DOI QR코드

DOI QR Code

Upgraded Malignancy from High-Risk and Borderline Breast Lesions: Immunohistochemical and Clinical Characteristics

고위험 및 경계성 유방 병변에서 업그레이드된 악성 종양: 면역조직화학적 및 임상적 특징

  • Park, Borim (Department of Radiology, Incheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea) ;
  • Kang, Bong Joo (Department of Radiology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea) ;
  • Baek, Ji Eun (Department of Radiology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea) ;
  • Kim, Sung Hun (Department of Radiology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea) ;
  • Lee, Hyun Sil (Department of Radiology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea)
  • 박보림 (가톨릭대학교 의과대학 인천성모병원 영상의학과) ;
  • 강봉주 (가톨릭대학교 의과대학 서울성모병원 영상의학과) ;
  • 백지은 (가톨릭대학교 의과대학 서울성모병원 영상의학과) ;
  • 김성헌 (가톨릭대학교 의과대학 서울성모병원 영상의학과) ;
  • 이현실 (가톨릭대학교 의과대학 서울성모병원 영상의학과)
  • Received : 2017.04.24
  • Accepted : 2017.08.18
  • Published : 2018.01.01

Abstract

Purpose: The purpose of this study was to investigate the immune-histochemical characteristics of upgraded malignancy from high-risk and borderline breast lesions, and to correlate the upgrade rates with clinical findings. Materials and Methods: We scrutinized image-guided biopsy records retrospectively, and included all women afflicted with high-risk and borderline breast lesions during the period, 2011 to 2015, inclusive. A total of 340 high-risk and borderline lesions were identified by the pathologist in biopsy samples and thereafter, surgical excision and/or image follow-up for at least 24 months was performed. We compared the clinical emanating from both high-risk and borderline lesions, and with and without cancer upgrade. In the instances of lesions with cancer upgrade, histologic and immuohistochemical reviews were performed. Results: Of the 340 high-risk or borderline lesions, 18.8% (64/340) were upgraded. The upgrade rates were higher in patients of more advanced age, larger body habitus and afflicted with atypical ductal hyperplasia rather than with other pathology (p < 0.05). In the lesions with cancer upgrade (n = 64), there was no lymph node metastasis. The estrogen receptor-positive (93.8%), progesterone receptor-positive (87.5%), human epidermal growth factor receptor type 2-negative (90.6%), Ki-67-negative (82.8%), and Luminal A (76.6%) types were seen more frequently. Conclusion: Most upgraded malignancies arising from high-risk and borderline breast lesions were found to be Luminal A-type with good prognostic factors, and the upgrade rates correlated with clinical characteristics.

목적: 이 연구의 목적은 고위험 및 경계성 유방 병변에서 업그레이드된 악성 종양의 면역조직화학적 특성을 조사하고 임상 소견과 암으로의 업그레이드율의 연관성을 알아보는 데 있다. 대상과 방법: 저자들은 영상유도하 생검 기록을 후향적으로 검토했으며 2011년부터 2015년까지 고위험과 경계성 유방 병변이 있는 모든 여성을 대상으로 하였다. 생검 샘플에서 병리학자에 의해 총 340개의 고위험 및 경계성 병변이 확인되었으며, 수술적 절제 혹은 24개월 이상 추적 검사가 시행되었다. 고위험 및 경계성 병변이 암으로 업그레이드된 경우와 아닌 경우의 임상 소견을 비교하였다. 암으로 업그레이드된 경우에 대하여, 병리조직학적 및 면역조직화학적 검사를 시행하였다. 결과: 340예의 고위험 또는 경계성 병변 중, 18.8%(64/340)가 암으로 업그레이드되었다. 업그레이드율은 고령의 환자, 크기가 큰 병변에서 더 높았고, 다른 병리학적 유형보다 atypical ductal hyperplasia에서 더 높았다(p < 0.05). 업그레이드 된 악성 종양(n = 64)에서는 림프절 전이가 없었다. Estrogen receptor 양성(93.8%), progesterone receptor 양성(87.5%), human epidermal growth factor receptor type 2 음성(90.6%), Ki-67 음성(82.8%), Luminal A (76.6%)형이 가장 흔하였다. 결론: 고위험 및 경계성 유방 병변에서 업그레이드된 악성 종양은 주로 Luminal A 면역조직화학형과 좋은 예후 인자를 가지며 업그레이드율은 임상 특성과 관련이 있다.

