BRCA testing delay during the COVID-19 pandemic: How to act?

Angelo Minucci1, Giovanni Scambia2,3, Maria De Bonis4

  • 1Molecular and Genomic Diagnostics Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy. angelo.minucci@policlinicogemelli.it.

Molecular Biology Reports
|December 14, 2020
PubMed

Insights

The COVID-19 pandemic significantly reduced germline BRCA1/2 (gBRCA) testing, with no recovery post-lockdown. This delay impacts cancer patient management and questions the future of oncogenetic testing.

Area of Science:

  • Oncology
  • Genetics
  • Epidemiology

Background:

  • The COVID-19 pandemic caused widespread disruption to healthcare services globally.
  • Germline BRCA1/2 (gBRCA) testing is crucial for managing hereditary cancers, including ovarian, breast, pancreas, and prostate cancers.
  • Initial reports indicated a significant drop in gBRCA testing during the early COVID-19 lockdown in Italy.

Purpose of the Study:

  • To evaluate the ongoing impact of the COVID-19 pandemic on gBRCA testing rates.
  • To analyze gBRCA testing trends post-lockdown and compare them with pre-pandemic years.
  • To assess the long-term implications of pandemic-related testing delays on cancer patient care.

Main Methods:

  • Retrospective analysis of gBRCA testing data from a referral center in Italy.
  • Comparison of testing volumes during lockdown (March-April 2020) and post-lockdown (May-October 2020).
  • Trend analysis of annual gBRCA testing data from 2017 to 2020.

Main Results:

  • gBRCA testing rates did not significantly increase after the initial lockdown period.
  • Testing volumes in May-October 2020 remained low, similar to the lockdown phase.
  • Overall gBRCA testing in 2020 (January-October) showed a significant decline compared to previous years, mirroring 2017 trends.
  • The pandemic has caused a notable delay in oncogenetic testing for both cancer patients and healthy individuals.

Conclusions:

  • The COVID-19 pandemic has severely impacted gBRCA testing, leading to significant delays in diagnosis and management.
  • The observed trends question the sustainability of advancements in hereditary cancer management.
  • Urgent measures are needed to ensure the continuity of oncogenetic testing services and integrate them into new diagnostic and clinical strategies.