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Should we give maintenance therapy in
NSCLC?
Factors influencing the decision
• Patient preference
• Risk of progression
– Response to front-line chemotherapy
– EGFR status
• Performance status
• Age
Maintenance therapy paradigm
First-line platinum-based chemotherapy x 4-6 cycles
No Progression-PS 0-1
In favor of therapyRefuse of any therapy
Prevent PS
deterioration: strict
FU (q 4-6 weeks)
Maintenance therapy
Maintenenance therapy more effective in
NSCLC with high risk of progression
OSprobability
1.0
0.8
0.6
0.4
0.2
0
0 3 6 9 12 15 18 21 24 27 30 33 36
Time (months)
9.6 11.9
1.0
0.8
0.6
0.4
0.2
0
0 3 6 9 12 15 18 21 24 27 30 33 36
Time (months)
12.0 12.5
Log-rank p=0.0019
HR=0.72 (0.59–0.89)
Erlotinib (n=252)
Placebo (n=235)
Log-rank p=0.6181
HR=0.94 (0.74–1.20)
Erlotinib (n=184)
Placebo (n=210)
SD CR/PR
*OS is measured from time of randomisation into the maintenance phase
SATURN: OS according to EGFR
mutation status
0 3 6 9 12 15 18 21 24 27 30 33 36
OSprobability
1.0
0.8
0.6
0.4
0.2
0
Time (months)
0 3 6 9 12 15 18 21 24 27 30 33 36
1.0
0.8
0.6
0.4
0.2
0
Time (months)
EGFR mutation+ EGFR wild-type
Log-rank p=0.6810
HR=0.83 (0.34–2.02)
Erlotinib (n=199)
Placebo (n=189)
Erlotinib (n=22)
Placebo (n=27)*
Log-rank p=0.0243
HR=0.77 (0.61–0.97)
*Note that 67% of patients with EGFR mutation+
disease in the placebo arm received a second-line
EGFR TKI
Maintenance treatment of
Gemcitabine +BSC vs. BSC
Gemcitabine +
Carboplatin X
4 cycles
R
A
N
D
O
M
I
Z
E
Gemcitabine q 21
days + BSC
N= 128
BSC
N= 127
CR, PR
SD
Off study
PD
Randomization factors:
• PS status
• Stage
• Best tumour repsonse
Primary Endpoint OS
Belani et al, ASCO 2010
~60% of PS2 Patients
Lack of survival benefit with maintenance
gemcitabine in PS 2 patients
Overall Survival (months)
0 6 12 18 24 30 36 42 48 54 60
1.0
0.9
0.8
0.7
0.6
0.5
0.4
0.3
0.2
0.1
0.0
Gemcitabine 8.0 mos.
BSC 9.3 mos.
HR=0.97 (95% CI:0.72, 1.30)
P =0.838
Maintenance Chemotherapy – OS:
Curves Separate Early and Come Together
by 20 Months
0.8
1
0.6
0.4
0.2
0
Placebo: 10.18 mos
(95% CI: 8.57-13.17)
Pemetrexed: 13.01 mos
(95% CI: 11.40-14.42)
0.8
1
0.6
0.4
0.2
0
Months 55% censored
OS HR = 0.798
(95% CI: 0.63-1.01)
0 3 6 9 12 15 18 21 24 27 30 0 4 8 12 16 20 24 28 32 36 40 44 48 52
Probability
Immediate
D
(N = 153)
Delayed D
(N = 156)
Median OS,
months
(95% CI)
12.3 9.7
12-month survival,
% (95% CI)
51.1% 43.5
Months
Pemetrexed vs. Placebo Docetaxel vs. Placebo
Ciuleanu T et al. The Lancet 2009;374(9699):1432-1440. Fidias PM, et al. J Clin Oncol. 2009;27(4):591-598.
Probability
Pemetrexed
Placebo
Immediate Docetaxel
Delayed Docetaxel
Maintenance Erlotinib – SATURN OS:
Curves Separate Late and Stay Separated for
Many Months
1.0
0.8
0.6
0.4
0.2
0
6 12 18 24 30 33 363 9 15 21 270
Erlotinib (N = 438)
Placebo (N = 451)
Months
HR = 0.81 (95% CI: 0.70-0.95);
Log-rank p = 0.0088
Probability

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That's cool - F. Cappuzzo 25 settembre 2010

