跳至主要内容
临床试验/NCT06135896
NCT06135896招募中2 期

An Open-label, Randomized, Multicenter, Phase II Tripegfilgrastim Trial to Reduce the Risk of Severe Neutropenia in Patients With Unresectable Pancreaticobiliary Cancers

National Cancer Center, Korea1 个研究点 分布在 1 个国家目标入组 98 人开始时间: 2024年1月16日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
98
试验地点
1
主要终点
Primary endpoint

研究概览

简要总结

  • Clinical trial phase: Phase 2
  • Intervention model: Control group
  • Group allocation: Randomized controlled trial
  • Research perspective: Prospective study
  • Participating centers: Multicenter study
  • Definition of the intervention period: Based on the RECIST 1.1 guidelines, patients will receive treatment until dropout due to disease progression or unacceptable toxicity related to the trial drug. Patients will be followed up with to assess survival every 2 months until either death or the end of the trial, whichever is first.
  • The intervention period is from the date of IRB approval to December 31st, 2025
  • The follow-up duration is one year, and the statistical analysis duration is six months
  • The total research period is from the date of IRB approval to June 30th, 2026

详细描述

Pancreatic cancer and Bile duct cancer are the 8th and 9th leading causes of all cancer in Korea, have 5-year survival rates of approximately 20%, and unresectable cancers show a poor prognosis of approximately 5%. The first-line treatment recommended for unresectable pancreaticobiliary cancer is chemotherapy. FOLFIRINOX or gemcitabine/nab-paclitaxel combination therapy is recommended for pancreatic cancer, and gemcitabine/cisplatin combination therapy is recommended for bile duct cancer. Recently, anticancer therapy advances have led to an increase in survival for pancreaticobiliary cancer patients, and more than half of patients receive secondary chemotherapy due to disease progression after first-line treatment. Recently, with the introduction of nanoliposomal irinotecan (nal-IRI) and the clinical outcomes of Phase 3 NAPOL-1 trial and the Phase 2b NIFTY trial, nal-IRI/5-FU/LV combination therapy is being used as second-line chemotherapy following gemcitabine treatment. Granulocyte colony-stimulating factors (G-CSFs) (filgrastim, pegfilgrastim, and tripegfilgrastim) can be used for neutropenia prevention and treatment. In particular, pegylated G-CSF can reduce patient discomfort due to its long retention time. In a retrospective study analyzing the use of G-CSF for primary neutropenia prevention in Korea, pancreatic cancer patients who received FOLFIRINOX treatment that exhibited neutropenia and FN were significantly reduced from 55.6% to 31.6% (P = 0.003) and from 18.5% to 1.8% (P = 0.002), respectively. Similarly, in a retrospective study in Japan, preventive pegylated G-CSF treatment reduced the incidence of FN from 23% to 0%, and in a double-blinded, randomized, phase 3 breast cancer clinical trial, pegylated G-CSF treatment significantly reduced the incidence of FN from 68.8% to 1.2%. In a retrospective study of non-small cell lung cancer, another solid cancer, the incidence of FN in the preventive pegylated G-CSF treatment group was 0%, compared to an incidence of 50% in the control group.

However, no studies have evaluated the efficacy of G-CSF in pancreaticobiliary cancer patients receiving nal-IRI/5-FU/LV combination therapy yet. Hence, our objective was to report the effects of pegylated G-CSF on preventing severe neutropenia in patients receiving nal-IRI/5-FU/LV combination chemotherapy for unresectable pancreaticobiliary cancer.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged at least 19 years old, diagnosed with unresectable pancreaticobiliary cancer, and scheduled to receive chemotherapy using nal-IRI/5-FU/LV combination chemotherapy

排除标准

  • Patients who refuse to sign the consent form Patients who have previously experienced severe neutropenia during chemotherapy

研究组 & 干预措施

Treatment Group

Experimental
  • Premedication: depending on the center (Ondansetron 8 mg +Dextrose 5% 50 mL, MIV, Dexamethason 10 mg IV, and Atropine sulfate 0.25 mg [0.5 amp] SC)
  • Onivyde 70 mg/m2 + Dextrose 5% 500 mL (bag), and MIV for 90 min
  • Leucovorin 400 mg/m2 + Dextrose 5% 500 mL (bag), and MIV for 30 min
  • 5-FU (2400 mg/m2) + Dextrose 5% 500 mL (bag) and MIV for 46 h
  • Tripegfilgrastim 6 mg SC administered 24 h after completing 5-FU infusion The above chemotherapy will be administered every two weeks

干预措施: Tripegfilgrastim (Drug)

结局指标

主要结局

Primary endpoint

时间窗: through study completion, an average of 1 year

Severe neutropenia incidence

次要结局

  • biomarkers(through study completion, an average of 1 year)
  • neutropenia incidence(through study completion, an average of 1 year)
  • emergency department visits(through study completion, an average of 1 year)
  • Overall survival(through study completion, an average of 1 year)
  • Progression-free survival(through study completion, an average of 1 year)
  • Febrile neutropenia(through study completion, an average of 1 year)

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Sang Myung Woo

medical doctor, Senior scientist

National Cancer Center, Korea

研究点 (1)

Loading locations...

相似试验

招募中
1 期
Evaluation of a Renin Inhibitor, Aliskiren, Compared to Enalapril, in C3 Glomerulopathy
CTIS2024-515892-36-00Region Skane30
进行中(未招募)
1 期
Controlled clinical trial to evaluate the clinical efficacy and safety of a drug that inhibits renin, aliskiren, compared to an angiotensin converting enzyme inhibitor enalapril in children and adults with the kidney disease C3 glomerulopathyC3 glomerulopathy
EUCTR2019-001440-22-SESkåne University Hospital30
进行中(未招募)
1 期
A multicenter, open-label, randomized, phase II/III study to evaluate the safety and efficacy of combretastatin a-4 phosphate in combination with paclitaxel and carboplatin in comparison with paclitaxel and carboplatin against anaplastic thyroid carcinoma - N/AAnaplastic Thyroid CarcinomaMedDRA version: 9.1 Level: PT Classification code 10002240 Term: Anaplastic thyroid cancer
EUCTR2007-002846-38-GBOXiGENE, Inc.180
进行中(未招募)
1 期
A study evaluating the safety and efficacy of an experimental drug for chronic lung disease against normally prescribed care in extremely premature babiesChronic Lung DiseaseMedDRA version: 21.1Level: LLTClassification code 10066204Term: Chronic lung disease of prematuritySystem Organ Class: 10038738 - Respiratory, thoracic and mediastinal disorders
EUCTR2018-001393-16-PTOHB Neonatology Ltd338
进行中(未招募)
1 期
A study evaluating the safety and efficacy of an experimental drug for chronic lung disease against normally prescribed care in extremely premature babiesChronic Lung DiseaseMedDRA version: 21.1Level: LLTClassification code 10066204Term: Chronic lung disease of prematuritySystem Organ Class: 10038738 - Respiratory, thoracic and mediastinal disorders
EUCTR2018-001393-16-DEOHB Neonatology Ltd338