RecruitingNCT06782789

An Italian Multicentric Retrospective Observational Study to Assess Effectiveness and Safety of the Combination of Tafasitamab and Lenalidomide in Diffuse Large B-cell Lymphoma Patients Treated Under Named Patient Program


Sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Enrollment

96 participants

Start Date

Mar 1, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

The study is pilot, observational, retrospective, Italian multicenter study.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Histologically confirmed diagnosis of R/R DLBCL.
  • Patientswho received at least one dose of tafasitamab in association with lenalidomide under the NPP (D.M. 7 Sep 2017), between April 2022 and December 2022.
  • Age ≥ 18 years at enrollment.
  • Signature of written informed consent (if applicable).

Exclusion Criteria1

  • \) R/R DLBCL patients who received tafasitamab in association with lenalidomide in a clinical trial context.

Locations(11)

IRCCS Azienda Ospedaliero - Universitaria di Bologna

Bologna, Bologna, Italy

AO Sant'Anna e San Sebastiano di Caserta

Caserta, Caserta, Italy

A.R.N.A.S. Garibaldi

Catania, Catania, Italy

Azienda Ospedaliera Universitaria Arcispedale S. Anna

Ferrara, Italy

Azienda Ospedaliero Universitaria Careggi

Florence, Italy

Irccs Ospedale San Raffaele

Milan, Italy

Azienda Ospedaliero-Universitaria Maggiore della Carità

Novara, Italy

Azienda Ospedaliera Villa Sofia Cervello

Palermo, Italy

Ospedale Guglielmo da Saliceto di Piacenza

Piacenza, Italy

IRCCS- Istituto Nazionale Tumori Regina Elena

Roma, Italy

Fondazione Policlinico Universitario A. Gemelli IRCCS

Roma, Italy

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NCT06782789


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