Mie Takafumi, Sasaki Takashi, Takeda Tsuyoshi, Okamoto Takeshi, Hamada Tsuyoshi, Ishitsuka Takahiro, Yamada Manabu, Nakagawa Hiroki, Furukawa Takaaki, Kasuga Akiyoshi, Matsuyama Masato, Ozaka Masato, Sasahira Naoki
Department of Hepato-Biliary-Pancreatic Medicine, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo 135-8550, Japan.
Cancers (Basel). 2023 Jan 5;15(2):358. doi: 10.3390/cancers15020358.
Outcomes and prognostic factors of second-line gemcitabine plus nab-paclitaxel (GnP) after modified FOLFIRINOX (mFFX) for unresectable pancreatic cancer were unclear. We retrospectively analyzed consecutive patients with unresectable pancreatic cancer treated with GnP after first-line mFFX treatment between March 2015 and March 2022 at our hospital. A total of 103 patients were included. Median overall survival (OS) from the start of first-line and second-line treatments was 14.9 months and 7.2 months, respectively. Median progression-free survival (PFS) was 3.6 months. Performance status, modified Glasgow prognostic score, and neutrophil-to-lymphocyte ratio were independently associated with OS. Our prognostic model using these parameters classifies patients into good (n = 70) and poor (n = 33) prognosis groups. Median OS and PFS were longer in the good prognosis group than in the poor prognosis group (OS: 9.3 vs. 3.8 months, p < 0.01; PFS: 4.1 vs. 2.3 months, p < 0.01). Grade 3/4 adverse events were observed in 70.9% of patients, with neutropenia being the most frequent. While GnP as second-line treatment was well-tolerated, efficacy of second-line gemcitabine plus nab-paclitaxel was notably limited, particularly in the poor prognosis group.
对于不可切除胰腺癌,在改良FOLFIRINOX(mFFX)治疗后使用二线吉西他滨联合白蛋白结合型紫杉醇(GnP)的疗效和预后因素尚不清楚。我们回顾性分析了2015年3月至2022年3月在我院接受一线mFFX治疗后使用GnP治疗的连续性不可切除胰腺癌患者。共纳入103例患者。从一线和二线治疗开始的中位总生存期(OS)分别为14.9个月和7.2个月。中位无进展生存期(PFS)为3.6个月。体能状态、改良格拉斯哥预后评分和中性粒细胞与淋巴细胞比值与OS独立相关。使用这些参数的我们的预后模型将患者分为预后良好组(n = 70)和预后不良组(n = 33)。预后良好组的中位OS和PFS长于预后不良组(OS:9.3对3.8个月,p < 0.01;PFS:4.1对2.3个月,p < 0.01)。70.9%的患者观察到3/4级不良事件,其中中性粒细胞减少最为常见。虽然GnP作为二线治疗耐受性良好,但二线吉西他滨联合白蛋白结合型紫杉醇的疗效明显有限,尤其是在预后不良组。