Proposed changes to the pathologic staging for colon cancer (CC): AJCC Colon Cancer Expert Panel (AJCCCCEP).

Q Qian Shi G George J. Chang (The University of Texas MD Anderson Cancer Center, Houston, TX) L Levi D. Pederson (1Division of Hematology, Mayo Clinic, Rochester, MN) E Elliot Amponsah Asare (University of Utah Huntsman Cancer Institute, Salt Lake City, UT) Z Zhaohui Jin R Romain Cohen (Sorbonne University; Department of Medical Oncology, Saint-Antoine Hospital, AP-HP, INSERM 938, SIRIC CURAMUS, Paris, France) J Jeffrey A. Meyerhardt T Thierry André J Jeanne Tie (Division of Personalized Oncology, Walter and Eliza Hall Institute of Medical Research) J Jesse G. Dixon (Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN) B Bryan E Palis (American College of Surgeons, Chicago, IL) K Karla V. Ballman (From the Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda (A.B.A., N.S., S.N., L.L., L.C.), the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore (J.H.-C.), and the Investigational Drug Branch, Cancer Therapy Evaluation Program, National Cancer Institute, National Institutes of Health, Rockville (H.S., E.S.) — all in Maryland; the Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN (K.V.B., M.O., C.M., G.P.B.); AdventHealth Cancer Institute and the University of Central Florida, Orlando (G.S.); Dana–Farber/Harvard Cancer Center, Boston (S.B., B.M.); UNC Lineberger Comprehensive Cancer Center, Chapel Hill (W.Y.K.), and Duke University Medical Center and Duke Cancer Institute, Durham (J.H., S.H.) — both in North Carolina; the University of Kansas Cancer Center, Westwood (R.P.); Memorial Sloan Kettering Cancer Center, New York (M.Y.T., M.J.M., J.E.R.), and Roswell Park Comprehensive Cancer Center, Buffalo (G.C.) — both in...) G Greg Yothers (NRG Oncology SDMC, Pittsburgh, PA) Z Zeliang Ma (Peking Union Medical College, Beijing, China) S Steven R. Alberts (Mayo Clinic Rochester, Rochester, MN) C Chanjuan Shi (Duke University Trent Center for Bioethics Humanities and History of Medicine, Durham, NC) M Mary Kay Washington (Vanderbilt University Medical Center, Nashville, TN) J Julien Taieb S Scott Steele (Cleveland Clinic, Cleveland, OH) R Richard M. Goldberg (Department of Hematology and Oncology, West Virginia University Cancer Institute, Morgantown)

