Abstract
Background
Occult breast cancer (OBC) is classified as carcinoma of an unknown primary site, and the adequate therapy for OBC remains controversial. This retrospective study aimed to reveal the transition in breast cancer therapy and the frequency of primary breast tumors after resection in clinical OBC (cT0N+) patients using the Japanese Breast Cancer Registry database.
Methods
We enrolled OBC patients with cT0N+ from the registry between 2010 and 2018. On the basis of the period of diagnosis, OBC patients were divided into the following two groups: 2010–2014 and 2015–2018. We described the transition in treatments and tumor characteristics. After breast resection, the frequency of pathological identification of primary tumors and tumor sizes was assessed.
Results
Of the 687,468 patients registered, we identified 148 cT0N+ patients with a median age of 61 years. Of these patients, 64.2% (n = 95) received breast surgery (2010–2014: 79.1%, 2015–2018: 50.0%). Axillary lymph node dissection was performed in 92.6% (n = 137, 2010–2014: 91.6%, 2015–2018: 93.4%). The breast tumor size in the resected breast was 0–7.0 cm (median: 0 cm, 2010–2014: 0–7.0 cm [median: 0 cm], 2015–2018: 0–6.2 cm [median: 0 cm]). The pathological identification rate of the primary tumor was 41.1% (n = 39, 2010–2014: 40.4%, 2015–2018: 42.1%).
Conclusions
Breast surgery for cT0N+ decreased between 2010 and 2018. Despite the high identification rate of primary tumors, most tumors were small, and there was no significant change in the identification rate or invasive diameter of the identified tumors after 2010.
Similar content being viewed by others
References
Rosen PP. Axillary lymph node metastases in patients with occult noninvasive breast carcinoma. Cancer. 1980;46:1298–306.
Patel J, Nemoto T, Rosner D, Dao TL, Pickren JW. Axillary lymph node metastasis from an occult breast cancer. Cancer. 1981;47:2923–7.
Galimberti V, Bassani G, Monti S, Simsek S, Villa G, Renne G, et al. Clinical experience with axillary presentation breast cancer. Breast Cancer Res Treat. 2004;88:43–7.
Baron PL, Moore MP, Kinne DW, Candela FC, Osborne MP, Petrek JA. Occult breast cancer presenting with axillary metastases. Updated management. Arch Surg. 1990;125:210–4.
Owen HW, Dockerty MB, Gray HK. Occult carcinoma of the breast. Surg Gynecol Obstet. 1954;98:302–8.
NCCN Clinical Practice Guidelines in Oncology [Internet]. https://www.nccn.org/professionals/physician_gls/pdf/occult.pdf. Accessed 22 Dec 2017.
Walker GV, Smith GL, Perkins GH, Oh JL, Woodward W, Yu T-K, et al. Population-based analysis of occult primary breast cancer with axillary lymph node metastasis. Cancer. 2010;116:4000–6.
Fayanju OM, Stoll CRT, Fowler S, Colditz GA, Jeffe DB, Margenthaler JA. Geographic and temporal trends in the management of occult primary breast cancer: a systematic review and meta-analysis. Ann Surg Oncol. 2013;20:3308–16.
Macedo FIB, Eid JJ, Flynn J, Jacobs MJ, Mittal VK. Optimal surgical management for occult breast carcinoma: a meta-analysis. Ann Surg Oncol. 2016;23:1838–44.
de Bresser J, de Vos B, van der Ent F, Hulsewé K. Breast MRI in clinically and mammographically occult breast cancer presenting with an axillary metastasis: a systematic review. Eur J Surg Oncol. 2010;36:114–9.
He M, Tang L-C, Yu K-D, Cao A-Y, Shen Z-Z, Shao Z-M, et al. Treatment outcomes and unfavorable prognostic factors in patients with occult breast cancer. Eur J Surg Oncol (EJSO). 2012;38:1022–8.
Blanchard DK, Farley DR. Retrospective study of women presenting with axillary metastases from occult breast carcinoma. World J Surg. 2004;28:535–9.
Vlastos G, Jean ME, Mirza AN, Mirza NQ, Kuerer HM, Ames FC, et al. Feasibility of breast preservation in the treatment of occult primary carcinoma presenting with axillary metastases. Ann Surg Oncol. 2001;8:425–31.
Wang X, Zhao Y, Cao X. Clinical benefits of mastectomy on treatment of occult breast carcinoma presenting axillary metastases. Breast J. 2010;16:32–7.
Ellerbroek N, Holmes F, Singletary E, Evans H, Oswald M, McNeese M. Treatment of patients with isolated axillary nodal metastases from an occult primary carcinoma consistent with breast origin. Cancer. 1990;66:1461–7.
Merson M, Andreola S, Galimberti V, Bufalino R, Marchini S, Veronesi U. Breast carcinoma presenting as axillary metastases without evidence of a primary tumor. Cancer. 1992;70:504–8.
van Ooijen B, Bontenbal M, Henzen-Logmans SC, Koper PC. Axillary nodal metastases from an occult primary consistent with breast carcinoma. Br J Surg. 1993;80:1299–300.
Foroudi F, Tiver KW. Occult breast carcinoma presenting as axillary metastases. Int J Radiat Oncol Biol Phys. 2000;47:143–7.
Hayashi N, Kumamaru H, Isozumi U, Aogi K, Asaga S, Iijima K, et al. Annual report of the Japanese Breast Cancer Registry for 2017. Breast Cancer. 2020;27:803–9.
