Adamczuk-Nurzyńska Agata, Nurzyński Paweł, Brzozowska Melania, Jewczak Maciej, Śliwczyński Andrzej
Department of Oncology, National Medical Institute of the Ministry of the Interior and Administration, 02-507 Warsaw, Poland.
National Medical Institute of the Ministry of the Interior and Administration, 02-507 Warsaw, Poland.
Cancers (Basel). 2025 Aug 28;17(17):2821. doi: 10.3390/cancers17172821.
Metastatic pancreatic cancer (mPC) is an aggressive disease with high morbidity and mortality, and long-term survival rates remain poor. New therapeutic options that demonstrate statistically significant improvements in overall survival (OS) and progression-free survival (PFS) are still being sought. Although many first-line (FL) treatment studies exist in the literature, there are almost no prospective studies on second-line (SL) therapy. The aim of this clinical study was to retrospectively analyze the medical history of 251 patients diagnosed with mPC, treated first-line (FL) with GEM-NAB between February 2017 and January 2025. After disease progression, 109 patients received SL treatment. We also present a multivariate analysis based on routinely collected data (demographic, clinical, and laboratory parameters) evaluating their impact on OS and PFS. The median age was 66 years (range 37-84 years). The median PFS was 2.33 months (95% CI 1.69-2.97). Specifically, the mPFS was 4.1 months (95% CI 1.31-6.90) for FOLFIRINOX; 2.8 months (95% CI 2.30-3.30) for FOLFIRI; 2.37 months (95% CI 1.66-3.08) for NALIRI; 1.47 months (95% CI 1.18-1.75) for FOLFOX 6; and 0.93 months (95% CI 0.00-2.64) for GEM-cisplatin. The median OS was 5.03 months (95% CI 3.75-6.31). Seven patients achieved a partial response (overall response rate 6%). The most frequent adverse events (AEs) included anemia, fatigue, peripheral neuropathy, neutropenia, and thrombocytopenia. As a result, SL treatments were compared, and some statistically significant difference was found between them in PFS time for chemotherapy FOLFIRINOX and GEM + cisplatin. The most frequent AEs occurred during treatment with FOLFIRINOX chemotherapy.
转移性胰腺癌(mPC)是一种侵袭性疾病,发病率和死亡率高,长期生存率仍然很低。目前仍在寻找能在总生存期(OS)和无进展生存期(PFS)方面显示出统计学显著改善的新治疗方案。尽管文献中有许多一线(FL)治疗研究,但几乎没有关于二线(SL)治疗的前瞻性研究。本临床研究的目的是回顾性分析2017年2月至2025年1月期间251例诊断为mPC并接受吉西他滨-纳米白蛋白结合型紫杉醇一线(FL)治疗的患者的病史。疾病进展后,109例患者接受了二线治疗。我们还基于常规收集的数据(人口统计学、临床和实验室参数)进行了多变量分析,评估其对OS和PFS的影响。中位年龄为66岁(范围37-84岁)。中位PFS为2.33个月(95%CI 1.69-2.97)。具体而言,FOLFIRINOX方案的mPFS为4.1个月(95%CI 1.31-6.90);FOLFIRI方案为2.8个月(95%CI 2.30-3.30);NALIRI方案为2.37个月(95%CI 1.66-3.08);FOLFOX 6方案为1.47个月(95%CI 1.18-1.75);吉西他滨-顺铂方案为0.93个月(95%CI 0.00-2.64)。中位OS为5.03个月(95%CI 3.75-6.31)。7例患者获得部分缓解(总缓解率6%)。最常见的不良事件(AE)包括贫血、疲劳、周围神经病变、中性粒细胞减少和血小板减少。结果,对二线治疗进行了比较,发现化疗FOLFIRINOX方案和吉西他滨+顺铂方案在PFS时间上存在一些统计学显著差异。最常见的不良事件发生在FOLFIRINOX化疗期间。