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CompletedNCT02945319Updated Jun 7, 2021

Integrated Molecular and Clinical Profiling to Optimize Outcome Prediction in Splenic Marginal Zone Lymphoma

An observational study in Splenic Marginal Zone Lymphoma, sponsored by International Extranodal Lymphoma Study Group (IELSG). Completed at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-06-07.

Sponsored by International Extranodal Lymphoma Study Group (IELSG) · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
373
Ages
18 Years and older
Sex
All
01

Study summary

The study aims at developing and validating an integrated clinico-molecular model for an accurate survival prognostication in newly diagnosed SMZL.

Already existing and coded tumor biological material and health-related personal data will be retrospectively collected. Mutation analysis will be performed by targeted deep next generation sequencing of tumor genomic DNA. Deletion of 7q will be assessed by FISH on nuclei isolated from tumor tissues. Immunoglobulin gene rearrangement and mutation status will be analyzed on tumor genomic DNA by PCR and Sanger sequencing. The methylation status of target genes will be assessed by methylation specific PCR on tumor genomic DNA.

The adjusted association between exposure variables and OS will be estimated by Cox regression. This approach will provide the covariates independently associated with OS that will be utilized in the development of a hierarchical molecular model to predict OS. The hierarchical order of relevance in predicting OS among covariates will be established by recursive partitioning analysis. An amalgamation algorithm will be used to merge terminal nodes showing homogenous OS. The discrimination capacity of the model will be assessed by calculating the c-index. Relative survival analysis will be used to provide a measure of the excess mortality experienced by patient's subgroups stratified according to the developed hierarchical molecular models, irrespective of whether the excess mortality is directly or indirectly attributable to the disease. The model developed in the training set will be tested in the validation sets and the model performance (c-index) in the validation set will be compared with that in the training set.

02

Conditions studied

  • Splenic Marginal Zone Lymphoma
03

In context

Lymphoma

5,578 studies on the registry are indexed under Lymphoma; 825 are open to participants now.

This study's enrollment of 373 is above the median of 136 across 625 observational studies indexed under Lymphoma.

Browse Lymphoma studies →

Lead sponsor

International Extranodal Lymphoma Study Group (IELSG) is the lead sponsor of 29 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients with diagnosis of SMZL on spleen histology.

Inclusion criteria

  • Male or female adults 18 years or older
  • Diagnosis of SMZL on spleen histology before Dec 31st 2010 (to provide the cohort with a minimum follow-up of at least 5 years)
  • Availability of tumor material (from spleen, peripheral blood or bone marrow) collected before initiation of medical therapy
  • Availability of the baseline and follow-up annotations

Exclusion criteria

Exclusion Criteria:

  • Having received any medical therapy including anti CD20 monoclonal antibody, chemotherapy or biological agents before splenectomy
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
373 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Overall survival (OS)

    Time frame: From date of enrollment to study ending at 2 years

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Study locations

1 site
  • IOSI
    Bellinzona, 6500, Switzerland
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 7, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02945319
Lead sponsor
International Extranodal Lymphoma Study Group (IELSG)
Responsible party
Sponsor
First posted
Oct 26, 2016
Start date
Jan 2017
Primary completion
Dec 2020
Completion
Dec 2020
Last update
Jun 7, 2021

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2021. You cannot join it, but the record below documents what was studied.

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