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Cancer Genetics for Primary Care. Sara Levene Registered Genetic Counsellor. Proportion of cancer that is inherited. Population risk: Breast cancer 1:10 Ovarian cancer 1:100 Colorectal cancer 1:25 - 35. Inherited susceptibility to cancer: ‘genetic’ Single genes. No family history of
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Cancer Genetics for Primary Care Sara Levene Registered Genetic Counsellor
Proportion of cancer that is inherited Population risk: Breast cancer 1:10 Ovarian cancer 1:100 Colorectal cancer 1:25 - 35 Inherited susceptibility to cancer: ‘genetic’ Single genes No family history of Cancer: ‘sporadic’ ?multi-factorial origins Family history of cancer: ‘familial’ ?multi-factorial origins
To make a long story short: All cancer is genetic Cancer is rarely inherited
cancer Sporadic cancer 1 normal gene 1 mutated gene 2 normal genes 2 mutated genes hormones viruses chemicals radiation Spontaneous mutations Inherited cancer 1 normal gene 1 mutated gene cancer 2 mutated genes hormones viruses chemicals radiation Spontaneous mutations
Inherited Mutations and Cancer • Inherited mutations relating to cancer do not cause cancer • Mutations are often found in genes that are ‘tumour suppressors’ • Mutations mean that protection from cancer is lost or reduced • Mutations lead to increased susceptibility to certain types of cancer
Autosomal dominant inheritance mother father child child Each child has 50:50 chance of inheriting the altered gene.
Cancer GenesMendelian Inheritance (AD) • In the last 10 years several genes relating to specific cancer syndromes have been identified • There are more cancer genes waiting to be ‘discovered’ • It is difficult to locate the exact mutation in a cancer gene for a particular family
Cancer GenesMulti-factorial Inheritance • More recently the search for other AD genes has led to the discovery of some ‘lower risk’ genes eg. CHEK2 • found in ~2% cases ca br • est doubles risk of ca br • ? Liability/threshold model with several similar genes (+ env factors) • This research is not yet applicable to clinical practice
Genetic Testing • Technically difficult • Can only be offered to high risk families • Can only search small number of high risk dominant genes • Can take more than a year to search for the mutation in a family • Often cannot locate the mutation for a family (?unknown genes)
Searching for the faulty gene cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt a cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt cgattgagg atcgtacgta ttaacggtag ctataccagtc gatccattgga gtcatcgatgtt
Genetic Testing • First test in family always done on person who has had the cancer (mutation search test) • If no living affected relatives available – cannot offer genetic test for family • If a mutation is found predictive testing can be offered to at-risk relatives: • If relative doesn’t carry familial mutation they are not at increased risk of cancer (still at population risk) • If a person does carry the familial mutation they are at increased risk of developing cancer
Breast and ovarian cancer Breast cancer risk ~80% Ovarian cancer risk ~45% Increased risk of second primary for women who have already had breast cancer Other cancers Prostate cancer Male breast cancer Pancreatic cancer Colorectal cancer Stomach cancer High RiskCancer risks associated with BRCA1 and BRCA2
Recent NICE Guidelines on Familial Breast Cancer • Women at or near population risk are cared for in primary care. • Women at moderate risk are cared for in secondary care. • Women at high risk are cared for in tertiary care.
Breast cancer case study 1 Ca breast, diag 70y Died 85y 68y Brain tumour, died 67y ? Prev breast cancer in 40s?
Breast cancer case study 1 Can this patient now be reassured? Ca breast, diag 70y Died 85y 68y Brain tumour, died 67y No record of prev ca br
Population riskScreening and management • National breast screening from 50y • Breast awareness • Reassure patient: • For most women, increasing age is the greatest risk factor. • The great majority of women with a family history of breast cancer do not fall into a high-risk category and do not develop breast cancer.
Breast cancer case study 2 Patient is requesting screening and is considering prophylactic mastectomies. What is her level of risk? What is appropriate management of her risk? Patient is also interested in genetic testing. Can this be offered? Ca breast, diag 54y Ca breast, diag 52y 20y
Moderate riskReferral to secondary care Female breast cancers • One 1st degree relative diagnosed before age 40 • Two 1st degree relatives (or one 1st degree relative and one 2nd degree relative) diagnosed after average age 50
Moderate riskScreening and management • Annual breast surveillance from age 40 – 50y • National Breast Screening from 50y. • ?Chemoprevention studies • Breast awareness
Breast cancer case study 3 Ca breast Died 40y Ca breast Diag 32y Considering prophylactic mastecomies What can we offer this family?
