Skip to main content
. 2021 Nov 16;5(6):pkab088. doi: 10.1093/jncics/pkab088

Table 3.

Efficacy outcomes for the use of IO as maintenance treatment for upper GI carcinomas compared with standard chemotherapy alonea

Setting No. of studies Study Investigational agent Overall survival
PFS
Response rate
HR (95% CI) P b HR (95% CI) P b OR (95% CI) P b
All studies 3 Bang et al., 2017c Ipilinumab 1.11 (0.68 to 1.80) 1.59 (0.90 to 2.81)d 0.24 (0.03 to 2.19)
JAVELIN-100 Avelumab 0.91 (0.74 to 1.13) 1.04 (0.86 to 1.27) 0.91 (0.55 to 1.51)
PLATFORM Durvalumab 0.92 (0.68 to 1.29) 0.79 (0.59 to 1.06)
Pooled evidence Any agent 0.94 (0.79 to 1.11) .46 1.02 (0.59 to 1.06) .92 0.83 (0.51 to 1.36) .47
Any PD-L1 status 2 Pooled evidence Any agent 0.94 (0.77 to 1.15) .55 1.09 (0.90 to 1.31) .37 0.83 (0.51 to 1.36) .47
PD-L1 CPS > 1% 1 JAVELIN-100 Avelumab 1.13 (0.57 to 2.23) 1.04 (0.53 to 2.02) 0.91 (0.55 to 1.51)
a

Only data for adenocarcinoma were available for analysis. CI = confidence interval; CPS = combined positive score; GI = gastrointestinal; HR = hazard ratio; IO = immunotherapy; OR = odds ratio; PD-L1 = programmed cell death ligand-1; PFS = progression-free survival.

b

Inverse-Variance and the Mantel-Haenszel statistical methods were applied for calculation of pooled hazard ratios and odds ratios, respectively. A 2-sided P value less than .05 was considered statistically significant.

c

Confidence interval for the hazard ratio was 92% in the original manuscript, recalculated to the 95% confidence interval for present comparisons.

d

Confidence interval for the hazard ratio was 80% in the original manuscript, recalculated as the 95% confidence interval for present comparisons.