Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Research
  • Published:

The presenting dental status of solid tumours with bone metastases requiring bone-targeting agents - part 2: breast cancer

Abstract

Introduction Patients with bony metastatic breast cancer (MBC) due to receive bone-targeting agents (BTA) are expected to undertake a dental assessment before commencing. The aim of this study was to determine the dental status of this tumour group and understand the challenges the dental practitioner faces in attempting to achieve 'dental fitness'.

Materials and methods Data were retrospectively collected from a dedicated pre-BTA dental assessment clinic and analysed for MBC. Statistical analysis and observational data were used to compare patient and tumour demographics.

Results A total of 229 patients were included in this cohort. On average, this cohort loses one tooth per decade (p = 0.003). Classifying the tumour sub-types provided observational differences in dental status with patients with triple negative MBC having the best dentition at presentation. These observations were more clinically profound when overlaid with survival following post-BTA dental assessment as patients with triple negative MBC had the lowest median survival (eight months, p = 0.002). In contrast, patients with luminal A breast cancer had a very complex presenting dentition with a median survival of 20 months.

Conclusion A clear difference exists in the outcomes of MBC patients and therefore a pre-BTA dental assessment should consider and integrate both patient and tumour demographics into dental treatment planning.

Key points

  • Annually, approximately 55,000 patients are diagnosed with breast cancer, with a significant proportion of them prescribed bone-targeting agents in either an adjuvant or metastatic setting.

  • In general, metastatic breast cancer patients have a higher survival rate than most other metastatic tumour groups.

  • Gene expression and hormone receptor status are key factors dictating oncology treatments and survival outcomes.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. World Health Organisation. Cancer. 2021. Available at https://www.who.int/news-room/fact-sheets/detail/cancer (accessed January 2022).

  2. Breast Cancer Now. Facts and Statistics 2021. 2021. Available at https://breastcancernow.org/about-us/media/facts-statistics#:~:text=One%2Dquarter%20of%20cases%20are,just%204%25%20of%20all%20cases (accessed January 2022).

  3. Redig A J, McAllister S S. Breast cancer as a systemic disease: a view of metastasis. J Intern Med 2013; 274: 113-126.

  4. O'Shaughnessy J. Extending survival with chemotherapy in metastatic breast cancer. Oncologist 2005; 10: 20-29.

  5. Coleman R E. Clinical features of metastatic bone disease and risk of skeletal morbidity. Clin Cancer Res 2006; DOI: 10.1158/1078-0432.CCR-06-0931.

  6. Coleman R E, Bertelli G, Beaumont T et al. UK guidance document: treatment of metastatic breast cancer. Clin Oncol (R Coll Radiol) 2012; 24: 169-176.

  7. Nielsen O S, Munro A J, Tannock I F. Bone metastases: pathophysiology and management policy. J Clin Oncol 1991; 9: 509-524.

  8. Yamashita K, Ueda T, Komatsubara Y et al. Breast cancer with bone-only metastases. Visceral metastases-free rate in relation to anatomic distribution of bone metastases. Cancer 1991; 68: 634-637.

  9. Coleman R E. Risks and benefits of bisphosphonates. Br J Cancer 2008; 98: 1736-1740.

  10. Ruggiero S L, Dodson T B, Fantasia J et al American Association of Oral and Maxillofacial Surgeons position paper on medication-related osteonecrosis of the jaw—2014 update. J Oral Maxillofac Surg 2014; 72: 1938-1956.

  11. Scottish Dental Clinical Effectiveness Programme. Oral Health Management of Patients at Risk of Medication-related Osteonecrosis of the Jaw. 2017. Available at https://www.sdcep.org.uk/published-guidance/medication-related-osteonecrosis-of-the-jaw/ (accessed January 2022).

  12. Patel V, Grossman S, Wali R et al. The presenting dental status of solid tumours with bone metastases requiring bone-targeting agents - part 1: an overview. Br Dent J 2022;DOI: 10.1038/s41415-021-3825-y.

  13. Early Breast Cancer Trialists' Collaborative Group. Adjuvant bisphosphonate treatment in early breast cancer: meta-analyses of individual patient data from randomised trials. Lancet 2015; 386: 1353-1361.

  14. Patel V, Mansi J, Ghosh S et al. MRONJ risk of adjuvant bisphosphonates in early stage breast cancer. Br Dent J 2018; 224: 74-79.

  15. Nicolatou-Galitis O, Papadopoulou E, Vardas E et al Alveolar bone histological necrosis observed before extractions in patients, who received bone-targeting agents. Oral Dis 2020; 26: 955-966.

  16. Bauer K R, Brown M, Cress R D, Parise C A, Caggiano V. Descriptive analysis of oestrogen receptor (ER)-negative, progesterone receptor (PR)-negative and HER2-negative invasive breast cancer, the so-called triple-negative phenotype: a population-based study from the California cancer Registry. Cancer 2007; 109: 1721-1728.

  17. Reis-Filho J S, Tutt A N J. Triple negative tumours: a critical review. Histopathology 2008; 52: 108-118.

  18. Perou C M, Sørlie T, Eisen M B et al. Molecular portraits of human breast tumours. Nature 2000; 406: 747-752.

  19. Sørlie T, Perou C M, Tibshirani R, Aas T, Geisler S, Johnsen H, Hastie T, Eisen M B, Van De Rijn M, Jeffrey S S, Thorsen T. Gene expression patterns of breast carcinomas distinguish tumour subclasses with clinical implications. Proc Natl Acad Sci U S A 2001; 98: 10869-10874.

