Table 1.
Primary author (year) | Data source | Sample size/ characteristics | Eligibility criteria | Year(s) of diagnosis | Follow-up period | Outcome variable(s) | Results | Operational definition of adherence/basis for definition a |
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Boehmer (2010) | Medical records | n = 253; ≤54 to ≥75y; 58% male; 54% White; safety net patients | Non-metastatic CRC; treated w/curative intent; no recurrence during study period | 2003–2007 | 5y post-dx | % COL 1/3y post-tx | 27/56% | COL 1 & 3y post-tx (referenced 2008 ACS, USMTFCC) |
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Borie (2004) | Regional cancer registry along with medical records | n = 231; mean age 64y (standard group) to 69y (minimal group); 56% male; French sample | CRC treated with potentially curative surgery; able to be classified into 1 of 2 (standard vs. minimal) follow-up groups | 1992 | 5y post-tx | Mean number PE (standard/minimal) | 20/7 | Standard follow-up: CEA every 4–6m for 3y, then once a year for 2y; PE every 3m for 2y, then every 6m for 3y; 1 COL every 3y; US every 4–6m for 3y, then once a year for 2y; annual CXR |
Mean number US (standard/minimal) | 6/2 | |||||||
Mean number COL (standard/minimal) | 5/2 | |||||||
Mean number CXR (standard/minimal) | 4/1 | Minimal follow-up: CEA & US once a year for 3y; PE every 6m for 5y; 1 COL every 3y; CXR once a year for 2y (based on 1998 French Consensus Guidelines) |
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Mean number CEA (standard/minimal) | 12/3 | |||||||
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Boulin (2005) | Regional cancer registry along with medical records and provider surveys as necessary | n = 409; mean age 71y; 55% male; 30% advanced stage CRC; French sample | Diagnosed with CRC Stage A, B, or C or Stage D with complete resection of liver metastasis; alive without recurrence ≥ 6m post-curative surgery | 1998 | 3y post-tx | % below/within/over standard for clinical exams | 35/23/42% | Clinical exam every 3m for first 2y; every 6m for next 3y |
% below/within/over standard for abdominal US | 65/35/1% | Abdominal US every 3–6m for first 3y; yearly for next 2y | ||||||
% below/within/over standard for CXR | 52/19/29% | CXR yearly for 5y | ||||||
% below/within/over standard/inappropriate time for COL | 20/27/24/29% | COL after 3y (or 1y if ≥ 3 adenomas with one > 1 cm diameter or presenting villous component | ||||||
Optional testing:
% CEA within 3y |
56% | Optional: CEA (based on 1998 French Consensus Guidelines) |
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Cluster analysis:
% “minimal/moderate/ intensive” surveillance |
47/24/29% | |||||||
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Brawarsky (2013) | SEER-Medicare | n = 38,889; 56% female; 88/7/5% White/Black/ Hispanic; median age 75y (White), 74y (Black/ Hispanic) | 66 to 85y; White, Black, or Hispanic; diagnosed with first CRC; stage I-III; treated with surgery; alive at end of study period | 1993–2005 | Through Dec 2007 | % COL 15m post-tx | 61% | At least 1 COL 15m post-surgery |
% PC visits 2y post-tx | 77% | At least 2 PC visits 2y post-surgery | ||||||
% CEA 2y post-tx | 68% | At least 2 CEA 2y post-surgery (stage II/III) | ||||||
% overall surveillance | 43% | Overall surveillance: COL and PC visits for stage I or COL, PC, and CEA for stage II/III (based on 2012 NCCN) |
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Cardella (2008) | Medical records | n = 96; median age 64y; 60% male; median time post-tx 34m; Canadian sample | 19 to 75y; curative intent resection of CRC; non-metastatic disease; able to go home and assume active daily living; alive and disease-free through end of study period | 2000–2002 | Through October 2004 | % clinic visits over follow-up period | 70% | Clinic visits every 6m for first 3y, followed by 12m intervals until 5y post-tx |
