Open Access

Are BRCA1- and BRCA2-related breast cancers associated with increased mortality?

Breast Cancer Research20036:E7

https://doi.org/10.1186/bcr748

Published: 25 November 2003

Abstract

There has been contradictory evidence as to whether BRCA1 associated breast cancers have a poorer prognosis than non-BRCA1 cancers. In this issue of Breast Cancer Research Robson and colleagues provide further evidence for poorer survival in BRCA1 carriers and show that it could be attributed to failure to treat small node-negative grade 3 breast cancers with chemotherapy. There still remains little evidence for a survival difference for BRCA2 related breast cancers. Although the high contralateral breast cancer risk is confirmed by this study there is no real evidence for an increase in ipsilateral recurrence or new primary breast cancers in mutation carriers up to the 10-year point.

Keywords

BRCA1BRCA2breast canceripsilateralsurvival

Introduction

In an article published in this issue of Breast Cancer Research, Robson and colleagues present important findings that show a decrease in long-term survival in breast cancer patients who carry BRCA1 mutations. The study also looked at ipsilateral recurrence and new primary breast cancers, and found no difference between those with BRCA1 mutations and those without [1]. A number of researchers have focused their research on the mortality associated with inherited mutations in BRCA1 and BRCA2. Apart from mere interest in the epidemiological aspects of breast malignancy, knowledge of the associated mortality is important to the families of patients with breast cancer, and to clinicians and scientists involved with improving the outcomes of breast cancer. We are entering the era of tailored therapies with targeted drugs such as Herceptin (trastuzumab), and a vital starting point in assessing the impact of interventions such as new drug therapy and screening is the mortality associated with standard care. Women making decisions about preventive options such as risk reducing surgery need to have reliable information on their chances of surviving breast cancer should it occur. Indeed, decisions about the type of surgery for an incident breast cancer will also depend on any difference in ipsilateral recurrence and new primary breast cancers between those opting for breast conserving treatment and those having mastectomy. These issues have been substantially addressed in the article by Robson and colleagues [1].

Methodological problems with BRCA1/2mortality studies

The purest study to assess mortality in BRCA1/2 carriers would be a prospective study of all incident breast cancer in an outbred population. In order for this to occur every woman would have had to give consent for testing of fresh biological tissue (usually blood) for genetic alterations. Many women do not wish to know their genetic status even if they have breast cancer and to counsel women adequately for the potential outcome of genetic testing at the very time they are weighing up different options regarding their treatment is distinctly problematic. Although an argument could be made that knowledge of BRCA1/2 status could alter treatment including management of the contralateral breast, the outcomes of the present study by Robson and colleagues [1] show that such a strategy may be misplaced. Indeed any change in treatment would confound the main aims of any prospective study.

An alternative strategy would be to test samples anonymously, by coding them and blinding any clinician involved in treatment of the patient to the results. This approach has some ethical problems, as many women would wish to know their mutation status. There is also likely to be a substantial refusal rate even to anonymous testing. This could lead to a significant bias if for instance those with a strong family history of breast cancers with poor outcomes were more likely to decline testing. Even in a large prospective study with very high ascertainment there are still the problems of accrual of follow-up time and the genetic testing process itself. The cost of testing a large enough cohort with a highly sensitive technique such as full sequencing is likely to be prohibitive. As only 2–3% of breast cancers in outbred populations are due to mutations in BRCA1 or BRCA2 [2], as many as 2,800 women would have to be accrued to arrive at a study with similar power to the one by Robson and colleagues [1]. Such a study would be likely to cost in excess of $3 million for the genetic testing aspect alone (over $7.7 million at full Myriad Genetic testing rates).

Flaws of previous mortality studies

The first studies to report on mortality associated with BRCA1 actually suggested a survival advantage [3, 4]. Although these studies were the best that could be achieved at that stage, these reports should be discounted as there was a substantial bias in the necessity of having a (and more likely several) living affected individual(s) in a family in order to identify linkage to chromosome 17q in the first instance. The next phase of reports were of studies based on mutation analysis. These studies were still subject to bias as individuals were either ascertained through existing proven BRCA1 families (the necessity again for a living affected individual) [57] or some time after diagnosis in Jewish families [8]. Interestingly the latter article [8] shares some authors with the present study [1] and it is likely that there is some overlap of patients. Nonetheless the potential bias in the older study will have been corrected by the methodologies of testing tumour material in the present study. Whilst there were trends to worse prognosis in BRCA1 carriers in these studies they were not significant after correction for other factors.

