Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2005 Feb;241(2):199-205.
doi: 10.1097/01.sla.0000151795.15068.27.

Detection of hematogenous tumor cell dissemination predicts tumor relapse in patients undergoing surgical resection of colorectal liver metastases

Affiliations

Detection of hematogenous tumor cell dissemination predicts tumor relapse in patients undergoing surgical resection of colorectal liver metastases

Moritz Koch et al. Ann Surg. 2005 Feb.

Abstract

Objective: To examine the prognostic significance of disseminated tumor cells in blood and bone marrow of patients undergoing surgical resection of colorectal liver metastases.

Summary background data: Despite curative hepatic resection of colorectal liver metastases, a high percentage of patients develop tumor recurrence. These recurrences probably originate from disseminated tumor cells released into the circulation before or during surgery.

Methods: Thirty-seven patients with potentially curative (R0) resection of colorectal liver metastases were prospectively enrolled into the study. Preoperative bone marrow samples and preoperative, intraoperative, and postoperative blood samples were examined for disseminated tumor cells by CK20 RT-PCR.

Results: Tumor cells were detected in preoperative blood samples in 11 of 37 (30%) patients, in intraoperative blood samples in 17 of 37 (46%) patients, and in postoperative blood samples in 8 of 37 (22%) patients. Four of 25 (16%) patients tested positive for disseminated tumor cells in bone marrow samples. Median follow-up time for all patients was 38 months (range, 10-63 months). Multivariate analysis confirmed tumor cell detection in intraoperative blood (P = 0.009) and in bone marrow samples (P = 0.013) to be independent prognostic factors of tumor relapse.

Conclusions: This is the first study demonstrating that detection of hematogenous tumor cell dissemination during hepatic resection of colorectal cancer metastases predicts tumor relapse. Detection of disseminated tumor cells may help to individualize adjuvant therapy for patients with colorectal liver metastases and to develop surgical strategies to prevent intraoperative hematogenous tumor cell shedding.

PubMed Disclaimer

Figures

None
FIGURE 1. Kaplan-Meier disease-free survival curves of patients (n = 37) after curative hepatic resection of colorectal liver metastases stratified according to CK20 RT-PCR results in intraoperative blood samples.
None
FIGURE 2. Kaplan-Meier disease-free survival curves of patients (n = 37) after curative hepatic resection of colorectal liver metastases stratified according to CK20 RT-PCR results in postoperative blood samples.
None
FIGURE 3. Kaplan-Meier disease-free survival curves of patients (n = 25) after curative hepatic resection of colorectal liver metastases stratified according to CK20 RT-PCR results in bone marrow samples.

Comment in

References

    1. Primrose JN. Treatment of colorectal metastases: surgery, cryotherapy, or radiofrequency ablation. Gut. 2002;50:1–5. - PMC - PubMed
    1. Rodgers MS, McCall JL. Surgery for colorectal liver metastases with hepatic lymph node involvement: a systematic review. Br J Surg. 2000;87:1142–1155. - PubMed
    1. Fong Y, Cohen AM, Fortner JG, et al. Liver resection for colorectal metastases. J Clin Oncol. 1997;15:938–946. - PubMed
    1. Pantel K, von Knebel Doeberitz M. Detection and clinical relevance of micrometastatic cancer cells. Curr Opin Oncol. 2000;12:95–101. - PubMed
    1. Johnson P, Burchill S, Selby P. The molecular detection of circulating tumor cells. Br J Cancer. 1995;72:268–276. - PMC - PubMed

Publication types

MeSH terms