% CEA over follow-up period | 49% | |||||||
% abdominal imaging over follow-up period | 62% | CEA, CXR, and abdominal imaging (CT or abdominal US) at each clinic visit | ||||||
% COL over follow-up period | 94% | COL 1y post-tx and every 3y thereafter (basis for adherence definition not reported) |
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Cheung (2008) | Academic and comm cancer center registries along with medical records | n = 341 (244 academic, 97 community); overall median age 62y; 58% male; 57% stage III; Canadian sample | Stage II or III CRC; referred to either cancer center for follow-up after curative resection; able to be monitored for ≥5y post-dx; not enrolled in clinical trials | 1999–2001 | 5y post-dx | Median CV (academic/ community) | 11/9 | Over the first 5y period of surveillance: 8–14 CV |
Median CEA (academic/ community) | 9/9 | 8–30 CEA 1 COL |
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Median COL (academic/ community) | 2/2 | Not routinely recommended: CBC, LFT, CXR, chest CT, abdominal CT, pelvic CT (based on 1999, 2000 ASCO) |
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% below CV recommendations (academic/community) | 23/23% | |||||||
% above CV recommendations (academic/community) | 17/0% | |||||||
% below CEA recommendations (academic/community) | 41/29% | |||||||
% above CEA recommendations (academic/community) | 0/0% | |||||||
% below COL recommendations (academic/community) | 15/3% | |||||||
% above COL recommendations (academic/community) | 67/76% | |||||||
Non-recommended testing: % non-recommended CBC/LFT/CXR/chest CT/ abdominal CT/pelvic CT in academic center |
94/91/70/42/9 3/91% | |||||||
% non-recommended CBC/LFT/CXR/chest CT/abdominal CT/pelvic CT in community center | 99/100/37/14/ 38/34% | |||||||
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Cooper (1999) | SEER-Medicare | n = 5716; mean age 75y; 51% female; 6% African-American | Medicare beneficiaries; local or regional CRC; underwent surgical resection; alive 6m post-dx; complete follow-up data | 1991 | Through 1994 | %/mean COL | 58%/2.8 | NR/NR |
%/mean abdominal CT | 29%/2.8 | |||||||
%/mean pelvic CT | 23%/2.6 | |||||||
%/mean CXR | 66%/4.2 | |||||||
%/mean abdominal US | 15%/14.8 | |||||||
%/mean liver enzymes | 74%/4.7 | |||||||
%/mean CEA | 38%/2.3 | |||||||
%/mean overall procedures | 87%/12.9 | |||||||
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Cooper (2000) | SEER-Medicare | n = 5716; mean age 75y; 51% female; 6% African-American | Medicare beneficiaries; local or regional CRC; underwent surgical resection; alive 6m post-dx; complete follow-up data | 1991 | Through 1994 | % 1 COL/>1 COL 7–12m post-dx | 22/14% | NR/NR |
% 1 COL/>1 COL 13–18m post-dx | 23/15% | |||||||
% 1 COL/>1 COL 19–24m post-dx | 15/10% | |||||||
% 1 COL/>1 COL 25–30m post-dx | 16/10% | |||||||
% 1 COL/>1 COL 31–36m post-dx | 12/8% | |||||||
Cooper (2006) | SEER-Medicare | n = 62,882; 55% female; 86% White | Medicare beneficiaries; ≥65y; treated w/curative intent; alive 1 & 3y post-dx | 1992–2002 | 3y post-dx | % COL 12/18/36m post-dx | 26/54/70% | COL 1 or 3y post-dx (referenced 1997 AGA; 1999, 2000 ASCO; 2001, 2003 ACS; 2003 AGA; 2004 ASCRS) |
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Cooper (2008) | SEER-Medicare | n = 9,426; 55% female; 87% White | Medicare beneficiaries; ≥66y; treated w/curative intent; alive 3.5y post-dx | 2000–2001 | 42m post-dx | % OV/COL/CEA 42m post-dx | 92/74/47% | ≥2 OV/y; ≥1 COL w/in 3y; ≥2 CEA in y1 & y2 (referenced 1989 AGA, ASGE; 1999, 2000, 2005 ASCO; 2004 ASCRS; 2006 ACS, ASGE, USMTFCC; 2008 NCCN) |
% testing below/at/above recommended levels | 60/17/23% | |||||||