Attempts to correct for these selection biases have been made in a cohort study of incident familial breast cancers [9] and in prospectively ascertained breast cancers in screened women in family history clinics [10]. These studies convincingly showed for the first time a worse prognosis in BRCA1 carriers in terms of survival. However, matching to other familial breast cancer cases may be problematic as non BRCA1/2 familial breast cancer may even have a better prognosis than sporadic breast cancer. A further case control study of early stage breast cancer failed to reveal a worse prognosis [11].

Results of increased mortality for BRCA2 are also conflicting, but less clear than for BRCA1. They are based on smaller numbers (total of only 70 patients), and have the same methodological flaws [5, 10, 12, 13].

The study by Robson and colleagues

The study reported in this issue of Breast Cancer Research [1] circumvents most of the methodological problems of the previous studies and expands on a previous report by some of the same authors [14]. Although retrospective a very high proportion (496/584) of incident cases have been tested for the three common Jewish BRCA1/2 mutations. As these mutations account for > 90% of involvement of BRCA1/2 in the Jewish population [15] such testing is equivalent to full gene sequencing in an outbred population. As the testing was based on tumour tissue, follow up was from diagnosis and there is little likelihood of selection bias.

The study has strengthened the evidence for worse prognosis in BRCA1 carriers, but shows that this survival disadvantage largely disappears if patients receive chemotherapy. The results do, nonetheless, depend on only 17 BRCA1 carriers of uncertain age who were not treated with chemotherapy. A further breakdown on age rather than just using under/over 50 years threshold would have been helpful. While data on grade and oestrogen receptor (ER) status were not testable, it is likely that the worse prognosis is associated with the known poor prognostic factors in BRCA1 carriers: high-grade ER negativity and postive p53 staining. Interestingly the authors have also recently reported on the increased presence of glomeruloid microvascular proliferation being associated with BRCA1 mutation carriers and poor prognosis [16]. If these results are borne out, it may well be that previous failure to treat small node negative BRCA1 patients with chemotherapy accounts for much of the survival disadvantage. Current treatment protocols are likely to address this with nearly all small grade 3 node negative tumours now receiving chemotherapy, but this might even be extended to grade 2 tumours. Not surprisingly, there was little evidence in this study for any efficacy for tamoxifen in a largely ER-negative group of tumours.

Unfortunately, the present study adds little to the limited information on BRCA2 with only 13 heterozygote carriers identified (this excludes the compound heterozygote carrying a BRCA1 mutation). On current evidence in some 83 BRCA2 mutation carriers prognosis does appear very similar to sporadic breast cancer and may well reflect the very similar tumour characteristics [17].

Ipsilateral and contralateral recurrence and new primary breast cancer

After a median follow up of nearly 10 years the current study has not shown an increase in ipsilateral risk in BRCA1 carriers, but has confirmed the known substantial contralateral risk. This is at variance with other studies, which show an increase in ipsilateral risk at longer follow up [18]. While the authors correctly point out that when considering treatment options at initial diagnosis it should be the patient's absolute risk of a further ipsilateral tumour that determines decision-making, the authors' own findings of increased survival in the more recent patients managed aggressively with chemotherapy mean that more women will be surviving to develop ipsilateral disease. It should not be forgotten that in most long-term follow-up studies of radiotherapy at other sites, the incidence of true new primary disease in the radiation field does not really occur until 10–15 years after therapy. It is nonetheless reassuring that the ipsilateral rates in BRCA1 are still substantially less than the contralateral rates. This means that the radio-therapy must be eliminating some of the new primary risk by destroying pre-existing tumours, and perhaps preventing cancers by eliminating a large proportion of breast epithelial cells. The final proof in this situation will only be from studies with in excess of 20 years follow up.

Conclusion

Robson and colleagues have provided further evidence to help in the management of breast cancer in BRCA1 mutation carriers. Whilst the population studied is limited to the two common BRCA1 mutations in the Jewish population, it is likely to extrapolate to other mutation carriers. It would appear that BRCA1 mutation carriers have substantially better survival when treated with chemotherapy, and even small node-negative tumours should be treated. Further evidence is needed to determine whether the type of chemotherapy is important. Greater numbers are required for firm evidence on prognosis related to BRCA2 breast cancers. While there is encouraging news for BRCA1/2 carriers opting for breast conserving surgery, longer follow up is required before a woman can reliably be told her ipsilateral risk is no different than average.

