Clinical Calculator Based on Molecular and Clinicopathologic Characteristics Predicts Recurrence Following Resection of Stage I-III Colon Cancer

Author:

Weiser Martin R.1ORCID,Hsu Meier2ORCID,Bauer Philip S.3ORCID,Chapman William C.3ORCID,González Iván A.4ORCID,Chatterjee Deyali4ORCID,Lingam Deepak4,Mutch Matthew G.3,Keshinro Ajaratu1ORCID,Shia Jinru5ORCID,Vakiani Efsevia5,Konishi Tsuyoshi16ORCID,Shimada Yoshifumi17ORCID,Stadler Zsofia8ORCID,Segal Neil H.8ORCID,Cercek Andrea8ORCID,Saltz Leonard8ORCID,Yaeger Rona8ORCID,Varghese Anna8ORCID,Widmar Maria1,Wei Iris H.1ORCID,Pappou Emmanouil P.1,Smith J. Joshua1ORCID,Nash Garrett1,Paty Philip1ORCID,Garcia-Aguilar Julio1,Gonen Mithat2ORCID

Affiliation:

1. Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY

2. Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY

3. Department of Surgery, Washington University, St Louis, MO

4. Department of Pathology and Immunology, Washington University, St Louis, MO

5. Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY

6. Department of Gastroenterological Surgery, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan

7. Division of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan

8. Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY

Abstract

PURPOSE Clinical calculators and nomograms have been endorsed by the American Joint Committee on Cancer (AJCC), as they provide the most individualized and accurate estimate of patient outcome. Using molecular and clinicopathologic variables, a third-generation clinical calculator was built to predict recurrence following resection of stage I-III colon cancer. METHODS Prospectively collected data from 1,095 patients who underwent colectomy between 2007 and 2014 at Memorial Sloan Kettering Cancer Center were used to develop a clinical calculator. Discrimination was measured with concordance index, and variability in individual predictions was assessed with calibration curves. The clinical calculator was externally validated with a patient cohort from Washington University's Siteman Cancer Center in St Louis. RESULTS The clinical calculator incorporated six variables: microsatellite genomic phenotype; AJCC T category; number of tumor-involved lymph nodes; presence of high-risk pathologic features such as venous, lymphatic, or perineural invasion; presence of tumor-infiltrating lymphocytes; and use of adjuvant chemotherapy. The concordance index was 0.792 (95% CI, 0.749 to 0.837) for the clinical calculator, compared with 0.708 (95% CI, 0.671 to 0.745) and 0.757 (0.715 to 0.799) for the staging schemes of the AJCC manual's 5th and 8th editions, respectively. External validation confirmed robust performance, with a concordance index of 0.738 (95% CI, 0.703 to 0.811) and calibration plots of predicted probability and observed events approaching a 45° diagonal. CONCLUSION This third-generation clinical calculator for predicting cancer recurrence following curative colectomy successfully incorporates microsatellite genomic phenotype and the presence of tumor-infiltrating lymphocytes, resulting in improved discrimination and predictive accuracy. This exemplifies an evolution of a clinical calculator to maintain relevance by incorporating emerging variables as they become validated and accepted in the oncologic community.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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