Analysis by TeloView® Technology Predicts the Response of Hodgkin’s Lymphoma to First-Line ABVD Therapy

Author:

Knecht Hans1ORCID,Johnson Nathalie1,Bienz Marc N.1ORCID,Brousset Pierre2,Memeo Lorenzo3ORCID,Shifrin Yulia4,Alikhah Asieh4,Louis Sherif F.4,Mai Sabine56ORCID

Affiliation:

1. Division of Hematology, Jewish General Hospital, McGill University, Montréal, QC H3A 0G4, Canada

2. Toulouse Cancer Center, Université de Toulouse, 31000 Toulouse, France

3. Pathology Unit, Department of Experimental Oncology, Mediterranean Institute of Oncology, 95029 Viagrande, Italy

4. Telo Genomics Corp., Toronto ON M5G 1L7, Canada

5. Department of Physiology and Pathophysiology, University of Manitoba, Winnipeg, MB R3T 2N, Canada

6. CancerCare Manitoba Research Institute, CancerCare Manitoba, Winnipeg, MB R3E 0V9, Canada

Abstract

Classic Hodgkin’s lymphoma (cHL) is a curable cancer with a disease-free survival rate of over 10 years. Over 80% of diagnosed patients respond favorably to first-line chemotherapy, but few biomarkers exist that can predict the 15–20% of patients who experience refractory or early relapsed disease. To date, the identification of patients who will not respond to first-line therapy based on disease staging and traditional clinical risk factor analysis is still not possible. Three-dimensional (3D) telomere analysis using the TeloView® software platform has been shown to be a reliable tool to quantify genomic instability and to inform on disease progression and patients’ response to therapy in several cancers. It also demonstrated telomere dysfunction in cHL elucidating biological mechanisms related to disease progression. Here, we report 3D telomere analysis on a multicenter cohort of 156 cHL patients. We used the cohort data as a training data set and identified significant 3D telomere parameters suitable to predict individual patient outcomes at the point of diagnosis. Multivariate analysis using logistic regression procedures allowed for developing a predictive scoring model using four 3D telomere parameters as predictors, including the proportion of t-stumps (very short telomeres), which has been a prominent predictor for cHL patient outcome in a previously published study using TeloView® analysis. The percentage of t-stumps was by far the most prominent predictor to identify refractory/relapsing (RR) cHL prior to initiation of adriamycin, bleomycin, vinblastine, and dacarbazine (ABVD) therapy. The model characteristics include an AUC of 0.83 in ROC analysis and a sensitivity and specificity of 0.82 and 0.78 respectively.

Funder

Telo Genomics, Toronto, Ontario, Canada

Publisher

MDPI AG

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