Investor Presentaiton
HER3-DXd
NSCLC Ph1 study cohort 2 data
ASCO 2022 Highlights
Daiichi-Sankyo
The promising clinical activity of HER3-DXd in patients with NSCLC harboring a
broad range of genomic alterations or without genomic alterations
Anti-tumor activity (With (A) or Without (B) genomic alterations)
(A)
(B)
Best percentage change in
sum of diameters
-40
-80
2202488
-20
CR
PR
BOR by BICR
SD
PD
NE
+ Treatment ongoing
Outcomes (BICR per RECIST 1.1)
Confirmed ORR (95% CI), %
-60
Disease control rate (95% CI), %
N=21
28.6 (11.3, 52.2)
76.2 (52.8, 91.8)
Time to response, median (range), mo
Duration of response, median (95% CI), mo
PFS, median (95% CI), mo
2.8 (1.3-4.6)
9.4 (4 2-NE)
10.8 (2.8-16.0)
-100
EGFR
Driver genomic ERBB2
alteration
AMP
MET EGFR KRAS EGFR ERBB2
AMP Ex20ins G12C Ex20ins D769Y
EGFR CD74:
Ex20ins ROS1
KRAS
CD74:
G12D
ROS1
EGFR
Ex20ins
T751 1759
delinsN
EGFR KRAS
L861R G12C
ERBB2
A775_6776
inSYVMA
RET
fusion
NRAS EML4
Q61L ALK
KRAS EML4
G12F
ALK
ALK
On-target
resistance
mechanism
Off-target resistance
mechanism
ROS1
D2033N
ROS1
G2032R
ALK
L1196M
G1202R
$1206F
S1206Y
BRAF
V600E
Best percentage change in
sum of diameters
CR
PR
BOR by BICR
SD
PD
NE
+ Treatment ongoing
40
20
0
-20
-40
Outcomes (BICR per RECIST 1.1)
N=26
-60
Confirmed ORR (95% CI), %
Disease control rate (95% CI), %
26.9 (11.6, 47.8)
73.1 (52.2, 88.4)
Time to response, median (range), mo
-80
9.6 (1.6-NE)
4.2 (2.5-10.8)
-100
+
Cohort 2
Patients with advanced NSCLC
without common EGFR mutations
■HER3-DXd showed promising
clinical activity and manageable
safety profile in patients with or
without genomic alterations
Presented cohort 1 data with EGFR
mutations at last year's ASCO
Duration of response, median (95% CI), mo
PFS, median (95% CI), mo
2.1 (1.2-6.0)
Data cutoff: January 28, 2022. Twenty of 21 patients with identified driver mutations, and 24 of 26 patients without, had best percentage change in sum of diameters data available.
BICR: blinded independent central review, BOR: best objective response,
NSCLC: non small cell lung cancer
27View entire presentation