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Review - Haymarket Media Group

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Commentary<br />

Inflammatory Breast Cancer: Still a Challenge<br />

Nancy U. Lin, MD<br />

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts<br />

Inflammatory breast cancer (IBC) is a relatively<br />

rare disease, comprising less than 3% of breast<br />

cancer cases in the United States. 1 Compared<br />

with locally advanced, noninflammatory breast cancer,<br />

IBC appears to be a distinct entity with a unique<br />

mode of presentation and underlying biology.<br />

Unfortunately, even with multimodality therapy, the<br />

prognosis for patients with IBC remains poor. 2<br />

Overexpression and/or amplification of HER2 is<br />

present in 25% to 30% of primary breast carcinomas. 3<br />

In contrast, HER2 is overexpressed in approximately<br />

half of IBC cases. 4,5 In all patients with breast cancer,<br />

Inflammatory breast cancer<br />

appears to be a distinct entity with<br />

a unique mode of presentation<br />

and underlying biology.<br />

overexpression of HER2 is associated with a higher<br />

risk of relapse and worse overall survival (OS) 3 ; however,<br />

the contribution of HER2 overexpression to the<br />

prognosis of patients with IBC is not well defined.<br />

Dawood and colleagues therefore set out to examine<br />

the prognostic significance of HER2 status in<br />

women with IBC diagnosed between 1989 and 2005<br />

20 The American Journal of Hematology/Oncology<br />

at the University of Texas M.D. Anderson Cancer<br />

Center. 6 In all, 179 patients fulfilled the inclusion/<br />

exclusion criteria for this retrospective analysis. A<br />

strength of the study is the relatively uniform treatment<br />

of the patients: all patients received an anthracycline,<br />

and nearly 80% received a taxane as part of<br />

their primary systemic chemotherapy. In addition,<br />

the exclusion of patients who received trastuzumab<br />

in the neoadjuvant or adjuvant setting allowed the<br />

authors to describe the impact of HER2 upon relapsefree<br />

survival (RFS) independent of an effective targeted<br />

therapy. Chemotherapy was followed by mastectomy<br />

and comprehensive radiotherapy in all patients,<br />

and hormonal therapy was given to patients with<br />

hormone receptor–positive disease. There was no difference<br />

in the rate of pathologic complete response<br />

(pCR) by HER2 status. After a median follow-up of 35<br />

months, 56% of patients with HER2-negative disease<br />

and 62% of patients with HER2-positive disease<br />

developed a disease recurrence, a difference that was<br />

not statistically significant.<br />

What could account for the lack of prognostic significance<br />

of HER2 for RFS described in this study<br />

compared with the reproducible influence of HER2<br />

status on prognosis in all-comers with breast cancer?<br />

One possibility relates to common characteristics of<br />

IBC present across breast cancer subtypes that lead to<br />

a more aggressive clinical phenotype. Using expression<br />

profiling, Bertucci and colleagues identified the<br />

same five molecular subtypes (luminal A and B,<br />

basal, HER2 positive, and normal breast-like) in IBC<br />

as have been observed in non-IBC. 7 At the same time,<br />

a single 109-gene set was able to distinguish between<br />

IBC and non-IBC within each subtype. These genes<br />

Dr Nancy U. Lin was invited to provide commentary on the following article: Dawood S, Broglio K, Gong Y, et al. Prognostic significance of<br />

HER-2 status in women with inflammatory breast cancer. Cancer. 2008;112:1905-1911.

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