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Efficacy and Safety Study of Bendamustine With or Without Rituximab in Chronic Lymphoproliferative Disorders

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Gruppo Italiano Studio Linfomi

Status

Completed

Conditions

Chronic Lymphocytic Leukaemia

Study type

Observational

Funder types

Other

Identifiers

NCT01832597
RetroBENDA

Details and patient eligibility

About

The purpose of this study is collect and evaluate the clinical experience reached in Italy on the use of bendamustine alone or combined with rituximab as treatment of patients with relapsed or refractory chronic lymphoproliferative disorders.

Full description

All patients who meet the criteria for inclusion will be included in the study. A specific database will be created to collect the following information: personal data, medical history, histology related to the underlying disease, comorbidities, laboratory data, initial staging, data on the dosage and the number of cycles administered, the recorded toxicity data, the clinical response and the main events (relapse, progression, death, and cause of death). These data will then be retrospectively examined in order to obtain information about the life-saving treatment.

Enrollment

109 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with relapsed or refractory chronic lymphoproliferative disorders
  • salvage treatment with Bendamustine +/- Rituximab
  • age ≥ 18 years

Exclusion criteria

  • previous treatment with Bendamustine

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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