Table 1. Description of included trials.
Study | Size (n) |
Follow-up (weeks) |
Age | Sex: F/M (n) | Baseline PC ´109/L | Duration of ITP (years) | Splenectomy (Y/N) | Outcomes | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TPO-RA | Control | TPO-RA | Control | TPO-RA | Control | TPO-RA | Control | TPO-RA | Control | ||||
Tarantino et al. 2016 | 62 | 25 | 10 (6–14) | 7.5 (6.5–13.5) | 24/18 | 11/9 | 17·8 (7·5–24·5) | 17·7 (9·8–24·1) | 1.9 (1.0–4.2) | 2.2 (1.5–3.7) | 1/41 | 1/19 | OR; DR; Rescue medication; Any bleeding events; Severe bleeding events; Severe AEs |
Mathias et al. 2016 | 62 | 25 | 9.7 ± 4.1 | 9.4 ± 4.7 | 24/18 | 11/9 | 19.9 ± 19.3 | 17.5 ± 10.7 | 3.0 ± 2.8 | 3.0 ± 2.3 | 1/41 | 1/19 | HqoL; Parental burden |
Klaassen et al. 2012 | 22 | 13 | 9 (1–17) | 11 (2–14) | 4/13 | 2/3 | 13 (2–27) | 9 (8–29) | 2.4 (0.8–14.0) | 4.1 (0.6–8.6) | 6/11 | 2/3 | HqoL; Parental burden |
Elalfy et al. 2011 |
18 | 12 | 9.5 (2.5–16) | 7 (4–15) | 2/10 | 3/3 | 10.5(2–20) | 10.5(6–20) | 2.3 (1.2–7.0) | 3.0 (1.5–6.5) | 0/12 | 0/6 | OR; Rescue medication; Severe bleeding events; All AEs; Severe AEs; |
Bussel et al. 2011 | 22 | 12 | 9 (1–17) | 11 (2–14) | 4/13 | 2/3 | 13 (2–27) | 9 (8–29) | 2.4 (0.8–14.0) | 4.1 (0.6–8.6) | 6/11 | 2/3 | OR; DR; Rescue medication; Any bleeding events; Severe bleeding events; Cilinical bleeding events; All AEs; Severe AEs |
Grainger et al. 2015 | 92 | 12 | 9.4 (8.2–10.5) | 9.8 (8.3–11.3) | 30/33 | 14/15 | < 30 | < 30 | 3.4 ± 2.8 | 4.4 ± 3.4 | 4/59 | 0/29 | OR; DR; Rescue medication; Any bleeding events; Cilinical bleeding events; All AEs; Severe AEs |
Bussel et al. 2015 | 67 | 7 | 9 (8–10) | 10 (8–12) | 27/18 | 13/9 | < 30 | < 30 | > 0.5 | > 0.5 | 5/40 | 0/22 | OR; DR; Rescue medication; Any bleeding events; Severe bleeding events; Cilinical bleeding events; All AEs; Severe AEs |
F/M: female/male; PC: platelet count; ITP: immune thrombocytopenia; Y/N: yes/no; OR: overall platelet response; DR: durable response; HqoL: health-related quality of life; AEs: adverse events.