Table 3.
Study characteristics
| Authors | Year | Study type | Participant characteristics | Sample size | Relevant Outcome(s) | Intervention(s) | Comparison | Duration |
|---|---|---|---|---|---|---|---|---|
| Gundermann et al. [28] | 2014 | RCT | Healthy, recreationally active males | 16 | Skeletal muscle maintenance/loss | Sirolimus, 16 mg, once 1 h prior to exercise | Control | 2 days |
| Dickinson et al. [29] | 2011 | RCT | Healthy, recreationally active | 8 | Skeletal muscle protein synthesis | Sirolimus, 16 mg, once 2 h following 1st muscle biopsy | Control | 4 days (2 days for 2 trials) |
| Dickinson et al. [30] | 2013 | RCT | Healthy young males and females | 6 | Skeletal muscle maintenance/loss | Sirolimus, 16 mg, 2 h following 1st muscle biopsy | Control | 4 days (2 days for 2 trials) |
| Drummond et al. [31] | 2009 | RCT | Healthy young males | 15 | Skeletal muscle maintenance/loss | Sirolimus, 12 mg, once 1 h after 1st muscle biopsy | Control | 2 days |
| Veasey-Rodrigues et al. [32] | 2013 | Non-randomized clinical trial | Had documented advanced solid tumors | 26 | Skeletal muscle maintenance/loss | Temsirolimus, 25 mg IV, weekly | Baseline | 8 weeks |
| Gyawali et al. [33] | 2016 | Cohort (retrospective) | Patients who had taken everolimus or Temsirolimus for at least 6 months as single drug therapy | 20 | Skeletal muscle maintenance/loss | Everolimus or Temsirolimus, single drug therapy for at least 6 months | Baseline | At least 6 months |
| Campistol et al. [23] | 2005 | RCT (secondary analysis) | Human renal transplant recipients | 115 | Bone metabolism |
Sirolimus, dose adjusted to maintain blood trough concentrations at 30 ng//ml for 2 months, 15 ng/ml after 2 months + All received glucocorticosteriods Study A received Azathioprine additionally Study B received Mycophenolate additionally |
Cyclosporin A (combination), dose adjusted to maintain blood trough concentrations at 200–400 mg/ml for 2 months, 100–200 ng/ml after 2 months | At least 24 weeks |
| Westenfeld et al. [24] | 2011 | Cross-sectional | Human renal transplant recipient (6–195 months after transplantation) | 42 | Bone metabolism | Triple therapy of steroids + Sirolimus + (Mycophenolate or Azathioprine), trough levels at 5–10 ng/ml | Calcineurin based triple therapy, (cyclosporine trough levels at 80–120 ng/ml, tacrolimus 8–12 ng/ml) | |
| Sessa et al. [25] | 2010 | Cohort (prospective) | Human renal transplant recipients | 24 | Impact on prevalence factors for post-renal transplant osteopathy | Sirolimus (combination with Mycophenolate or steroid) | Multiple groups with different immunosuppressive protocols | |
| Gnant et al. [26] | 2013 | RCT (exploratory analysis) | Postmenopausal women with metastatic or locally advanced, oestrogen positive HER2 breast cancer | 724 | Bone turnover |
Everolimus, 10 mg, each day + Exemestane, 25 mg, each day |
Placebo control (placebo + exemestane), 25 mg, each day | 18 months |
| Hadji et al. [27] | 2018 | Non-randomized clinical trial (exploratory analysis) | Postmenopausal women with HR + , HER2-negative locally advanced or metastatic breast cancer | 299 | Bone turnover |
Everolimus, 10 mg, each day + Exemestane, 25 mg, each day |
Baseline | 48 weeks |
| Bruyn et al. [34] | 2007 | RCT | Rheumatoid arthritis patients | 121 | Rheumatoid arthritis response |
Everolimus, 6 mg, each day + Methotrexate + (NSAIDs and prednisone if stable dose) |
Placebo control | 3 months |
| Wen et al. [35] | 2019 | RCT | Rheumatoid arthritis patients | 62 | Rheumatoid arthritis response, Impact on immune cells |
Sirolimus, 0.5 mg, once every two days + (Combination with other immunosuppressants based on participant) |
Control (receiving other immunosuppressives) | 24 weeks |
| Niu et al. [36] | 2020 | Non-randomized clinical trial | Rheumatoid arthritis patients | 115 | Rheumatoid arthritis response, Impact on immune cells |
Sirolimus, 0.5 mg, once every two days + (Combination with other immunosuppressants based on participant) |
RA patients under conventional treatment, Healthy volunteers |
12 weeks |