Association of Body Mass Index Changes during Neoadjuvant Chemotherapy with Pathologic Complete Response and Clinical Outcomes in Patients with Locally Advanced Breast Cancer

被引:18
|
作者
Kogawa, Takahiro [1 ]
Fouad, Tamer M. [1 ]
Wei, Caimiao [2 ]
Masuda, Hiroko [1 ]
Kai, Kazuharu [1 ]
Fujii, Takeo [1 ]
El-Zein, Randa [3 ]
Chavez-MacGregor, Mariana [1 ]
Litton, Jennifer K. [1 ]
Brewster, Abenaa [1 ]
Alvarez, Ricardo H. [1 ]
Hortobagyi, Gabriel N. [1 ]
Valero, Vicente [1 ]
Theriault, Richard [1 ]
Ueno, Naoto T. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Breast Med Oncol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX 77030 USA
来源
JOURNAL OF CANCER | 2015年 / 6卷 / 04期
基金
美国国家卫生研究院;
关键词
Breast cancer; Inflammatory breast cancer; Body mass index; Body mass index change; Predictive factor; Pathological complete response; DISEASE-FREE SURVIVAL; WEIGHT-GAIN; ADJUVANT CHEMOTHERAPY; DIAGNOSIS; OBESITY; WOMEN; CARCINOMA; STAGE; NUTRITION; PROGNOSIS;
D O I
10.7150/jca.10580
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this study was to determine the association between body mass index (BMI) measurements (baseline BMI and changes in BMI during neoadjuvant systemic treatment [NST]) and clinical efficacy (pathologic complete response [pCR] rate and survival outcomes) in locally advanced breast cancer (LABC). We hypothesized that high baseline BMI and increases in BMI during NST are associated with lower pCR rates and poorer clinical outcomes in LABC. We retrospectively reviewed the medical records of 1002 patients, 204 with primary inflammatory breast cancer (IBC) and 798 with stage III non-IBC, who underwent standard NST and definitive surgery between November 1, 2006, and December 31, 2012. The median follow-up time for the survivors was 19.6 months (0.4 - 67.8 months). The pCR rates of patients whose BMI increased or decreased were 23.2% and 18.1%, respectively, (p=0.048). The unadjusted overall survival (OS) was significantly better in the group with increased BMI (p=0.006). However, increased BMI was not an independent predictor of pCR and clinical outcomes (recurrence-free survival and OS) after adjusting for other clinical variables. In subset analyses, increased BMI as a continuous variable was an independent predictor of higher pCR rates in the normal BMI/underweight group (odds ratio [OR]=1.35, 95% confidence interval [CI]: 1.06-0.71, p=0.015). Increased BMI (BMI change >= 0 vs. < 0) was also an independent predictor of pCR (OR=1.65, 95% CI: 1.00-2.72, p=0.049) in the postmenopausal group. Our results show that increasing BMI shows improved clinical outcome in terms of better pCR rates in normal BMI/underweight group and in the postmenopausal group. These results contradict previously reported findings on the association between high BMI and poor clinical efficacy regarding pCR rate and survival outcomes in early-stage breast cancer. Thus, the role of BMI in breast cancer may depend on patients' clinical characteristics such as advanced stage.
引用
收藏
页码:310 / 318
页数:9
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