Literature DB >> 31786057

The efficacy and toxicity of chemotherapy in the elderly with advanced pancreatic cancer.

Xiang Li1, Da-Bing Huang1, Qi Zhang1, Cheng-Xiang Guo1, Qi-Han Fu2, Xiao-Chen Zhang2, Tian-Yu Tang1, Wei Su1, Yi-Wen Chen1, Wei Chen1, Tao Ma1, Shun-Liang Gao1, Ri-Sheng Que1, Xue-Li Bai3, Ting-Bo Liang4.   

Abstract

OBJECTIVES: FOLFIRINOX (FFX) or abraxane plus gemcitabine (AG)-based chemotherapy is used widely as firstline treatment for patients with pancreatic cancer. However, their use in the elderly is discouraged because of adverse events. More clinical data about the therapeutic response and tolerability to FFX or AG in elderly patents (over 70 years old) are required.
METHODS: Patients with advanced pancreatic cancer (n = 203; 131 metastatic pancreatic cancer patients (MPC) and 72 locally advanced pancreatic cancer patients (LAPC)) were treated using modified-FFX (mFFX) or AG and mFFX sequentially. The patients were grouped according to their age, patients below 70 years old and patients above 70 years old. The objective response rate (ORR), disease control rate (DCR), progression free survival (PFS), overall survival (OS) and adverse events were compared between the groups.
RESULTS: The ORRs in the elderly and in patients below 70 were similar (30.0% versus 32.3%). The median OS and PFS were also similar between the groups (mOS 13.3 m vs 12.7 m, p = 0.729, HR 0.874 (95% CI 0.5310 to 1.438); mPFS mPFS 10.6 m vs 10.3 m, p = 0.363, HR 0.800 (95% CI 0.4954 to 1.293)). However, the elderly patients suffered a higher incidence of severe adverse events (50% vs. 28.3%).
CONCLUSIONS: These data could provide guidance for chemotherapy use in elderly patients with advanced pancreatic cancer. Age did not affect treatment outcome; however, supportive treatment is very important for elderly patients receiving chemotherapy.
Copyright © 2019 IAP and EPC. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Abraxane plus gemcitabine; Chemotherapy; Elderly; Modified-FOLFIRINOX; Tolerability

Mesh:

Substances:

Year:  2019        PMID: 31786057     DOI: 10.1016/j.pan.2019.11.012

Source DB:  PubMed          Journal:  Pancreatology        ISSN: 1424-3903            Impact factor:   3.996


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