The impact of CA 19-9 on survival in patients with clinical stage I pancreatic cancer.

Authors

null

Alexa D. Melucci

Division of General Surgery, University of Rochester, Rochester, NY

Alexa D. Melucci , Alexander C Chacon , Paul R. Burchard , Nicholas A. Ullman , Vasleios Tsagkalidis , Anthony S. Casabianca , Alexandra Reitz , David A. Swift , Subir Goyal , Jeffrey M. Switchenko , Darren R. Carpizo , Mihir Maheshkumar Shah

Organizations

Division of General Surgery, University of Rochester, Rochester, NY, Department of Surgery, University of Rochester Medical Center, Rochester, NY, Emory University, Atlanta, GA, Winship Cancer Institute and Rollins School of Public Health at Emory University, Atlanta, GA, Emory University, Department of Biostatistics and Bioinformatics, Atlanta, GA, Division of Surgical Oncology, University of Rochester, Rochester, NY, Emory University School of Medicine, Atlanta, GA

Research Funding

No funding received

Background: Standard of care for early-stage resectable pancreatic cancer (PC) includes a combination of surgical resection and chemotherapy. Frequently, CA 19-9 is used as a biomarker to monitor treatment effect and has prognostic significance. We evaluated the impact of CA 19-9 on overall survival (OS) in patients with clinical stage I PC (cT1N0 and cT2N0) utilizing the National Cancer Database (NCDB). Methods: The NCDB was queried between 2010 and 2014 to identify patients with clinical stage I PC. Patients who had missing or undocumented CA 19-9 value at diagnosis were excluded. Demographic and clinical characteristics were analyzed. Patients were stratified into two cohorts based on the CA 19-9 value at diagnosis – CA 19-9 < 98 U/mL and CA 19-9 > 98 U/mL. Univariable and multivariable analyses were performed, and variables associated with OS were identified. Kaplan-Meier survival curves were computed to compare the OS between the two cohorts. Results: A total of 12,480 patients met our inclusion criteria. A majority of patients were female (51.9%), white (84.4%), with a median age of 70 years. Nearly, half the patients received care in an academic/research program (49.5%). A majority of patients had tumors located in the head of the pancreas (71.9%), and received single-agent (35.1%) or multiagent (22.9%) chemotherapy. Over half the patients (6505 patients, 52.1%) had a CA 19-9 value > 98 U/mL. A CA 19-9 value > 98 U/mL in patients predicted a significantly shorter median OS of 12.1 months compared to 19.4 months in patients with a CA 19-9 < 98 U/mL, p<0.0001 (Table). The 5-year OS rate was 9.9% in patients with a CA 19-9 value of > 98 U/mL compared to a 5-year OS rate of 18.1% for patients with a CA 19-9 value < 98 U/mL. On multivariable analysis, CA 19-9 > 98 compared to CA 19-9 < 98 (HR 1.53, p<0.001) and black race compared to white race (HR 1.10, p<0.001) was associated with worse survival, whereas tumor location in the body and tail compared to the head (HR 0.82, p<0.001), single-agent (HR 0.55, p<0.001) and multiagent (HR 0.55, p<0.001) chemotherapy compared to no chemotherapy, independently predicted improved OS. Conclusions: This is the first National Cancer Database study to demonstrate the prognostic value of CA 19-9 in patients with clinical stage I pancreatic cancer, with a value < 98 U/mL predicting improved survival. Clinical stage I pancreatic cancer patients appear to derive a significant benefit from chemotherapy, including single and multiagent chemotherapy, irrespective of the CA 19-9 value.

Survival comparison between the two Cohorts based on the CA 19-9 value.


CA 19-9
Subjects

(n= 12,480)
Median Survival (95%CI) (months)
Overall Survival (months)
Survival Rate (95% CI)
p-value
<98 U/ml
5975
19.4 (18.8, 20.3)
60

120
18.1% (16.8%, 19.4%)

0.0% (NA, NA)


<0.0001
> 98 U/ml
6505
12.1 (11.7, 12.5)
60

120
9.9% (8.9%, 10.9%)

0.0% (NA, NA)

CA 19-9: carbohydrate antigen 19-9; CI: confidence interval.

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2022 ASCO Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session B: Cancers of the Pancreas, Small Bowel, and Hepatobiliary Tract

Track

Pancreatic Cancer,Hepatobiliary Cancer,Neuroendocrine/Carcinoid,Small Bowel Cancer

Sub Track

Tumor Biology, Biomarkers, and Pathology

DOI

10.1200/JCO.2022.40.4_suppl.606

Abstract #

606

Poster Bd #

Online Only

Abstract Disclosures