Impact of intensity of post-treatment surveillance on survival in colorectal cancer.

Authors

Rebecca Snyder

Rebecca A Snyder

Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX

Rebecca A Snyder , Chung-Yuan Hu , Amanda Cuddy , Amanda B. Francescatti , Jessica R. Schumacher , Y. Nancy You , Deborah Schrag , Daniel McKellar , David P Winchester , Benjamin D. Kozower , Caprice Christian Greenberg , George J. Chang

Organizations

Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, The University of Texas MD Anderson Cancer Center, Houston, TX, American College of Surgeons, Chicago, IL, Department of Surgery, University of Wisconsin, Madison, WI, Dana-Farber Cancer Institute, Boston, MA, Wright State University, Dayton, OH, Cancer Programs, American College of Surgeons, Chicago, IL, Division of Cardiothoracic Surgery, Washington University, St. Louis, MO, Departments of Surgical Oncology and Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, TX

Research Funding

Other

Background: The optimal strategy for CRC post-treatment surveillance is unknown. The frequency and type of testing remains controversial, and it is unclear whether surveillance impacts rates of detection or survival. The purpose of this study was to determine if the intensity of post-treatment surveillance is associated with time to recurrence detection, treatment, or overall survival (OS). Methods: Primary records of a random sample of 10,636 Stage I-III CRC patients from Commission on Cancer accredited hospitals (2006-2007) were abstracted, and detailed results of surveillance testing were reviewed. Data was merged with records in the National Cancer Database (NCDB). A predicted and observed number of imaging and CEA tests per patient were determined and clustered by hospital to categorize patients into high (HI, O/E ≥ 1) or low intensity (LI, O/E < 1) categories. Results: 6,279 patients underwent imaging or CEA surveillance in the 3 years after CRC treatment. Patients with HI imaging (50.6%) or CEA (51.2%) had a mean of 2.9 imaging studies and 4.7 CEA tests. Patients with LI imaging underwent a mean of 1.4 imaging studies and 1.6 CEA tests. 5-year recurrence rates did not differ based on intensity of surveillance. Stage II and III patients who underwent HI imaging and CEA testing had a slightly higher resection rate, but this did not translate into an improvement in 5-year OS. Conclusions: High vs. low intensity surveillance was not associated with earlier detection of recurrent disease or improved OS. HI surveillance was associated with a slightly higher resection rate, but this did not result in a survival benefit. Our findings within a national hospital registry cohort failed to demonstrate a survival benefit of HI surveillance and suggest that an effective surveillance strategy may involve less frequent testing.

Imaging
P-valueCEA
P-value
LIHILIHI
Observed # tests in 3 years
Mean (SD) (n = 6279)
1.4 (1.46)2.9 (2.4)< .0011.7 (2.6)4.7 (4.4)< .001
3-year recurrence rate
(n = 8542)
17.7%17.4%0.67317.7%17.4%0.816
Resection of recurrence in
3 years (n = 3393)
3.9%4.8%0.054.2%4.5%0.40
Adjusted 3 and 5-yr OS
(n = 8542)
87.1%,77.8%87.3%,78.1%HR = 0.98,
p = 0.687
86.9%,77.5%87.4%,78.4%HR = 0.95,
p = 0.301

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Abstract Details

Meeting

2017 ASCO Annual Meeting

Session Type

Poster Discussion Session

Session Title

Patient and Survivor Care

Track

Patient and Survivor Care

Sub Track

Survivorship

Citation

J Clin Oncol 35, 2017 (suppl; abstr 10016)

DOI

10.1200/JCO.2017.35.15_suppl.10016

Abstract #

10016

Poster Bd #

5

Abstract Disclosures

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