la malattia metastatica 2 parte ‘immunoterapia nel ... · loi s et al, jco 2013 luen s et al,...
TRANSCRIPT
Luisa Carbognin 1University of Verona, Verona, Italy
2Division of Gynecologic Oncology, Department of Woman and Child Health,
Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy
La Malattia Metastatica – 2° Parte
‘Immunoterapia nel carcinoma
metastatico Triplo Negativo’
• Rational for Immunotherapy in advanced Triple Negative Breast Cancer (TNBC)
• Single Agent anti-PD1/PD-L1Trials Biomarkers from single agent anti- PD1/PD-L1
• Combination Strategies Chemotherapy
PARP inhibitors
• Conclusion and Future Directions
Outline
TNBC ER+ (Luminal A)
Mutation rate higher in basal-like and HER2-enriched subtypes compared to other subtypes
Are all cancers equally suitable for immunotherapy?
ER+ (Luminal B)
Banerji S et al, Nature 2012
TILs expression and Mutational Load according to BC subtypes
Higher TILs rates in TNBC Higher Mutational Load in TNBC
Loi S et al, JCO 2013 Luen S et al, Breast 2016
TILs expression as a prognostic marker
Higher TILs rates ad better OS: TIL effect is linear
OS
HR 0.84 0.77-0.92
Loi S et al, SABCS 2015
Loi S et al, JCO 2013; Loi S et al, AO 2014
• Rational for Immunotherapy in advanced Triple Negative Breast Cancer (TNBC)
• Single Agent anti-PD1/PD-L1Trials Biomarkers from single agent anti- PD1/PD-L1
• Combination Strategies Chemotherapy
PARP inhibitors
• Conclusion and Future Directions
Outline
Phase I and II studies in advanced TNBC
Phase I studies
• PD-L1 +
• mDOR n.r.
• mPFS 1.9 months
• mOS 11.2 months
• PD-L1 +/-
• mDOR 21 (1L) and 19 months (2L+)
• mPFS 1.4 months
• mOS 8.9 months
Nanda R et al, J Clin Oncol 2016 Emens LA et al, Jama Oncol 2018
ORR%
OS according to response and treatment line (ATEZO)
Emens LA et al, Jama Oncol 2018; Schmid et al, AACR 2017
Phase I and II studies in advanced TNBC
JAVELIN Study
• Phase I
• Avelumab as single agent
• n=168 MBC pts
• PD-L1 +/-
• 1L-4L
• ORR 3% in overall population
• 58 TNBC pts
• 62% PD-L1 + (≥1% IC)
• ORR 5.2%
Phase I and II studies in advanced TNBC
KEYNOTE-086 study
Adams S et al, ASCO 2017; Adams S et al, AACR 2018
*
• Phase II
• 254 TNBC pts
• mOS 16.1 months (Cohort B)
• Rational for Immunotherapy in advanced Triple Negative Breast Cancer (TNBC)
• Single Agent anti-PD1/PD-L1Trials Biomarkers from single agent anti-PD1/PD-L1
• Combination Strategies Chemotherapy
PARP inhibitors
• Conclusion and Future Directions
Outline
19%
9%
TIL high1
Ob
jec
tive
Res
po
ns
e R
ate
(%
)
10%
20%
30%
0%
6.4%
1.9%
Pembrolizumab (Cohort A)
Atezolizumab
TIL low
39.1%
8.7%
TIL low TIL high
Pembrolizumab (Cohort B)
4%
1 ≥ IC 10%; 2</≥ Median (5% in Cohort A and 17.5% in Cohort B)
TIL high2
TIL low
TILs and Response to single agent therapy
Emens LA et al, Jama Oncol 2018; Adams S et al, ASCO 2017; Loi S et al, ESMO 2017
TIL positive patients present higher response rate
KEYNOTE-086 study
OS according to PD-L1 and TILs (ATEZO)
Emens LA et al, Jama Oncol 2018
12%
0%
PDL1- PDL1+*
