Neoadjuvant Systemic Therapy in Early Breast Cancer: Results of a Prospective Observational Multicenter BRIDE Study.
criteria of choice of neoadjuvant therapy
early breast cancer
pathological response
types of neoadjuvant therapy
Journal
Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829
Informations de publication
Date de publication:
04 Oct 2023
04 Oct 2023
Historique:
received:
30
08
2023
revised:
26
09
2023
accepted:
28
09
2023
medline:
14
10
2023
pubmed:
14
10
2023
entrez:
14
10
2023
Statut:
epublish
Résumé
To evaluate the rate of early breast cancer (EBC) patients treated with neoadjuvant systemic therapy (NAT) in Italy, criteria of patient selection and types of therapies delivered, an analysis of 1276 patients with stage I-II-III was conducted out of 1633 patients enrolled in the multicenter prospective observational BRIDE study. A total of 177 patients (13.9%) were treated with NAT and 1099 (85.9%) with surgery; in multivariate analysis, menopausal status, cT, cN, grade, HER2-positive and Triple negative (TN) subgroups were significantly associated with the decision to administer NAT. The type of NAT delivered was influenced by EBC subtype. NAT was administered to 53.2% of HER2+/HR-negative, 27.9% of HER2+/HR+, 7.1% of HER2-negative/HR+ and 30.3% of TN EBC patients. The pCR rates were similar to the ones reported in the literature: 74.2% in HER2+/HR-negative, 52.3% in HER2+/HR+, 17.2% in HER2-negative/HR+ and 37.9% in TN. In clinical practice, patient and tumor characteristics influenced oncologists in the decision to administer NAT in EBC and in the choice of the type of systemic therapy, according to ESMO and AIOM Guidelines. Currently, it is recommended always to evaluate the use of NAT in EBC, mainly in HER2+ and TN patients, considering that pCR is associated with significantly better survival of the patient and that effective therapies are now available for residual disease.
Identifiants
pubmed: 37835546
pii: cancers15194852
doi: 10.3390/cancers15194852
pmc: PMC10572070
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Roche (Italy)
ID : ML 40011
Références
Breast. 2003 Oct;12(5):320-7
pubmed: 14659147
J Clin Oncol. 2020 Apr 20;38(12):1346-1366
pubmed: 31928404
Med Oncol. 2022 Nov 9;40(1):16
pubmed: 36352293
Ann Oncol. 2022 Dec;33(12):1250-1268
pubmed: 36228963
J Clin Oncol. 2006 May 1;24(13):2019-27
pubmed: 16606972
BMJ. 2012 Apr 26;344:e2718
pubmed: 22539013
J Clin Oncol. 2007 Jan 1;25(1):118-45
pubmed: 17159189
J Clin Oncol. 2003 Nov 15;21(22):4165-74
pubmed: 14559892
J Clin Oncol. 2023 Apr 1;41(10):1795-1808
pubmed: 36989610
N Engl J Med. 2020 Feb 27;382(9):810-821
pubmed: 32101663
J Clin Oncol. 2023 Jun 1;41(16):2998-3008
pubmed: 37075276
J Clin Oncol. 2011 May 20;29(15):1956-62
pubmed: 21482989
J Clin Oncol. 1997 Jul;15(7):2483-93
pubmed: 9215816
J Clin Oncol. 2006 Mar 1;24(7):1037-44
pubmed: 16505422
Lancet Oncol. 2022 Jan;23(1):149-160
pubmed: 34902335
J Clin Oncol. 2008 Jan 10;26(2):246-52
pubmed: 18056680
N Engl J Med. 2022 Feb 10;386(6):556-567
pubmed: 35139274
CA Cancer J Clin. 2021 May;71(3):209-249
pubmed: 33538338
J Clin Oncol. 2007 Oct 1;25(28):4414-22
pubmed: 17785706
Ann Surg Oncol. 2010 Jun;17(6):1471-4
pubmed: 20180029
N Engl J Med. 2019 Feb 14;380(7):617-628
pubmed: 30516102
JAMA Oncol. 2021 Nov 01;7(11):1654-1663
pubmed: 34529000
Clin Cancer Res. 2020 Jun 15;26(12):2838-2848
pubmed: 32046998
Lancet. 2014 Jul 12;384(9938):164-72
pubmed: 24529560
J Clin Oncol. 2023 Jun 1;41(16):2988-2997
pubmed: 36977286
Lancet Oncol. 2023 Jan;24(1):77-90
pubmed: 36493792
Ann Oncol. 2019 Aug 1;30(8):1194-1220
pubmed: 31161190
N Engl J Med. 2017 Jun 1;376(22):2147-2159
pubmed: 28564564
J Clin Oncol. 2020 Dec 1;38(34):3987-3998
pubmed: 32954927
Breast. 2012 Jun;21(3):261-6
pubmed: 22204930
J Clin Oncol. 2008 Feb 10;26(5):778-85
pubmed: 18258986
J Clin Oncol. 2010 Jun 1;28(16):2784-95
pubmed: 20404251
N Engl J Med. 2021 Jun 24;384(25):2394-2405
pubmed: 34081848