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改良 FOLFIRINOX 方案在 75 岁或以上的胰腺癌患者中的应用。

Modified FOLFIRINOX in pancreatic cancer patients Age 75 or older.

机构信息

The University of Texas MD Anderson Cancer Center, USA.

The University of Texas MD Anderson Cancer Center, USA.

出版信息

Pancreatology. 2020 Apr;20(3):501-504. doi: 10.1016/j.pan.2020.01.005. Epub 2020 Jan 9.

Abstract

BACKGROUND

Although FOLFIRINOX (5-Fluorouracil + leucovorin + irinotecan + oxaliplatin) is now the standard of care for patients (pts) with metastatic pancreatic cancer (PC) based on the 2011 study by Conroy et al. which demonstrated improved median overall survival (mOS), pts > 75 yrs old were excluded from this study. The purpose of this study was to assess the safety and efficacy of modified FOLFIRINOX (mFOLFIRINOX) in this population.

METHODS

We retrospectively analyzed unresectable PC pts, age ≥ 75, treated with mFOLFIRINOX at MD Anderson from 2011 to 2017. Primary outcome was rate of grade 3 or 4 hematologic toxicity (HT).

RESULTS

24 pts were included. Grade 3 or 4 HT occurred in 11 pts 6 pts required hospitalization for any toxicity, and 10 stopped mFOLFIRINOX due to toxicity. The most frequently used starting doses of infusional 5-FU, irinotecan and oxaliplatin were 2400, 150 and 75 mg/m, respectively. Median PFS was 3.7 months (95% CI: 3.0-5.7) with a median OS of 11.6 months (95% CI: 6.14-15.7). For first line pts, median PFS and OS were 5.1 (95% CI: 2.0-12.8) and 12.2 months (95% CI: 4.8-30.8), respectively.

CONCLUSIONS

In this single-center retrospective analysis of unresectable PC pts age 75 or older given mFOLFIRINOX, toxicities and survival outcomes were similar to those reported in the initial study. These data indicate that the use of modified dosing FOLFIRINOX in advanced PC pts older than 75 appears to maintain similar toxicity and efficacy when compared to younger pts.

摘要

背景

尽管基于 Conroy 等人 2011 年的研究结果,FOLFIRINOX(5-氟尿嘧啶+亚叶酸+伊立替康+奥沙利铂)已成为转移性胰腺癌(PC)患者的标准治疗方法,该研究中排除了年龄>75 岁的患者。本研究旨在评估改良 FOLFIRINOX(mFOLFIRINOX)在这一人群中的安全性和疗效。

方法

我们回顾性分析了 2011 年至 2017 年在 MD 安德森接受 mFOLFIRINOX 治疗的年龄≥75 岁的不可切除 PC 患者。主要结局是 3 级或 4 级血液学毒性(HT)的发生率。

结果

共纳入 24 例患者。11 例患者发生 3 级或 4 级 HT,6 例患者因任何毒性需要住院治疗,10 例患者因毒性停止 mFOLFIRINOX。输注 5-FU、伊立替康和奥沙利铂的起始剂量分别为 2400mg、150mg 和 75mg/m。中位无进展生存期(PFS)为 3.7 个月(95%CI:3.0-5.7),中位总生存期(OS)为 11.6 个月(95%CI:6.14-15.7)。对于一线治疗患者,中位 PFS 和 OS 分别为 5.1 个月(95%CI:2.0-12.8)和 12.2 个月(95%CI:4.8-30.8)。

结论

在这项针对年龄 75 岁或以上的不可切除 PC 患者使用 mFOLFIRINOX 的单中心回顾性分析中,毒性和生存结果与最初研究报告的结果相似。这些数据表明,与年轻患者相比,在年龄>75 岁的晚期 PC 患者中使用改良剂量 FOLFIRINOX 似乎可以保持相似的毒性和疗效。

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