Table 2.
Characteristics of included studies, *median
| Study ID | Country | Number of participants | Design | Treatment | Males-to-females ratio (%/%) | Mean age (SD or range) | Duration | Cancer type | Previous treatment | Summarized effects of donepezil treatment |
|---|---|---|---|---|---|---|---|---|---|---|
| Rapp 2024 | USA | 276 | Placebo-controlled RTC | Single daily 5 mg for 6 weeks, escalated to single daily 10 mg for 18 weeks | 0/100 | 57.1 (10.5) | Up to 24 weeks | Breast |
≥ 4 cycles of adjuvant/neoadjuvant cytotoxic chemotherapy 1–5 years before enrollment |
No significant effect on memory, cognitive function, or subjective cognitive function compared to placebo |
| Lawrance 2015 | USA | 62 | Placebo-controlled RTC | Single daily 5 mg for 6 weeks, escalated to single daily 10 mg for 18 weeks | 0/100 | 55.8 (39–79) | Up to 36 weeks | Breast |
> 4 cycles of adjuvant/neoadjuvant cytotoxic chemotherapy 1–5 years before enrollment |
Improved verbal memory and executive function in patients with poorer baseline cognitive performance compared to placebo |
| Bruera 2003 | USA | 27 | Observational | Single daily 5 mg | 33.3/66.7 | 52*(24–75) | 1 week | Hematological, gastrointestinal, lung, head and neck, breast | N/A, during study patients were given oral morphine-equivalent daily dose of 180 mg per day | Significantly improved sedation, fatigue, well-being, anxiety, and constipation in cancer patients receiving opioids |
| Bruera 2007 | USA | 142 | Placebo-controlled RTC | Single daily 5 mg | 35.2/64.8 | 56 (12.2) | 1 week | Breast, gynecologic, gastrointestinal, lung, and others | N/A | Not superior to placebo in the management of cancer-related fatigue |