Pre-Implementation Assessment of the Acceptability of Using Circulating Micrornas for Follow-Up of Malignant Germ-Cell Tumors

MicroRNAs are short, non-protein-coding RNAs. Circulating microRNA testing is likely to transform future management of patients with testicular cancer, including diagnosis, disease monitoring, and follow-up. Here, we undertook patient and public involvement workshops to explore consumer views on replacing routine serial computed tomography (CT) scans with non-invasive, blood-based microRNA testing. Our user consultation study suggests high acceptability of this test with benefits versus traditional CT scan-based follow-up. Background: MicroRNAs from the miR-371(similar to)373 and miR-302/367 clusters, particularly miR-371 a-3p, are promising biomarkers for blood-based diagnosis and disease monitoring of malignant germ cell tumors (GCTs) and are nearing clinical implementation. These biomarkers have superior sensitivity and specificity compared with current markers alpha-fetoprotein (AFP) and human chorionic gonadotropin (HCG). We explored patient acceptability of using circulating microRNAs to replace multiple serial computed tomography (CT) scans in malignant GCT follow-up. Patients and Methods: Two workshops involved interactive presentations and focus groups. Discussions were digitally recorded and transcribed verbatim. Qualitative thematic analysis of transcripts identified the key themes. Results: Prior to the workshops, potential participants expressed concern about the adoption of new blood tests due to personal experiences of the limitations of existing (AFP/HCG) markers. Twelve males (22-57 years of age; currently, 26-59 years of age) with a malignant GCT diagnosis participated; all were in follow-up. Three had experienced recurrence. Participants had cumulative exposure of between 1 and 15 CT scans. Data saturation was reached at the second workshop; five themes emerged underpinning preference for microRNA testing versus CT scans: (1) increased sensitivity and safety, (2) reduced financial costs, (3) reduced time for testing and results, (4) practicalities, and (5) reduced anxiety. However, some participants perceived an increased diagnostic capacity of CT scans versus blood testing. Conclusion: This first user consultation of circulating microRNA testing for future malignant GCT follow-up suggests high acceptability with potential patient and healthcare system benefits. (C) 2021 Elsevier Inc. All rights reserved.