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Ellison (2003) | SEER-Medicare | n = 52,105; 53% female; 86% White | Medicare beneficiaries; ≥65y; stage I-III CRC; treated w/ curative intent | 1986–1996 | Through 998 | % CE 18m/3y/5y post-tx | 57/67/74% | NR/NR |
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Elston Lafata (2001) | Medical records | n = 251; mean age 65y; 62% male; 63% White; HMO members | ≥40y; stage I-III CRC; treated w/ curative intent | 1990–1995 | 8y post-dx | % CE 18m/3y/5y post-tx | 55/65/77% | CE (COL, SIG & BE, BE only) 1y post-tx, every 3–5y thereafter (referenced 1992 ASCRS; 1996 NCCN; 1997 AGA; 1999 ASCO) |
% CEA 18m/3y/5y post-tx | 71/79/87% | |||||||
Elston Lafata (2005) | Medical records | n = 100; 56% male; 68% White; HMO members | Enrolled ≥ 1y or ≥1 PCP visit pre-dx; ≥30y; new primary CRC; alive ≥6m post-dx | 1990–1995 | 5y post-dx | % PE 18m post-tx/within 18m of initial | 78/85% | 2 PE/y, 1 CE (COL, SIG, or BE) in y1 & y3-y5 |
% CE 18m post-tx/within 18m of initial | 61/62% | 4 CEA/yr (based on 1999 ASCO; 2001, 2002 NCCN) |
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% CEA 18m post-tx/within 18m of initial | 17/12% | |||||||
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Foley (2011) | State cancer registry-Medicaid | n = 1,044; <65 to ≥75y; 68% female; 57% White | Medicaid beneficiaries; stage I to III CRC; alive ≥18m post-dx | 1999–2002 | 18m post-tx | % COL/CEA 3–18m post-tx | 42/25% | COL 1y post-tx (referenced 1999 ASCO; 2008 ACS, USMTFCC, ACR) |
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Fox (2013) | Military Health System claims data (TRICARE) | n = 345; 73% ≥50y; 55% male; 62% Southern US region | 18 to 61y; underwent curative treatment for CRC; enrolled in TRICARE Prime managed care program; ≥ 1 health claim per year | 2005–2007 | Through Sept 2010 | % PE 1y/2y/3y follow-up | 95/93/89% | 1y follow-up: 2 PE, 2 CEA, 1 COL |
% PE each year | 52% | |||||||
% CEA 1y/2y/3y follow-up | 59/49/43% | 2y follow-up: 2 PE, 2 CEA | ||||||
% 1+ COL in 3y | 69% | 3y follow-up: 2 PE, 2 CEA (based on 2009 NCCN) |
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% all recommended care each year | 26% | |||||||
High-cost imaging:
% PET 1y/2y/3y/overall |
16/14/11/24% | |||||||
% CT 1y/2y/3y/overall | 60/54/50/78% | |||||||
% MRI 1y/2y/3y/overall | 18/15/15/35% | |||||||
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Haggstrom (2009) | Cross-sectional survivor survey | n = 416; 52% ≥65y; 52% male; 70% White | No treatment in past 6m; no evidence of recurrence | 1999–2001 | April 2003–Nov 2004 | % 1/2/≥3 OV in past 12m | 27/34/39% | Regular history and physicals during the first 3 years post-tx (referenced 2005 ASCO) |
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Hilsden (2004) | Provincial cancer registry linked with ministry of health admin databases and medical records | n = 3918; 46% ≥ 70y; 56% male; 85% rural residence; Canadian sample | ≥30y; first CRC treated w/curative resection; survived ≥270d post-surgery; eligible for Alberta insurance plan at dx; able to be linked to admin databases | 1983–1995 | Through March 2000 | % COL within 5y post-tx | 51% | NR/NR |
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Hu (2011) | SEER-Medicare | n = 7,348; 60% female; 89% White | Medicare beneficiaries; ≥66y; stage I-III CRC; treated w/ curative intent w/in 3m of dx; alive 3.5y post-tx | 2000–2002 | Through 2005 | % OV 1/2/3y post-tx | 93/88/84% | ≥2 OV/y for 3y; ≥2 CEA/y for 2y; ≥1 COL w/in 3y (referenced 1999 ASCO; 2010 NCCN) |
% CEA 1/2y post-tx | 42/29% | |||||||
% COL 1/2/3y post-tx | 59/68/74% | |||||||
% testing at recommended levels | 25% | |||||||
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Jackson (2010) | Medical records | n = 2,492; 98% male; 72% White; VA patients | Stage I-III CRC; treated w/ curative intent | 2003–2006 | Through March 2006 | % COL 7–18m post-tx | 44% | COL 7–18m post-tx (based on 2003 NCCN) |
