Table 2. Protocols of rhuIL-2 treatment.
Source | Tan et al. [28] | Johnson et al. [29] | Chu et al. [30] | Johnson et al. [18] |
---|---|---|---|---|
Year of publication | 2017 | 2003 | 2003 | 1997 |
Intervention group | ||||
-Source | China | Canada | China | Canada |
-Beginning time | After inclusion and allocation | After inclusion and allocation | After inclusion and allocation | After inclusion and allocation |
-Delivery method | Subcutaneous injection | Intradermal injection | Intradermal injection | Intradermal injection |
-Bolus dose | 50 × 104 U/mL | 225,000 IU | 200,000 IU |
DRG: 225,000 IU PRG: 450,000 IU |
- Schedule | Once every other day for 30 days separately during months 1, 3, 5, and 7. | Twice daily during the first 30 days of anti-TB treatment | Once daily for 30 days, followed by 30 days 'rest', for two cycles. |
DRG: Twice daily for 30 consecutive days PRG: Daily at 12-h intervals for 5 days, followed by 9 days 'rest', for three cycles. |
-Therapy period | 7 months | 30 days | 90 days | 30 days |
Control group | Background drug regimen (chemotherapy) | Standard short-course chemotherapy with sterile 5% dextrose | Standard chemotherapy | Standard chemotherapy with diluent |
TB: tuberculosis; DRG: Daily rhuIL-2 groups; PRG: Pulse-therapy rhuIL-2 group.