Department of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, Guangdong, China.
Department of Oncology, Chongqing University Three Gorges Hospital/Chongqing Three Gorges Central Hospital, Chongqing, 404100, China.
J Cancer Res Clin Oncol. 2023 Mar;149(3):1185-1193. doi: 10.1007/s00432-022-03935-0. Epub 2022 Apr 4.
Primary pulmonary lympho-epithelioma-like carcinoma (PPLELC) is a rare subtype of primary non-small cell lung cancer (NSCLC). Currently, there is still lack of research data on anti-angiogenic therapy of advanced PPLELC. The purpose of this study was to investigate the efficacy and safety of anti-angiogenic therapy combined with chemotherapy compared with traditional chemotherapy for these patients.
Advanced PPLELC patients admitted to six grade A hospitals from January 2013 to January 2021 were selected. The patients received anti-angiogenic therapy combined with chemotherapy (AT group) or chemotherapy (CT group) alone.
A total of 65 patients were included in this study, including 31 patients in the AT group treated with anti-angiogenic therapy combined with chemotherapy and 34 patients in the CT group treated with chemotherapy alone. As of October 1, 2021, the median progression-free survival (PFS) in the AT group was 11.2 months [95% confidence interval (CI), 5.9-16.5]. The median PFS in the CT group was 7.0 months [95%CI, 5.1-8.9] [Hazard Ratio (HR), 0.49; 95%CI, 0.29-0.83; P = 0.008]. The 1-year PFS rates were 41.9% and 17.6%, respectively. The overall response rates (ORR) of two groups were 45.2% (95% CI, 0.27-0.64), 38.2% (95% CI, 0.21-0.56), (P = 0.571). The disease control rates (DCR) of two groups were 93.5% (95% CI, 0.84-1.03), 88.2% (95% CI, 0.77-1.00), (P = 0.756).
Among patients with advanced PPLELC, the PFS of patients with anti-angiogenic therapy combined with chemotherapy is better than that of patients with chemotherapy alone. Anti-angiogenic therapy combined with chemotherapy is an optional treatment scheme.
原发性肺淋巴上皮样癌(PPLELC)是一种罕见的原发性非小细胞肺癌(NSCLC)亚型。目前,针对晚期 PPLELC 的抗血管生成治疗研究数据仍较为缺乏。本研究旨在探讨抗血管生成治疗联合化疗与传统化疗相比,对这些患者的疗效和安全性。
选择 2013 年 1 月至 2021 年 1 月期间,6 家 A 级医院收治的晚期 PPLELC 患者。患者接受抗血管生成治疗联合化疗(AT 组)或单独化疗(CT 组)。
本研究共纳入 65 例患者,其中 AT 组 31 例患者接受抗血管生成治疗联合化疗,CT 组 34 例患者接受单独化疗。截至 2021 年 10 月 1 日,AT 组的中位无进展生存期(PFS)为 11.2 个月[95%置信区间(CI),5.9-16.5]。CT 组的中位 PFS 为 7.0 个月[95%CI,5.1-8.9] [风险比(HR),0.49;95%CI,0.29-0.83;P=0.008]。两组的 1 年 PFS 率分别为 41.9%和 17.6%。两组的总缓解率(ORR)分别为 45.2%(95%CI,0.27-0.64)和 38.2%(95%CI,0.21-0.56)(P=0.571)。两组的疾病控制率(DCR)分别为 93.5%(95%CI,0.84-1.03)和 88.2%(95%CI,0.77-1.00)(P=0.756)。
在晚期 PPLELC 患者中,抗血管生成治疗联合化疗组的 PFS 优于单纯化疗组。抗血管生成治疗联合化疗是一种可选的治疗方案。