TY - JOUR
T1 - Invasive lobular vs. ductal breast cancer
T2 - A stage-matched comparison of outcomes
AU - Wasif, Nabil
AU - Maggard, Melinda A.
AU - Ko, Clifford Y.
AU - Giuliano, Armando E.
N1 - Funding Information:
ACKNOWLEDGMENT Work was supported by grants from the Gonda (Goldschmied) Research Laboratories of the John Wayne Cancer Institute at Saint John’s Health Center. Also supported by funding from QVC and the Fashion Footwear Association of New York Charitable Foundation (New York, NY), the Margie and Robert E. Petersen Foundation (Los Angeles, CA), Mrs. Lois Rosen (Los Angeles, CA), the Associates for Breast and Prostate Cancer Studies (Santa Monica, CA), the Family of Robert Novick (Los Angeles, CA), Ruth and Martin H. Weil Fund (Los Angeles, CA), and the Wrather Family Foundation (Los Alamos, CA).
PY - 2010/7
Y1 - 2010/7
N2 - Background. Invasive lobular breast cancer (ILC) is less common than invasive ductal breast cancer (IDC), more difficult to detect mammographically, and usually diagnosed at a later stage. Does delayed diagnosis of ILC affect survival? We used a national registry to compare outcomes of patients with stage-matched ILC and IDC. Methods. Query of the National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) tumor registry identified 263,408 women diagnosed with IDC or ILC between 1993 and 2003. Survival of patients matched by T and N stage was compared using Kaplan-Meier curves and log-rank analysis. Results. When compared with IDC, ILC was more likely to be >2 cm (43.1 vs. 32.6%; P<0.001), lymph node positive (36.8 vs. 34.4%; P<0.001), and ER positive (93.1 vs. 75.6%; P<0.001). The 5-year disease-specific survival (DSS) was significantly better for patients with ILC than for those with IDC, before (90 vs. 88%; P<0.001) and after matching for stage T1N0 (98 vs. 96%; P<0.001), T2N0 (94 vs. 88%; P<0.001), and T3N0 (92 vs. 83%, P<0.001). The 5-year DSS for patients with nodal metastasis of ILC vs. IDC was 89% vs. 88% (P = NS) for stage T1N1, 81 vs. 73% (P<0.001) for T2N1, and 72 vs. 56% (P<0.001) for T3N1. Multivariate analysis identified a 14% survival benefit for ILC (hazard ratio 0.86, 95% confidence interval 0.80-0.92). Conclusions. Stage-matched prognosis is better for patients with ILC than for those with IDC. Our findings support a different biology for ILC and are important for counseling and risk stratification.
AB - Background. Invasive lobular breast cancer (ILC) is less common than invasive ductal breast cancer (IDC), more difficult to detect mammographically, and usually diagnosed at a later stage. Does delayed diagnosis of ILC affect survival? We used a national registry to compare outcomes of patients with stage-matched ILC and IDC. Methods. Query of the National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) tumor registry identified 263,408 women diagnosed with IDC or ILC between 1993 and 2003. Survival of patients matched by T and N stage was compared using Kaplan-Meier curves and log-rank analysis. Results. When compared with IDC, ILC was more likely to be >2 cm (43.1 vs. 32.6%; P<0.001), lymph node positive (36.8 vs. 34.4%; P<0.001), and ER positive (93.1 vs. 75.6%; P<0.001). The 5-year disease-specific survival (DSS) was significantly better for patients with ILC than for those with IDC, before (90 vs. 88%; P<0.001) and after matching for stage T1N0 (98 vs. 96%; P<0.001), T2N0 (94 vs. 88%; P<0.001), and T3N0 (92 vs. 83%, P<0.001). The 5-year DSS for patients with nodal metastasis of ILC vs. IDC was 89% vs. 88% (P = NS) for stage T1N1, 81 vs. 73% (P<0.001) for T2N1, and 72 vs. 56% (P<0.001) for T3N1. Multivariate analysis identified a 14% survival benefit for ILC (hazard ratio 0.86, 95% confidence interval 0.80-0.92). Conclusions. Stage-matched prognosis is better for patients with ILC than for those with IDC. Our findings support a different biology for ILC and are important for counseling and risk stratification.
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U2 - 10.1245/s10434-010-0953-z
DO - 10.1245/s10434-010-0953-z
M3 - Article
C2 - 20162457
AN - SCOPUS:77954955272
SN - 1068-9265
VL - 17
SP - 1862
EP - 1869
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
IS - 7
ER -