Miyata H, Gotoh M, Hashimoto H, Motomura N, Murakami A, Tomotaki A, et al. Challenges and prospects of a clinical database linked to the board certification system. Surg Today. 2014;44:1991–9.
Greene. AJCC cancer staging manual, 6th edn. New York: Springer; 2003.
World Health Organization. Tumours of the breast and female genital organs. Oxford: Oxford University Press; 2003.
Kim H, Park W, Kim SS, Ahn SJ, Kim YB, Kim TH, et al. Outcome of breast-conserving treatment for axillary lymph node metastasis from occult breast cancer with negative breast MRI. Breast. 2019;49:63–9.
Terada M, Adachi Y, Sawaki M, Hattori M, Yoshimura A, Naomi G, et al. Occult breast cancer may originate from ectopic breast tissue present in axillary lymph nodes. Breast Cancer Res Treat. 2018;172:1–7.
McCartan DP, Zabor EC, Morrow M, Zee KJV, El-Tamer MB. Oncologic outcomes after treatment for MRI occult breast cancer (pT0N+). Ann Surg Oncol. 2017;24:3141–7.
Rueth NM, Black DM, Limmer AR, Gabriel E, Huo L, Fornage BD, et al. Breast conservation in the setting of contemporary multimodality treatment provides excellent outcomes for patients with occult primary breast cancer. Ann Surg Oncol. 2015;22:90–5.
Kim BH, Kwon J, Kim K. Evaluation of the benefit of radiotherapy in patients with occult breast cancer: a population-based analysis of the SEER database. Cancer Res Treat. 2018;50:551–61.
Kuroki-Suzuki S, Kuroki Y, Nasu K, Nawano S, Moriyama N, Okazaki M. Detecting breast cancer with non-contrast MR imaging: combining diffusion-weighted and STIR imaging. Magn Reson Med Sci. 2007;6:21–7.
Malur S, Wurdinger S, Moritz A, Michels W, Schneider A. Comparison of written reports of mammography, sonography and magnetic resonance mammography for preoperative evaluation of breast lesions, with special emphasis on magnetic resonance mammography. Breast Cancer Res. 2001;3:55–60.
Orel SG, Weinstein SP, Schnall MD, Reynolds CA, Schuchter LM, Fraker DL, et al. Breast MR imaging in patients with axillary node metastases and unknown primary malignancy. Radiology. 1999;212:543–9.
Ambaye AB, MacLennan SE, Goodwin AJ, Suppan T, Naud S, Weaver DL. Carcinoma and atypical hyperplasia in reduction mammaplasty: increased sampling leads to increased detection. A prospective study. Plast Reconstr Surg. 2009;124:1386–92.
Usón Junior PLS, Callegaro Filho D, Bugano DDG, Geyer FC, de Nigro Corpa MV, Gonçalves PDS, et al. Incidental findings in reduction mammoplasty specimens in patients with no prior history of breast cancer. An analysis of 783 specimens. Pathol Oncol Res. 2018;24:95–9.
Waldner M, Klein HJ, Künzi W, Guggenheim M, Plock JA, Giovanoli P. Occurrence of occult malignancies in reduction mammoplasties. Front Surg [Internet]. 2018 [cited 2021 Mar 17];5. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850823/. Accessed 17 Mar 2021.
Acevedo F, Armengol VD, Deng Z, Tang R, Coopey SB, Braun D, et al. Pathologic findings in reduction mammoplasty specimens: a surrogate for the population prevalence of breast cancer and high-risk lesions. Breast Cancer Res Treat. 2019;173:201–7.
Kuehlmann B, Vogl FD, Kempny T, Djedovic G, Huemer GM, Hüttinger P, et al. Occult pathologic findings in reduction mammaplasty in 5781 patients—an international multicenter study. J Clin Med. 2020;9:2223.
Acknowledgements
We would like to thank the JBCS staff and National Clinical Database office staff for their support in this study. MT would like to thank Yayoi Adachi and Hiroji Iwata at Aichi Cancer Center for their support in the application of this research proposal. We thank Melissa Crawford, PhD, from Edanz (https://en-author-services.edanz.com/ac) for editing a draft of this manuscript.
Funding
This work was supported by the Japanese Breast Cancer Society.
Author information
Authors and Affiliations
Contributions
MT, MM, HK, HM, KT, MY, EO MD, MN, SA, YK, TK, KA, NN, KI, NH MK, YY, and HJ were involved in study design and data interpretation. MT, MM and HM were involved in the data analysis. All authors critically revised the report, commented on drafts of the manuscript, and approved the final report.
Corresponding author
Ethics declarations
Conflict of interest
HK, and HM are affiliated with the Department of Healthcare Quality Assessment at The University of Tokyo, which is a social collaboration department supported by the National Clinical Database, Johnson & Johnson K.K., and Nipro Corporation. MT, MM, KT, MY, EO MD, MN, SA, YK, TK, KA, NN, KI, NH MK, YY, and HJ declare no conflicts of interest associated with this manuscript.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Terada, M., Miyashita, M., Kumamaru, H. et al. Surgical treatment trends and identification of primary breast tumors after surgery in occult breast cancer: a study based on the Japanese National Clinical Database—Breast Cancer Registry. Breast Cancer 29, 698–708 (2022). https://doi.org/10.1007/s12282-022-01348-y
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12282-022-01348-y