Efficacy of adding levofloxacin to gemcitabine and nanoparticle-albumin-binding paclitaxel combination therapy in patients with advanced pancreatic cancer: study protocol for a multicenter, randomized phase 2 trial (T-CORE2201)

被引:3
|
作者
Imai, Hiroo [1 ,9 ]
Sakamoto, Yasuhiro [2 ]
Takahashi, Shin [3 ]
Shibata, Hiroyuki [4 ]
Sato, Atsushi [5 ]
Otsuka, Kazunori [6 ]
Amagai, Kenji [7 ]
Takahashi, Masanobu [1 ,9 ]
Yamaguchi, Takuhiro [8 ]
Ishioka, Chikashi [1 ,9 ]
机构
[1] Tohoku Univ Hosp, Dept Med Oncol, Sendai, Japan
[2] Osaki Citizen Hosp, Dept Med Oncol, Osaki City, Japan
[3] Sendai Kousei Hosp, Chemotherapeut Ctr, Sendai, Japan
[4] Akita Univ, Dept Clin Oncol, Grad Sch Med, Akita, Japan
[5] Hirosaki Univ, Dept Med Oncol, Grad Sch Med, Hirosaki City, Japan
[6] Miyagi Canc Ctr, Dept Med Oncol, Natori City, Japan
[7] Ibaraki Cent Hosp, Dept Gastroenterol & Med Oncol, Kasama City, Japan
[8] Tohoku Univ Hosp, Clin Res Innovat & Educ Ctr, Sendai, Japan
[9] Tohoku Univ, Dept Clin Oncol, Grad Sch Med, Sendai, Japan
关键词
Pancreatic cancer; Multicenter randomized phase 2 study; Levofloxacin; Gemcitabine; Nanoparticle albumin binding paclitaxel; BACTERIA;
D O I
10.1186/s12885-024-11973-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundAdvanced pancreatic cancer is one of the leading causes of cancer-related deaths. For patients with advanced pancreatic cancer, gemcitabine and nanoparticle albumin-binding paclitaxel (nabPTX) combination (GEM/nabPTX) therapy is one of the recommended first-line treatments. Several retrospective studies have suggested that the addition of levofloxacin improves the efficacy of GEM/nabPTX therapy in patients with advanced pancreatic cancer. This prospective study aims to evaluate whether the addition of antibiotics improves the treatment efficacy of GEM/nabPTX as a first-line chemotherapy in patients with advanced pancreatic cancer.MethodsThis multicenter, prospective, randomized, phase 2 trial will included 140 patients. Patients with advanced pancreatic cancer will be randomized in a 1:1 ratio to either the GEM/nabPTX therapy group or the GEM/nabPTX plus levofloxacin group. The primary endpoint for the two groups is median progression-free survival time (mPFS) for the full analysis set (FAS). The secondary endpoints for the two groups are median overall survival (mOS), response rate (RR), disease control rate (DCR), and adverse event (AE) for the FAS and mPFS, mOS, RR, DCR, and AE for the per-protocol set. This study will enroll patients treated with GEM/nabPTX as the first-line chemotherapy for stage IV pancreatic adenocarcinoma.DiscussionGEM/nabPTX is a standard first-line chemotherapy regimen for patients with advanced pancreatic cancer. Recently, the superiority of 5-fluorouracil, liposomal irinotecan, and oxaliplatin combination therapy (NALIRIFOX) to GEM/nabPTX as first-line therapy for pancreatic cancer has been reported. However, the efficacy of NALIRIFOX is inadequate. Based on previous retrospective studies, it is hypothesized that treatment efficacy will improve when levofloxacin is added to GEM/nabPTX therapy. If the AEs (such as leukopenia, neutropenia, and peripheral neuropathy) that occur at an increased rate with levofloxacin and GEM/nabPTX combination therapy can be carefully monitored and properly managed, this simple intervention can be expected to improve the prognosis of patients with advanced pancreatic cancer.Trial registrationThis study was registered with the Japan Registry of Clinical Trials (jRCT; registry number: jRCTs021230005).
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页数:8
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