Breast cancer case study 3 Ca breast Died 40y Ca breast Diag 32y Blood taken for BRCA1/2 testing Recommend screening Recommend screening
Breast cancer case study 3 Ca breast Died 40y Ca breast Diag 32y BRCA1/2 testing on-going Ca breast Diag 35y
Breast cancer case study 3 Ca breast Died 40y Ca breast Diag 32y BRCA1 mutation found Ca breast Diag 35y
Breast cancer case study 3 Ca breast Died 40y N Ca breast Diag 32y BRCA1 mutation found Ca breast Diag 35y BRCA1 mutation carrier BRCA1 mutation carrier
High riskReferral to secondary care, then tertiary care • Two 1st degree relatives (OR one 1st degree relative and one 2nd degree relative) with breast cancer, av age <50 • Three or more 1st or 2nd degree relatives with breast cancer at any age • One 1st degree male relative with breast cancer at any age • One 1st degree relative with bilateral breast cancer where 1st primary diagnosed <50 • One 1st or 2nd degree relative with ovarian cancer at any age and one 1st or 2nd degree relative with breast cancer at any age
High riskScreening and management • 30-39y: may be eligible for annual mammograms • 40-49y: annual mammograms • >50y: NBSP, plus may be eligible for additional screening • Refer to genetics to discuss genetic testing • ?MRI screening in the future • ?Prophylactic surgery • ?Ovarian screening
Breast cancer case study 4 What should we do for this family? Ca ?type Ca breast, diag 51y Died 53y Ca breast, diag 41y
Breast cancer case study 4 Ca ovary, died 48y Ca breast, diag 51y Died 53y Breast & ovarian screening Ca breast, diag 41y
Breast cancer case study 4 Ca ovary, died 48y Ca breast, diag 51y Died 53y Breast & ovarian screening Ca breast, diag 41y Blood taken for BRCA1/2 testing
Breast cancer case study 4 Ca ovary, died 48y Ca breast, diag 51y Died 53y Considering surgery Ca breast, diag 41y BRCA1/2 tested No mutations found
Other factors to consider: • Paternal history: two or more breast cancers on father’s side of family • Unusual cancers: Bilateral breast cancer Male breast cancer Ovarian cancer Sarcoma <45y Glioma or childhood adrenal cortical carcinoma Complicated patterns of multiple cancers at young age • Jewish ancestry Women with Jewish ancestry are around 5–10 times more likely to carry BRCA1 or BRCA2 mutations than women in non-Jewish populations.
100% affected by 35y Hundreds/thousands of polyps in colon Mutation on APC gene Accounts for <1% colon cancers Other cancer risks: duodenal, gastric Up to 80% lifetime risk Less than 10 polyps found At least 5 genes found Accounts for up to 5% of colon cancers Other cancer risks: endometrial, ovarian, gastric HNPCC Hereditary Non-Polyposis Colon Cancer FAPFamilial AdenomatousPolyposis
CRC FH Risk categorisation Low risk One FDR with CRC at > 45 (No screening required, bowel awareness) Low-Moderate risk Two FDRs with CRC at average age > 60. Screening: One colonoscopy at 35y-40y and one at 55y High-Moderate risk One FDR with CRC <45, or three older FDRs i.e. >50. Screening: Begins at 45 or 5yrs prior to youngest diagnosis (not prior to 35). Repeat 5yrly to 75y.
What is High Risk? • A known polyposis syndrome e.g. FAP Be sure to ask if there is any history of polyposis in the family. • HNPCC (Amsterdam positive families). • At least 3 of HNPCC related cancers (CRC, endometrium, ovarian, small bowel, ureter or renal pelvis) • One should be a FDR of the other two • At least two successive generations affected • At least one cancer diagnosed < 50 years
HNPCC Colonoscopies from 25y, continuing 2 yearly to 75y ?Endometrial/ovarian screening annually from 35y (research) FAP Colonoscopies annually from teens (or younger depending on family history) Prophylactic colectomy offered ?Upper GI screening annually (research) High risk screening/management
Summary • Most cancer is not due to dominant, high-risk genes. • Most patients with a family history of cancer can be reassured and possibly referred for screening. • For most patients with a family history of cancer, current genetic testing is not helpful and is not available. • Patients with a high risk of cancer due to family history can have screening, and genetic testing may be available. • Patients who inherit a mutation in a high risk gene have a high risk of developing cancer themselves.
Take-home messages • Young diagnoses of cancer (<45y) may be significant • Three or more cases of the same / related types of cancer, in one family (even if older ages) may be significant • Genetic testing may or may not be available / informative for a given family • Genetic testing must start with a living affected relative • Screening may be available
If you have enquiries about a family history : Contact your local Clinical Genetics dept: Clinical Genetics Great Ormond Street Hospital London WC1N 3JH Tel: 0207 905 2138 Clinics held at Barts and The London.