Journals / Journal of Medicine and Palliative Care / 2026 / Volume: 7 Issue: 4

Clinicopathological features and survival of early-onset colon cancer: a SEER-based analysis of 156,031 curative-intent surgical patients

Faruk Recep Özalp(DOKUZ EYLÜL ÜNİVERSİTESİ, TIP FAKÜLTESİ)0000-0002-2863-3243
Özge Yetginoğlu(DOKUZ EYLÜL ÜNİVERSİTESİ, TIP FAKÜLTESİ)0000-0002-0684-8710
Şerife Sivridemir(Osmaniye Eğitim Araştırma Hastanes,)0000-0002-4766-220X
Erkut Demirciler(DOKUZ EYLÜL ÜNİVERSİTESİ, TIP FAKÜLTESİ)0000-0001-9747-3784
Oktay Halit Aktepe(DOKUZ EYLÜL ÜNİVERSİTESİ, TIP FAKÜLTESİ)0000-0003-3540-0701
Hüseyin Salih Semiz(DOKUZ EYLÜL ÜNİVERSİTESİ, TIP FAKÜLTESİ)0000-0002-7083-8517
Aziz Karaoğlu(DOKUZ EYLÜL ÜNİVERSİTESİ, TIP FAKÜLTESİ)0000-0001-5500-156X
Pages
—
Publication Date
2026-08-15
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Although EOCC was associated with more advanced stage and adverse pathological features, younger age remained associated with better CSS after multivariable adjustment.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Aims: To analyze the clinicopathological features and survival outcomes of early-onset colon cancer (EOCC, <50 years) compared with late-onset colon cancer (LOCC, ≥50 years) in a large curative-intent surgical cohort.
📊
Key Findings & Data:Methods: We retrospectively analyzed 156,031 stage I-III colon cancer patients from the SEER database (2010-2015 and 2018-2022) who underwent therapeutic surgical resection.
💡
Conclusion & Impact:Although EOCC was associated with more advanced stage and adverse pathological features, younger age remained associated with better CSS after multivariable adjustment.
🔬Design:Research Article
📍Scope:2010-2015 Verileri
⚙️Variables:Early-onset colon cancer · SEER · cause-specific survival

Abstract

Aims: To analyze the clinicopathological features and survival outcomes of early-onset colon cancer (EOCC, <50 years) compared with late-onset colon cancer (LOCC, ≥50 years) in a large curative-intent surgical cohort. Methods: We retrospectively analyzed 156,031 stage I-III colon cancer patients from the SEER database (2010-2015 and 2018-2022) who underwent therapeutic surgical resection. Patients with stage 0/IV, appendiceal tumors, or unknown staging were excluded. Clinicopathological characteristics and cause-specific survival (CSS) were compared. Multivariable Cox proportional hazards regression was performed to identify independent prognostic factors. Results: EOCC accounted for 9.0% (n=14,028) of the curative surgical population. The proportion of EOCC significantly increased from 8.4% in 2010 to 11.6% in 2022 (p<0.001 for trend). EOCC patients were more likely to present with stage III disease (45.2% vs. 33.8%), distal tumor location (57.5% vs. 37.2%), and higher perineural invasion (12.9% vs. 8.9%) (p<0.001 for all). Despite advanced presentation, EOCC demonstrated superior 5-year CSS (88.1% vs. 81.4%, log-rank p<0.001). After multivariable adjustment, EOCC was associated with a 42.3% lower risk of cancer-specific death (HR: 0.577; 95% CI: 0.548-0.608; p<0.001). Conclusion: In this curative-intent surgical cohort, the proportion of EOCC increased over time. Although EOCC was associated with more advanced stage and adverse pathological features, younger age remained associated with better CSS after multivariable adjustment.

🔖

Cite This Article

Özalp, F. R., Yetginoğlu, Ö., Sivridemir, Ş., Demirciler, E., Aktepe, O. H., Semiz, H. S., Karaoğlu, A. (2026). Clinicopathological features and survival of early-onset colon cancer: a SEER-based analysis of 156,031 curative-intent surgical patients. Journal of Medicine and Palliative Care, Volume: 7 Issue: 4. https://doi.org/10.47582/jompac.1969236

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (27)

