Skip to main content

Advertisement

Log in

Tumor phenotype and concordance in synchronous bilateral breast cancer in young women

  • Epidemiology
  • Published:
Breast Cancer Research and Treatment Aims and scope Submit manuscript

Abstract

Purpose

Synchronous bilateral breast cancer is uncommon, and its pattern and incidence among younger women is unknown. Here we report the incidence, phenotypes, and long-term oncologic outcomes of bilateral breast cancer in women enrolled in the Young Women’s Breast Cancer Study (YWS).

Methods

The YWS is a multi-center, prospective cohort study of women with breast cancer diagnosed at age ≤ 40 years. Those with synchronous bilateral breast cancer formed our study cohort. Tumor phenotypes were categorized as luminal A (hormone receptor (HR)+/HER2−/grade 1/2), luminal B (HR+ /HER2+ or HER2− and grade 3), HER2-enriched (HR−/HER2+), or basal-like (HR−/HER2−). Descriptive statistics were used to evaluate tumor phenotypes of bilateral cancers for concordance.

Results

Among 1302 patients enrolled in the YWS, 21 (1.6%) patients had synchronous bilateral disease. The median age of diagnosis was 38 years (range 18–40 years). Seventeen (81.0%) underwent genetic testing with 6 found to have pathogenic germline mutations in BRCA1, BRCA2, or TP53. The majority of patients (76.2%) underwent bilateral mastectomy. On pathology, 2 patients had bilateral in-situ disease, 6 had unilateral invasive and contralateral in-situ disease, and 13 had bilateral invasive disease. Of those with bilateral invasive disease, 10 (76.9%) had bilateral luminal tumors and, when fully characterized, 6 were of the same luminal subtype. Only 1 patient had bilateral basal-like breast cancer. At median follow-up of 8.2 years, 14 patients are alive with no recurrent disease.

Conclusions

Bilateral breast cancer is uncommon among young women diagnosed with breast cancer at age ≤ 40. In our cohort, the majority of invasive tumors were of the luminal phenotype, though some differed by grade or HER2 status. These findings support the need for thorough pathologic workup of bilateral disease when it is found in young women with breast cancer to determine risk and tailor treatment.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Data availability

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

References

  1. de la Rochefordiere A, Asselain B, Scholl S, Campana F, Ucla L, Vilcoq JR, Durand JC, Pouillart P, Fourquet A (1994) Simultaneous bilateral breast carcinomas: a retrospective review of 149 cases. Int J Radiat Oncol Biol Phys 30(1):35–41. https://doi.org/10.1016/0360-3016(94)90516-9

    Article  PubMed  Google Scholar 

  2. Heron DE, Komarnicky LT, Hyslop T, Schwartz GF, Mansfield CM (2000) Bilateral breast carcinoma: risk factors and outcomes for patients with synchronous and metachronous disease. Cancer 88(12):2739–2750

    Article  CAS  Google Scholar 

  3. Sakai T, Ozkurt E, DeSantis S, Wong SM, Rosenbaum L, Zheng H, Golshan M (2019) National trends of synchronous bilateral breast cancer incidence in the United States. Breast Cancer Res Treat 178(1):161–167. https://doi.org/10.1007/s10549-019-05363-0

    Article  PubMed  Google Scholar 

  4. Hartman M, Czene K, Reilly M, Adolfsson J, Bergh J, Adami HO, Dickman PW, Hall P (2007) Incidence and prognosis of synchronous and metachronous bilateral breast cancer. J Clin Oncol 25(27):4210–4216. https://doi.org/10.1200/jco.2006.10.5056

    Article  PubMed  Google Scholar 

  5. Ruddy KJ, Gelber SI, Tamimi RM, Ginsburg ES, Schapira L, Come SE, Borges VF, Meyer ME, Partridge AH (2014) Prospective study of fertility concerns and preservation strategies in young women with breast cancer. J Clin Oncol 32(11):1151–1156. https://doi.org/10.1200/jco.2013.52.8877

    Article  PubMed  PubMed Central  Google Scholar 

  6. Goldhirsch A, Winer EP, Coates AS, Gelber RD, Piccart-Gebhart M, Thurlimann B, Senn HJ (2013) Personalizing the treatment of women with early breast cancer: highlights of the St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2013. Ann Oncol 24(9):2206–2223. https://doi.org/10.1093/annonc/mdt303

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  7. Rosenberg SM, Greaney ML, Patenaude AF, Partridge AH (2019) Factors affecting surgical decisions in newly diagnosed young women with early-stage breast cancer. J Adolescent Young Adult Oncol 8(4):463–468. https://doi.org/10.1089/jayao.2019.0002

