progression-free survival. There was a statistically significant increase in median progression-free survival from 4.5 (95% CI 3.9–5.1) to 6.9 (95% CI 5.6–8.2) months when the neutrophil to lymphocyte ratio was < 3. A significant decrease in median progression-free survival – 5.0 (95% CI 3.5–6.5) months was also observed in patients with blood group B (III) vs 6.2 (95% CI 4.7–7.7) months for patients with a different blood group (p = 0.047). Factors such as leukocytosis, thrombocytosis, fibrinogen level, lactate dehydrogenase level and neutrophil to lymphocyte ratio did not have a significant impact on overall survival. Patients with blood type B (III) showed significantly worse survival: median overall survival was 12.1 (95% CI 9.3–14.9) months in blood group B (III) and was not achieved in patients with other blood groups (p = 0.017).Conclusion. The significance of the identified predictors of the immunochemotherapy effectiveness in patients with advanced small cell lung cancer should be confirmed with the larger sampling size using a multivariate analysis. The study continues a recruitment of patients.
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