  1. Roshandel G, Ghasemi-Kebria F, Malekzadeh R. Colorectal cancer: epidemiology, risk factors, and prevention. Cancers (Basel). 2024;16(8): 1530. doi:10.3390/cancers16081530
  2. Siegel RL, Miller KD, Wagle NS, Jemal A. Cancer statistics, 2023. CA Cancer J Clin. 2023;73(1):17-48. doi:10.3322/caac.21763
  3. Bailey CE, Hu C-Y, You YN, et al. Increasing disparities in the age-related incidences of colon and rectal cancers in the United States, 1975-2010. JAMA Surg. 2015;150(1):17-22. doi:10.1001/jamasurg.2014.1756
  4. Stoffel EM, Murphy CC. Epidemiology and mechanisms of the increasing incidence of colon and rectal cancers in young adults. Gastroenterology. 2020;158(2):341-353. doi:10.1053/j.gastro.2019.07.055
  5. Vuik FE, Nieuwenburg SA, Bardou M, et al. Increasing incidence of colorectal cancer in young adults in Europe over the last 25 years. Gut. 2019;68(10):1820-1826. doi:10.1136/gutjnl-2018-317592
  6. You YN, Xing Y, Feig BW, Chang GJ, Cormier JN. Young-onset colorectal cancer: is it time to pay attention? Arch Intern Med. 2012;172(3):287-289. doi:10.1001/archinternmed.2011.602
  7. Wolf AMD, Fontham ETH, Church TR, et al. Colorectal cancer screening for average-risk adults: 2018 guideline update from the American Cancer Society. CA Cancer J Clin. 2018;68(4):250-281. doi:10.3322/caac.21457
  8. US Preventive Services Task Force, Davidson KW, Barry MJ, et al. Screening for colorectal cancer: US preventive services task force recommendation statement. JAMA. 2021;325(19):1965-1977. doi:10.1001/jama.2021.6238
  9. Sinicrope FA. Increasing incidence of early-onset colorectal cancer. N Engl J Med. 2022;386(16):1547-1558. doi:10.1056/NEJMra2200869
  10. Chang SH, Patel N, Du M, Liang PS. Trends in early-onset vs late-onset colorectal cancer incidence by race/ethnicity in the United States cancer statistics database. Clin Gastroenterol Hepatol. 2022;20(6):e1365-1377. doi:10.1016/j.cgh.2021.07.035
  11. Patel SG, Karlitz JJ, Yen T, Lieu CH, Boland CR. The rising tide of early-onset colorectal cancer: a comprehensive review of epidemiology, clinical features, biology, risk factors, prevention, and early detection. Lancet Gastroenterol Hepatol. 2022;7(3):262-274. doi:10.1016/S2468-1253(21)00426-X
  12. Surveillance, Epidemiology, and End Results (SEER) Program. National Cancer Institute. [Internet]. [cited 2026 Mar 16]. Available from: https://www.seer.cancer.gov.
  13. Ricciardiello L, Ferrari C, Cameletti M, et al. Impact of SARS-CoV-2 pandemic on colorectal cancer screening delay: effect on stage shift and increased mortality. Clin Gastroenterol Hepatol. 2021;19(7):1410-1417.e9. doi:10.1016/j.cgh.2020.09.008
  14. Toes-Zoutendijk E, Vink G, Nagtegaal ID, et al. Impact of COVID-19 and suspension of colorectal cancer screening on incidence and stage distribution of colorectal cancers in the Netherlands. Eur J Cancer. 2022;161:38-43. doi:10.1016/j.ejca.2021.11.008
  15. Carbone F, Spinelli A, Ciardiello D, et al. Prognosis of early-onset versus late-onset sporadic colorectal cancer: systematic review and meta-analysis. Eur J Cancer. 2025;215:115172. doi:10.1016/j.ejca.2024.115172
  16. Fritz CDL, Otegbeye EE, Zong X, et al. Red-flag signs and symptoms for earlier diagnosis of early-onset colorectal cancer. J Natl Cancer Inst. 2023;115(8):909-916. doi:10.1093/jnci/djad068
  17. Demb J, Kolb JM, Dounel J, et al. Red flag signs and symptoms for patients with early-onset colorectal cancer: a systematic review and meta-analysis. JAMA Netw Open. 2024;7(5):e2413157. doi:10.1001/jamanetworkopen.2024.13157
  18. Segev L, Kalady MF, Church JM. Left-sided dominance of early-onset colorectal cancers: a rationale for screening flexible sigmoidoscopy in the young. Dis Colon Rectum. 2018;61(8):897-902. doi:10.1097/DCR.0000000000001062
  19. Ugai T, Akimoto N, Haruki K, et al. Prognostic role of detailed colorectal location and tumor molecular features: analyses of 13,101 colorectal cancer patients including 2994 early-onset cases. J Gastroenterol. 2023; 58(3):229-245. doi:10.1007/s00535-023-01955-2
  20. Zhang B, Lin Y, Wang C, et al. Combining perineural invasion with staging improve the prognostic accuracy in colorectal cancer: a retrospective cohort study. BMC Cancer. 2023;23(1):675. doi:10.1186/s12885-023-11114-8
  21. Dienstmann R, Vermeulen L, Guinney J, Kopetz S, Tejpar S, Tabernero J. Consensus molecular subtypes and the evolution of precision medicine in colorectal cancer. Nat Rev Cancer. 2017;17(2):79-92. doi:10.1038/nrc.2016.126
  22. Mouillet-Richard S, Cazelles A, Sroussi M, Gallois C, Taieb J, Laurent-Puig P. Clinical challenges of consensus molecular subtype CMS4 colon cancer in the era of precision medicine. Clin Cancer Res. 2024;30(11): 2351-2358. doi:10.1158/1078-0432.CCR-23-3964
  23. Wang S, Yuan Z, Ni K, et al. Young patients with colorectal cancer have higher early mortality but better long-term survival. Clin Transl Gastroenterol. 2022;13(12):e00543. doi:10.14309/ctg.0000000000000543
  24. Jeri-Yabar A, Vittini-Hernandez L, Prado-Nuñez S, Dharmapuri S. Survival analysis of metastatic early-onset colorectal cancer compared to metastatic average-onset colorectal cancer: a SEER database analysis. Cancers (Basel). 2024;16(11):2004. doi:10.3390/cancers16112004
  25. Murphy CC, Wallace K, Sandler RS, Baron JA. Racial disparities in incidence of young-onset colorectal cancer and patient survival. Gastroenterology. 2019;156(4):958-965. doi:10.1053/j.gastro.2018.11.060
  26. Holowatyj AN, Ruterbusch JJ, Rozek LS, Cote ML, Stoffel EM. Racial/ethnic disparities in survival among patients with young-onset colorectal cancer. J Clin Oncol. 2016;34(18):2148-2156. doi:10.1200/JCO.2015.65.0994
  27. Kneuertz PJ, Chang GJ, Hu C-Y, et al. Overtreatment of young adults with colon cancer: more intense treatments with unmatched survival gains. JAMA Surg. 2015;150(5):402-409. doi:10.1001/jamasurg.2014.3572