Constitutional pathogenic variants in TP53 are associated with Li-Fraumeni syndrome or the more recently described heritable TP53-related cancer syndrome and are associated with increased lifetime risks of a wide spectrum of cancers. Due to the broad tumour spectrum, surveillance for this patient group has been limited. To date, the only recommendation in the UK has been for annual breast MRI in women; however, more recently, a more intensive surveillance protocol including whole-body MRI (WB-MRI) has been recommended by International Expert Groups. To address the gap in surveillance for this patient group in the UK, the UK Cancer Genetics Group facilitated a 1-day consensus meeting to discuss a protocol for the UK. Using a preworkshop survey followed by structured discussion on the day, we achieved consensus for a UK surveillance protocol for TP53 carriers to be adopted by UK Clinical Genetics services. The key recommendations are for annual WB-MRI and dedicated brain MRI from birth, annual breast MRI from 20 years in women and three-four monthly abdominal ultrasound in children along with review in a dedicated clinic.
- clinical genetics
- paediatric oncology
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Li-Fraumeni syndrome (LFS) is a rare inherited cancer predisposition syndrome, first described by Frederick Li and Joseph Fraumeni in 1969.1 LFS is caused by pathogenic variants (PVs) in the TP53 gene.2 Individuals with LFS have a very substantially increased lifetime risk of cancer, with risks reported to be as high as 22% by 5 years of age, 41% by 18 years of age and approaching 100% by 70 years of age.3 4 The most frequent cancers that occur in patients with LFS are bone and soft tissue sarcomas, very early-onset breast cancer, malignant tumours of the central nervous system and adrenocortical cancers (ACCs). However, of note, with expanded testing of cancer predisposition genes outside the context of a strong family history of cancer and identification of TP53 PVs in population databases, there is widening recognition that the phenotypical spectrum and cancer risk for individuals with a constitutional TP53 PV may be both broader and lower than initially described.5–7 This has led to recent suggestions to expand the clinical description of constitutional TP53 PVs from LFS to a wider cancer predisposition syndrome designated heritable TP53-related cancer syndrome (hTP53rc) (GD Evans from GENTURIS expert group, personal communication).
Most TP53 carriers in the UK have been identified through referral to clinical genetics services due to a strong personal or family history of cancer, where genetic testing has largely been recommended on clinical criteria such as the ‘Chompret criteria’.3 Once a PV has been identified within a family, predictive genetic testing can be offered to at-risk relatives.
There has been a long-standing hesitancy to offer genetic testing of TP53 due to the absence of surveillance recommendations should a TP53 PV be identified. To date, the only nationally agreed surveillance recommendation for individuals with a TP53 PV has been for breast surveillance with annual breast MRI from age 20 in women.8 However, over the past 5 years, recommendations for more comprehensive surveillance for TP53 carriers have been made, most notably the Toronto protocol, an intensive protocol involving clinical, biochemical and radiological surveillance that has demonstrated a survival benefit.9 10 One of the unique aspects of this protocol is the use of whole-body MRI (WB-MRI). WB-MRI has been separately studied in a number of centres across North America, Canada and Europe, and a meta-analysis of the data from 13 studies in 578 TP53 carriers from six countries, including the UK SIGNIFY study, evidences a 7% (95% CI 5% to 9%) new cancer detection rate, with the majority of cancers being detected at a sufficiently early stage to allow treatment with curative intent.11 12
In 2017, an expert international group published recommendations on surveillance for individuals with LFS.13 This publication necessitated a review of current UK practice. Therefore, the UK Cancer Genetics Group (UKCGG), with support from the George Pantziarka TP53 Trust (the UK LFS patient advocacy group), organised a national consensus meeting on 6 July 2018 to agree on a consistent approach to the management of TP53 carriers across the UK.
Preparation for the meeting included a systematic review of the literature to identify key publications on surveillance in LFS to inform discussion. As there is limited literature available on this topic, only five key publications were selected for discussion at the meeting: publications relating to the Toronto protocol, recent International Recommendations, results of a meta-analysis of baseline WB-MRI and results from a UK study of WB-MRI.9 11–13
Prior to the meeting, these publications and a survey (online supplementary information 1) were sent out to the 24 UK Regional Genetics centres. This approach has been successful for other UKCGG guidelines.14 The survey focused on questions relating to current practice and sought opinion on the surveillance recommendations made by the International TP53 Consensus Group.13 The response rate to the survey was 22/24 (91.7%). The themes arising from the survey were then used to create a series of key questions to be addressed at the consensus meeting.
