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. 2019 Nov 26;39(11):BSR20193319. doi: 10.1042/BSR20193319

Table 1. Clinical information from the eligible trials in the meta-analysis.

Included studies Tumor stage/KPS Patients Con/Exp Therapeutic regimen Dosage of kanglaite Parameter types
Experimental Control (drugs)
Ao, M. (2017) ≥60 38/38 Con+ kanglaite1 TACE (DDP, 5-Fu, E-ADM) 20 g/time, 1 time/day ORR, DCR, AE
Feng, Y.Z. (2001) II–IV 21/11 Con+KLT1 TAE 20 g/time, 1 time/day ORR, DCR, IF
Hu, J.B. (2003) II–IV 25/31 Con+KLT1 TACE (DDP, 5-Fu, THP) 20 g/time, 1 time/day ORR, DCR, AE, CS, AFP, QoL
Jiang, Y.B. (2006) I–III 51/105 Con+KLT1 TACE (DDP, 5-Fu, ADM) 20 g/time, 1 time/day ORR, DCR, CS, QoL
Li, D.J. (2009) II–III 32/30 Con+KLT2 TACE (DDP, 5-Fu, ADM) 2.7 g /time, 4 times/day OS, ORR, DCR, AE, AFP, QoL
Li, M. (2015) II-III 23/24 Con+KLT1 CT (Oxaliplatin) 20 g/time, 1 time/day OS, ORR, DCR, IF, CS, QoL
Li, Y. (2014) I–IV 75/75 Con+KLT1 CT (Meccnu, ADM, 5-Fu) 20 g/time, 1 time/day OS, ORR, DCR, AE, QoL
Liang, S.M. (2006) II-III 25/31 Con+KLT1 TAE unknown ORR, DCR, CS, AFP
Lu, D.P. (2017) Unknown 43/51 Con+KLT1 TACE (Oxaliplatin, 5-Fu) 20 g/time, 1 time/day OS, ORR, DCR, QoL
Lu, H. (2006) I–III 24/24 Con+KLT1 TACE (DDP, 5-Fu, MMC) 20 g/time, 1 time/day OS, ORR, DCR, AE, QoL
Lv, D.Z. (2004) II–III 38/38 Con+KLT1 TACE (unknown), SST 20 g/time, 1 time/day IF, CS, QoL
Ma, W.L. (2017) Unknown 43/43 Con+KLT1 CT (FOLFOX) 20 g/time, 1 time/day ORR, DCR, IF
Qin, G.Y. (1998) Unknown 20/18 Con+KLT1 TACE (DDP, 5-Fu, THP) 10-20 g/time, 1 time/day ORR, DCR, CS
Qin, Y.T. (2001) Unknown 42/52 Con+KLT1 SST 20 g/time, 1 time/day IF
Shao, L. (2017) II–III 25/25 Con+KLT1 SRT 20 g/time, 1 time/day ORR, AE, QoL
Wang, C.H. (2001) I–III 50/50 Con+KLT1 TACE (DDP, ADM, HCPT) 10 g/time, 1 time/day ORR, DCR
Wang, X.F. (2012) III–IV 24/34 Con+KLT1 TACE (unknown) FOLFOX 10 g/time, 1 time/day ORR, AE, QoL
Wei, Q.C. (2009) Unknown 24/24 Con+KLT1 SST 10 g/time, 1 time/day QoL
Wu, D.H. (2009) II–III 30/30 Con+KLT1 CT (Oxaliplatin, FUDR) 20 g/time, 1 time/day ORR, DCR, AE, CS, QoL
Wu, J.L. (2015) Unknown 60/60 Con+KLT1 TACE (unknown) 10 g/time, 1 time/day ORR, DCR, QoL
Xi, D.S. (2001) I–III 20/20 Con+KLT1 CT (E-ADM, 5-Fu, HCPT, ACTD) 20 g/time, 1 time/day ORR, DCR, AE
Xu, J. (2018) Unknown 54/54 Con+KLT1 CT (Meccnu, ADM, 5-Fu) 20 g/time, 1 time/day ORR, DCR
Xu, X.H. (2010) II–III 37/38 Con+KLT1 CT (Capecitabine) 20 g/time, 1 time/day OS, ORR, DCR, AE, CS
Yang, T. (2013) ≥60 30/60 Con+KLT1 TACE (DDP, 5-Fu, E-ADM) 10 g/time, 1 time/day ORR, DCR, AE, CS, QoL
Ye, X. (2003) III-IV 17/19 Con+KLT1 TACE (DDP, 5-Fu, ADM, MMC) 20 g/time, 1 time/day ORR, DCR, AE, CS, AFP, QoL
Yin, R.R. (2009) Unknown 32/40 Con+KLT1 TACE (unknown) 10 g/time, 1 time/day ORR, DCR
Yu, Z.H. (2016) ≥50 20/20 Con+KLT1 Thalidomide 20 g/time, 1 time/day OS, ORR, DCR, AE, QoL
Zhang, Y. (2012) >50 31/31 Con+KLT1 SST 10 g/time, 1 time/day AFP, QoL
Zhang, Y.J. (2017) II–III 48/49 Con+KLT1 TACE (DDP, 5-Fu, ADM, MMC) 20 g/time, 1 time/day ORR, DCR, AE, AFP, QoL
Zhou, S.F. (2018) III–IV 54/54 Con+KLT1 Sorafenib 20 g/time, 1 time/day ORR, DCR, IF
Zhu, X.F. (2006) I–IV 40/40 Con+KLT1 TACE (DDP, 5-Fu, THP) 20 g/time, 1 time/day ORR, DCR, CS, QoL

Con, control group (CTs alone group); Exp, experimental group (CTs and kanglaite group). Abbreviations: ACTD, actinomycin D; ADM, adriamycin; AE, adverse event; CF, calcium folinate; CS, clinical symptom; DDP, cisplatin; E-ADM, epirubicin; FOLFOX, qxaliplatin+CF+5-Fu; HCPT, hydroxycamptothecin; IF, immune function; MMC, mitomycin C; ORR, overall response rate; THP, pirarubicin; 5-Fu, 5-Fluorouracil.

1Kanglaite injection.

2Kanglaite capsules.

HHS Vulnerability Disclosure