Abstract

3520 Background: Recent analyses highlight nonhierarchical outcomes using the 8 th Edition AJCC staging system for CC. For instance, the 5-year survival rate for stages I and IIIa patients (pts) closely align. Additionally, tumor deposits (TDs) have been established as significant prognostic indicators. The AJCCCCEP commissioned this study to develop an updated pathological staging system for CC focused specifically on pts without distant metastasis (M0), while retaining the existing stage IV classification. Methods: Individual patient data (IPD) from pts diagnosed with cc (2010- 2017) in the NCDB were divided into training (70%) and internal validation (30%) datasets. External validation used IPD from clinical trials. The primary endpoint was overall survival (OS). Risk classification development for M0 pts incorporated ungrouped data on pathologic T categories, the number of involved regional lymph nodes (LN+), and TD counts. Recursive partitioning and regression tree analyses were applied to construct hierarchical staging levels. Pre-specified criteria required survival probabilities to be consecutive and show clear separations using Kaplan-Meier (KM) estimates with pairwise log-rank test P of < 0.005 for the training and < 0.05 for validation analyses. Results: Data from 281,997 pts (median age 67 years, 50% male, 81% white, 55% T3, 19% T4, 44% N+, 26% M+, and 11% with ≥1 TD) were analyzed, with a median follow-up of 7.3 years. The updated staging system (Table) met pre-specified criteria, with all observed pairwise P < 0.0001 in the development and internal validation sets. KM OS curves displayed a hierarchical separation across all sub-levels after the 1 st year of diagnosis. Consistent results were seen in pts treated with adjuvant chemotherapy in 4 trials (all pair-wise P < 0.0001). Conclusions: The proposed pathological staging system for M0 pts fulfills pre-specified criteria for hierarchical risk stratification, validated both internally and externally, and provides an evidence-based update. Pending review process, the AJCCCCEP will recommend that these changes be made to the Version 9 staging protocol for colon cancer to improve prognostication for CC pts. Stage T, # of LN+, # of TD M % of pts 1y OS (CI), % 3y OS (CI), % 5y OS (CI), % I T1, 0, 0 0 5 96 (95-97) 91 (90-92) 84 (83-86) IIa T2, 0, 0 0 10 95 (94-95) 88 (88-89) 80 (79-81) IIb T1, 0, 1+T1, 1+, 0T2, 0, 1+T2, 1-4, 0T3, 0, 0 0 27 93 (92-93) 84 (84-85) 75 (75-76) IIIa T1, 1+, 1+T2, 1-4, 1+T2, 5+, 0T3, 0, 1+T3, 1-4, 0 0 14 92 (91-92) 80 (80-81) 71 (70-72) IIIb T2, 5+, 1+T3, 1-4, 1+T3, 5+, 0T4a, 0-4, 0T4b, 0-2, 0 0 13 86 (86-87) 69 (68-70) 58 (57-59) IIIc T3, 5+, 1+T4a, 0-4, 1+T4a, 5+, anyT4b, 0-2, 1+T4b, 3+, any 0 5 78 (77-80) 53 (51-54) 40 (38-41) IVa Any 1a 19 59 (58-60) 28 (28-29) 17 (16-18) IVb Any 1b 7 43 (42-44) 14 (13-14) 6 (6-7) CI: 95% confidence internal; Peritoneum involvement data were not available before 2018 in NCDB. Thus, IVa/b were based on 7 th Edition.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 3520-3520
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

Q

Qian Shi

G

George J. Chang

The University of Texas MD Anderson Cancer Center, Houston, TX

L

Levi D. Pederson

1Division of Hematology, Mayo Clinic, Rochester, MN

E

Elliot Amponsah Asare

University of Utah Huntsman Cancer Institute, Salt Lake City, UT

Z

Zhaohui Jin

R

Romain Cohen

Sorbonne University; Department of Medical Oncology, Saint-Antoine Hospital, AP-HP, INSERM 938, SIRIC CURAMUS, Paris, France

J

Jeffrey A. Meyerhardt

T

Thierry André

J

Jeanne Tie

Division of Personalized Oncology, Walter and Eliza Hall Institute of Medical Research

J

Jesse G. Dixon

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN

B

Bryan E Palis

American College of Surgeons, Chicago, IL

K

Karla V. Ballman

From the Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda (A.B.A., N.S., S.N., L.L., L.C.), the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore (J.H.-C.), and the Investigational Drug Branch, Cancer Therapy Evaluation Program, National Cancer Institute, National Institutes of Health, Rockville (H.S., E.S.) — all in Maryland; the Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN (K.V.B., M.O., C.M., G.P.B.); AdventHealth Cancer Institute and the University of Central Florida, Orlando (G.S.); Dana–Farber/Harvard Cancer Center, Boston (S.B., B.M.); UNC Lineberger Comprehensive Cancer Center, Chapel Hill (W.Y.K.), and Duke University Medical Center and Duke Cancer Institute, Durham (J.H., S.H.) — both in North Carolina; the University of Kansas Cancer Center, Westwood (R.P.); Memorial Sloan Kettering Cancer Center, New York (M.Y.T., M.J.M., J.E.R.), and Roswell Park Comprehensive Cancer Center, Buffalo (G.C.) — both in...

G

Greg Yothers

NRG Oncology SDMC, Pittsburgh, PA

Z

Zeliang Ma

Peking Union Medical College, Beijing, China

S

Steven R. Alberts

Mayo Clinic Rochester, Rochester, MN

C

Chanjuan Shi

Duke University Trent Center for Bioethics Humanities and History of Medicine, Durham, NC

M

Mary Kay Washington

Vanderbilt University Medical Center, Nashville, TN

J

Julien Taieb

S

Scott Steele

Cleveland Clinic, Cleveland, OH

R

Richard M. Goldberg

Department of Hematology and Oncology, West Virginia University Cancer Institute, Morgantown