Consensus Group participants
Forty-three stakeholders attended from across the UK and Ireland, including patient support group representatives (n=3), clinical cancer geneticists (n=19), genetic counsellors (n=6), paediatric oncologists (n=2), oncologists (n=3), radiologists (n=8), psychologists (n=1) and pathologists (n=1). Each of the 24 UK genetics centres was represented.
Presentation of current knowledge
The first part of the meeting was structured into a series of talks. The talks covered the history of LFS and TP53 the associated cancer risks, surveillance suggested by other expert groups, a UK perspective on WB-MRI and the survey results. These lectures provided a review of the available evidence and equipped the Consensus Group, who were from a variety of backgrounds with up-to-date evidence on which to base their recommendations. The agenda and presentations from the day are available online https://www.ukcgg.org/information-education/ukcgg-consensus-meetings/
The group was then divided into three small working groups to discuss three key questions listed as follows. Participants in each group were selected to include a range of the multidisciplinary team. Each group had a nominated facilitator and scribe. After each discussion, there was feedback and discussion and debate by the wider group until a consensus was reached. Once all delegates had discussed the three key questions, the final part of the day was a group forum to agree on a UK surveillance protocol.
Following the meeting, the agreed statements were circulated to the group and presented at the UK-CGG Winter Meeting 2018 for further comments to ensure that the statements were an accurate representation of the day and consensus had been reached. A summary of the meeting was posted on the UKCGG website in March 2019 (https://www.ukcgg.org/information-education/ukcgg-consensus-meetings/).
Most centres who responded to the survey (17/22) were not currently offering any surveillance other than the recommended annual breast MRI from age 20 years, which was available by direct referral to the NHS Breast Screening Programme. Four centres were offering adrenal ultrasound (US) in children, and three centres were able to offer WB-MRI or were in the process of trying to set this up.
With regard to opinion on the International Consensus guidelines, the main themes that arose from survey respondents were either disagreement or concern with specific areas of the guidelines and/or the implementation of any agreed recommendations within the NHS. Specifically, there was concern about the requirement for general anaesthetic for WB-MRI in childhood and uncertainty about the requirement for brain MRI, in addition to WB-MRI and the use of gadolinium in imaging. There was also strong disagreement with the recommendation for upper gastrointestinal (GI) endoscopy and lower GI colonoscopy. More general comments were the lack of clinical evidence for benefit of early detection on long-term outcome of patients and concern over the high false-positive rate of WB-MRI.
Regarding implementation of any guidelines, survey respondents wanted to address who should be responsible for coordinating surveillance and whether this should be undertaken in all centres or in specialist clinics. The change in practice towards offering predictive testing in childhood if surveillance was available was also discussed.
The results and questions raised by the survey were then split into three main themes to be discussed on the day.
Question 1: what surveillance should we recommend?
The group reviewed the International Consensus recommendations based on the Toronto Protocol.13 For the majority of the recommendations, consensus was reached that we should adopt the same recommendations. However, there was further discussion of a number of key areas; clinical breast examination, US of the abdomen and pelvis in adults, upper and lower GI endoscopy and annual dermatological examination.
Clinical breast examination has not been proven to be an effective screening tool,15 and the Department of Health issued advice that clinical breast examination was not an appropriate screening technique in February 1998 (PL/CMO/98/1). Instead the recommendation of the Consensus Group would be to ensure that women are educated in breast self-examination and to recommend annual breast MRI surveillance, and the option of risk-reducing mastectomy was discussed.
