Department of Gastroenterology, University Hospital Pontchaillou, Rennes 1 University, INSERM U1242 "Chemistry Oncogenesis Stress Signalling," Rennes, France.
Department of Digestive Oncology, La Timone, AMU, Marseille, France.
Oncologist. 2024 Sep 6;29(9):e1149-e1158. doi: 10.1093/oncolo/oyae079.
Predictive markers of LV5FU2 maintenance benefit after first-line induction with FOLFIRINOX in patients with metastatic pancreatic cancer are necessary to select patients who will not be harmed by this strategy.
We focused on patients who received 12 cycles of FOLFIRINOX (arm A, N = 88) or 8 cycles of FOLFIRINOX followed by LV5FU2 maintenance in controlled patients (arm B, N = 91) from the PRODIGE-35 trial. Prognostic factors and predictors of efficiency were identified by using Cox regression. Median progression-free survival (PFS), overall survival (OS), and time to deterioration of quality of life (TTD-QoL) were evaluated.
Poor independent prognostic factors were primary tumor in place, age <65 years and the presence of liver metastases for PFS, a baseline neutrophil/lymphocyte ratio (NLR) ≥5 and CA19.9 ≥500 UI/L for OS, independent of the treatment arm. Patients with one metastatic site had a longer PFS in arm A, whereas patients with ≥2 metastatic sites had a longer PFS in arm B. We also identified predictors of OS and TTD-QoL in arm B but these differences were not statistically significant.
Except for patients with one metastatic site who benefited more from 12 cycles of FOLFIRINOX, a maintenance strategy with LV5FU2 should be widely offered to mPC patients whose survival and QoL are preserved after 4 months of FOLFIRINOX. (ClinicalTrials.gov: NCT02352337).
对于转移性胰腺癌患者,一线应用 FOLFIRINOX 诱导治疗后,需要预测性标志物来确定哪些患者能从 LV5FU2 维持治疗中获益,避免该策略带来的伤害。
我们主要关注 PRODIGE-35 试验中接受 12 个周期 FOLFIRINOX(A 组,N=88)或 8 个周期 FOLFIRINOX 后接受 LV5FU2 维持治疗的患者(B 组,N=91)。采用 Cox 回归识别预后因素和疗效预测因子。评估中位无进展生存期(PFS)、总生存期(OS)和生活质量恶化时间(TTD-QoL)。
独立预后不良因素包括原发肿瘤位置、年龄<65 岁和肝转移存在与 PFS 相关,基线中性粒细胞/淋巴细胞比值(NLR)≥5 和 CA19.9≥500 UI/L 与 OS 相关,与治疗分组无关。A 组中,转移灶数为 1 个的患者 PFS 较长,而 B 组中,转移灶数≥2 个的患者 PFS 较长。我们还确定了 B 组中 OS 和 TTD-QoL 的预测因子,但差异无统计学意义。
除了转移灶数为 1 个的患者从 12 个周期的 FOLFIRINOX 治疗中获益更多外,对于 4 个月 FOLFIRINOX 治疗后生存和生活质量得到保存的 mPC 患者,应广泛提供 LV5FU2 维持治疗策略。(ClinicalTrials.gov:NCT02352337)。