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Six-Year Follow-Up of Patients With Microinvasive, T1a, and T1b Breast Carcinoma

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Abstract

Background: Management of patients with breast cancers ≤1 cm remains controversial. Reports of infrequent nodal metastases in tumors ≤5 mm has led to suggestions that axillary dissection should be selective, and that tumor characteristics should guide adjuvant therapy.

Methods: A retrospective review of 290 patients with breast cancer 1 cm in size or smaller from 1989 to 1991 was done. Distant disease-free survival (DDFS) was the primary outcome measure.

Results: There were 95 T1a (≤5 mm) and 196 T1b (6–10 mm) cancers. Nodal metastases were found in 8 T1a and 26 T1b tumors. Larger size, poorer differentiation, and lymphovascular invasion (LVI) were associated with more nodal metastases, but none of these trends reached statistical significance. The 6-year DDFS was 93% for node-negative and 87% for node-positive patients (P = .02). Overall, breast cancers with poorer differentiation and LVI trended toward a poorer outcome. For patients with node-negative tumors, LVI was associated with a poorer outcome (P = .03). The size of the primary tumor was not predictive of outcome. There were no nodal metastases or recurrences in the 18 patients with microinvasive breast cancer.

Conclusions: Lymph node status is the major determinant of outcome in breast cancers 1 cm in size or smaller. Accurate axillary assessment remains crucial in management of small breast cancer.

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REFERENCES

  1. NIH Consensus Conference. Treatment of early-stage breast cancer. JAMA 1991;265:391–4.

    Google Scholar 

  2. Silverstein M, Gierson E, Waisman J, Senofsky G, Colburn W, Gamagami P. Axillary lymph node dissection for T1a breast carcinoma: is it indicated? Cancer 1994;73:664–7.

    Google Scholar 

  3. Cady B. Is axillary lymph node dissection necessary in routine management of breast cancer? No. The Breast Journal 1997;3:246–60.

    Google Scholar 

  4. Chontos A, Maher D, Ratzer E, Fenoglio M. Axillary lymph node dissection: is it required in T1a breast cancer? J Am Coll Surg 1997;184:493–8.

    Google Scholar 

  5. Velanovich V. Axillary lymph node dissection for breast cancer: a decision analysis of T1 lesions. Ann Surg Oncol 1998;5:131–9.

    Google Scholar 

  6. Mustafa I, Bland K. Indications for axillary dissection in T1 breast cancer. Ann Surg Oncol 1998;5:4–8.

    Google Scholar 

  7. Walls J, Boggis C, Wilson M, Asbury D, Roberts J, Bundred N, Mansel R. Treatment of the axilla in patients with screen-detected breast cancer. Br J Surg 1993;80:436–8.

    Google Scholar 

  8. Silverstein M, Gierson E, Waisman J, Colburn W, Gamagami P. Predicting axillary node positivity in patients with invasive carcinoma of the breast by using a combination of T category and palpability. J Am Coll Surg 1995;180:700–7004.

    Google Scholar 

  9. Dowlatshahi K, Snider H, Kim R. Axillary node status in nonpalpable breast cancer. Ann Surg Oncol 1995;2:424–428.

    Google Scholar 

  10. Barth A, Craig P, Silverstein M. Predictors of axillary lymph node metastases in patients with T1 breast cancer. Cancer 1997;79:1918–1922.

    Google Scholar 

  11. Carter C, Allen C, Henson D. Relation of tumor size, lymph node status, and survival in 24,740 breast cancer cases. Cancer 1989; 63:181–187.

    Google Scholar 

  12. Giuliano A, Barth A, Spivack B, Beitsch PD, Evans SW. Incidence, and predictors of axillary metastasis in T1 carcinoma of the breast. J Am Coll Surg 1996;183:185–189.

    CAS  PubMed  Google Scholar 

  13. Shetty M, Reiman H Jr. Tumor size and axillary metastasis, a correlative occurrence in 1244 cases of breast cancer between 1980 and 1995. Eur J Surg Oncol 1997;23:139–141.

    Google Scholar 

  14. White R, Vezeridis M, Konstadoulakis M, Cole B, Wanebo H, Bland K. Therapeutic options and results for the management of minimally invasive carcinoma of the breast: influence of axillary dissection for treatment of T1a and T1b lesions. J Am Coll Surg 1996;183:575–582.

    Google Scholar 

  15. Rush Port E, Tan L, Borgen P, Van Zee K. Incidence of axillary lymph node metastases in T1a and T1b breast carcinoma. Ann Surg Oncol 1998;5:23–27.