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Knopf (2001) | SEER-Medicare | n = 52,283; 53% female | Medicare beneficiaries; ≥65y; stage I-III CRC; treated w/curative intent | 1986–1996 | Through 1998 | % CE 1y/1–4y/ 4–7y/7+y post-dx | 46/48/40/31% | CE (COL, SIG, or BE) 1y post-tx & every 3–5y thereafter (referenced 1989 AGA, ASGE; 1996 NCCN; 1997 ACS, AGA; 1999 ASCO) |
% testing below/above recommended levels | 17/18% | |||||||
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Parsons (2012) | SEER-Medicare | n = 17,906; 59% female; 85% White | Medicare beneficiaries; ≥ 66y; stage III CRC; treated w/curative intent | 1992–2007 | 3y post-tx | % COL/CEA 3y post-tx | 49/72% | COL w/in 3 y post-tx |
Any CEA w/in 3 y post-tx (referenced 2003 GCP; 2005 ASCO; 2006 ACS, USMTFCC; 2007 NCCN) | ||||||||
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Pollack (2009) | SEER-Medicare along with UPIN registry and AMA Physician file | n = 16,671; 86% 65+y; 56% female; 86% White; 84% metropolitan residence | First CRC dx at ≥ 60y; survived ≥ 5y; no recurrence or multiple cancers | 1992–1997 | Through Dec 2003 | % PV with cancer specialist | 28% | ≥ 1 PV during 6th to 12th year post-dx (basis for adherence definition not reported) |
% PV with hematologist/oncologist | 26% | |||||||
% PV with radiation oncologist | 2% | |||||||
% PV with surgical oncologist | 1% | |||||||
% PV with gynecologic oncologist | 0.2% | |||||||
% PV with cancer-related specialist | 37% | |||||||
% PV with general surgeon | 8% | |||||||
% PV with colorectal surgeon | 6% | |||||||
% PV with gastroenterologist | 26% | |||||||
% PV with PCP | 73% | |||||||
% PV with medical specialist | 66% | |||||||
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Ramsey (2007) | SEER-Medicare | n = 28,209; 52% female; 86% White | Medicare beneficiaries; ≥ 65y; stage I-III CRC; treated w/ curative intent | 1986–1996 | Through 2003 | % testing below/at/above recommended levels | 47/25/28% | ≥ 1 CE (COL, SIG, or BE) over study period (referenced 2006 ACS, USMTFCC) |
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Rolnick (2005) | Medical records | n = 881; 48% ≥ 70y; 57% male; 75% White; HMO members | ≥ 40y; stage 0-III CRC; White or African-American | 1990–2000 | 5y post-tx | % CE 1/3/5y post-tx | 18/60/67% | CE (COL or SIG & BE) 1, 3, & 5y post-dx (referenced 1989 AGA, ASGE; 1996 NCCN; 1997 AGA; 1999, 2000 ASCO; 2003 AGA) |
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Rulyak (2004) | Medical records linked with SEER | n = 1,002; <50 to 80+y; 50% male; 93% White; HMO members | Stage 0-III new primary CRC | 1993–1999 | 8.7y post-dx | % CE 18m post-dx/within 18m of initial/5 y post-dx | 61/38/80% | NR/NR |
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Rulyak (2007) | Medical records linked with SEER | n = 1002; 78% ≥ 60y at dx; 50% male; 93% White; HMO members | Stage 0-III; treated w/curative intent; survived ≥ 6m post-dx | 1993–1999 | Through Dec 2001 | % ≥ 1 CE during study period | 65% | NR/NR |
Mean exams during study period | 1.4 | |||||||
% CE 18m/5y post-dx | 61/80% | |||||||
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Salloum (2012) | Medical records linked to tumor registry | n = 2,297; mean age 68.6y; 51% female; 81% White; HMO members | ≥ 18y; enrolled in HMO plan ≥ 1y pre-dx; treated w/curative intent | 2000–2008 | 8y post-dx | % PE 18m post-tx/within 18m of initial | 98/91% | 2 PE 18m post-tx; 1 CE (COG, SIG, or BE) |
% CE 18m post-tx/within 18m of initial | 55/16.7% | 18m post-tx (based on 2011 NCCN; 1999 ASCO) |
