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Disseminated Tumor Cells in Bone Marrow Following Definitive Radiotherapy for Intermediate or High-Risk Prostate Cancer
被引:4
作者:
Berg, Arne
[1
]
Bruland, Oyvind S.
[1
,2
]
Fossa, Sophie D.
[1
,2
]
Nesland, Jahn M.
[1
,3
]
Berner, Aasmund
[3
]
Schirmer, Cecilie
[3
]
Lilleby, Wolfgang
[2
]
机构:
[1] Univ Oslo, Fac Div Norwegian Radium Hosp, Fac Med, N-0310 Oslo, Norway
[2] Univ Hosp, Rikshosp, Div Canc Med & Radiotherapy, Oslo, Norway
[3] Univ Hosp, Rikshosp, Div Pathol, Oslo, Norway
来源:
关键词:
metastasis;
prostate-specific antigen;
cytokeratin;
immunocytochemistry;
disease progression;
D O I:
10.1002/pros.20826
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
BACKGROUND. The purpose of this study was to explore the prevalence of disseminated tumor cells (DTCs) in bone marrow (BM) of clinically progression-free prostate cancer (PC) patients at least 2 years after curatively intended radiotherapy (RT) with or without adjuvant hormone treatment. METHODS. All patients were T1-3N0M0 with intermediate or high risk of progression. Median time from RT to BM sampling was 5 years (2-8). A standardized immunocytochemical method applying the anticytokeratin antibodies AE1/AE3 was used for DTCs detection in 130 patients. Morphological characterization of immunostained cells was performed to exclude false positive cells. The post-treatment BM was explored in relation to pre-treatment risk factors, treatment strategy and serum levels of Testosterone and PSA at the time of BM sampling. Longitudinal changes in BM status were studied in a sub-group of 109 patients who also had donated BM prior to treatment. RESULTS. Post-treatment BM-aspirates were positive for DTCs in 17% of cases without correlation to any of the tested variables. Out of 14 patients who had DTCs in BM prior to treatment, all but one had become post-treatment negative. Out of 95 patients with pretreatment negative BM status, 18 (19%) had become post-treatment positive. CONCLUSIONS. DTCs in BM were found in 17% of clinically progression-free PC patients following RT. The detection of these cells may provide PSA-independent prognostic information remaining to be explored by prolonged follow-up. Prostate 68: 1607-1614, 2008. (C) 2008 Wiley-Liss, Inc.
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页码:1607 / 1614
页数:8
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