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Evaluation of Patient and Lesion Specific Prognostic Factors for Standard Radioimmunotherapy (MERIT-NHL)

U

University Hospital, Saarland

Status

Unknown

Conditions

Follicular Lymphoma

Study type

Observational

Funder types

Other

Identifiers

NCT01151358
MERIT-NHL

Details and patient eligibility

About

MERIT-NHL as an addendum to the International Registry of Radioimmunotherapy (RIT registry) pooling clinical data of patients who suffered from a non-Hodgkin´s lymphoma also includes the documentation of the respective FDG-PET and CT-image files in an online archive.

Based on these documented clinical and imaging data, the MERIT study group centrally performs an intra- as well as interindividual evaluation of follicular CD20+ lymphoma lesions before and after radioimmunotherapy. According to this, the aim of the MERIT-NHL study is to prospectively identify yet unknown patient- and lesion specific prognostic factors predicting patient´s outcome in line with the therapeutic modality radioimmunotherapy.

Enrollment

150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • standard radioimmunotherapy with 90-yttrium-labeled anti-CD20-antibodies in treatment of relapsed and/or refractory follicular NHL or partial remission after induction chemotherapy
  • finding of at least one image-guided measurable lymphoma lesion
  • existence of FDG-PET- and CT-image data of at most 8 weeks before treatment
  • signed patient´s agreement for RIT registry and MERIT-NHL

Exclusion criteria

  • other therapy modalities than standard radioimmunotherapy (e.g. consolidation)
  • solely CNS-lymphoma or primary effusion lymphoma

Trial contacts and locations

4

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Central trial contact

Anja Hoock; Aleksandar Grgic, MD

Data sourced from clinicaltrials.gov

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