Published in:
03-02-2024 | Cancer Biomarker | Peritoneal Surface Malignancy
Preoperative CA 19-9 Predicts Disease Progression in Colorectal Peritoneal Metastases Treated with Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy: An Analysis from the US HIPEC Collaborative
Authors:
Nadege T. Fackche, MD, Ryan K. Schmocker, MD, MS, Richard Nudotor, MD, PMH, Boateng Kubi, BS, Jordan M. Cloyd, MD, Travis E. Grotz, MD, Keith F. Fournier, MD, Sean P. Dineen, MD, Jula Veerapong, MD, Joel M. Baumgartner, MD, MAS, Callisia N. Clarke, MD, Sameer H. Patel, MD, Gregory C. Wilson, MD, Laura A. Lambert, MD, Courtney Pokrzywa, MD, Daniel E. Abbott, MD, Byrne Lee, MD, Charles A. Staley, MD, Mohammad Y. Zaidi, MD, Fabian M. Johnston, MD, MHS, Jonathan B. Greer, MD
Published in:
Annals of Surgical Oncology
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Issue 5/2024
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Abstract
Introduction
Patients with colorectal peritoneal metastases (CRPM) are increasingly treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CRS/HIPEC). Unfortunately, data identifying preoperative risk factors for poor oncologic outcomes after this procedure are limited. We aimed to determine the prognostic value of preoperative CEA, CA 125, and CA 19-9 on disease progression after CRS/HIPEC.
Methods
Patients with CRPM treated with curative intent CRS/HIPEC from 12 participating sites in the United States from 2000 to 2017 were identified. Progression-free survival (PFS), defined as disease progression or recurrence, was the primary outcome.
Results
In 279 patients who met inclusion criteria, the rate of disease progression was 63.8%, with a median PFS of 11 months (interquartile range [IQR] 5–20). Elevated CA 19-9 was associated with dismal PFS at 2 years (8.9% elevated vs. 30% not elevated, p < 0.01). In 113 patients who underwent upfront CRS/HIPEC, CA 19-9 emerged as the sole tumor marker independently predictive of worse PFS (hazard ratio [HR] 2.88, p = 0.048). In the subgroup of patients who had received neoadjuvant therapy (NAT), no variable was independently predictive of PFS. CA 19-9 levels over 37 U/ml were highly specific for accelerated disease progression after CRS/HIPEC. Lastly, there was no association between PFS and elevated CEA or CA 125.
Conclusions
Elevated CA 19-9 is associated with decreased PFS in patients with CRPM. While traditionally CEA is the main tumor marker assessed in colon cancer, we found that CA 19-9 may better inform preoperative risk stratification for poor oncologic outcomes in patients with CRPM. However, prospective studies are required to confirm this association.