AI Article Synopsis

  • Researchers studied circulating tumor cells in patients with biliary-pancreatic cancer during surgeries to understand their link to metastases.
  • Blood samples from 67 patients were analyzed, showing a significant presence of CEA-mRNA in nearly half of them, while it was absent in healthy individuals and those with benign conditions.
  • Those with detectable CEA-mRNA had a higher incidence of post-surgery metastases and poorer survival rates compared to those without detectable tumor cells, indicating a connection between these markers and prognosis.

Article Abstract

Background: Circulating tumor cells in the blood were frequently detected by reverse transcription-polymerase chain reaction during operation in patients with biliary-pancreatic cancer. We investigated the relationship between circulating tumor cells during operation and hematogenous metastases.

Methods: Blood samples from 67 patients with biliary-pancreatic cancer were obtained from the portal vein, peripheral artery, and superior vena cava during operation. After total RNA was extracted from each blood sample, carcinoembryonic antigen (CEA)-specific reverse transcription-polymerase chain reaction was performed.

Results: Intraoperative CEA-messenger RNA (mRNA) expression was detected in the blood of 32 (47.8%) of 67 patients with biliary-pancreatic cancer, although it was not detected in the blood obtained from 20 healthy volunteers or 15 patients with benign disease of the biliary pancreas. The incidence (37.5%) of hematogenous metastases after surgery in the CEA-mRNA-positive group (n = 32) was significantly higher than that (11.4%) in the negative group (n = 35; P =.01). In stage I, II, and III patients, survival of the CEA-mRNA-positive group was significantly worse compared with that of negative group (P =.03).

Conclusions: Intraoperative molecular detection of circulating tumor cells in patients with biliary-pancreatic cancer relates to a high risk of hematogenous metastasis and is associated with unfavorable prognosis even after curative resection.

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Source
http://dx.doi.org/10.1007/BF02573871DOI Listing

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