  • 1. Should we give maintenance therapy in NSCLC? Factors influencing the decision • Patient preference • Risk of progression – Response to front-line chemotherapy – EGFR status • Performance status • Age
  • 2. Maintenance therapy paradigm First-line platinum-based chemotherapy x 4-6 cycles No Progression-PS 0-1 In favor of therapyRefuse of any therapy Prevent PS deterioration: strict FU (q 4-6 weeks) Maintenance therapy
  • 3. Maintenenance therapy more effective in NSCLC with high risk of progression OSprobability 1.0 0.8 0.6 0.4 0.2 0 0 3 6 9 12 15 18 21 24 27 30 33 36 Time (months) 9.6 11.9 1.0 0.8 0.6 0.4 0.2 0 0 3 6 9 12 15 18 21 24 27 30 33 36 Time (months) 12.0 12.5 Log-rank p=0.0019 HR=0.72 (0.59–0.89) Erlotinib (n=252) Placebo (n=235) Log-rank p=0.6181 HR=0.94 (0.74–1.20) Erlotinib (n=184) Placebo (n=210) SD CR/PR *OS is measured from time of randomisation into the maintenance phase
  • 4. SATURN: OS according to EGFR mutation status 0 3 6 9 12 15 18 21 24 27 30 33 36 OSprobability 1.0 0.8 0.6 0.4 0.2 0 Time (months) 0 3 6 9 12 15 18 21 24 27 30 33 36 1.0 0.8 0.6 0.4 0.2 0 Time (months) EGFR mutation+ EGFR wild-type Log-rank p=0.6810 HR=0.83 (0.34–2.02) Erlotinib (n=199) Placebo (n=189) Erlotinib (n=22) Placebo (n=27)* Log-rank p=0.0243 HR=0.77 (0.61–0.97) *Note that 67% of patients with EGFR mutation+ disease in the placebo arm received a second-line EGFR TKI
  • 5. Maintenance treatment of Gemcitabine +BSC vs. BSC Gemcitabine + Carboplatin X 4 cycles R A N D O M I Z E Gemcitabine q 21 days + BSC N= 128 BSC N= 127 CR, PR SD Off study PD Randomization factors: • PS status • Stage • Best tumour repsonse Primary Endpoint OS Belani et al, ASCO 2010 ~60% of PS2 Patients
  • 6. Lack of survival benefit with maintenance gemcitabine in PS 2 patients Overall Survival (months) 0 6 12 18 24 30 36 42 48 54 60 1.0 0.9 0.8 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0.0 Gemcitabine 8.0 mos. BSC 9.3 mos. HR=0.97 (95% CI:0.72, 1.30) P =0.838
  • 7. Maintenance Chemotherapy – OS: Curves Separate Early and Come Together by 20 Months 0.8 1 0.6 0.4 0.2 0 Placebo: 10.18 mos (95% CI: 8.57-13.17) Pemetrexed: 13.01 mos (95% CI: 11.40-14.42) 0.8 1 0.6 0.4 0.2 0 Months 55% censored OS HR = 0.798 (95% CI: 0.63-1.01) 0 3 6 9 12 15 18 21 24 27 30 0 4 8 12 16 20 24 28 32 36 40 44 48 52 Probability Immediate D (N = 153) Delayed D (N = 156) Median OS, months (95% CI) 12.3 9.7 12-month survival, % (95% CI) 51.1% 43.5 Months Pemetrexed vs. Placebo Docetaxel vs. Placebo Ciuleanu T et al. The Lancet 2009;374(9699):1432-1440. Fidias PM, et al. J Clin Oncol. 2009;27(4):591-598. Probability Pemetrexed Placebo Immediate Docetaxel Delayed Docetaxel
  • 8. Maintenance Erlotinib – SATURN OS: Curves Separate Late and Stay Separated for Many Months 1.0 0.8 0.6 0.4 0.2 0 6 12 18 24 30 33 363 9 15 21 270 Erlotinib (N = 438) Placebo (N = 451) Months HR = 0.81 (95% CI: 0.70-0.95); Log-rank p = 0.0088 Probability

Notas del editor

  1. Key Eligibility Criteria Stage IIB (wuth pleural effusion and or positive spravclavicular nodes or stage IV Age greater than or equal to 18 ECOG PS 0-2 Adequate renal, hepatic and bone marrow function Asymptomatic or treated and controlled brain mets were allowed Presence of measurable disease No prior chemotherapy
  2. Early docetaxel significantly prolonged PFS; OS was slightly longer in the immediate docetaxel arm but the prolongation was not significant (p=0.07) Pemetrexed significantly prolonged PFS (HR = 0.6) and OS (HR = 0.79) but not in squamous tumors For both chemo agents, PFS benefit occurs early and is less impressive at later time points