Archives of Surgery · 1995 · 268 citations · 18 references
MedicineOncologySurgeryMedical OncologyOncologic SurgerySurgical OncologyCirculating Tumor CellsIntraoperative CytologyMalignant NeoplasmsMalignant TumorsTumor BiologyTumor MarkersAbdominal Oncologic SurgeryCirculating Tumor BiomarkersCirculating Tumor Cell BiomarkersCirculating Tumor Cell CharacterizationCirculating Tumor Cell EnumerationCirculating Tumor Cell Proteomic AnalysisCirculating Tumor MarkersOncologic Cell Salvage
The study analyzes tumor cells in blood shed during oncologic surgery and evaluates their functional properties. Tumor cells were isolated from salvaged blood by density‑gradient centrifugation and identified via cytokeratin and nucleolar organizer region staining with a sensitivity of 10 cells per 500 mL. Tumor cells were detected in 93 % of patients, exhibited clonogenic, invasive, and tumorigenic properties, and were present in quantities ranging from 10 to 7 million cells per 500 mL, with no link to blood loss; these findings support avoiding intraoperative autotransfusion during tumor surgery.
To analyze blood shed from the surgical field during oncologic surgery for tumor cells and to assess functional characteristics of these cells.Series of 61 patients with cancer who underwent surgery for an abdominal, orthopedic, urological, gynecological, or head and neck malignant tumor, and blinded comparison with 15 patients with benign diseases undergoing surgery.A 500-bed tumor center and a tertiary care hospital.Tumor cells were isolated from intraoperatively salvaged and washed blood by density gradient centrifugation. They were identified in cytospin specimens by their content of cytokeratins and nucleolar organizer regions with a sensitivity of 10 cells in 500 mL of blood. Clonogenicity was tested in a cell colony assay; invasiveness, in Boyden chambers; and tumorigenicity, in nude mice.In 57 of 61 patients, tumor cells were detected in the blood shed during oncologic surgery. They demonstrated proliferation capacity, invasiveness, and tumorigenicity. The total number of tumor cells identified ranged from 1 x 10(1) to 7 x 10(6), with no close correlation to the amount of blood loss. Circulating tumor cells were demonstrated in only 26% of these patients and in small numbers.Malignant cells identified regularly in the blood shed during tumor surgery and different from circulating tumor cells are of concern, since at the surgical site they may cause local tumor recurrence, or in the salvaged blood they may cause hematogenic metastasis after retransfusion. Therefore, the contraindication of intraoperative autotransfusion in tumor surgery is strongly supported, and a review of surgical procedures and adjuvant therapy may be indicated, as the passage of the identified cells to the shed blood is yet unknown.
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RUPERT B. TUHNBULL, Kenneth Kyle, FRANK R. WATSON et al. · Annals of Surgery · 1967 · 905 citations · Full text
Medicine, Oncology, Gastroenterology +15