Atypical Ductal Hyperplasia (ADH)

  • ADH and atypical lobular hyperplasia are now frequently diagnosed with use of core-needle biopsy
  • Although atypia can be difficult to distinguish from carcinoma in situ:
    • Pathologic criteria exist to distinguish the two entities
  • This distinction is important because, while in situ carcinoma is malignant and may progress to invasive disease:
    • ADH is a non-obligate cancer precursor and often represents a marker of an elevated future breast cancer risk
  • ADH is most frequently found by mammography
  • Atypia alone, with no other risk factors, confers an approximate:
    • Four-fold to five-fold risk of the development of breast cancer
  • Although breast MRI is more sensitive to detect intermediate- and high-grade ductal carcinoma in situ (DCIS) as well as invasive cancers:
    • Breast MRI lacks sufficient diagnostic ability to differentiate ADH versus DCIS or invasive cancers
  • Excision is indicated for ADH found on core needle biopsy:
    • As concomitant in situ or invasive cancer will be found in approximately 15% of cases
  • The 10-year risk of developing a breast cancer after a diagnosis of ADH:
    • Is approximately 17%:
      • Risk is bilateral yet breast cancers developing within 5 years of a biopsy of ADH more likely to occur in the ipsilateral breast than those developing more than 5 years (82% ipsilateral in the first 5 years vs 58% ipsilateral after 5 years)
  • The National Surgical Adjuvant Breast and Bowel Project (NSABP) P-1 trial:
    • Showed that when atypia is found on a sample obtained with needle biopsy and excision rules out cancer:
      • Tamoxifen reduces the risk of developing breast cancer by about 86%:
        • These patients should therefore be referred for discussion about this endocrine prophylaxis
  • Similarly, the Study of Tamoxifen and Raloxifene (STAR, NSABP P-2) trial:
    • Which randomized post-menopausal women to tamoxifen or raloxifene, found that raloxifene provided equivalent risk reduction to tamoxifen with less toxicity (e.g., endometrial cancer)
  • References:
    • Coopey SB, Mazzola E, Buckley JM, et al. The role of chemoprevention in modifying the risk of breast cancer in women with atypical breast lesions. Breast Cancer Res Treat. 2012;136:627-633.
    • 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.
    • Krishnamurthy S, Bevers T, Kuerer H, Yang WT. Multidisciplinary considerations in the management of high-risk breast lesions. AJR Am J Roentgenol. 2012;198:W132-140.
    • Hartmann LC, Radisky DC, Frost MH, et al. Understanding the premalignant potential of atypical hyperplasia through its natural history: a longitudinal cohort study. Cancer Prev Res (Phila). 2014;7:211-217.
    • Vogel VG, Costantino JP, Wickerham DL, et al; National Surgical Adjuvant Breast and Bowel Project. Update of the National Surgical Adjuvant Breast and Bowel Project Study of Tamoxifen and Raloxifene (STAR) P-2 Trial: Preventing breast cancer. Cancer Prev Res (Phila). 2010;3:696-706.

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