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. Author manuscript; available in PMC: 2017 Nov 1.
Published in final edited form as: Psychooncology. 2015 Aug 27;25(11):1261–1270. doi: 10.1002/pon.3954

Table 2.

Illustrative studies examining mental health outcomes during long-term colorectal cancer survivorship

Reference Sample demographics at baseline Cancer site and stage Study design Theoretical framework Mental health measures Results
Caravati- Jouvenceaux et al., 2011 [35] N = 542, 57% male, mean age = 71 years, France 63% colon cancer, 37% rectal cancer, 41% stage I, 26% stage II, 19% stage III, 2% stage IV, 12% unknown Cross-sectional, population-based, case-controlled (N = 1,181 controls), surveyed at 5, 10, and 15 years post- diagnosis None SF-36: MCS, EORTC QLQ-C30: Emotional functioning scale, STAI There were no significant differences between survivors and non-cancer controls in overall mental health or anxiety.
Dunn et al., 2013 [28]* N = 1,703, 60% male, 71% aged between 60 and 80 years, Australia Type of CRC not reported, 55% stage 0, I, or II, 35% stage III or IV, 11% unknown Longitudinal, surveyed at 5, 12, 24, 36, 48, 60 months post- diagnosis, population-based None BSI Rates of high psychological distress were between 32% and 44% over the 5-year study period. Four different distress trajectories were identified, including: (1) constantly low distress (19%); (2) medium distress that fluctuated across time points (30%); (3) medium distress that increased gradually over time (39%); and (4) high decrease in distress over time (13%). Men reported more distress than women. The most distressed men were more likely to be younger and have lower levels of education, poor social support, and late-stage disease.
Goldzweig et al., 2009 [37] N = 339, 55% male, mean age = 71 years, Israel Type of CRC not reported, 18% stage 0 or I, 62% stage II, 20% stage III Cross-sectional, surveyed between 2 and 6 years post- treatment None BSI, IES, MAC Unmarried, male survivors reported the highest rates of distress and helplessness. Levels of family support were comparable between married and unmarried survivors; however, greater family support was only related to less distress among married survivors.
Jansen et al., 2011 [33] N = 439, 57% male, mean age = 65 years, Germany 59% colon cancer, 41% rectal cancer, 51% local, 31% regional, 17% distal, 1% unknown Longitudinal, surveyed at 1, 3, 5, and 10 years post- diagnosis, population-based, case-controlled (N = 2,028 controls) None EORTC QLQ-C30: Emotional functioning scale At 1, 3, and 10 years post-diagnosis, survivors reported significantly worse emotional functioning compared to controls; however, the differences were not clinically meaningful (i.e., >10 points). Compared to older survivors (age ≥ 70 years at diagnosis), younger survivors (age < 60 years) reported significantly worse emotional functioning at 1 and 3 years post-diagnosis, and these differences were clinically meaningful.
Krouse et al., 2009 [42] N = 491, 62% male, mean age = 72 years, 76% non-Hispanic White, USA 100% rectal cancer, 53% local, 41% regional, 1% distal, 5% unknown Cross-sectional, surveyed at least 5 years post- diagnosis, case- controlled: ostomies (n = 246 cases) vs. anastomoses (n = 245 controls) None Modified COH-QOL- Ostomy, SF- 36 version 2: MCS Females with ostomies reported worse psychological well-being compared to females with anastomoses. Male and female survivors with ostomies were also more likely to report depressive symptoms following their surgery compared to those with anastomoses.
Thong et al., 2013 [30] N = 1,419, 53% male, mean age = 70 years, Netherlands 59% colon cancer, 41% rectal, 33% stage I, 38% stage II, 26% stage III, 2% stage IV, 1% unknown Cross-sectional, surveyed at an average of 8 years post-diagnosis (minimum of 5 years post- diagnosis), population-based, case-controlled (N = 338 normative population controls) None HADS Using a cut-off of ≥ 8 on the HADS, 20% of survivors reported clinical levels of anxiety compared to 10% of the normative population; similarly, 18% of survivors reported clinical levels of depressive symptoms compared to 12% of the normative population. Using a more stringent cut-off of ≥ 11, 8% of survivors reported clinical levels of anxiety compared to 3% of the normative population; additionally, 7% of survivors reported clinical levels of depressive symptoms compared to 3% of the normative population.

BSI, Brief Symptom Inventory; COH-QOL-Ostomy, City of Hope Quality of Life-Ostomy; CRC = colorectal cancer; EORTC QLQ-C30, European Organization for Research and Treatment of Cancer Quality-of-Life Questionnaire-Core 30; HADS, Hospital Anxiety and Depression Scale; IES, Impact of Event Scale; MAC, Mental Adjustment to Cancer; SF-36: MCS, Medical Outcomes Study 36-Item Short-Form Health Survey: Mental Component Summary; STAI, State-Trait Anxiety Inventory.

*

Study sample overlaps with Lynch et al., 2008 [3] sample.