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May 2, 20262 citations

Bridging the distance in precision oncology: a nationwide survey on institutional perspectives toward telemedicine and decentralized trials in Japan.

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HTHiroya TaniguchiTKTakeshi KawakamiHSHironaga Satake

Key Points

  • The survey aims to assess institutional challenges in implementing genomic profiling and the perceived effectiveness of telemedicine and decentralized trials.
  • Nationwide web-based questionnaire sent to professionals at government-designated cancer genomic hospitals.
  • Responses focused on institutional data and barriers to CGP access, telemedicine use, and trial participation.
  • Data collected between December 2024 and February 2025 from 194 professionals across 140 hospitals.
  • 23.5% of CGP-tested patients referred from non-designated hospitals faced multiple visits.
  • 58% of respondents supported using telemedicine for informed consent and result disclosure, citing reduced travel burden.
  • 61% reported that over half of eligible patients declined genotype-matched trials due to travel distance.

Abstract

BACKGROUND: Comprehensive genomic profiling (CGP) has been reimbursed under Japan's universal health coverage since 2019, yet access remains uneven because designated institutions are concentrated in urban areas. Although CGP can identify actionable alterations, fewer than 10% of patients receive matched therapies, often due to geographic barriers to clinical trial enrollment. This nationwide survey evaluated institutional challenges in CGP implementation and explored the perceived role of telemedicine and decentralized clinical trials (DCTs) in improving equitable access. METHODS: A web-based questionnaire was distributed to professionals involved in CGP across government-designated hospitals for cancer genomic medicine between December 2024 and February 2025. Respondents provided institutional data and perceptions regarding CGP access, telemedicine use, and barriers to trial participation. RESULTS: A total of 194 professionals from 140 hospitals responded. On average, 23.5% of CGP-tested patients were referred from non-designated hospitals, often requiring multiple in-person visits. Fifty-eight percent of respondents supported telemedicine for both informed consent and result disclosure, citing reduced travel burden, while concerns included digital literacy and institutional workload. Sixty-one percent reported that over half of eligible patients declined genotype-matched trials due to travel distance. Institutions facing higher dropout rates expressed greater support for DCTs (67% "strongly needed"). CONCLUSION: This nationwide study identified major geographic and logistical barriers to equitable precision oncology in Japan. Most institutions view telemedicine and DCTs as essential to expanding access to genomic testing and clinical trials. Japan's experience may offer insights for other healthcare systems considering integration of telemedicine into national precision oncology frameworks under universal health coverage.

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Cite This Study

Taniguchi et al. (2026) studied this question.

synapsesocial.com/papers/69f5941871405d493affef4ehttps://doi.org/10.1007/s10147-026-03034-x
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