With regard to abdominal US in adults, it was not felt that US would offer additional benefit over WB-MRI in adults, particularly as the incidence of ACC in adults is low. In the Toronto study, while US in childhood was found to be beneficial, abdominal and pelvic US did not detect any cancers in adults.9
Consensus was reached not to offer surveillance of the upper GI tract. The main reason for this decision is that current data suggest that only a small number of TP53 carriers develop an upper GI malignancy. Recent data suggest that 2% of TP53 carriers develop stomach cancer and 0.6% develop oesophageal cancer.3 This risk is comparable to the general population risk of developing gastric cancer from birth to age 74 of 1.87% in men and 0.79% in women worldwide.16 Upper GI endoscopy is also not recommended in the Toronto protocol, and there is limited evidence to suggest that it results in any survival benefit.17 Although there is no specific data relating to Helicobacter pylori (HP) eradication in TP53 carriers, it is recognised that HP is a risk factor for gastric cancer and evidence that eradication reduces gastric cancer risk.18 Therefore, the group felt that advice on testing and eradication of HP should be specifically recommended, as well as more general advice not to smoke.
Consensus was reached not to offer surveillance of the lower GI tract. Colorectal cancer has been postulated to be associated with LFS; however, review of the relevant literature provides little supporting evidence for this. Sixteen cases of colorectal cancer were reported in a series of 397 patients with cancer from 64 families with LFS, giving a similar risk to general population risk (4%), although admittedly at younger ages.19 Of note, many of the patients with colorectal cancer were not proven TP53 carriers. Another study reported 6/497 TP53 carriers in a series of patients with colorectal cancer at age 40 years or younger, but evaluation of the identified variants showed that only 1/6 variants would be classified as likely pathogenic or pathogenic based on current guidelines.20 Therefore, the opinion of the Consensus Group is that there is no sufficient evidence that colorectal cancer risk is increased in LFS and that colonoscopic surveillance should only be considered if there is a family history of colorectal tumours according to recently published guidelines and investigation for other inherited causes of colorectal cancer if appropriate.21
Regarding annual dermatological review, the group recognised the resource implications for this, and it was felt that this could be undertaken by the patient’s general practitioner with a low threshold for referral to dermatology.
The Consensus Group also felt that it was important to ensure there was detailed discussion of ‘red flag’ symptoms in both children and adults and provide information on relevant resources and to discuss the importance of making positive lifestyle choices, for example, not smoking, eating a healthy diet and being physically active.
The concern raised through the premeeting survey regarding the requirement for general anaesthetic for WB-MRI in childhood was also discussed. Data on cancer risk were reviewed, and it was strongly felt that due to the high risks of cancer reported in infancy,3 general anaesthetic was acceptable in order to provide the appropriate surveillance. This position was supported by the patient advocates present at the meeting.
The group also discussed the requirement for dedicated brain MRI. Malignant tumours of the central nervous system are a core cancer in LFS. The meta-analysis of WB-MRI compared the outcomes of WB-MRI with dedicated brain MRI and demonstrated that of 10 brain tumours identified in individuals having both WB-MRI and brain MRI, 5 tumours were missed by WB-MRI.12 The Consensus Group therefore agreed that both dedicated brain MRI and WB-MRI should be included in the surveillance protocol. The use of gadolinium was felt to be necessary for the first but not subsequent scans.
The surveillance protocol agreed by the Consensus Group is detailed in table 1.
Question 2: who should we offer surveillance to?
TP53 PVs are identified in approximately 30% patients fulfilling Chompret criteria and up to 75% of patients with classic LFS.3 This discussion focused on whether we would offer surveillance only to patients with confirmed PVs in TP53, those who meet clinical criteria for LFS but do not have a confirmed TP53 PV or those with PVs predicted to be of lower penetrance for example, the Brazilian founder PV c.1010G>A, p.ArgR337His. In addition, we also considered the situation of patients who are at 50% risk of a familial TP53 PV but do not wish to proceed with predictive testing.
The Consensus Group felt that for patients with classic LFS but without a confirmed TP53 PV, surveillance should be offered for patients affected with a relevant cancer. It was felt that Li-Fraumeni-like (LFL) criteria had largely been designed to broaden the clinical criteria and increase sensitivity for testing of TP53. Therefore, for LFL families without a TP53 PV, the lifetime risks of cancer were unlikely to be in the range of that observed for classic LFS and surveillance of this patient group was not supported. With regards to lower-penetrance variants, it was felt that at present without the benefit of clear genotype phenotype correlations, the surveillance protocol should be offered to all patients with a TP53 PV, recognising that more reliable phenotype–genotype data may lead to genotype-specific modifications of these recommendations in the future.
