TABLE 2

General methodological characteristics of the trials

First author [ref.]PhasePrimary outcomeSecondary outcomesIAAdjustment for IA
First-line setting
 Negoro [13]IIIOSResponseNoNA
Duration of response
TTP
Toxicity
QoL
 Rosell [14]IIIResponseToxicityNoNA
QoL
OS
 Fossella [15]IIIOSResponseYesReported
Duration of response
TTP
Toxicity
QoL
 Ohe [16]III1-year OSResponseNoNA
Duration of response
TTF
TTP
Toxicity
QoL
 Novello [17]IIIOSResponse rateNoNA
1-year OS
Toxicity
QoL
 Park [18]IIIOSResponseNoNA
TTP
Toxicity
QoL
 Scagliotti [19]IIIOSResponseNoNA
Duration of response
TTF
TTP
PFS
Toxicity
 Heymach [20]IIPFSResponseYesNot reported
Disease control
Toxicity
OS
 Mok [21]IIIPFSResponseNoNA
Reduction in symptoms
Toxicity
OS
QoL
 Okamoto [22]IIIOSResponseYesReported
PFS
Toxicity
QoL
 Lee [23]IIBResponsePFSNoNA
Toxicity
OS
Second-line setting
 Schuette [24]III1-year OSResponseNoNA
TTP
Toxicity
QoL
 Hanna [25]IIIOSResponseNoNA
Duration of CB
TTF
TTP
PFS
QoL
 Ramlau [26]III1-year OSResponseNoNA
Duration of response
TTR
TTP
Toxicity
OS
QoL
Drug exposure
 Krzakowski [27]IIIPFSResponseNoNA
CB
Toxicity
OS
QoL
 Maruyama [28]IIIOSPFSYesReported
Toxicity
QoL
 Kim [29]IIIOSResponseYesReported
PFS
Toxicity
QoL
 Li [30]II#ResponseDisease controlNoNA
Performance index scores
Toxicity
 Natale [31]IIIPFSResponseYesReported
Time to symptom deterioration
 Shi [32]IIIPFSResponseNoNA
TTP
Toxicity
OS
QoL
  • IA: interim analysis; OS: overall survival; TTP: time to progression; QoL: quality of life; NA: not applicable; TTF: time to treatment failure; PFS: progression-free survival; CB: clinical benefit; TTR: time to response. #: stated as exploratory.