Clinical Significance of Circulating Tumor Cells in Hormone Receptor-positive Metastatic Breast Cancer Patients who Received Letrozole with or Without Bevacizumab.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
15 09 2020
Historique:
received: 10 04 2020
revised: 08 06 2020
accepted: 19 06 2020
pubmed: 27 6 2020
medline: 15 12 2021
entrez: 27 6 2020
Statut: ppublish

Résumé

We evaluated the prognostic and predictive value of circulating tumor cells (CTCs) hormone receptor-positive (HR Blood samples were collected at pretreatment and three additional time points during therapy. The presence of ≥5 CTCs per 7.5 mL of blood was considered CTC positive. Association of CTCs with progression-free survival (PFS) and overall survival (OS) was assessed using Cox regression models. Of 343 patients treated, 294 had CTC data and were included in this analysis. Median follow-up was 39 months. In multivariable analysis, CTC-positive patients at baseline (31%) had significantly reduced PFS [HR, 1.49; 95% confidence interval (CI), 1.12-1.97] and OS (HR, 2.08; 95% CI, 1.49-2.93) compared with CTC negative. Failure to clear CTCs during treatment was associated with significantly increased risk of progression (HR, 2.2; 95% CI, 1.58-3.07) and death (HR, 3.4; 95% CI, 2.36-4.88). CTC-positive patients who received only letrozole had the worse PFS (HR, 2.3; 95% CI, 1.54-3.47) and OS (HR, 2.6; 95% CI, 1.59-4.40). Median PFS in CTC-positive patients was significantly longer (18.0 vs. 7.0 months) in letrozole plus bevacizumab versus letrozole arm ( CTCs were highly prognostic for the addition of bevacizumab to first-line letrozole in patients with HR+ MBC in CALGB 40503. Further research to determine the potential predictive value of CTCs in this setting is warranted.

Identifiants

pubmed: 32586939
pii: 1078-0432.CCR-20-1329
doi: 10.1158/1078-0432.CCR-20-1329
pmc: PMC7501177
mid: NIHMS1607185
doi:

Substances chimiques

Receptors, Estrogen 0
Receptors, Progesterone 0
Bevacizumab 2S9ZZM9Q9V
Letrozole 7LKK855W8I

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4911-4920

Subventions

Organisme : NCI NIH HHS
ID : UG1 CA233290
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233329
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180821
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233373
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233180
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180882
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA196171
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180820
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180888
Pays : United States

Informations de copyright

©2020 American Association for Cancer Research.

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Auteurs

Mark Jesus M Magbanua (MJM)

University of California at San Francisco, San Francisco, California. mark.magbanua@ucsf.edu.

Oleksandr Savenkov (O)

Weill Medical College of Cornell University, New York, New York.

Erik J Asmus (EJ)

Alliance Statistics and Data Center, Mayo Clinic, Rochester, Minnesota.

Karla V Ballman (KV)

Alliance Statistics and Data Center, Weill Medical College of Cornell University, New York, New York.

Janet H Scott (JH)

University of California at San Francisco, San Francisco, California.

John W Park (JW)

University of California at San Francisco, San Francisco, California.

Maura Dickler (M)

Lilly Oncology, Indianapolis, Indiana.

Ann Partridge (A)

Dana-Farber/Partners CancerCare, Boston, Massachusetts.

Lisa A Carey (LA)

UNC Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina.

Eric P Winer (EP)

Dana-Farber/Partners CancerCare, Boston, Massachusetts.

Hope S Rugo (HS)

University of California at San Francisco, San Francisco, California.

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Classifications MeSH