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Completed

NCT Number: NCT03083613

Raltitrexed and Paclitaxel for Gastric or Gastroesophageal Junction Adenocarcinoma

This is a single-arm clinical trial.The purpose of this study is to evaluate the efficacy and safety of Raltitrexed and Paclitaxel as second-line chemotherapy for patients with unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma .The primary endpoint of this study is objective response rate.The secondary endpoint of this study is safety,progression-free survival and overall survival.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Chinese Academy of Medical Sciences

Beijing, 10000, China

About this study

Raltitrexed is an antifolate thymidylate synthase inhibitor that has shown efficacy and good safety profile in the treatment of colorectal cancer. To our knowledge, there has been no study published with the Raltitrexed and Paclitaxel regimen as second-line chemotherapy for patients with unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma.The aim of our study was to evaluate the efficacy, safety and survival of this regimen in patients with unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically or cytologically confirmed unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma;
  • Patients failed first-line chemotherapy containing fluoropyrimidines and platinums;
  • ECOG (Eastern Cooperative Oncology Group)performance status 0-1;
  • At least 1 measurable lesion should be present(RECIST1.1)
  • Available Organ function: Neutrophils>2g/L, Hemoglobin>9g/L, Blood platelet >100g/L; Alanine aminotransferase(ALT) and Aspartate aminotransferase(AST)<1.5 ULN(upper limit of normal); Total bilirubin(TBIL)<1.0 ULN; Cr <1.0ULN
  • Signed informed consent.
  • Life expectancy ≥3 months;

Exclusion criteria

  • Previous treatment with Raltitrexed or Paclitaxel;
  • Known history of allergic reaction to Raltitrexed or Paclitaxel;
  • Known brain metastases;
  • Pregnant or breast feeding women;
  • Severe diarrhea,intestinal obstruction;
  • other co-existing malignancies or malignancies diagnosed within the last 5 years(except cured cutaneum carcinoma or carcinoma in situs of cervix);
  • Previous myocardial infarction, unstable angina, stroke ,or uncontrollable Arrhythmia;
  • Kown HIV infecton.

Treatment and study plan

Raltitrexed

Drug

Raltitrexed:3mg/m2,iv,d1, Every 3 weeks

Other names: RTX

paclitaxel

Drug

Paclitaxel:80mg/m2,iv,d1,d8, Every 3 weeks

Primary outcomes

  1. Objective Response Rate

    Time frame: 18-26 months

Secondary outcomes

  1. Overall Survival

    Time frame: 18-26 months

    From date of randomization until date of death

  2. Progression-free survival

    Time frame: 18-26 months

    From date of randomization until date of first documented PD, date of death

Sponsors and collaborators

Lead sponsor

Chinese Academy of Medical Sciences

Other

Registry information

Official study title

Phase II Trial of Raltitrexed and Paclitaxel as Second-line Chemotherapy for Patients With Unresectable or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma

Important dates

Study start
2015
Primary completion
2017
Study completion
2018
First posted
Mar 20, 2017
Registry last updated
Feb 1, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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