The prognostic value of HER2-positive circulating tumor cells in breast cancer patients: a systematic review and meta-analysis
Abstract Introduction A meta-analysis was conducted to determine the prognostic value of human epidermal growth receptor (HER)2-positive circulating tumor cells (CTCs) in patients with breast cancer. Materials and methods Medline, Central, and Embase databases were search. Inclusion criteria were: 1...
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Published in: | Clinical breast cancer Vol. 17; no. 5; pp. 341 - 349 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Elsevier Inc
01-08-2017
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Subjects: | |
Online Access: | Get full text |
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Summary: | Abstract Introduction A meta-analysis was conducted to determine the prognostic value of human epidermal growth receptor (HER)2-positive circulating tumor cells (CTCs) in patients with breast cancer. Materials and methods Medline, Central, and Embase databases were search. Inclusion criteria were: 1) Randomized controlled trials (RCTs), 2-arm prospective studies, and retrospective studies; 2) Patients with breast cancer; 3) HER2-positive CTCs were examined; 4) Hazard ratio of survival between patients with HER2-positive and HER2-negative CTCs was reported. Results Four studies with a total of 550 patients with stage I-IV breast cancer were included. HER2-positive CTCs were not associated with worse overall survival (OS) (hazard ratio [HR] = 1.489, 95% CI: 0.873-2.540, P = .144) or progression-free survival (PFS) (HR = 1.543, 95% CI: 0.636-3.744, P = .338). In patients without metastasis, Her2-positive CTCs were associated with worse OS (HR: 2.273, 95% CI: 1.340-3.853, P = .002) and worse PFS (HR = 2.870, 95% CI: 1.298-6.343, P = .009). There is no significant relationship between HER2-positive CTCs and survival in subgroup of patients with metastasis. Conclusion HER2-positive CTCs have prognostic value in patients with breast cancer and without distant metastasis. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 ObjectType-Review-4 content type line 23 ObjectType-Undefined-3 |
ISSN: | 1526-8209 1938-0666 |
DOI: | 10.1016/j.clbc.2017.02.002 |