  20. Sotiriou C, Neo S Y, McShane L M et al. Breast cancer classification and prognosis based on gene expression profiles from a population-based study. Proc Natl Acad Sci U S A 2003; 100: 10393-10398.

  21. Stephens P J, Tarpey P S, Davies H et al. The landscape of cancer genes and mutational processes in breast cancer. Nature 2012; 486): 400-404.

  22. Walters S, Maringe C, Butler J et al. Breast cancer survival and stage at diagnosis in Australia, Canada, Denmark, Norway, Sweden and the UK, 2000-2007: a population-based study. Br J Cancer 2013; 108: 1195-1208.

  23. National Cancer Institute. SEER Cancer Statistics Review, 1975-2013. 2016. Available at https://seer.cancer.gov/archive/csr/1975_2013/ (accessed January 2022).

  24. National Cancer Institute. Cancer Stat Facts: Female Breast Cancer. 2022. https://seer.cancer.gov/statfacts/html/breast.html (accessed January 2022).

  25. Selvaggi G, Scagliotti G V. Management of bone metastases in cancer: a review. Critical reviews in oncology/haematology. Crit Rev Oncol Hematol 2005; 56: 365-378.

  26. Bowen R L, Duffy S W, Ryan D A, Hart I R, Jones J L. Early onset of breast cancer in a group of British black women. Br J Cancer 2008; 98: 277-281.

  27. Partridge A H, Rumble R B, Carey L A et al. Chemotherapy and targeted therapy for women with human epidermal growth factor receptor 2-negative (or unknown) advanced breast cancer: American Society of Clinical Oncology Clinical Practice Guideline. J Clin Oncol. 2014; 32: 3, 3307-3329.

  28. Lobbezoo D J A, van Kampen R J W, Voogd A C et al. Prognosis of metastatic breast cancer subtypes: the hormone receptor/HER2-positive subtype is associated with the most favourable outcome. Breast Cancer Res Treat 2013; 141: 507-514.

  29. Galasko C S B: Skeletal metastases. London: Butterworths, 1986.

  30. Patanaphan V, Salazar O M, Risco R. Breast cancer: metastatic patterns and their prognosis. South Med J 1988; 81: 1109-1112.

  31. Solomayer E F, Diel I J, Meyberg G C, Gollan C, Bastert G. Metastatic breast cancer: clinical course, prognosis and therapy related to the first site of metastasis. Breast Cancer Res Treat 2000; 59: 271-278.

  32. King R, Zebic L, Patel V. Deciphering novel chemotherapy and its impact on dentistry. Br Dent J 2020; 228: 415-421.

  33. Jung T Y. Osteonecrosis of jaw after anti-angiogenic agent administration in a renal cell carcinoma patient. Oral Maxillofac Surg Cases 2017; 3: 27-33.

  34. Lee C Y S, Lee K L, Hirata K Y, Suzuki J B. Medication-Related Osteonecrosis Of The Jaw With The Mtor Inhibitor Everolimus In A Patient With Oestrogen-Receptor Positive Breast Cancer: A Case Report. Int J Oral Dent Health 2016; 2: 1-5.

  35. Yamamoto D, Tsubota Y, Utsunomiya T et al. Osteonecrosis of the jaw associated with everolimus: A case report. Mol Clin Oncol 2017; 6: 255-257.

  36. Giancola F, Campisi G, Russo L L, Muzio L L, Di Fede O. Osteonecrosis of the jaw related to everolimus and bisphosphonate: a unique case report?. Ann Stomatol (Roma) 2013; 4: 20-21.

  37. Kim D W, Jung Y-S, Park H-S, Jung H-D. Osteonecrosis of the jaw related to everolimus: a case report. Br J Oral Maxillofac Surg 2013; DOI: 10.1016/j.bjoms.2013.09.008.

  38. Himelstein A L, Foster J C, Khatcheressian J L et al. Effect of longer-interval vs standard dosing of zoledronic acid on skeletal events in patients with bone metastases: a randomized clinical trial. JAMA 2017; 317: 48-58.

  39. Stopeck A T, Fizazi K, Body J-J et al. Safety of long-term denosumab therapy: results from the open label extension phase of two phase 3 studies in patients with metastatic breast and prostate cancer. Support Care Cancer 2016; 24: 447-455.

  40. Barrett-Lee P, Casbard A, Abraham J et al. Oral ibandronic acid versus intravenous zoledronic acid in treatment of bone metastases from breast cancer: a randomised, open label, non-inferiority phase 3 trial. Lancet Oncol 2014; 15: 114-122.

  41. Stopeck A T, Lipton A, Body J-J et al. Denosumab compared with zoledronic acid for the treatment of bone metastases in patients with advanced breast cancer: a randomized, double-blind study. J Clin Oncol 2010; 28: 5132-5139.

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Vinod Patel.

Ethics declarations

19/LO/1600 - Dental status of oncology patients requiring bone modulating therapy - a retrospective cohort study.

There are no conflicts of interest to declare by any of the authors for this submitted work.

Supplementary Information

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Patel, V., Wali, R., Burns, M. et al. The presenting dental status of solid tumours with bone metastases requiring bone-targeting agents - part 2: breast cancer. Br Dent J 232, 95–100 (2022). https://doi.org/10.1038/s41415-022-3875-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41415-022-3875-9

This article is cited by

Search

Quick links