Constitutional Oncogenetics

Noureddine Boukhatem

• Publisher: Wiley-ISTE
• Year: 2021
• Print ISBN: 9781789450163
• eBook ISBN: 9781119818182
• Edition: 1
• Topic: Medicine
• Subtopic: Medical Theory, Practice & Reference

In the age of genomics, oncogenetics is a growing discipline. It is defined as the identification and management of families where there is a suspected hereditary risk of cancer. This relatively new discipline is part of a modern medicine that aims to be both preventive and predictive.

Constitutional Oncogenetics gives precise descriptions of the main syndromes that cause a predisposition for cancer. The first part examines the most common syndromes in the majority of the world, including the heightened hereditary risk of breast and ovarian cancer and Lynch syndrome. The second part introduces less common infracentesimal syndromes, such as Bloom syndrome and Fanconi syndrome. This book is intended for oncogenetic practitioners and other specialists, as well as medical students.

PART 1
Major Syndromes

1
Hereditary Breast and Ovarian Cancer Syndrome Including Isolated Ovarian Cancers

In this chapter, we will describe the genetic predisposition to breast and ovarian cancers, including situations where the only cancers encountered are ovarian cancers.

1.1. Introduction

Inherited cancer syndromes are characterized by germline genetic mutations, which are associated with a high risk of cancer development. These mutations are usually inherited in an autosomal dominant manner and often induce cancers at a relatively early age. Hereditary cancer syndromes are rare, accounting for only about 5–10% of all breast cancers.

In addition to hereditary breast and ovarian cancer (HBOC, BRCA1/BRCA2) syndrome, breast and ovarian cancers are components of several autosomal dominant cancer syndromes: Li–Fraumeni syndrome (TP53), Cowden syndrome (PTEN) and hereditary diffuse gastric cancer syndrome (CDH1). The risk of breast cancer is higher in people diagnosed with these syndromes and there is a risk of developing tumors in other organs.

Other genetic syndromes may include breast cancer as an associated trait: the heterozygous carriers of the deleterious mutations of the ATM gene (ataxia-telangiectasia) and the STK11 gene (Peutz–Jeghers syndrome).

Lynch syndrome (LS) is primarily associated with colorectal and endometrial cancer, although several studies have shown that patients with LS have a higher risk of developing breast cancer.

Ovarian cancer is also associated with LS and Gorlin syndrome.

Mutations in other genes are also associated with an increased risk of developing breast cancer (checkpoint kinase 2 [CHEK2], PALB2, NBN and BARD1) or ovarian cancer (BRCA1 interacting protein 1 [BRIP1], RAD51C and RAD51D).

Recent studies have shown that half of the pathogenic mutations identified in individuals who meet only the HBOC test criteria were in genes other than BRCA1/2. Similarly, half of the pathogenic mutations identified in individuals who meet only the criteria for LS testing were in genes that are not part of the LS predisposition genes.

These same studies have shown the usefulness of testing people suspected of developing or who have developed HBOC for a list of 25 genes (BRCA1, BRCA2, ATM, CHEK2, PALB2, NBN, BARD1, BRIP1, RAD51C, RAD51D, MLH1, MSH2, EPCAM, MSH6, PMS2, APC, MUTYH (biallelic), BMPR1A, SMAD4, TP53, PTEN, STK11, CDH1, CDKN2A and CDK4).

While MUTYH biallelic mutations are known to cause MYH polyposis-associated syndrome with a 28-fold increased risk of colorectal adenocarcinoma, monoallelic carriers have been reported to have only a slight increase in colorectal cancer risk (odds ratio of ~1.34), but together with an increased risk of breast cancer.

The most recent studies have confirmed the association of 15 genes with an increased risk (>2.0 times) of breast cancer (ATM, BARD1, BRCA1, BRCA2, CDH1, CDKN2A, CHEK2 (except p.I157T), MLH1, MSH2, MSH6, NF1, PALB2, PTEN, RAD51D and TP53). Eleven genes were associated with an increased risk (>2.0 times) of ovarian cancer (ATM, BRCA1, BRCA2, BRIP1, MSH2, MSH6, NBN, PMS2, RAD51C, RAD51D and TP53).

In this section, we will discuss the roles of BRCA1 and BRCA2 genes in predisposition to both breast and ovarian cancers; CHEK2, PALB2, NBN and BARD1 in predisposition to breast cancer; and BRIP1, RAD51C and RAD51D in predisposition to ovarian cancer.

1.2. Prevalence

Approximately one in 300–400 people in the general population is born with an inherited mutation in the BRCA1 or BRCA2 gene. The frequency of BRCA1 or BRCA2 mutation is approximately one in 40 in the Ashkenazi Jewish population.

PALB2 pathogenic variants have been examined in multiple small studies of familial and early breast cancer in multiple populations. The prevalence of pathogenic variants ranged from 0.4% to 3.9%. Similar to BRIP1 and CHEK2, there was incomplete segregation of PALB2 pathogenic variants in families with hereditary breast cancer.

It is estimated that mutations in RAD51C increase the risk of ovarian cancer by 9% and occur in approximately 1–5.7% of women with ovarian cancer (without considering any selection criteria).

It is estimated that one in 200 people with ovarian cancer will have a constitutional mutation in the RAD51D gene.

When should one suspect a genetic predisposition? The following section outlines the criteria for referral for an oncogenetic consultation, according to the National Comprehensive Cancer Network (NCCN).

1.2.1. Genetic risk assessment criteria¹

1.2.1.1. A person with cancer

For a diagnosed patient, the reasons for referral for an oncogenetic consultation, according to the NCCN, are as follows:

1. 1) a person with ovarian cancer²;
2. 2) a person diagnosed with breast cancer who meets one of the following criteria:
   • – a mutation known in the family in a cancer predispositi...

Table of contents

• Cover
• Table of Contents
• Copyright
• Foreword
• Introduction
• PART 1: Major Syndromes
• PART 2: Infracentesimal Syndromes
• Appendix: Summary of the Book
• References
• Index
• End User License Agreement