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Letter
Management strategies for the colonoscopic surveillance of people with Lynch syndrome during the COVID-19 pandemic
  1. Kevin J Monahan1,2,
  2. Anne Lincoln3,
  3. James E East4,
  4. Sally Benton5,
  5. John Burn6,
  6. Bianca DeSouza7,
  7. Helen Hanson8,
  8. Fiona Lalloo9,
  9. Terri McVeigh10,
  10. Matthew D Rutter11,12,
  11. Katie Snape8,
  12. Huw J W Thomas1,2,
  13. Peter Sasieni3
  1. 1The Lynch Syndrome and Family Cancer Clinic, St Mark's Hospital and Academic Institute, Harrow, London, UK
  2. 2Imperial College London, London, UK
  3. 3Comprehensive Cancer Centre, King's College London, London, UK
  4. 4Translational Gastroenterology Unit, John Radcliffe Hospital, Oxford, UK
  5. 5NHS Bowel Cancer Screening South of England Hub, Royal Surrey County Hospital NHS Foundation Trust, Guildford, Surrey, UK
  6. 6Institute of Human Genetics, Newcastle upon Tyne, UK
  7. 7Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, UK
  8. 8Clinical Genetics, St George's University Hospitals NHS Foundation Trust, London, UK
  9. 9Genetic Medicine, Central Manchester University Hospitals Foundation Trust, Manchester, UK
  10. 10Cancer Genetics Unit, Royal Marsden NHS Foundation Trust, London, UK
  11. 11Gastroenterology, University Hospital of North Tees, Stockton-on-Tees, UK
  12. 12Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK
  1. Correspondence to Dr Kevin J Monahan, The Lynch Syndrome and Family Cancer Clinic, St Mark's Hospital and Academic Institute, Harrow HA1 3UJ, London, UK; k.monahan{at}imperial.ac.uk

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The recent publication of UK guidelines for the management of hereditary colorectal cancer1 immediately preceded the COVID-19 pandemic.

We commend the response by the British Society of Gastroenterology (BSG) relating to GI endoscopy activity amidst this pandemic.2 Such urgent measures are required to curtail the rate and breadth of coronavirus transmission throughout the country, and we are of the belief that the adherence to these guidelines during the early stages of this global pandemic was crucial in saving lives, and further guidance relating to the ‘recovery’ phase will be crucial in delivering diagnostic and cancer preventing endoscopic interventions.

Though the emergency endoscopy COVID-19 guidance expressed clear and justified recommendations for the suspension of these services in non-urgent or routine screening populations, the management of patients deemed as being ‘high risk’ and subsequently prioritised for colonoscopy during this time is not currently well defined. For example, specific guidance for surveillance of individuals with conditions such as Lynch syndrome appeared vague in some statements and altogether omitted from early guidance announcements.3

Lynch syndrome is an inherited cancer predisposition syndrome defined by the presence of pathogenic or germline variants within any one of the mismatch repair (MMR) genes. Lynch syndrome is known to affect up to 1:125 of the UK population and presents a high lifetime risk of colorectal cancer (observed anywhere between 10% and 47% dependent on age and MMR mutation).4

In this patient population, routine 2-yearly colonoscopy may have been cancelled or postponed until further notice in response to emergency COVID-19 guidelines, and given the present backlog of patients awaiting colonoscopy, we imagine that local centres may opt to classify these patients as falling into a ‘category 3’, that is, potentially deferred for colonoscopy for the indefinite future.

The cancer prevalence in the Lynch syndrome patient population undergoing 2-yearly colonoscopy is observed at 4%–5%,4 5 with an annual incidence rate of 1%–4% (depending on age and affected MMR gene). These surveillance-detected cancers are usually identified at an early stage and are thus associated with good survival outcomes. The prevalence of colorectal cancer in this patient population at the time of their scheduled screening colonoscopy is therefore higher than the 3% threshold used for urgent 2-week wait (2WW) referred of patients with suspected cancer symptoms according to National Institute for Health and Care Excellence guidelines (NG12).6

We therefore propose, as in interim solution, the use of faecal immunochemical test (FIT) as a method of risk stratification of individuals with Lynch syndrome who are due surveillance colonoscopy, which may not currently be possible to provide easily. FIT, with a low cut-off at 10 µg/g faeces detects 90% of cancers in low-risk symptomatic primary care populations.7 However, with the roll-out of FIT in secondary care for symptomatic 2WW patients, endoscopy services throughout the country are now inundated with the task of deploying FIT kits as a strategic intervention in colonoscopy prioritisation.

In addressing the need of people with Lynch syndrome, we have collectively developed and are rolling out a clinical service pilot proposal entitled ‘Rapid evaluation of FIT levels in individuals with a Lynch syndrome pathogenic variant to determine a revised threshold for colonoscopy in response to the COVID-19 pandemic’. In our interim testing pathway, patients with a FIT level of 10 µg/g faeces or greater will be prioritised for urgent colonoscopic surveillance. We do not envisage that FIT will permanently replace colonoscopy as the primary method of surveillance for people with Lynch syndrome, but suggest that it is an appropriate solution during a public health emergency. Additionally, the role of FIT as a less invasive surveillance strategy has the potential to avoid harm to these patients and complement colonoscopy as the primary modality.

References

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Footnotes

  • Twitter @kevinjmonahan

  • Contributors The document was written by the lead author with edits from all authors.

  • Funding The pilot study ‘Rapid evaluation of FIT levels in individuals with a Lynch syndrome pathogenic variant to determine a revised threshold for colonoscopy in response to the COVID-19 pandemic’ is supported by St Mark's Hospital Foundation and funded by the 40tude charity. James E. East was funded by the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre. The views expressed are those of the authors and not necessarily those of the National Health Service, the NIHR or the Department of Health.

  • Competing interests KJM: Medical advisory board of Bowel Cancer UK, Lynch Syndrome UK, Funding for Lynch colonoscopic surveillance study awarded by 40tude charity. FL: FAP trial (now closed) with funding awarded to NHS trust research facility. JE: Advisory board Lumendi, Boston Scientific; Speaker feesOlympus, Falk. MDR: speaker fees: SwissSCWeb, Pentax; Research Grant: Olympus; Consultancy: Norgine. JB: a patent for high-speed low-cost tumour profiling pending to John Burn and QuantuMDx.

  • Patient and public involvement Patients and/or the public were not involved in the design, conduct, reporting or dissemination plans of this research.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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