Abbreviations

ER: 

Oestrogen receptor.

Declarations

Authors’ Affiliations

(1)
Academic Unit of Medical Genetics and Regional Genetics Service, St Mary's Hospital
(2)
Department of Medical Oncology, Christie Hospital

References

  1. Robson ME, Chappuis PO, Satagopan J, Wong N, Boyd J, Goffin JR, Hudis C, Roberge D, Norton L, Bégin LR, Offit K, Foulkes WD: A combined analysis of outcome following breast cancer: differences in survival based on BRCA1/2 mutation status and administration of adjuvant treatment. Breast Cancer Res. 2004, 6: R8-R17. 10.1186/bcr658.View ArticlePubMedGoogle Scholar
  2. Ford D, Easton DF, Stratton M, Narod S, Goldgar D, Devilee P, Bishop DT, Weber B, Lenoir G, Chang-Claude J, Sobol H, Teare MD, Struewing J, Arason A, Scherneck S, Peto J, Rebbeck TR, Tonin P, Neuhausen S, Barkardottir R, Eyfjord J, Lynch H, Ponder BAJ, Gayther SA, Birch JM, Lindblom A, Stoppa-Lyonnet D, Bignon Y, Borg A, Hamann U, Haites N, Scott RJ, Maugard CM, Vasen H, Seitz S, Cannon-Albright LA, Schofield A, Zelada-Hedman M: Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet. 1998, 62: 676-689. 10.1086/301749.View ArticlePubMedPubMed CentralGoogle Scholar
  3. Porter DE, Cohen BB, Wallace MR, Smyth E, Chetty U, Dixon JM, Steel CM, Carter DC: Breast cancer incidence, penetrance and survival in probable carriers of BRCA1 gene mutation in families linked to BRCA1 on chromosome 17q12-21. Br J Surg. 1994, 81: 1512-1515.View ArticlePubMedGoogle Scholar
  4. Marcus JN, Watson P, Page DL, Narod SA, Lenoir GM, Tonin P, Linder-Stephenson L, Salerno G, Conway TA, Lynch HT: Hereditary breast cancer: pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage. Cancer. 1996, 77: 697-709. 10.1002/(SICI)1097-0142(19960215)77:4<697::AID-CNCR16>3.0.CO;2-W.View ArticlePubMedGoogle Scholar
  5. Eerola H, Vahteristo P, Sarantaus L, Kyyronen P, Pyrhonen S, Blomqvist C, Pukkala E, Nevanlinna H, Sankila R: Survival of breast cancer patients in BRCA1, BRCA2, and non-BRCA1/2 breast cancer families: a relative survival analysis from Finland. Int J Cancer. 2001, 93: 368-372. 10.1002/ijc.1341.View ArticlePubMedGoogle Scholar
  6. Hamann U, Sinn HP: Survival and tumor characteristics of German hereditary breast cancer patients. Breast Cancer Res Treat. 2000, 59: 185-192. 10.1023/A:1006350518190.View ArticlePubMedGoogle Scholar
  7. Verhoog LC, Brekelmans CT, Seynaeve C, van den Bosch LM, Dahmen G, van Geel AN, Tilanus-Linthorst MM, Bartels CC, Wagner A, van den Ouweland A, Devilee P, Meijers-Heijboer EJ, Klijn JG: Survival and tumor characteristics of breast-cancer patients with germline mutations of BRCA1. Lancet. 1998, 351: 316-321. 10.1016/S0140-6736(97)07065-7.View ArticlePubMedGoogle Scholar
  8. Robson M, Gilewski T, Haas B, Levin D, Borgen P, Rajan P, Hirschaut Y, Pressman P, Rosen PP, Lesser ML, Norton L, Offit K: BRCA-associated breast cancer in young women. J Clin Oncol. 1998, 16: 1642-1649.PubMedGoogle Scholar
  9. Stoppa-Lyonnet D, Ansquer Y, Dreyfus H, Gautier C, Gauthier-Villars M, Bourstyn E, Clough KB, Magdelenat H, Pouillart P, Vincent-Salomon A, Fourquet A, for the Institute Curie Breast Cancer Group, Asselian B: Familial invasive breast cancer: worse outcome related to BRCA1 mutations. J Clin Oncol. 2000, 18: 4053-4059.PubMedGoogle Scholar
