4.4 Article

A Comprehensive Comparison of Early-Onset and Average-Onset Colorectal Cancers

Journal

JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
Volume 113, Issue 12, Pages 1683-1692

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/jnci/djab124

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Funding

  1. National Cancer Institute [P30 CA008748]
  2. National Institutes of Health [T32 GM132083, R25 CA233208]
  3. Stand Up to Cancer Colorectal Cancer Dream Team Translational Research Grant [SU2CAACR-DT22-17]

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The study found that patients with early-onset colorectal cancer are more likely to have left-sided tumors, present with rectal bleeding and abdominal pain, but are otherwise clinically and genomically indistinguishable from average-onset colorectal cancer. Aggressive treatment regimens based solely on the age at colorectal cancer diagnosis are not warranted.
Background: The causative factors for the recent increase in early-onset colorectal cancer (EO-CRC) incidence are unknown. We sought to determine if early-onset disease is clinically or genomically distinct from average-onset colorectal cancer (AO-CRC). Methods: Clinical, histopathologic, and genomic characteristics of EO-CRC patients (2014-2019), divided into age 35 years and younger and 36-49 years at diagnosis, were compared with AO-CRC (50 years and older). Patients with mismatch repair deficient tumors, CRC-related hereditary syndromes, and inflammatory bowel disease were excluded from all but the germline analysis. All statistical tests were 2-sided. Results: In total, 759 patients with EO-CRC (35 years, n = 151; 36-49 years, n = 608) and AO-CRC (n = 687) were included. Left-sided tumors (35 years and younger = 80.8%; 36-49 years = 83.7%; AO = 63.9%; P<.001 for both comparisons), rectal bleeding (35 years and younger = 41.1%; 36-49 years = 41.0%; AO = 25.9%; P =.001 and P<.001, respectively), and abdominal pain (35 years and younger = 37.1%; 36-49 years = 34.0%; AO = 26.8%; P =.01 and P =.005, respectively) were more common in EO-CRC. Among microsatellite stable tumors, we found no differences in histopathologic tumor characteristics. Initially, differences in TP53 and Receptor Tyrosine Kinase signaling pathway (RTKRAS)alterations were noted by age. However, on multivariate analysis including somatic gene analysis and tumor sidedness, no statistically significant differences at the gene or pathway level were demonstrated. Among advanced microsatellite stable CRCs, chemotherapy response and survival were equivalent by age cohorts. Pathogenic germline variants were identified in 23.3% of patients 35 years and younger vs 14.1% of AO-CRC (P =.01). Conclusions: EO-CRCs are more commonly left-sided and present with rectal bleeding and abdominal pain but are otherwise clinically and genomically indistinguishable from AOCRCs. Aggressive treatment regimens based solely on the age at CRC diagnosis are not warranted.

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