Association of Inflammatory Biomarkers With Survival Among Patients With Stage III Colon Cancer

Author:

Cheng En1,Shi Qian2,Shields Anthony F.3,Nixon Andrew B.4,Shergill Ardaman P.5,Ma Chao6,Guthrie Katherine A.7,Couture Felix8,Kuebler Philip9,Kumar Pankaj10,Tan Benjamin11,Krishnamurthi Smitha S.12,Ng Kimmie6,O’Reilly Eileen M.13,Brown Justin C.14,Philip Philip A.3,Caan Bette J.1,Cespedes Feliciano Elizabeth M.1,Meyerhardt Jeffrey A.6

Affiliation:

1. Division of Research, Kaiser Permanente Northern California, Oakland

2. Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota

3. Department of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, Michigan

4. Department of Medicine, Duke University Medical Center, Durham, North Carolina

5. Department of Medicine, University of Chicago, Pritzker School of Medicine, Chicago, Illinois

6. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts

7. SWOG Statistics and Data Management Center, Fred Hutchinson Cancer Research Center, Seattle, Washington

8. Department of Medicine, Hôtel-Dieu de Québec, Quebec, Canada

9. Columbus NCI Community Oncology Research Program, Columbus, Ohio

10. Illinois CancerCare PC, Peoria

11. Siteman Cancer Center, Washington University School of Medicine in St Louis, St Louis, Missouri

12. Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, Ohio

13. Memorial Sloan Kettering Cancer Center, Weill Cornell Medical Center, New York, New York

14. Cancer Metabolism Program, Pennington Biomedical Research Center, Baton Rouge, Louisiana

Abstract

ImportanceThe association of chronic inflammation with colorectal cancer recurrence and death is not well understood, and data from large well-designed prospective cohorts are limited.ObjectiveTo assess the associations of inflammatory biomarkers with survival among patients with stage III colon cancer.Design, Setting, and ParticipantsThis cohort study was derived from a National Cancer Institute–sponsored adjuvant chemotherapy trial Cancer and Leukemia Group B/Southwest Oncology Group 80702 (CALGB/SWOG 80702) conducted between June 22, 2010, and November 20, 2015, with follow-up ending on August 10, 2020. A total of 1494 patients with plasma samples available for inflammatory biomarker assays were included. Data were analyzed from July 29, 2021, to February 27, 2022.ExposuresPlasma inflammatory biomarkers (interleukin 6 [IL-6], soluble tumor necrosis factor α receptor 2 [sTNF-αR2], and high-sensitivity C-reactive protein [hsCRP]; quintiles) that were assayed 3 to 8 weeks after surgery but before chemotherapy randomization.Main Outcomes and MeasuresThe primary outcome was disease-free survival, defined as time from randomization to colon cancer recurrence or death from any cause. Secondary outcomes were recurrence-free survival and overall survival. Hazard ratios for the associations of inflammatory biomarkers and survival were estimated via Cox proportional hazards regression.ResultsOf 1494 patients (median follow-up, 5.9 years [IQR, 4.7-6.1 years]), the median age was 61.3 years (IQR, 54.0-68.8 years), 828 (55.4%) were male, and 327 recurrences, 244 deaths, and 387 events for disease-free survival were observed. Plasma samples were collected at a median of 6.9 weeks (IQR, 5.6-8.1 weeks) after surgery. The median plasma concentration was 3.8 pg/mL (IQR, 2.3-6.2 pg/mL) for IL-6, 2.9 × 103 pg/mL (IQR, 2.3-3.6 × 103 pg/mL) for sTNF-αR2, and 2.6 mg/L (IQR, 1.2-5.6 mg/L) for hsCRP. Compared with patients in the lowest quintile of inflammation, patients in the highest quintile of inflammation had a significantly increased risk of recurrence or death (adjusted hazard ratios for IL-6: 1.52 [95% CI, 1.07-2.14]; P = .01 for trend; for sTNF-αR2: 1.77 [95% CI, 1.23-2.55]; P < .001 for trend; and for hsCRP: 1.65 [95% CI, 1.17-2.34]; P = .006 for trend). Additionally, a significant interaction was not observed between inflammatory biomarkers and celecoxib intervention for disease-free survival. Similar results were observed for recurrence-free survival and overall survival.Conclusions and RelevanceThis cohort study found that higher inflammation after diagnosis was significantly associated with worse survival outcomes among patients with stage III colon cancer. This finding warrants further investigation to evaluate whether anti-inflammatory interventions may improve colon cancer outcomes.Trial RegistrationClinicalTrials.gov Identifier: NCT01150045

Publisher

American Medical Association (AMA)

Subject

Oncology,Cancer Research

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