Ob
jec
tive
Re
sp
on
se
Ra
te (
%)
10%
20%
30%
0%
5.7% 4.7%
Pembrolizumab (Cohort A)
Atezolizumab
*PD-L1+: baseline PD-L1 expression on ICs ≥ 1%
PDL1- PDL1+
Emens LA et al, Jama Oncol 2018; Adams S et al, ASCO 2017; Loi S et al, ESMO 2017
PD-L1 expression & Response to single
agent therapy
PD-L1 expression not good predictive of response
#PD-L1+: baseline combined positive score [PD-L1 expression on ICs or TCs ≥ 1%]
#
13%
18%
TMBlow TMBhigh
OR
R R
ate
(%
)
10%
20%
0%
8%
15%
BCRA- BRCA+
18%
13%
LOHlow LOHhigh
0 20 40 60 800
5
10
15
20
TILs (% tumor area)
TM
B (M
ut/M
b)
TMB vs TILs
r = 0.13
p = 0.24TMBHigh
TMBLow
<14% ≥14%0
10
20
30
40
50
Genomic Loss
of Hetezygosity
TIL
s (%
tu
mo
r a
rea
)
LOH and TILsns
0 5 10 150
5
10
15
20
TMB vs CD8
CD8 (% tumor center)
TM
B (M
ut/M
b)
r = 0.10
p = 0.38TMBHigh
TMBLow
<14% ≥14%0
2
4
6
8
10
Genomic Loss
of Hetezygosity
CD
8
(% o
f T
um
or
Ce
nte
r)
LOH and CD8
0 10 20 30 40 500
5
10
15
20
PDL1 IC (% tumor area)
TM
B (M
ut/M
b)
TMB vs PDL1 IC
r = 0.13
p = 0.24TMBHigh
TMBLow
<14% ≥14%0
10
20
30
40
50
Genomic Loss
of Hetezygosity
PD
-L1
IC (%
tu
mo
r a
rea
)
LOH and PDL1 ICns
0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
0
5
10
15
20
TMB (Mutations/Megabase)
Fre
qu
en
cy
(%
)Distribution of Mutations/Megabase
0 20 40 60 800
5
10
15
20
TILs (% tumor area)
TM
B (M
ut/M
b)
TMB vs TILs
r = 0.13
p = 0.24TMBHigh
TMBLow
<14% ≥14%0
10
20
30
40
50
Genomic Loss
of Hetezygosity
TIL
s (%
tu
mo
r a
rea
)
LOH and TILsns
0 5 10 150
5
10
15
20
TMB vs CD8
CD8 (% tumor center)
TM
B (M
ut/M
b)
r = 0.10
p = 0.38TMBHigh
TMBLow
<14% ≥14%0
2
4
6
8
10
Genomic Loss
of Hetezygosity
CD
8
(% o
f T
um
or
Ce
nte
r)
LOH and CD8
0 10 20 30 40 500
5
10
15
20
PDL1 IC (% tumor area)
TM
B (M
ut/M
b)
TMB vs PDL1 IC
r = 0.13
p = 0.24TMBHigh
TMBLow
<14% ≥14%0
10
20
30
40
50
Genomic Loss
of Hetezygosity
PD
-L1
IC (%
tu
mo
r a
rea
)
LOH and PDL1 ICns
TILs PDL1
Molinero L et al, SABCS 2017
Mutational load & Response to Atezolizumab
• Rational for Immunotherapy in advanced Triple Negative Breast Cancer (TNBC)
• Single Agent anti-PD1/PD-L1Trials Biomarkers from single agent anti- PD1/PD-L1
• Combination Strategies Chemotherapy
PARP inhibitors
• Conclusion and Future Directions
Outline
Chemotherapy as a trigger for immune activation
Modified from Curigliano G, ESMO 2018
Modified from Curigliano G, ESMO 2018
Chemotherapy and Immune System
Phase Ib, n=33
PD-L1 +/-
mFU 21.4 months
50% PD-L1 +
ORR 39%
mPFS 5.5 months
mOS 14.7 months
Nab-paclitaxel plus Atezolizumab
Pohlmann PR et al, AACR 2018; Adams J et al, JAMA Oncol 2018
OS
Eribulin plus Pembrolizumab
(ENHANCE study)
Phase Ib/II, n=107
PD-L1 +/-
ORR 26%
• ORR 1L 29.2%
• ORR 2L+ 22%
mPFS 4.2 months
mOS 17.7 months
Tolaney S et al, SABCS 2017
TONIC Trial
ORR
Phase II, n=66 Max 3 lines for MBC; 23% 1L 85% prior anthracyclines (operable); 58% prior platinum (metastatic) Induction Nivolumab The doxorubicin cohort as an «immune induction» will be expanded in the stage II of the trial.