Offering the full surveillance protocol for those at 50% risk was not considered appropriate due to the intensity of the surveillance protocol. However, women at 50% of a TP53 PV can still be offered breast MRI in line with National Institute for Clinical Excellence (NICE) guidelines.8 Children at 50% risk should be reviewed in a specialist clinic, ideally with a paediatric oncologist and clinical geneticist, to discuss the surveillance and testing, red flag symptoms. If predictive testing is not pursued open access back to the clinic should be offered for when the family wish to pursue testing or if they have further questions.
The Consensus Group noted that the recommendation of a surveillance protocol will likely change both clinician and patients’ perspectives of having a genetic test for TP53 and also that it would be appropriate to offer predictive testing in childhood for a familial PV.
The recommendations for who should be offered surveillance are set out in box 1.
Eligibility for surveillance
The aforementioned screening programme should be offered to
Patients with a TP53 PV (class 4 or 5 according to American College of Medical Genetics ACMG guidelines).
Patients with constitutional (germline) mosaicism for a TP53 PV (verified by confirmation in two tissues).
Patients with low-penetrance TP53 PVs, until further data on cancer risk available.
Patients affected with cancer fulfilling classic Li-Fraumeni syndrome (LFS) criteria#* without a pathogenic TP53 variant (confirmation of cancer diagnoses required).
The above screening programme should not be offered to
Patients at 50% risk of familial TP53 PV. Patients at 50% risk should have appropriate counselling and support but should be encouraged to consider testing in order to access cancer screening.
Paediatric patients at 50% risk of familial TP53 PV should continue to be offered support and review in a specialist clinic, but screening is not appropriate unless they are confirmed to have inherited the familial PV.
Adult patients at 50% risk.*†
*Classic LFS criteria=proband with a sarcoma diagnosed before age 45 years and a first-degree relative with any cancer before age 45 years and a first-degree or second-degree relative with any cancer before age 45 years or a sarcoma at any age.
†Women at 50% risk of a TP53 PV can be offered annual breast MRI from age 20 years.
Patients with an LFL family history. Screening should be offered on the basis of cancer in the family according to other recommended guidelines, for example, breast cancer.
Question 3: where should surveillance be offered?
It was felt by the Consensus Group that due to the expertise required in surveillance and assessment of symptoms in childhood that coordination of screening in children should managed through specialist paediatric oncology clinics.
For adults, the opinion was that coordination of screening should ideally be through clinical genetics services, provided appropriate resources where in place.
It was recognised that the ability to offer surveillance to unaffected TP53 carriers in a non-oncology setting would be preferable but not always possible due to local arrangements.
Overall, the opinion was that a small number of national specialist clinics would be best placed to manage this work and prospectively audit the surveillance protocol. However, it was recognised that the funding of such a service may be difficult.
It was agreed that WB-MRI should only be undertaken where there is sufficient radiology expertise to report the imaging and that local clinical genetics centres should consider referral for WB-MRI to another centre if their local department were unable to work to the radiology working group standards (table 1 footnote).
This is the first UK clinical guideline for the surveillance and management of TP53 carriers. The strength of the guidance is that opinion was sought prior to the meeting to identify key areas of discussion, and the Consensus Group was formed from a broad range of medical specialties and patient advocates who were given equal voice during discussion. The different perspectives and expertise of the group enriched the discussion and allowed the group to achieve a consensus view.
Our key recommendations are that a UK surveillance protocol based on international guidelines should be offered to TP53 carriers from birth. The major limitation of the guidelines is the lack of robust evidence on which to base our discussions and recommendations. However, it was recognised that due to the rarity of LFS and TP53 PVs, there is, and likely always will be, a limited evidence base to support screening recommendations in terms of early detection and cancer mortality. It is, therefore, recommended that discussion of the screening recommendations with patients should include a thorough discussion of the pros and cons of screening, consideration of the family history of cancer and that future screening recommendations may change as more data become available, particularly with respect to surveillance for specific variants. It is also recommended that screening data are prospectively collected and audited to inform future practice and fill gaps in our understanding.
