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Micrometastases in esophagogastric cancer: High detection rate in resected rib segments
被引:130
作者:
O'Sullivan, GC
Sheehan, D
Clarke, A
Stuart, R
Kelly, J
Kiely, MD
Walsh, T
Collins, JK
Shanahan, F
[1
]
机构:
[1] Cork Univ Hosp, Dept Med, Cork, Ireland
[2] Cork Univ Hosp, Dept Surg, Cork, Ireland
[3] Mercy Hosp, Dept Surg, Cork, Ireland
[4] Mercy Hosp, Dept Med, Cork, Ireland
[5] Natl Univ Ireland Univ Coll Cork, Cork, Ireland
[6] Univ Glasgow, Glasgow Royal Infirm, Dept Surg, Glasgow G31 2ER, Lanark, Scotland
[7] Beaumont Hosp, Dept Surg, Dublin 9, Ireland
[8] Royal Coll Surgeons Ireland, Dublin 2, Ireland
关键词:
D O I:
10.1016/S0016-5085(99)70175-7
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Background & Aims: Micrometastases within bone marrow indicate a poor prognosis. We prospectively examined micrometastases in patients undergoing resection of esophagogastric cancers for (1) prevalence in rib marrow; (2) comparative detection rates in rib and iliac crest marrow; (3) responsiveness to neoadjuvant therapy; and (4) viability and tumorigenicity. Methods: In 50 consecutive patients, marrow was obtained before manipulation of the primary tumor. Micrometastatic cells were detected by staining contaminant cytokeratin-18-positive cells. Viability and tumorigenicity were determined by culture and xenograft. Results: Micrometastases were detected in rib marrow from 88% of patients (44 of 50). When bilateral iliac crest marrow was also obtained, micrometastases were found in 15% (4 of 27) compared with 89% (24 of 27) for ribs (P < 0.001). Detection rates were independent of histological type or nodal status and were similar in patients with and without neoadjuvant therapy. Metastatic cells were cultured from rib marrow of 5 of 7 patients and were tumorigenic in nude mice. Conclusions: Most patients undergoing resection of esophagogastric malignancies have micrometastases in rib marrow, Detection rates based on iliac crest marrow are underestimates. Hematogenous spread of metastatic cells is independent of histological type or nodal status. The metastatic cells are viable, tumorigenic, and resistant to neoadjuvant therapy.
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页码:543 / 548
页数:6
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