Ibrutinib Combined With R-CHOP/R-DHAP in Newly Diagnosed Mantle Cell Lymphoma Patients Who Aged ≤65 Years

NCT05429918 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2022-06-23

No results posted yet for this study

Summary

The purpose of the study is to better and systematically collect clinical data on the treatment of ibrutinib combined with R-CHOP/DHAP regimen for more scientific and accurate evaluation, our center has carried out the R-CHOP/R-DHAP alternative regimen combined with ibrutinib at age ≤ An observational clinical study on the safety and effectiveness of 65-year-old mantle cell lymphoma. Through this study, young mantle cell lymphomas in the Chinese population can be collected. Ibrutinib combined with R-CHOP/R-DHAP is used in the initial treatment. 2 and 6 cycles of ORR were used to evaluate survival indicators, and collect adverse reactions during treatment and recurrence rate after treatment.

Conditions

Sponsors & Collaborators

  • The Second Affiliated Hospital of Dalian Medical University

    collaborator OTHER
  • Peking University First Hospital

    collaborator OTHER
  • Beijing Hospital

    collaborator OTHER_GOV
  • Beijing Tsinghua Changgeng Hospital

    collaborator OTHER
  • China-Japan Friendship Hospital

    collaborator OTHER
  • Chinese PLA General Hospital

    collaborator OTHER
  • First Affiliated Hospital of Harbin Medical University

    collaborator OTHER
  • Baotou Cancer Hospital

    collaborator OTHER
  • Beijing Shijitan Hospital, Capital Medical University

    collaborator OTHER
  • Shanxi Province Cancer Hospital

    collaborator OTHER
  • Beijing Naval General Hospital

    collaborator OTHER
  • First Hospital of China Medical University

    collaborator OTHER
  • Jilin Provincial Tumor Hospital

    collaborator OTHER
  • Shengjing Hospital

    collaborator OTHER
  • 307 Hospital of PLA

    collaborator OTHER
  • Peking Union Medical College Hospital

    collaborator OTHER
  • Harbin Medical University

    collaborator OTHER
  • Beijing Tongren Hospital

    collaborator OTHER
  • Peking University Third Hospital

    lead OTHER

Principal Investigators

  • Hongmei Jing, Professor · Peking University Third Hospital

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-12-30
Primary Completion
2023-12-30
Completion
2024-06-30

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05429918 on ClinicalTrials.gov