The Consensus Group meeting was funded by the UK Cancer Genetics Group and The George Pantziarka TP53 Trust.
Collaborators *Consensus Group Members Dr Muna Ahmed, Clinical Genetics, Great Ormond Street Hospital; Dr Paola Angelini, Paediatric Oncology, The Royal Marsden NHS Foundation Trust; Dr Angela Brady, Clinical Genetics, North West Thames Regional Genetics Service; Dr Paul Brennan, Northern Genetics Service, Newcastle-upon-Tyne; Dr Carole Brewer, Clinical Genetics, Exeter; Dr Jackie Cook, Clinical Genetics, Sheffield; Dr Gillian Crawford, Clinical Genetics, Southampton; Dr Rosemarie Davidson, Clinical Genetics, Glasgow; Dr Mark Davis Oncology/ Clinical Genetics, Cardiff; Dr Bianca de Souza, Clinical Genetics, Guys and St Thomas’ NHS Foundation Trust; Mrs Verity Easton, Patient representative, George Pantziarka TP53 Trust; Professor Ros Eeles, Oncology/Clinical Genetics, The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust; Professor Gareth Evans, Clinical Genetics, Manchester; Dr Ian Frayling, Pathology, Cardiff; Dr Angela George, Oncology/Clinical Genetics, Royal Marsden Hospital NHS Foundation Trust; Miss Sarah Gibson, Clinical Genetics, Exeter; Dr Andrew Gogbashian, Adult Radiology, Mount Vernon; Professor Vicky Goh, Cancer Imaging, King’s College London and Clinical Radiology, Guy’s and St Thomas’ NHS Foundation Trust; Professor Andrew Green, Clinical Genetics, Dublin; Dr Lynn Greenhalgh, Clinical Genetics, Liverpool; Mr Michael Farrell; Clinical Genetics, Mater Private Hospital, Dublin; Dr Dorothy Halliday, Clinical Genetics, Oxford; Dr Helen Hanson, Clinical Genetics, St Georges NHS Foundation Trust ; Dr Louise Izatt Clinical Genetics, Guy’s and St Thomas’ NHS Foundation Trust; Dr Rosalyn Jewell, Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust; Dr Robin Jones, Oncology/Sarcoma, Royal Marsden NHS Foundation Trust; Dr Mette Jorgensen, Paediatric Oncology, Great Ormond Street Hospital; Dr Claire Lloyd, Paediatric Radiology, Guys and St Thomas’ NHS Foundation Trust; Miss Baharak Mohammadi, Clinical Genetics; Dr Alex Murray, Clinical Genetics, Cardiff; Dr Kai Ren Ong, Genetics, Birmingham; Dr Erika Pace, Paediatric Radiology, Royal Marsden NHS Foundation Trust; Dr Pan Pantziarka, Patient representative, George Pantziarka TP53 Trust; Mrs Michelle Potter, Patient representative, George Pantziarka TP53 Trust; Miss Sarah Pugh, Clinical Genetics, Bristol; Dr Gillian Rea, Clinical Genetics, Belfast; Dr Aslam Sohaib, Adult Radiology, Royal Marsden NHS Foundation Trust; Ms Beverley Speight, Clinical Genetics, Cambridge; Dr Stavros Stivros, Paediatric Neuroradiology, Manchester; Dr David Swienton, Adult Radiology, Leicester; Professor Clare Turnbull, Clinical Genetics, Genomics England; Professor Leslie Walker, Psychology, Hull; Dr Richard Whitehouse, Adult Radiology, Manchester.
Contributors HH developed and administered the premeeting survey, collated and presented the results, organised and chaired the consensus meeting and drafted the manuscript. AFB, GC, SG and LI helped in the organisation of the meeting and acted as group facilitators on the day. RE, MJ and AS presented data at the consensus meeting and provided expert opinion. GE and MT reviewed and critically appraised the manuscript. All named authors and members of the Consensus Group contributed to the discussion at the meeting and reviewed and contributed to the final manuscript.
Funding HH is supported by the Cancer Research CRUK Catalyst Award, CanGene-CanVar (C61296/A27223).
Competing interests None declared.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
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