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Immunotherapy in previously treated patients:

efficacy by PD-L1 status

*TC3 or IC3: ≥50% of TCs or ≥10% of ICs; TC2/3 or IC2/3: ≥5% of TCs or ICs;

TC1/2/3 or IC1/2/3: ≥1% of TCs or ICs; TC0 and IC0: <1% of TCs and ICs

1. Brahmer, et al. N Engl J Med 2015; 2. Borghaei, et al. N Engl J Med 2015

3. Herbst, et al. Lancet 2015; 4. Barlesi, et al. ESMO 2016

CheckMate 017 (phase

III)

1

2L nivo vs doc (n=272)

CheckMate 057 (phase

III)

2

2/3L nivo vs doc

(n=582)

KEYNOTE-010 (phase

II/III)

3

≥2L pembro

vs doc

(n=1,033)

OAK (phase

III)

4

≥2L atezo vs doc (n=850)

Histology

Squamous

Non-squamous

All comers

All comers

PD-L1

selected

No

No

Yes (TPS ≥1%)

No

Efficacy by

PD-L1

status

PD-L1

assay

28-8 (Dako) on TCs

22C3 (Dako) on TCs SP142 (Ventana) on ICs and

TCs

0.53

0.76

HR

1–49% (n=591)

≥50% (n=442)

Subgroup

(pooled doses)

doc

HR

pembro

0.1

1

2

0.5

0.2

0.67

ITT (n=1,033)

≥5% (n=81)

<5% (n=144)

≥10% (n=69)

<10% (n=156)

≥1% (n=119)

<1% (n=106)

ITT (

n=272

)

0.69

0.58

0.53

0.70

0.50

0.70

0.39

0.59

HR

Subgroup

doc

HR

nivo

0.1

1 2

0.5

0.2

NQ (n=47)

≥5% (n=181)

<5% (n=274)

≥10% (n=165)

<10% (n=290)

≥1% (n=246)

<1% (n=209)

ITT (n=582)

0.58

0.87

0.43

0.96

0.40

0.96

0.72

HR

Subgroup

doc

HR

nivo

0.1

1

2

0.5

0.2

doc

atezo

HR

TC1/2/3 or IC1/2/3 (n=463)

TC0 and IC0 (n=379)

TC3 or IC3 (n=137)

TC2/3 or IC2/3 (n=265)

ITT (n=850)

0.73

0.41

0.67

0.74

0.75

HR

Subgroup*

<1% not available

study design

2

1

0.1

0.2

0.5