    Google Scholar 

  16. Robinson D, Senofsky G, Ketcham A. Role, and extent of lymphadenectomy for early breast cancer. Semin Surg Oncol 1992;8:78–82.

    Google Scholar 

  17. Morrow M. Role of axillary dissection in breast cancer management. Ann Surg Oncol 1996;3:233–234.

    Google Scholar 

  18. Shetty M. Axillary lymph node metastasis in carcinoma of the breast. J Am Coll Surg 1997;184:671–672.

    Google Scholar 

  19. Baxter N, McCready D, Chapman J, et al. Clinical behavior of untreated axillary nodes after local treatment for primary breast cancer. Ann Surg Oncol 1996;3:235–240.

    Google Scholar 

  20. Sosa J, Diener-West M, Gusev Y, Choti M, Lange J, Dooley W, Zeiger M. Association between extent of axillary lymph node dissection and survival in patients with stage I breast cancer. Ann Surg Oncol 1998;5:140–149.

    Google Scholar 

  21. Giuliano A, Jones R, Brennan M, Statman R. Sentinel lymphadenectomy in breast cancer. J Clin Oncol 1997;15:2345–2350.

    Google Scholar 

  22. Veronesi U, Paganelli G, Galimberti V, et al. Sentinel-node biopsy to avoid axillary dissection in breast cancer with clinically negative lymph-nodes. Lancet 1997;349:1864–1867.

    Article  CAS  PubMed  Google Scholar 

  23. Kiricuta C, Tausch J. A mathematical model of axillary lymph node involvement based on 1446 complete axillary dissections in patients with breast carcinoma. Cancer 1992;69:2496–2501.

    Google Scholar 

  24. Chadha M, Chabon A, Friedmann P, Vikram B. Predictors of axillary lymph node metastases in patients with T1 breast cancer. Cancer 1993;73:350–353.

    Google Scholar 

  25. Fein D, Fowble B, Hanlon A, et al. Identification of women with T1–T2 breast cancer at low risk of positive axillary nodes. J surg Oncol 1997;65:34–39.

    Google Scholar 

  26. Olivotto I, Jackson J, Mates D, Anderson S, Davidson W, Bryce C, Ragaz J. Prediction of axillary lymph node involvement of women with invasive breast carcinoma: a multivariate analysis. Cancer 1998;83:948–955.

    Google Scholar 

  27. Leitner S, Swern A, Weinberger D, Duncan L, Hutter R. Predictors of recurrence for patients with small (one centimeter or less) localized breast cancer (T1a,b N0 M0). Cancer 1995;76:2266–2274.

    Google Scholar 

  28. International Breast Cancer Study Group. Prognostic importance of occult axillary lymph node micrometastases from breast cancers. Lancet 1990;335:1565–1568.

    Google Scholar 

  29. Kinne D, Petrek J, Osborne M, Fracchia A, DePalo A, Rosen P. Breast carcinoma in situ. Arch Surg 1989;124:33–36.

    Google Scholar 

  30. Wong J, Kopald K, Morton D. The impact of microinvasion on axillary node metastases and survival in patients with intraductal breast cancer. Arch Surg 1990;125:1298–1302.

    Google Scholar 

  31. Silverstein M, Waisman J, Gamagami P, et al. Intraductal carcinoma of the breast (208 cases): clinical factors influencing treatment choice. Cancer 1990;66:102–108.

    Google Scholar 

  32. Solin L, Fowble B, Yeh I, Kowalyshyn M, Schultz D, Weiss M, Goodman R. Microinvasive ductal carcinoma of the breast treated with breast-conserving surgery and definitive irradiation. Int J Radiat Oncol Biol Phys 1992;23:961–968.

    Google Scholar 

  33. Harris JR, Osteen RT. Patients with early breast cancer benefit from effective axillary treatment. Breast Cancer Res Treat 1985; 5:17–21.

    Google Scholar 

  34. Hayward J, Caleffi M. The significance of local control in the primary treatment of breast cancer. Arch Surg 1987;122:1244–1247.

    Google Scholar 

  35. Ruffin WK, Stacey-Clear A, Younger J, Hoover HC Jr. Rationale for routine axillary dissection in carcinoma of the breast. J Am Coll Surg 1995;180:245–251.

    Google Scholar 

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Mann, G.B., Port, E.R., Rizza, C. et al. Six-Year Follow-Up of Patients With Microinvasive, T1a, and T1b Breast Carcinoma. Ann Surg Oncol 6, 591–598 (1999). https://doi.org/10.1007/s10434-999-0591-5

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  • DOI: https://doi.org/10.1007/s10434-999-0591-5

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