Racial differences in acute toxicities of neoadjuvant or adjuvant chemotherapy in patients with early-stage breast cancer

被引:51
作者
Han, Hyo Sook [2 ]
Reis, Isildinha M. [3 ,4 ]
Zhao, Wei [4 ]
Kuroi, Katsumasa [5 ]
Toi, Masakazu [6 ]
Suzuki, Eiji [5 ]
Syme, Rachel [7 ]
Chow, Louis [8 ,9 ]
Yip, Adrian Y. S. [8 ]
Glueck, Stefan [1 ]
机构
[1] Univ Miami, Leonard M Miller Sch Med, Sylvester Comprehens Canc Ctr, Div Hematol & Oncol,Dept Internal Med, Miami, FL 33152 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Breast Program, Dept Womens Oncol, Tampa, FL USA
[3] Univ Miami, Miller Sch Med, Div Biostat, Dept Epidemiol & Publ Hlth, Miami, FL 33136 USA
[4] Univ Miami, Sylvester Comprehens Canc Ctr, Miami, FL USA
[5] Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Dept Surg, Tokyo, Japan
[6] Kyoto Univ, Grad Sch Med, Dept Breast Surg, Kyoto, Japan
[7] Univ Calgary, Dept Oncol, Tom Baker Canc Ctr, Alberta Hlth Serv, Calgary, AB T2N 1N4, Canada
[8] Org Oncol & Translat Res, Hong Kong, Hong Kong, Peoples R China
[9] Univ Hong Kong, Li Ka Shing Fac Med, Clin Trials Ctr, Hong Kong, Hong Kong, Peoples R China
关键词
Breast cancer; Racial/ethnic difference; Toxicity; Chemotherapy; DOSE INTENSITY; SURVIVAL; ETHNICITY; CYCLOPHOSPHAMIDE; HAWAII; OBESE; WOMEN; RACE;
D O I
10.1016/j.ejca.2011.06.027
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Racial disparities in breast cancer outcomes are attributed to differences in baseline tumour characteristics and biology, stage, age, ethnic background and socioeconomic factors. However, little is known about racial differences in treatment-related toxicities. We hypothesised that racial/ethnic differences result in differential tolerance to chemotherapy potentially, leading to compromised dose intensity/density of chemotherapy in patients with early-stage breast cancer. Methods: Data were collected from patients treated at five international centers for early breast cancer with the same adjuvant/neoadjuvant chemotherapy (FEC 100: fluorouracil 500 mg/m(2), epirubicin 100 mg/m(2), and cyclophosphamide 500 mg/m(2),every 21 d for 3-6 cycles). Toxicities were assessed by first episode of >= grade 2 toxicity. Results: Toxicities were compared according to four race/ethnicity groups (103 Caucasian, 30 African American, 164 Asian, and 34 Hispanic patients). Tumour characteristics across four race/ethnicity groups were similar. Asians had a significantly higher rate of grade 3 haematologic toxicity than Caucasians, African Americans or Hispanic women (32%, 16%, 10%, and 15%, respectively; p < 0.05). In multivariate analysis, only lower BMI was associated with a higher incidence of >= grade 3 toxicities. However, no significant differences in chemotherapy dose intensity/density were shown across the four race/ethnicity groups. Conclusion: Racial differences in acute toxicity were noted in women with breast cancer who were treated with FEC 100 chemotherapy, suggesting that extrapolating toxicities from chemotherapy across ethnicities is not possible and emphasising the need to validate safety of chemotherapeutic regimens in patients of different ethnicities by enhancing the participation of minorities in clinical trials. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2537 / 2545
页数:9
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