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TEST:
LymphoTrack® Dx IGK Assay

Type:
Laboratory Developed Test
Related tests:
Evidence

News

15d
Measurable Residual Disease Monitoring for Philadelphia Positive Acute Lymphoblastic Leukemia (Ph+ALL) in the Setting of the Gimema ALL2820 Trial (ASH 2024)
Samples derived from cases from both the experimental and the control arm, based respectively on ponatinib followed by blinatumomab and on a combination of imatinib and conventional chemotherapy. While some groups reported a higher predictive prognostic power of IG/TR monitoring, our findings do not confirm these data, also in view of the very low rate of relapses so far observed. Nevertheless, a double-hit strategy may be informative for MRD monitoring and possibly for the distinction between typical/lymphoid Ph+ ALL vs multilineage/CML-like Ph+ ALL.
IO biomarker
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ABL1 (ABL proto-oncogene 1) • IKZF1 (IKAROS Family Zinc Finger 1)
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ABL1 fusion
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LymphoTrack® Dx IGH Assay • LymphoTrack® Dx IGK Assay
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imatinib • Iclusig (ponatinib) • Blincyto (blinatumomab)
almost1year
Next-Generation Sequencing of Vitreoretinal Lymphoma by Vitreous Liquid Biopsy: Diagnostic Potential and Genotype/Phenotype Correlation. (PubMed, Invest Ophthalmol Vis Sci)
Overall, NGS of the vitreous demonstrated high sensitivity among conventional diagnostic tests. VRL and CNSL appeared to have both shared and distinct genetic variations, which may suggest site-specific variations from a common origin.
Journal • Liquid biopsy • Next-generation sequencing • Biopsy
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CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) • MYD88 (MYD88 Innate Immune Signal Transduction Adaptor) • IGH (Immunoglobulin Heavy Locus) • ETV6 (ETS Variant Transcription Factor 6) • IL6 (Interleukin 6) • IL10 (Interleukin 10) • PIM1 (Pim-1 Proto-Oncogene) • IGLL5 (Immunoglobulin Lambda Like Polypeptide 5)
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MYD88 mutation • MYD88 L265P
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LymphoTrack® Dx IGH Assay • LymphoTrack® Dx IGK Assay
over1year
NON-INVASIVE MINIMAL RESIDUAL DISEASE ANALYSIS BY IMMUNOGLOBULIN GENE REARRANGEMENTS ON CIRCULATING TUMOR DNA PREDICTS THE OUTCOME OF PATIENTS WITH DIFFUSE LARGE B-CELL LYMPHOMA (EHA 2023)
A multicenter cohort of 53 consecutive newly diagnosed DLBCL treated with R-CHOP was included in this study... In most DLBCL patients at diagnosis, ctDNA was suitable for IG-based biomarker identification by NGS and was comparable to diagnostic LN biopsies. ctDNA MRD evaluation both at interim and at EOT allowed to predict theoutcome of DLBCL patients. ctDNA MRD can refine the CT/PET-CT-based response.
Clinical • Minimal residual disease • Circulating tumor DNA
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LymphoTrack® Dx IGH Assay • LymphoTrack® Dx IGK Assay
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Rituxan (rituximab)
2years
Clinical implication of minimal residual disease assessment by next-generation sequencing-based immunoglobulin clonality assay in pediatric B-acute lymphoblastic leukemia. (PubMed, Front Oncol)
"Our study demonstrated that MRD assessment by NGS-based Ig clonality assay could be applied in most pediatric B-ALL patients. Normalized post-induction MRD <0.01% was a significant prognostic indicator."
Journal • Minimal residual disease
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LymphoTrack® Dx IGH Assay • LymphoTrack® Dx IGK Assay