Cascade Testing for Hereditary Cancer Syndromes: Should We Move Toward Direct Relative Contact? A Systematic Review and Meta-Analysis

Author:

Frey Melissa K.1ORCID,Ahsan Muhammad Danyal1ORCID,Bergeron Hannah1ORCID,Lin Jenny1ORCID,Li Xuan1ORCID,Fowlkes Rana K.1ORCID,Narayan Priyanka1,Nitecki Roni2ORCID,Rauh-Hain Jose Alejandro2,Moss Haley A.3ORCID,Baltich Nelson Becky1ORCID,Thomas Charlene1ORCID,Christos Paul J.1,Hamilton Jada G.4ORCID,Chapman-Davis Eloise1,Cantillo Evelyn1,Holcomb Kevin1ORCID,Kurian Allison W.5ORCID,Lipkin Steven1ORCID,Offit Kenneth4,Sharaf Ravi N.1ORCID

Affiliation:

1. Weill Cornell Medicine, New York, NY

2. MD Anderson Cancer Center, Houston, TX

3. Duke University Medical Center, Durham, NC

4. Memorial Sloan Kettering Cancer Center, New York, NY

5. Stanford University School of Medicine, Palo Alto, CA

Abstract

PURPOSE Evidence-based guidelines recommend cascade genetic counseling and testing for hereditary cancer syndromes, providing relatives the opportunity for early detection and prevention of cancer. The current standard is for patients to contact and encourage relatives (patient-mediated contact) to undergo counseling and testing. Direct relative contact by the medical team or testing laboratory has shown promise but is complicated by privacy laws and lack of infrastructure. We sought to compare outcomes associated with patient-mediated and direct relative contact for hereditary cancer cascade genetic counseling and testing in the first meta-analysis on this topic. MATERIALS AND METHODS We conducted a systematic review and meta-analysis in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines (PROSPERO No.: CRD42020134276). We searched key electronic databases to identify studies evaluating hereditary cancer cascade testing. Eligible trials were subjected to meta-analysis. RESULTS Eighty-seven studies met inclusion criteria. Among relatives included in the meta-analysis, 48% (95% CI, 38 to 58) underwent cascade genetic counseling and 41% (95% CI, 34 to 48) cascade genetic testing. Compared with the patient-mediated approach, direct relative contact resulted in significantly higher uptake of genetic counseling for all relatives (63% [95% CI, 49 to 75] v 35% [95% CI, 24 to 48]) and genetic testing for first-degree relatives (62% [95% CI, 49 to 73] v 40% [95% CI, 32 to 48]). Methods of direct contact included telephone calls, letters, and e-mails; respective rates of genetic testing completion were 61% (95% CI, 51 to 70), 48% (95% CI, 37 to 59), and 48% (95% CI, 45 to 50). CONCLUSION Most relatives at risk for hereditary cancer do not undergo cascade genetic counseling and testing, forgoing potentially life-saving medical interventions. Compared with patient-mediated contact, direct relative contact increased rates of cascade genetic counseling and testing, arguing for a shift in the care delivery paradigm, to be confirmed by randomized controlled trials.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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