    Article  Google Scholar 

  8. Kheirelseid EA, Jumustafa H, Miller N, Curran C, Sweeney K, Malone C, McLaughlin R, Newell J, Kerin MJ (2011) Bilateral breast cancer: analysis of incidence, outcome, survival and disease characteristics. Breast Cancer Res Treat 126(1):131–140. https://doi.org/10.1007/s10549-010-1057-y

    Article  PubMed  Google Scholar 

  9. Baykara M, Ozturk SC, Buyukberber S, Helvaci K, Ozdemir N, Alkis N, Berk V, Koca D, Coskun U, Oksuzoglu B, Uncu D, Arpaci E, Ustaalioglu BO, Demirci U, Kucukoner M, Dogu GG, Alici S, Akman T, Ozkan M, Aslan UY, Durnali AG, Benekli M (2012) Clinicopathological features in bilateral breast cancer. Asian Pac J Cancer Prev 13(9):4571–4575

    Article  Google Scholar 

  10. Rosenberg SM, Ruddy KJ, Tamimi RM, Gelber S, Schapira L, Come S, Borges VF, Larsen B, Garber JE, Partridge AH (2016) BRCA1 and BRCA2 mutation testing in young women with breast cancer. JAMA Oncol 2(6):730–736. https://doi.org/10.1001/jamaoncol.2015.5941

    Article  PubMed  PubMed Central  Google Scholar 

  11. Narod SA (2014) Bilateral breast cancers. Nat Rev Clin Oncol 11(3):157–166. https://doi.org/10.1038/nrclinonc.2014.3

    Article  PubMed  CAS  Google Scholar 

  12. Sandberg ME, Hartman M, Klevebring D, Eloranta S, Ploner A, Hall P, Czene K (2012) Prognostic implications of estrogen receptor pattern of both tumors in contralateral breast cancer. Breast Cancer Res Treat 134(2):793–800. https://doi.org/10.1007/s10549-012-2096-3

    Article  PubMed  CAS  Google Scholar 

  13. Coradini D, Oriana S, Mariani L, Miceli R, Bresciani G, Marubini E, Di Fronzo G (1998) Is steroid receptor profile in contralateral breast cancer a marker of independence of the corresponding primary tumour? Eur J Cancer 34(6):825–830. https://doi.org/10.1016/s0959-8049(97)10121-6

    Article  PubMed  CAS  Google Scholar 

  14. Begg CB, Ostrovnaya I, Geyer FC, Papanastasiou AD, Ng CKY, Sakr RA, Bernstein JL, Burke KA, King TA, Piscuoglio S, Mauguen A, Orlow I, Weigelt B, Seshan VE, Morrow M, Reis-Filho JS (2018) Contralateral breast cancers: Independent cancers or metastases? Int J Cancer 142(2):347–356. https://doi.org/10.1002/ijc.31051

    Article  PubMed  CAS  Google Scholar 

  15. Packwood K, Martland G, Sommerlad M, Shaw E, Moutasim K, Thomas G, Bateman AC, Jones L, Haywood L, Evans DG, Birch JM, Alsalmi OA, Henderson A, Poplawski N, Eccles DM (2019) Breast cancer in patients with germline TP53 pathogenic variants have typical tumour characteristics: the Cohort study of TP53 carrier early onset breast cancer (COPE study). J Pathol Clin Res 5(3):189–198. https://doi.org/10.1002/cjp2.133

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  16. Kuba MG, Lester SC, Bowman T, Stokes SM, Taneja KL, Garber JE, Dillon DA (2020) Histopathologic features of breast cancer in Li-Fraumeni syndrome. Mod Pathol. https://doi.org/10.1038/s41379-020-0610-4

    Article  PubMed  Google Scholar 

  17. Voduc KD, Cheang MC, Tyldesley S, Gelmon K, Nielsen TO, Kennecke H (2010) Breast cancer subtypes and the risk of local and regional relapse. J Clin Oncol 28(10):1684–1691. https://doi.org/10.1200/jco.2009.24.9284

    Article  PubMed  Google Scholar 

  18. Guzman-Arocho YD, Rosenberg SM, Poorvu P, Ruddy KJ, Kirkner G, Snow C, Tamimi RM, Peppercorn J, Schapira L, Borges VF, Come SE, Brachtel EF, Warner E, Partridge AH, Collins LC (2020) Abstract P4-07-02: clinicopathological features and BRCA 1/2 status in a large prospective cohort of young women with breast cancer. https://cancerres.aacrjournals.org/content/80/4_Supplement/P4-07-02.

Download references

Funding

None.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ann H. Partridge.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Research involving human participants

The YWS was approved by the Institutional Review Board at Dana-Farber Cancer Institute and other participating sites.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pak, L.M., Gaither, R., Rosenberg, S.M. et al. Tumor phenotype and concordance in synchronous bilateral breast cancer in young women. Breast Cancer Res Treat 186, 815–821 (2021). https://doi.org/10.1007/s10549-020-06027-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10549-020-06027-0

Keywords

Navigation