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N Engl J Med.
2004 Aug 19;351(8):781-91.
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Comment in:
N Engl J Med. 2004 Aug 19;351(8):824-6.
N Engl J Med. 2004 Dec 2;351(23):2452-4; author reply 2452-4.
N Engl J Med. 2004 Dec 2;351(23):2452-4; author reply 2452-4.
N Engl J Med. 2004 Dec 2;351(23):2452-4; author reply 2452-4.
N Engl J Med. 2004 Dec 2;351(23):2452-4; author reply 2452-4.
Circulating tumor cells, disease progression, and survival in metastatic breast cancer.
Cristofanilli M
,
Budd GT
,
Ellis MJ
,
Stopeck A
,
Matera J
,
Miller MC
,
Reuben JM
,
Doyle GV
,
Allard WJ
,
Terstappen LW
,
Hayes DF
.
Department of Breast Medical Oncology, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. mcristof@mdanderson.org
BACKGROUND: We tested the hypothesis that the level of circulating tumor cells can predict survival in metastatic breast cancer. METHODS: In a prospective, multicenter study, we tested 177 patients with measurable metastatic breast cancer for levels of circulating tumor cells both before the patients were to start a new line of treatment and at the first follow-up visit. The progression of the disease or the response to treatment was determined with the use of standard imaging studies at the participating centers. RESULTS: Outcomes were assessed according to levels of circulating tumor cells at baseline, before the patients started a new treatment for metastatic disease. Patients in a training set with levels of circulating tumor cells equal to or higher than 5 per 7.5 ml of whole blood, as compared with the group with fewer than 5 circulating tumor cells per 7.5 ml, had a shorter median progression-free survival (2.7 months vs. 7.0 months, P<0.001) and shorter overall survival (10.1 months vs. >18 months, P<0.001). At the first follow-up visit after the initiation of therapy, this difference between the groups persisted (progression-free survival, 2.1 months vs. 7.0 months; P<0.001; overall survival, 8.2 months vs. >18 months; P<0.001), and the reduced proportion of patients (from 49 percent to 30 percent) in the group with an unfavorable prognosis suggested that there was a benefit from therapy. The multivariate Cox proportional-hazards regression showed that, of all the variables in the statistical model, the levels of circulating tumor cells at baseline and at the first follow-up visit were the most significant predictors of progression-free and overall survival. CONCLUSIONS: The number of circulating tumor cells before treatment is an independent predictor of progression-free survival and overall survival in patients with metastatic breast cancer. Copyright 2004 Massachusetts Medical Society
Publication Types:
Clinical Trial
Multicenter Study
PMID: 15317891 [PubMed - indexed for MEDLINE]
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