Overall survival differences between patients with inflammatory and noninflammatory breast cancer presenting with distant metastasis at diagnosis

被引:0
作者
Tamer M. Fouad
Takahiro Kogawa
Diane D. Liu
Yu Shen
Hiroko Masuda
Randa El-Zein
Wendy A. Woodward
Mariana Chavez-MacGregor
Ricardo H. Alvarez
Banu Arun
Anthony Lucci
Savitri Krishnamurthy
Gildy Babiera
Thomas A. Buchholz
Vicente Valero
Naoto T. Ueno
机构
[1] The University of Texas MD Anderson Cancer Center,Department of Breast Medical Oncology
[2] The University of Texas MD Anderson Cancer Center,Department of Biostatistics
[3] The University of Texas MD Anderson Cancer Center,Department of Epidemiology
[4] The University of Texas MD Anderson Cancer Center,Department of Radiation Oncology
[5] The University of Texas MD Anderson Cancer Center,Department of Surgical Oncology
[6] The University of Texas MD Anderson Cancer Center,Department of Pathology
[7] The University of Texas MD Anderson Cancer Center,Morgan Welch Inflammatory Breast Cancer Research Program and Clinic
[8] Cairo University,Department of Medical Oncology, The National Cancer Institute
来源
Breast Cancer Research and Treatment | 2015年 / 152卷
关键词
Stage IV; Breast cancer; Inflammatory breast cancer; IBC; Prognosis; Metastasis;
D O I
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中图分类号
学科分类号
摘要
Inflammatory breast cancer (IBC) is a rare and aggressive disease. Previous studies have shown that among patients with stage III breast cancer, IBC is associated with a worse prognosis than noninflammatory breast cancer (non-IBC). Whether this difference holds true among patients with stage IV breast cancer has not been studied. We tested the hypothesis that overall survival (OS) is worse in patients with IBC than in those with non-IBC among patients with distant metastasis at diagnosis (stage IV disease). We reviewed the records of 1504 consecutive patients with stage IV breast cancer (IBC: 206; non-IBC: 1298) treated at our institution from 1987 through 2012. Survival curves for IBC and non-IBC subcohorts were compared. The Cox proportional hazards model was used to determine predictors of OS. The median follow-up period was 4.7 years. IBC was associated with shorter median OS time than non-IBC (2.27 vs. 3.40 years; P = 0.0128, log-rank test). In a multicovariate Cox model that included 1389 patients, the diagnosis of IBC was a significant independent predictor of worse OS (hazard ratio = 1.431, P = 0.0011). Other significant predictors of worse OS included Black (vs. White) ethnicity, younger age at diagnosis, negative HER2 status, and visceral (vs. nonvisceral) site of metastasis. IBC is associated with shorter OS than non-IBC in patients with distant metastasis at diagnosis. The prognostic impact of IBC should be taken into consideration among patients with stage IV breast cancer.
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页码:407 / 416
页数:9
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