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Salz (2010) | Medical records | n = 1,423 56% ≥ 65y; 56% male; 67% White; multi-region cohort including VA & managed care patients | Stage I-III CRC; treated w/curative intent w/in 1m of dx; alive 14m post-tx w/out recurrence | 2003–2005 | 15m post-dx | % COL 14m post-tx | 49% | COL 14m post-tx (based on 2003 ACS; 2006 ACS, NCCN, USMTFCC) |
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Singh (2013) | SEER-Medicare | n = 70,419; 36% ≥ 80y; 55% female; 85% White | ≥ 66y; stage I-III CRC; no history of IBD; Medicare beneficiaries enrolled in Part A & B; not HMO members | 1992–2005 | 1992–2003 (second COL cohort), 1992–2002 (third COL cohort) | % early surveillance COL after first/second normal COL | 32/27% | COL 1y post-tx, 3- and 5y later |
Median time between first and second COL | 29m | “Early surveillance”: COL 3m to 2y after previous COL | ||||||
Median time between second and third COL | 33m | (referenced 1997 AGA, 2000 ASCO, 2004 ASCRS, 2006 USMTFCC) | ||||||
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Sisler (2012) | Provincial cancer registry linked with pop health research data | n = 250; median age = 70y; 53% male; Canadian sample | Stage II and III new CRC; treated with definitive surgery; alive 42m post-dx | 2004 | July 2004–June 2008 | % COL within 3y period | 80% | At least 1 COL in 3y study period; at least 1 liver imaging (CT, US, or MRI of the abdomen) in each 1y interval; at least 3 CEA tests in each 1y interval (based on 2005 ASCO) |
% liver imaging (CT, US, or MRI) in each 1y interval | 47% | |||||||
% CEA in each 1y interval | 22% | |||||||
% adherent to all 3 tests over study period | 12% | |||||||
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Spratlin (2008) | Provincial cancer registry along with medical records | n = 152; mean age 66y; 66% male; 57% stage II; Canadian sample | Resected stage II/III CRC w/clear surgical margins; discharged to community; no second malignancy ≤5y post-dx | 2001 | 3y post-dx | % minimum CEA follow-up | 7% | CEA every 4m for ≥2y (based on clinical practice and informed by 2000 ASCO) |
Adherence to surveillance was judged according to the particular guideline(s) mentioned in the individual studies. Individual studies’ definitions of adherence varied. The majority of studies explicitly stated that they based their definition of adherence on a specific guideline(s) (n = 12), yet other studies only referenced published guidelines (n = 12). A few studies did not provide any basis for the definitions of adherence (n = 7).
ABBREVIATIONS: CRC, colorectal cancer; d, days; m, months; y, years; admin, administrative; comm, community; pop, population; post-dx, post-diagnosis; post-tx, post-treatment; NR, not reported; OV, office visits; PE, physical examination; CE, colon examination (i.e., colonoscopy, sigmoidoscopy, and/or barium enema; majority of exams, 77–99%, were colonoscopy); COL, colonoscopy; SIG, sigmoidoscopy; BE, barium enema; CEA, carcinoembryonic antigen test; CBC, complete blood counts; CT, computed tomography; CXR, chest x-rays; LFT, liver function tests; US, ultrasound; OMD, other metastatic disease testing (e.g., x-ray, ultrasound, CT scan, MRI ); ACR, American College of Radiology; AMA, American Medical Association; AGA, American Gastroenterological Association; ASCO, American Society of Clinical Oncology; ASCRS, American Society of Colon and Rectal Surgeons; ASGE, American Society for Gastrointestinal Endoscopy; CanCORS, Cancer Care Outcomes Research and Surveillance Consortium; HMO, health maintenance organization; IBD, inflammatory bowel disease; NSABP, National Surgical Adjuvant Breast and Bowel Project; NCCN, National Comprehensive Cancer Network; SSO, Society of Surgical Oncology; USMTFCC, United States Multi-Society Task Force on Colorectal Cancer; GCP, Gastrointestinal Consortium Panel; UPIN, Unique Physician Identification Number.