Tumor cells in blood shed from the surgical field
E. Hansen, N. Wolff, R. Knuechel, J. Ruschoff, F. Hofstaedter and K. Taeger
Department of Anesthesiology, University of Regensburg, Germany.
OBJECTIVES: To analyze blood shed from the surgical field during oncologic
surgery for tumor cells and to assess functional characteristics of these
cells. DESIGN AND PATIENTS: 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. SETTING: A 500-bed tumor center and a
tertiary care hospital. MAIN OUTCOME MEASURES: 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.
RESULTS: 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. CONCLUSIONS: 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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