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  Vol. 141 No. 6, June 2006 TABLE OF CONTENTS
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A Single-Center Experience With Inflammatory Breast Cancer, 1985-2003

Rory L. Smoot, MD; Cody A. Koch, MA; Amy C. Degnim, MD; Sylvester Sterioff, MD; John H. Donohue, MD; Clive S. Grant, MD; Sunni A. Barnes, PhD; Rachel E. Gullerud, BS; Timothy J. Hobday, MD; David R. Farley, MD

Arch Surg. 2006;141:567-573.

Hypothesis  "Up-front" surgery improves survival in inflammatory breast cancer (IBC).

Design  Retrospective cohort, 1985-2003.

Setting  Tertiary referral center.

Patients  Consecutive patients with a primary occurrence of IBC.

Main Outcome Measures  All-cause and disease-free survival.

Results  One-hundred fifty-six patients were identified with IBC; 28 patients with metastatic disease were excluded from further analysis. The mean age of the remaining 128 patients was 53 years; 57% of women were postmenopausal. One hundred twenty-two patients had clinically apparent IBC. Tumors were palpable in 83 patients (mean diameter, 9.1 cm). Neoadjuvant chemotherapy was the initial therapy in 106 patients, while surgery was the initial therapy in 22 patients. The overall median survival was 37 months, with a median disease-free interval of 23 months. The 5-year survival was 42%, with a disease-free survival of 21%. Univariate analysis of recurrence identified previous hormone therapy (relative risk [RR], 0.50; P = .03), menopause (RR, 0.55; P = .01), and palpable adenopathy (RR, 1.57; P = .04) as significant factors. Univariate survival analysis highlighted previous hormone therapy (RR, 0.48; P = .04), radiotherapy (RR, 0.39; P = .02), sequence of therapy (P = .001), family history (RR, 0.47; P = .01), and palpable adenopathy (RR, 2.22; P<.001) as being important. Multivariate analysis of recurrence identified menopausal status as the key factor. Adenopathy at the initial examination was associated with decreased length of survival, while radiotherapy was associated with better survival.

Conclusions  Survival from IBC remains poor. Although adenopathy and radiotherapy affected survival by multivariate analysis, the sequence of therapy was not associated with improved outcome.


Author Affiliations: Departments of Surgery (Drs Smoot, Degnim, Sterioff, Donohue, Grant, and Farley) and Medical Oncology (Dr Hobday) and Division of Biostatistics (Drs Barnes and Ms Gullerud), Mayo Clinic College of Medicine (Mr Koch), Rochester, Minn.







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