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Clinical Trials/NCT02992223
NCT02992223
Completed
Not Applicable

Retrospective Collection of Data on Patient With Relapsed/Refractory Aggressive Non Hodgkin Lymphoma Treated With Y90 Ibritumomab Tiuxetan Radioimmunotherapy Plus High-Dose Chemotherapy and Autologous Stem Cell Transplant

A.O.U. Città della Salute e della Scienza0 sites58 target enrollmentJuly 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Refractory B-Cell Non-Hodgkin Lymphoma
Sponsor
A.O.U. Città della Salute e della Scienza
Enrollment
58
Primary Endpoint
Overall Survival
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Evaluate if Y90 Ibritumomab Tiuxetan Radioimmunotherapy in addition to standard high dose chemotherapy followed by autologous stem cell transplant could improve prognosis in patients affected by relapsed/refractory aggressive non Hodgkin lymphoma

Registry
clinicaltrials.gov
Start Date
July 2014
End Date
July 2015
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
A.O.U. Città della Salute e della Scienza
Responsible Party
Principal Investigator
Principal Investigator

Barbara Botto

MD

A.O.U. Città della Salute e della Scienza

Eligibility Criteria

Inclusion Criteria

  • High Risk Relapsed/refractory aggressive non-hodgkin lymphoma defined as:
  • Progressive disease
  • Early relapse (within 12 months from response)
  • Recurrent relapse
  • Treated with salvage chemotherapy followed by Y90 Ibritumomab Tiuxetan plus high-dose chemotherapy and Autologous stem cell transplant
  • Age \> 18 years
  • Previous treatment with Rituximab
  • Written informed consent

Exclusion Criteria

  • Patient with no complete data available for collection

Outcomes

Primary Outcomes

Overall Survival

Time Frame: Date of last follow-up for at least 18 months (up to 78 months)

Time to last follow-up or death

Progression Free Survival

Time Frame: From first response to last follow-up for at least 18 month (up to 78 months)

Time from last response to nearest relapse or follow-up

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