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Significance of Circulating Tumor Cells in Metastatic Triple-Negative Breast Cancer Patients within a Randomized, Phase II Trial: TBCRC 019.
Paoletti, Costanza; Li, Yufeng; Muñiz, Maria C; Kidwell, Kelley M; Aung, Kimberly; Thomas, Dafydd G; Brown, Martha E; Abramson, Vandana G; Irvin, William J; Lin, Nancy U; Liu, Minetta C; Nanda, Rita; Nangia, Julie R; Storniolo, Anna M; Traina, Tiffany A; Vaklavas, Christos; Van Poznak, Catherine H; Wolff, Antonio C; Forero-Torres, Andres; Hayes, Daniel F.
Afiliação
  • Paoletti C; Comprehensive Cancer Center and the Department of Internal Medicine, University of Michigan Health and Hospital System, Ann Arbor, Michigan.
  • Li Y; University of Alabama at Birmingham, Birmingham, Alabama.
  • Muñiz MC; Comprehensive Cancer Center and the Department of Internal Medicine, University of Michigan Health and Hospital System, Ann Arbor, Michigan.
  • Kidwell KM; Comprehensive Cancer Center and the Department of Internal Medicine, University of Michigan Health and Hospital System, Ann Arbor, Michigan. Univeristy of Michigan, Department of Biostatistics, Ann Arbor, Michigan.
  • Aung K; Comprehensive Cancer Center and the Department of Internal Medicine, University of Michigan Health and Hospital System, Ann Arbor, Michigan.
  • Thomas DG; Comprehensive Cancer Center and the Department of Internal Medicine, University of Michigan Health and Hospital System, Ann Arbor, Michigan.
  • Brown ME; Comprehensive Cancer Center and the Department of Internal Medicine, University of Michigan Health and Hospital System, Ann Arbor, Michigan.
  • Abramson VG; Vanderbilt-Ingram Cancer Center, Nashville, Tennessee.
  • Irvin WJ; University of North Carolina, Chapel Hill, North Carolina. Bon Secours Cancer Institute, Midlothian, Virginia.
  • Lin NU; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Liu MC; Georgetown University Hospital, Washington, District of Columbia.
  • Nanda R; University of Chicago, Chicago, Illinois.
  • Nangia JR; Baylor College of Medicine, Houston, Texas.
  • Storniolo AM; Indiana University Simon Cancer Center, Indianapolis, Indiana.
  • Traina TA; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Vaklavas C; University of Alabama at Birmingham, Birmingham, Alabama.
  • Van Poznak CH; Comprehensive Cancer Center and the Department of Internal Medicine, University of Michigan Health and Hospital System, Ann Arbor, Michigan.
  • Wolff AC; Johns Hopkins Kimmel Comprehensive Cancer Center, Baltimore, Maryland.
  • Forero-Torres A; University of Alabama at Birmingham, Birmingham, Alabama.
  • Hayes DF; Comprehensive Cancer Center and the Department of Internal Medicine, University of Michigan Health and Hospital System, Ann Arbor, Michigan. hayesdf@umich.edu.
Clin Cancer Res ; 21(12): 2771-9, 2015 Jun 15.
Article em En | MEDLINE | ID: mdl-25779948
ABSTRACT

PURPOSE:

Circulating tumor cells (CTC) are prognostic in metastatic breast cancer (MBC). We tested whether EpCAM-based capture system (CellSearch) is effective in patients with triple-negative (TN) MBC, and whether CTC apoptosis and clustering enhances the prognostic role of CTC. EXPERIMENTAL

DESIGN:

CTC enumeration and apoptosis were determined using the CXC CellSearch kit at baseline and days 15 and 29 in blood drawn from TN MBC patients who participated in a prospective randomized phase II trial of nanoparticle albumin-bound paclitaxel (nab-paclitaxel) with or without tigatuzumab. Association between levels of CTC and patient outcomes was assessed using logistic regression, Kaplan-Meier curves, and Cox proportional hazards modeling.

RESULTS:

Nineteen of 52 (36.5%), 14 of 52 (26.9%), and 13 of 49 (26.5%) patients who were evaluable had elevated CTC (≥5 CTC/7.5 mL whole blood) at baseline and at days 15 and 29, respectively. Patients with elevated versus not elevated CTC at each time point had worse progression-free survival (PFS; P = 0.005, 0.0003, 0.0002, respectively). The odds of clinical benefit response for those who had elevated versus low CTC at baseline and days 15 and 29 were 0.25 (95% CI 0.08-0.84; P = 0.024), 0.19 (95% CI 0.05-0.17; P = 0.014), and 0.06 (95% CI 0.01-0.33; P = 0.001), respectively. There was no apparent prognostic effect comparing CTC apoptosis versus non-apoptosis. Presence of CTC cluster at day 15 and day 29 was associated with shorter PFS.

CONCLUSIONS:

CTC were detected using CellSearch assay in approximately one-third of TN MBC patients. Elevated CTC at baseline and days 15 and 29 were prognostic, and reductions in CTC levels reflected response.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias de Mama Triplo Negativas / Células Neoplásicas Circulantes Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias de Mama Triplo Negativas / Células Neoplásicas Circulantes Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article