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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.
Fackche, Nadege T; Schmocker, Ryan K; Nudotor, Richard; Kubi, Boateng; Cloyd, Jordan M; Grotz, Travis E; Fournier, Keith F; Dineen, Sean P; Veerapong, Jula; Baumgartner, Joel M; Clarke, Callisia N; Patel, Sameer H; Wilson, Gregory C; Lambert, Laura A; Pokrzywa, Courtney; Abbott, Daniel E; Lee, Byrne; Staley, Charles A; Zaidi, Mohammad Y; Johnston, Fabian M; Greer, Jonathan B.
Affiliation
  • Fackche NT; Department of Gastrointestinal Oncology, Moffitt Cancer Center, Department of Oncologic Sciences, Morsani College of Medicine, Tampa, FL, USA.
  • Schmocker RK; Department of Surgery, Johns Hopkins University, Baltimore, MD, USA.
  • Nudotor R; Department of Surgery, Johns Hopkins University, Baltimore, MD, USA.
  • Kubi B; Department of Surgery, Johns Hopkins University, Baltimore, MD, USA.
  • Cloyd JM; Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Grotz TE; Division of Hepatobiliary and Pancreas Surgery, Mayo Clinic, Rochester, MN, USA.
  • Fournier KF; Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Dineen SP; Department of Gastrointestinal Oncology, Moffitt Cancer Center, Department of Oncologic Sciences, Morsani College of Medicine, Tampa, FL, USA.
  • Veerapong J; Division of Surgical Oncology, Department of Surgery, University of California, San Diego, CA, USA.
  • Baumgartner JM; Division of Surgical Oncology, Department of Surgery, University of California, San Diego, CA, USA.
  • Clarke CN; Division of Surgical Oncology, Department of Surgery, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Patel SH; Department of Surgery, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Wilson GC; Department of Surgery, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Lambert LA; Division of Surgical Oncology, Department of Surgery, University of Massachusetts Medical School, Worcester, MA, USA.
  • Pokrzywa C; Division of Surgical Oncology, Department of Surgery, University of Wisconsin, Madison, WI, USA.
  • Abbott DE; Division of Surgical Oncology, Department of Surgery, University of Wisconsin, Madison, WI, USA.
  • Lee B; Division of Surgical Oncology, Department of Surgery, City of Hope National Medical Center, Duarte, CA, USA.
  • Staley CA; Division of Surgical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA, USA.
  • Zaidi MY; Division of Surgical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA, USA.
  • Johnston FM; Department of Surgery, Johns Hopkins University, Baltimore, MD, USA.
  • Greer JB; Department of Surgery, Johns Hopkins University, Baltimore, MD, USA. jgreer13@jhmi.edu.
Ann Surg Oncol ; 31(5): 3314-3324, 2024 May.
Article de En | MEDLINE | ID: mdl-38310181
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.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du péritoine / Tumeurs colorectales / Hyperthermie provoquée Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Humans Langue: En Journal: Ann Surg Oncol Sujet du journal: NEOPLASIAS Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du péritoine / Tumeurs colorectales / Hyperthermie provoquée Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Humans Langue: En Journal: Ann Surg Oncol Sujet du journal: NEOPLASIAS Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique