Impact of race, ethnicity, and BMI on achievement of pathologic complete response following neoadjuvant chemotherapy for breast cancer: a pooled analysis of four prospective Alliance clinical trials (A151426)
- PMID: 27449492
- PMCID: PMC5011019
- DOI: 10.1007/s10549-016-3918-5
Impact of race, ethnicity, and BMI on achievement of pathologic complete response following neoadjuvant chemotherapy for breast cancer: a pooled analysis of four prospective Alliance clinical trials (A151426)
Abstract
Previous studies demonstrated poor response to neoadjuvant systemic therapy (NST) for breast cancer among black women and women who are overweight or obese, but this may be due to chemotherapy underdosing. We assessed associations of race, ethnicity, and body mass index (BMI) with pathologic complete response (pCR) in clinical trial populations. 1797 women enrolled in four NST trials (CALGB 40601, 40603; ACOSOG Z1041, Z1071) were included. Tumor subtypes were defined by estrogen receptor (ER) and HER2 status. Logistic regression generated odds ratios (OR) and 95 % confidence intervals (CI) for the associations of race, ethnicity, and BMI with in-breast pCR adjusting for subtype, study arm, lymph node status, tumor size, and tumor grade. 253 (14.1 %) were black, 199 (11.1 %) Hispanic, 520 (28.9 %) overweight, and 743 (41.4 %) obese. Compared to whites, Blacks and Hispanics were more likely to be obese and Blacks were more likely to have triple-negative cancer. pCR rates differed significantly by tumor subtype. In multivariate analyses, neither race (black vs white: OR 1.18, 95 % CI 0.85-1.62) nor ethnicity (Hispanic vs non-Hispanic; OR 1.30, 95 % CI 0.67-2.53) were significant predictors of pCR overall or by subtype. Overweight and obese women had lower pCR rates in ER+/HER2+, but higher pCR rates in ER-/HER2+ cancers. There was no difference in pCR according to race or ethnicity. Overall, there was no major difference in pCR rates by BMI. These findings suggest that pCR with optimally dosed NST is a function of tumor, rather than patient, biology.
Keywords: Body mass index; Breast cancer; Ethnicity; Pathologic complete response; Race.
Conflict of interest statement
Conflict of Interests The authors declare that they have no conflict of interests.
Similar articles
-
Impact of body mass index on pathological response after neoadjuvant chemotherapy: results from the I-SPY 2 trial.Breast Cancer Res Treat. 2024 Apr;204(3):589-597. doi: 10.1007/s10549-023-07214-5. Epub 2024 Jan 12. Breast Cancer Res Treat. 2024. PMID: 38216819 Free PMC article.
-
A Multicenter Study of the Impact of Body Mass Index (BMI) on the incidence of Pathologic Complete Response (pCR) Among Saudi Patients with locally advanced Breast cancer (LABC) post Neoadjuvant Chemotherapy (NAC).Gulf J Oncolog. 2019 May;1(30):33-42. Gulf J Oncolog. 2019. PMID: 31242980
-
Obesity is an independent prognostic factor of decreased pathological complete response to neoadjuvant chemotherapy in breast cancer patients.Breast. 2017 Apr;32:237-244. doi: 10.1016/j.breast.2016.05.013. Epub 2016 Jun 16. Breast. 2017. PMID: 27318645
-
The role of quantitative estrogen receptor status in predicting tumor response at surgery in breast cancer patients treated with neoadjuvant chemotherapy.Breast Cancer Res Treat. 2017 Jul;164(2):285-294. doi: 10.1007/s10549-017-4269-6. Epub 2017 May 2. Breast Cancer Res Treat. 2017. PMID: 28466123 Review.
-
BMI, physical activity, and breast cancer subtype in white, black, and Sea Island breast cancer survivors.Adv Cancer Res. 2020;146:83-102. doi: 10.1016/bs.acr.2020.01.005. Epub 2020 Mar 12. Adv Cancer Res. 2020. PMID: 32241393 Free PMC article. Review.
Cited by
-
Racial disparity in distant recurrence-free survival in patients with localized breast cancer: A pooled analysis of National Surgical Adjuvant Breast and Bowel Project trials.Cancer. 2022 Jul 15;128(14):2728-2735. doi: 10.1002/cncr.34241. Epub 2022 May 17. Cancer. 2022. PMID: 35578919 Free PMC article.
-
Obesity Is an Independent Prognostic Factor That Reduced Pathological Complete Response in Operable Breast Cancer Patients.Medicina (Kaunas). 2024 Nov 27;60(12):1953. doi: 10.3390/medicina60121953. Medicina (Kaunas). 2024. PMID: 39768835 Free PMC article.
-
Disparities in breast cancer: a multi-institutional comparative analysis focusing on American Hispanics.Cancer Med. 2018 Jun;7(6):2710-2717. doi: 10.1002/cam4.1509. Epub 2018 May 7. Cancer Med. 2018. PMID: 29733543 Free PMC article.
-
Response to Treatment, Racial and Ethnic Disparity, and Survival in Patients With Breast Cancer Undergoing Neoadjuvant Chemotherapy in the US.JAMA Netw Open. 2023 Mar 1;6(3):e235834. doi: 10.1001/jamanetworkopen.2023.5834. JAMA Netw Open. 2023. PMID: 36995711 Free PMC article.
-
An Overview of the Impact of Body Mass Index on Pathological Complete Response Following Neoadjuvant Chemotherapy in Operable Breast Cancer in a Tertiary Care Centre in South India.Eur J Breast Health. 2022 Jul 1;18(3):271-278. doi: 10.4274/ejbh.galenos.2022.2022-2-5. eCollection 2022 Jul. Eur J Breast Health. 2022. PMID: 35855193 Free PMC article.
References
-
- Sparano JA, Wang M, Zhao F, Stearns V, Martino S, Ligibel JA, Perez EA, Saphner T, Wolff AC, Sledge GW, Jr, Wood WC, Fetting J, Davidson NE. Obesity at diagnosis is associated with inferior outcomes in hormone receptor-positive operable breast cancer. Cancer. 2012 doi: 10.1002/cncr.27527. - DOI - PMC - PubMed
-
- Ligibel JA, Cirrincione CT, Liu M, Citron M, Ingle JN, Gradishar W, Martino S, Sikov W, Michaelson R, Mardis E, Perou CM, Ellis M, Winer E, Hudis CA, Berry D, Barry WT. Body Mass Index, PAM50 Subtype, and Outcomes in Node-Positive Breast Cancer: CALGB 9741 (Alliance) J Natl Cancer Inst. 2015;107(9) doi: 10.1093/jnci/djv179. - DOI - PMC - PubMed
-
- Warner ET, Tamimi RM, Hughes ME, Ottesen RA, Wong YN, Edge SB, Theriault RL, Blayney DW, Niland JC, Winer EP, Weeks JC, Partridge AH. Racial and Ethnic Differences in Breast Cancer Survival: Mediating Effect of Tumor Characteristics and Sociodemographic and Treatment Factors. J Clin Oncol. 2015;33(20):2254–2261. doi: 10.1200/JCO.2014.57.1349. - DOI - PMC - PubMed
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Research Materials
Miscellaneous