Serum Tumor Markers and Outcomes in Patients With Appendiceal Adenocarcinoma

Abdelrahman Yousef(The University of Texas MD Anderson Cancer Center), Mahmoud Yousef(The University of Texas MD Anderson Cancer Center), Mohammad A. Zeineddine(The University of Texas MD Anderson Cancer Center), Aditya More(The University of Texas MD Anderson Cancer Center), Mohammad Mahdi Fanaeian(The University of Texas MD Anderson Cancer Center), Saikat Chowdhury(The University of Texas MD Anderson Cancer Center), Mark Knafl(The University of Texas MD Anderson Cancer Center), Paul Edelkamp(The University of Texas MD Anderson Cancer Center), Ichiaki Ito(The University of Texas MD Anderson Cancer Center), Yue Gu(The University of Texas MD Anderson Cancer Center), Vinay K. Pattalachinti(The University of Texas MD Anderson Cancer Center), Zahra Alavi Naini(The University of Texas MD Anderson Cancer Center), Fadl A. Zeineddine(Methodist Hospital), Jennifer Peterson(The University of Texas MD Anderson Cancer Center), Kristin D Alfaro(The University of Texas MD Anderson Cancer Center), Wai Chin Foo(The University of Texas MD Anderson Cancer Center), Fengyi Jin(The University of Texas MD Anderson Cancer Center), Neal Bhutiani(The University of Texas MD Anderson Cancer Center), Victoria Serpas Higbie(The University of Texas MD Anderson Cancer Center), Christopher P. Scally(The University of Texas MD Anderson Cancer Center), Bryan K. Kee(The University of Texas MD Anderson Cancer Center), Scott Kopetz(The University of Texas MD Anderson Cancer Center), Drew Goldstein, Madeleine C. Strach(The University of Sydney), Andrew Williamson(National Health Service), Omer Aziz(University of Manchester), Jorge Barriuso(University of Manchester), Abhineet Uppal(The University of Texas MD Anderson Cancer Center), Michael G. White(The University of Texas MD Anderson Cancer Center), Beth A. Helmink(The University of Texas MD Anderson Cancer Center), Keith F. Fournier(The University of Texas MD Anderson Cancer Center), Kanwal Raghav(The University of Texas MD Anderson Cancer Center), Melissa W. Taggart(The University of Texas MD Anderson Cancer Center), Michael J. Overman(The University of Texas MD Anderson Cancer Center), John Paul Shen(The University of Texas MD Anderson Cancer Center)
JAMA Network Open
February 28, 2024
Cited by 29Open Access
Full Text

Abstract

Importance: Serum tumor markers carcinoembryonic antigen (CEA), carbohydrate antigen 19-9 (CA19-9), and cancer antigen 125 (CA125) have been useful in the management of gastrointestinal and gynecological cancers; however, there is limited information regarding their utility in patients with appendiceal adenocarcinoma. Objective: To assess the association of serum tumor markers (CEA, CA19-9, and CA125) with clinical outcomes and pathologic and molecular features in patients with appendiceal adenocarcinoma. Design, Setting, and Participants: This is a retrospective cohort study at a single tertiary care comprehensive cancer center. The median (IQR) follow-up time was 52 (21-101) months. Software was used to query the MD Anderson internal patient database to identify patients with a diagnosis of appendiceal adenocarcinoma and at least 1 tumor marker measured at MD Anderson between March 2016 and May 2023. Data were analyzed from January to December 2023. Main Outcomes and Measures: Association of serum tumor markers with survival in patients with appendiceal adenocarcinoma. Cox proportional hazards regression analyses were also performed to assess associations between clinical factors (serum tumor marker levels, demographics, and patient and disease characteristics) and patient outcomes (overall survival). Results: A total of 1338 patients with appendiceal adenocarcinoma were included, with a median (range) age at diagnosis of 56.5 (22.3-89.6) years. The majority of the patients had metastatic disease (1080 patients [80.7%]). CEA was elevated in 742 of the patients tested (56%), while CA19-9 and CA125 were elevated in 381 patients (34%) and 312 patients (27%), respectively. Individually, elevation of CEA, CA19-9, or CA125 were associated with worse 5-year survival; elevated vs normal was 81% vs 95% for CEA (hazard ratio [HR], 4.0; 95% CI, 2.9-5.6), 84% vs 92% for CA19-9 (HR, 2.2; 95% CI, 1.4-3.4), and 69% vs 93% for CA125 (HR, 4.6; 95% CI, 2.7-7.8) (P < .001 for all). Quantitative evaluation of tumor markers was associated with outcomes. Patients with highly elevated (top 10th percentile) CEA, CA19-9, or CA125 had markedly worse survival, with 5-year survival rates of 59% for CEA (HR, 9.8; 95% CI, 5.3-18.0), 64% for CA19-9 (HR, 6.0; 95% CI, 3.0-11.7), and 57% for CA125 (HR, 7.6; 95% CI, 3.5-16.5) (P < .001 for all). Although metastatic tumors had higher levels of all tumor markers, when restricting survival analysis to 1080 patients with metastatic disease, elevated CEA, CA19-9, or CA125 were all still associated worse survival (HR for CEA, 3.4; 95% CI, 2.5-4.8; P < .001; HR for CA19-9, 1.8; 95% CI, 1.2-2.7; P = .002; and HR for CA125, 3.9; 95% CI, 2.4-6.4; P < .001). Interestingly, tumor grade was not associated with CEA or CA19-9 level, while CA-125 was slightly higher in high-grade tumors relative to low-grade tumors (mean value, 18.3 vs 15.0; difference, 3.3; 95% CI, 0.9-3.7; P < .001). Multivariable analysis identified an incremental increase in the risk of death with an increase in the number of elevated tumor markers, with an 11-fold increased risk of death in patients with all 3 tumor markers elevated relative to those with none elevated. Somatic mutations in KRAS and GNAS were associated with significantly higher levels of CEA and CA19-9. Conclusions and Relevance: In this retrospective study of serum tumor markers in patients with appendiceal adenocarcinoma, CEA, CA19-9, and CA125 were associated with overall survival in appendiceal adenocarcinoma. Given their value, all 3 biomarkers should be included in the initial workup of patients with a diagnosis of appendiceal adenocarcinoma.


Related Papers

No related papers found

Powered by citation graph analysis