Kok M et al, ASCO 2018
IMpassion130 study design
Statistical design
Baseline characteristics
PFS Analysis
Schmid P et al, ESMO 2018
OS Analysis
Schmid P et al, ESMO 2018
Secondary Efficacy Endpoints
Toxicity
PFS subgroup analysis: ITT population
• First Phase III trial demonstrated a benefit with first-line immunotherapy in advanced TNBC • Atezolizumab + Nab-paclitaxel resulted in statistically significant
PFS benefit in ITT (HR=0.80) and PD-L1+ population (HR=0.62)
• At the first interim analysis, OS improvement in PD-L1+ population (mOS 15.5 vs 25.0 months)
• No detrimental effect in PD-L1 negative sub-groups
• The combination was well tolerated
Open Question
• Nab-paclitaxel is the optimal chemo backbone? • Dose of Nab-paclitaxel?
• Formal OS testing in PD-L1+ pts not permitted according to study design
• Duration of atezolizumab (longer=better?)
• Role of Atezolizumab alone?
• BRCA status?
IMpassion130 Conclusions
• Rational for Immunotherapy in advanced Triple Negative Breast Cancer (TNBC)
• Single Agent anti-PD1/PD-L1Trials Biomarkers from single agent anti- PD1/PD-L1
• Combination Strategies Chemotherapy
PARP inhibitors
• Conclusion and Future Directions
Outline
Rationale for Parp + Checkpoint Inhibitors
Rationale for combining PARP inhibitors and immune checkpoint inhibitors
Jiao et al, Clin Cancer Res 2017
Accumulating DNA damage has the potential to modify tumor immunogenicity
Phase II Basket study gBRCAmut HER2 neg MBC (n=25)
MEDIOLA study
Domcheck et al, SABCS 2017
12/25 (48%) DCR at 7 months Median DOR/PFS/OS not yet reached Response independent of HR status and BRCA mutation type
TOPACIO: Niraparib + Pembrolizumab (n=46)
Presented By Kevin Kalinsky at 2018 ASCO Annual Meeting
ORR: 28% all; 60% tBRCAmut, 36% PD-L1+
• Rational for Immunotherapy in advanced Triple Negative Breast Cancer (TNBC)
• Single Agent anti-PD1/PD-L1Trials Biomarkers from single agent anti- PD1/PD-L1
• Combination Strategies Chemotherapy
PARP inhibitors
• Conclusion and Future Directions
Outline
Single-agent anti-PD-L1/PD1
• Durable response
• Better response in earlier lines of therapy
• Well tolerated
• Biomarkers not good predictive of response
Combination of CT and anti-PD-L1/PD1
• First promising results from combination IO + CT for 1st line PD-L1+ advanced TNBC (IMpassion130 study)
• Well tolerated
• Ongoing phase III in metastatic, neoadjuvant and adjuvant studies
Combination of PARPi and anti-PD-L1/PD1
• Further evaluation (small cohort with heterogenous population) and maturity of data in BRCAmut HER2- are needed
Conclusions-1
Biomarkers:
• Optimize patients selection
• Higher evidence for TILs than PD-L1 status as a predictive biomarker of response
• Advanced TNBC presents ‘low’ TILs levels
• Need to increase host anti-tumor immunity
• How to define and best to test PD-L1 positive population?
• Mutational load is not predictive of response
• MSI? MSI-H less than 2%
• Gut microbiome? Ongoing studies in BC
Conclusions-2
Title of the slide
Thank you for your attention