Division of Pulmonary, Critical Care and Allergy, Department of Internal Medicine, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Thorac Cancer. 2022 Dec;13(23):3384-3392. doi: 10.1111/1759-7714.14697. Epub 2022 Oct 23.
The phase III trial IMpower133 showed that platinum and etoposide plus atezolizumab was associated with improved overall survival (OS) and progression free-survival (PFS) when compared to the placebo group in treatment-naïve extensive stage (ES) small cell lung cancer (SCLC). Due to superiority in clinical outcomes, combination immunotherapy plus chemotherapy have become mainstay treatment modalities as first-line treatment in ES-SCLC. Nevertheless, real-world data are still lacking and the search for potential biomarkers is essential. This study aimed to evaluate potential predictive biomarkers applicable in ES-SCLC under combination therapy.
Patients with ES-SCLC under etoposide-platinum-atezolizumab enrolled from seven university hospitals affiliated to the Catholic University of Korea were evaluated. Pretreatment clinical parameters were evaluated for association with OS and PFS. Adverse events (AEs) during induction and maintenance phases were also evaluated. p-values below 0.05 were considered statistically significant.
A total of 41 patients were evaluated. Six-month survival was 68.6%. As best response to treatment, 26 (63.4%) showed partial response, nine (22.0%) showed stable disease, and four (9.8%) showed progressive disease. During the induction phase, grade I-II AEs occurred in 22 (53.7%) patients, and grade III-IV AEs occurred in 26 (63.4%) patients. During the maintenance phase, nine out of 25 (36.0%) patients experienced any grade AEs. In multivariate analysis for OS, lactate dehydrogenase (LDH), c-reactive protein (CRP), and forced vital capacity (%) were significant factors. In multivariate analysis for PFS, sex, and LDH were significant.
In ES-SCLC under etoposide-platinum-atezolizumab, pretreatment CRP, LDH and FVC (%) were independent predictive factors.
III 期 IMpower133 试验表明,与安慰剂组相比,在未经治疗的广泛期(ES)小细胞肺癌(SCLC)患者中,铂类药物和依托泊苷加阿替利珠单抗联合治疗可改善总生存期(OS)和无进展生存期(PFS)。由于临床疗效的优势,联合免疫治疗加化疗已成为 ES-SCLC 一线治疗的主要治疗方式。然而,目前仍缺乏真实世界的数据,寻找潜在的生物标志物至关重要。本研究旨在评估 ES-SCLC 患者接受联合治疗时潜在的预测性生物标志物。
评估来自韩国天主教大学附属的 7 所大学医院的接受依托泊苷-铂类药物-阿替利珠单抗治疗的 ES-SCLC 患者。评估治疗前的临床参数与 OS 和 PFS 的相关性。还评估了诱导和维持阶段的不良事件(AE)。p 值<0.05 被认为具有统计学意义。
共评估了 41 例患者。6 个月生存率为 68.6%。作为最佳治疗反应,26 例(63.4%)患者显示部分缓解,9 例(22.0%)患者显示稳定疾病,4 例(9.8%)患者显示疾病进展。在诱导阶段,22 例(53.7%)患者出现 1-2 级 AE,26 例(63.4%)患者出现 3-4 级 AE。在维持阶段,25 例中有 9 例(36.0%)患者出现任何级别的 AE。在 OS 的多变量分析中,乳酸脱氢酶(LDH)、C 反应蛋白(CRP)和用力肺活量(%)是显著因素。在 PFS 的多变量分析中,性别和 LDH 是显著因素。
在接受依托泊苷-铂类药物-阿替利珠单抗治疗的 ES-SCLC 患者中,治疗前 CRP、LDH 和 FVC(%)是独立的预测因素。