Keywords

Acknowledgement

Supported by : Ministry of Health & Welfare

References

  1. Londero V, Zuiani C, Linda A, Battigelli L, Brondani G, Bazzocchi M. Borderline breast lesions: comparison of malignancy underestimation rates with 14-gauge core needle biopsy versus 11-gauge vacuum-assisted device. Eur Radiol 2011;21:1200-1206 https://doi.org/10.1007/s00330-010-2053-7
  2. Londero V, Zuiani C, Linda A, Girometti R, Bazzocchi M, Sardanelli F. High-risk breast lesions at imaging-guided needle biopsy: usefulness of MRI for treatment decision. AJR Am J Roentgenol 2012;199:W240-W250 https://doi.org/10.2214/AJR.11.7869
  3. Menes TS, Rosenberg R, Balch S, Jaffer S, Kerlikowske K, Miglioretti DL. Upgrade of high-risk breast lesions detected on mammography in the Breast Cancer Surveillance Consortium. Am J Surg 2014;207:24-31 https://doi.org/10.1016/j.amjsurg.2013.05.014
  4. Krishnamurthy S, Bevers T, Kuerer H, Yang WT. Multidisciplinary considerations in the management of high-risk breast lesions. AJR Am J Roentgenol 2012;198:W132-W140 https://doi.org/10.2214/AJR.11.7799
  5. Sewell CW. Pathology of high-risk breast lesions and ductal carcinoma in situ. Radiol Clin North Am 2004;42:821-830 https://doi.org/10.1016/j.rcl.2004.03.013
  6. Linda A, Zuiani C, Bazzocchi M, Furlan A, Londero V. Borderline breast lesions diagnosed at core needle biopsy: can magnetic resonance mammography rule out associated malignancy? Preliminary results based on 79 surgically excised lesions. Breast 2008;17:125-131 https://doi.org/10.1016/j.breast.2007.11.002
  7. Heller SL, Moy L. Imaging features and management of high-risk lesions on contrast-enhanced dynamic breast MRI. AJR Am J Roentgenol 2012;198:249-255 https://doi.org/10.2214/AJR.11.7610
  8. Pediconi F, Padula S, Dominelli V, Luciani M, Telesca M, Casali V, et al. Role of breast MR imaging for predicting malignancy of histologically borderline lesions diagnosed at core needle biopsy: prospective evaluation. Radiology 2010;257: 653-661 https://doi.org/10.1148/radiol.10100732
  9. Kohr JR, Eby PR, Allison KH, DeMartini WB, Gutierrez RL, Peacock S, et al. Risk of upgrade of atypical ductal hyperplasia after stereotactic breast biopsy: effects of number of foci and complete removal of calcifications. Radiology 2010; 255:723-730 https://doi.org/10.1148/radiol.09091406
  10. Lips EH, Mulder L, de Ronde JJ, Mandjes IA, Koolen BB, Wessels LF, et al. Breast cancer subtyping by immunohistochemistry and histological grade outperforms breast cancer intrinsic subtypes in predicting neoadjuvant chemotherapy response. Breast Cancer Res Treat 2013;140:63-71 https://doi.org/10.1007/s10549-013-2620-0
  11. Ko ES, Lee BH, Kim HA, Noh WC, Kim MS, Lee SA. Triple-negative breast cancer: correlation between imaging and pathological findings. Eur Radiol 2010;20:1111-1117 https://doi.org/10.1007/s00330-009-1656-3
  12. Bae MS, Park SY, Song SE, Kim WH, Lee SH, Han W, et al. Heterogeneity of triple-negative breast cancer: mammographic, US, and MR imaging features according to androgen receptor expression. Eur Radiol 2015;25:419-427 https://doi.org/10.1007/s00330-014-3419-z
  13. Kim SH, Seo BK, Lee J, Kim SJ, Cho KR, Lee KY, et al. Correlation of ultrasound findings with histology, tumor grade, and biological markers in breast cancer. Acta Oncol 2008; 47:1531-1538 https://doi.org/10.1080/02841860801971413
  14. Philpotts LE, Shaheen NA, Jain KS, Carter D, Lee CH. Uncommon high-risk lesions of the breast diagnosed at stereotactic core-needle biopsy: clinical importance. Radiology 2000; 216:831-837 https://doi.org/10.1148/radiology.216.3.r00se31831
  15. Esserman L, Yau C. Rethinking the standard for ductal carcinoma in situ treatment. JAMA Oncol 2015;1:881-883 https://doi.org/10.1001/jamaoncol.2015.2607
  16. Narod SA, Iqbal J, Giannakeas V, Sopik V, Sun P. Breast cancer mortality after a diagnosis of ductal carcinoma in situ. JAMA Oncol 2015;1:888-896 https://doi.org/10.1001/jamaoncol.2015.2510
  17. Carels N, Spinasse LB, Tilli TM, Tuszynski JA. Toward precision medicine of breast cancer. Theor Biol Med Model 2016; 13:7 https://doi.org/10.1186/s12976-016-0035-4
  18. Abdel-Fatah TM, Powe DG, Hodi Z, Reis-Filho JS, Lee AH, Ellis IO. Morphologic and molecular evolutionary pathways of low nuclear grade invasive breast cancers and their putative precursor lesions: further evidence to support the concept of low nuclear grade breast neoplasia family. Am J Surg Pathol 2008;32:513-523 https://doi.org/10.1097/PAS.0b013e318161d1a5
  19. Sinn HP, Elsawaf Z, Helmchen B, Aulmann S. Early breast cancer precursor lesions: lessons learned from molecular and clinical studies. Breast Care (Basel) 2010;5:218-226 https://doi.org/10.1159/000319624
  20. Sanders ME, Schuyler PA, Dupont WD, Page DL. The natural history of low-grade ductal carcinoma in situ of the breast in women treated by biopsy only revealed over 30 years of long-term follow-up. Cancer 2005;103:2481-2484 https://doi.org/10.1002/cncr.21069
  21. Goldhirsch A, Wood WC, Coates AS, Gelber RD, Thurlimann B, Senn HJ, et al. Strategies for subtypes--dealing with the diversity of breast cancer: highlights of the St. Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2011. Ann Oncol 2011;22:1736-1747 https://doi.org/10.1093/annonc/mdr304
  22. Bild AH, Parker JS, Gustafson AM, Acharya CR, Hoadley KA, Anders C, et al. An integration of complementary strategies for gene-expression analysis to reveal novel therapeutic opportunities for breast cancer. Breast Cancer Res 2009;11:R55 https://doi.org/10.1186/bcr2344