  10. Moller P, Borg A, Evans DG, Haites N, Reis MM, Vasen H, Anderson E, Steel CM, Apold J, Goudie D, Howell A, Lalloo F, Maehle L, Gregory H, Heimdal K: Survival in prospectively ascertained familial breast cancer: analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomy. Int J Cancer. 2002, 101: 555-559. 10.1002/ijc.10641.View ArticlePubMedGoogle Scholar
  11. Pierce LJ, Strawderman M, Narod SA, Oliviotto I, Eisen A, Dawson L, Gaffney D, Solin LJ, Nixon A, Garber J, Berg C, Isaacs C, Heimann R, Olopade OI, Haffty B, Weber BL: Effect of radio-therapy after breast-conserving treatment in women with breast cancer and germline BRCA1/2 mutations. J Clin Oncol. 2000, 18: 3360-3369.PubMedGoogle Scholar
  12. Verhoog LC, Brekelmans CT, Seynaeve C, Dahmen G, van Geel AN, Bartels CC, Tilanus-Linthorst MM, Wagner A, Devilee P, Halley DJ, van den Ouweland AM, Meijers-Heijboer EJ, Klijn JG: Survival in hereditary breast cancer associated with germline mutations of BRCA2. J Clin Oncol. 1999, 17: 3396-3402.PubMedGoogle Scholar
  13. Loman N, Johannsson O, Bendahl PO, Dahl N, Einbeigi Z, Gerdes A-M, Borg A, Olsson H: Prognosis and clinical presentation of BRCA2-associated breast cancer. Eur J Cancer. 2000, 36: 1365-1373. 10.1016/S0959-8049(00)00098-8.View ArticlePubMedGoogle Scholar
  14. Foulkes WD, Wong N, Brunet JS, Begin LR, Zhang JC, Martinez JJ, Rozen F, Tonin PN, Narod SA, Karp SE, Pollak MN: Germ-Line BRCA1 Mutation is an Adverse Prognostic Factor in Ashkenazi Jewish Women with Breast Cancer. Clin Cancer Res. 1997, 3: 2465-2469.PubMedGoogle Scholar
  15. Kauff ND, Perez-Segura P, Robson ME, Scheuer L, Siegel B, Schluger A, Rapaport B, Frank TS, Nafa K, Ellis NA, Parmigiani G, Offit K: Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families. J Med Genet. 2002, 39: 611-614. 10.1136/jmg.39.8.611.View ArticlePubMedPubMed CentralGoogle Scholar
  16. Goffin JR, Straume O, Chappuis PO, Brunet JS, Begin LR, Hamel N, Wong N, Akslen LA, Foulkes WD: Glomeruloid microvascular proliferation is associated with p53 expression, germline BRCA1 mutations and an adverse outcome following breast cancer. Br J Cancer. 2003, 89: 1031-1034. 10.1038/sj.bjc.6601195.View ArticlePubMedPubMed CentralGoogle Scholar
  17. Lakhani SR, Jacquemier J, Sloane JP, Gusterson BA, Anderson TJ, van de Vijver MJ, Farid LM, Venter D, Antoniou A, Storfer-Isser A, Smyth E, Steel CM, Haites N, Scott RJ, Goldgar D, Neuhausen S, Daly PA, Ormiston W, McManus R, Scherneck S, Ponder BAJ, Ford D, Peto J, Stoppa-Lyonnet D, Bignon YJ, Struewing JP, Spurr NK, Bishop DT, Klijn JGM, Devilee P, Cornelisse CJ, Lasset C, Lenoir G, Barkardottir RB, Egilsson V, Hamann U, Chang-Claude J, Sobol H, Weber B, Stratton MR, Easton DF: Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations. J Natl Cancer Inst. 1998, 90: 1138-1145. 10.1093/jnci/90.15.1138.View ArticlePubMedGoogle Scholar
  18. Haffty BG, Harrold E, Khan AJ, Pathare P, Smith TE, Turner BC, Glazer PM, Ward B, Carter D, Matloff E, Bale AE, Alvarez-Franco M: Outcome of conservatively managed early-onset breast cancer by BRCA1/2 status. Lancet. 2002, 359: 1471-1477. 10.1016/S0140-6736(02)08434-9.View ArticlePubMedGoogle Scholar

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© BioMed Central Ltd 2004