TY - JOUR
T1 - Consolidation nivolumab and ipilimumab versus observation in limited-disease small-cell lung cancer after chemo-radiotherapy – results from the randomised phase II ETOP/IFCT 4-12 STIMULI trial
AU - ETOP/IFCT 4-12 STIMULI Collaborators
AU - Peters, S.
AU - Pujol, J. L.
AU - Dafni, U.
AU - Dómine, M.
AU - Popat, S.
AU - Reck, M.
AU - Andrade, J.
AU - Becker, A.
AU - Moro-Sibilot, D.
AU - Curioni-Fontecedro, A.
AU - Molinier, O.
AU - Nackaerts, K.
AU - Insa Mollá, A.
AU - Gervais, R.
AU - López Vivanco, G.
AU - Madelaine, J.
AU - Mazieres, J.
AU - Faehling, M.
AU - Griesinger, F.
AU - Majem, M.
AU - González Larriba, J. L.
AU - Provencio Pulla, M.
AU - Vervita, K.
AU - Roschitzki-Voser, H.
AU - Ruepp, B.
AU - Mitchell, P.
AU - Stahel, R. A.
AU - Le Pechoux, C.
AU - De Ruysscher, D.
AU - Hiltbrunner, A.
AU - Pardo-Contreras, M.
AU - Gasca-Ruchti, A.
AU - Giacomelli, N.
AU - Kammler, R.
AU - Marti, N.
AU - Pfister, R.
AU - Piguet, A. C.
AU - Roux, S.
AU - Troesch, S.
AU - Schneider, M.
AU - Schweri, R.
AU - Zigomo, I.
AU - Tsourti, Z.
AU - Zygoura, P.
AU - Tsouprou, S.
AU - Kassapian, M.
AU - Dimopoulou, G.
AU - Andriakopoulou, C.
AU - Barlesi, F.
AU - Aix, S. P.
N1 - Publisher Copyright:
© 2021 European Society for Medical Oncology
PY - 2022/1/1
Y1 - 2022/1/1
N2 - Background: Concurrent chemotherapy and thoracic radiotherapy followed by prophylactic cranial irradiation (PCI) is the standard treatment in limited-disease small-cell lung cancer (LD-SCLC), with 5-year overall survival (OS) of only 25% to 33%. Patients and methods: STIMULI is a 1:1 randomised phase II trial aiming to demonstrate superiority of consolidation combination immunotherapy versus observation after chemo-radiotherapy plus PCI (protocol amendment-1). Consolidation immunotherapy consisted of four cycles of nivolumab [1 mg/kg, every three weeks (Q3W)] plus ipilimumab (3 mg/kg, Q3W), followed by nivolumab monotherapy (240 mg, Q2W) for up to 12 months. Patient recruitment closed prematurely due to slow accrual and the statistical analyses plan was updated to address progression-free survival (PFS) as the only primary endpoint. Results: Of the 222 patients enrolled, 153 were randomised (78: experimental; 75: observation). Among the randomised patients, median age was 62 years, 60% males, 34%/65% current/former smokers, 31%/66% performance status (PS) 0/1. Up to 25 May 2020 (median follow-up 22.4 months), 40 PFS events were observed in the experimental arm, with median PFS 10.7 months [95% confidence interval (CI) 7.0-not estimable (NE)] versus 42 events and median 14.5 months (8.2-NE) in the observation, hazard ratio (HR) = 1.02 (0.66-1.58), two-sided P = 0.93. With updated follow-up (03 June 2021; median: 35 months), median OS was not reached in the experimental arm, while it was 32.1 months (26.1-NE) in observation, with HR = 0.95 (0.59-1.52), P = 0.82. In the experimental arm, median time-to-treatment-discontinuation was only 1.7 months. CTCAE v4 grade ≥3 adverse events were experienced by 62% of patients in the experimental and 25% in the observation arm, with 4 and 1 fatal, respectively. Conclusions: The STIMULI trial did not meet its primary endpoint of improving PFS with nivolumab-ipilimumab consolidation after chemo-radiotherapy in LD-SCLC. A short period on active treatment related to toxicity and treatment discontinuation likely affected the efficacy results.
AB - Background: Concurrent chemotherapy and thoracic radiotherapy followed by prophylactic cranial irradiation (PCI) is the standard treatment in limited-disease small-cell lung cancer (LD-SCLC), with 5-year overall survival (OS) of only 25% to 33%. Patients and methods: STIMULI is a 1:1 randomised phase II trial aiming to demonstrate superiority of consolidation combination immunotherapy versus observation after chemo-radiotherapy plus PCI (protocol amendment-1). Consolidation immunotherapy consisted of four cycles of nivolumab [1 mg/kg, every three weeks (Q3W)] plus ipilimumab (3 mg/kg, Q3W), followed by nivolumab monotherapy (240 mg, Q2W) for up to 12 months. Patient recruitment closed prematurely due to slow accrual and the statistical analyses plan was updated to address progression-free survival (PFS) as the only primary endpoint. Results: Of the 222 patients enrolled, 153 were randomised (78: experimental; 75: observation). Among the randomised patients, median age was 62 years, 60% males, 34%/65% current/former smokers, 31%/66% performance status (PS) 0/1. Up to 25 May 2020 (median follow-up 22.4 months), 40 PFS events were observed in the experimental arm, with median PFS 10.7 months [95% confidence interval (CI) 7.0-not estimable (NE)] versus 42 events and median 14.5 months (8.2-NE) in the observation, hazard ratio (HR) = 1.02 (0.66-1.58), two-sided P = 0.93. With updated follow-up (03 June 2021; median: 35 months), median OS was not reached in the experimental arm, while it was 32.1 months (26.1-NE) in observation, with HR = 0.95 (0.59-1.52), P = 0.82. In the experimental arm, median time-to-treatment-discontinuation was only 1.7 months. CTCAE v4 grade ≥3 adverse events were experienced by 62% of patients in the experimental and 25% in the observation arm, with 4 and 1 fatal, respectively. Conclusions: The STIMULI trial did not meet its primary endpoint of improving PFS with nivolumab-ipilimumab consolidation after chemo-radiotherapy in LD-SCLC. A short period on active treatment related to toxicity and treatment discontinuation likely affected the efficacy results.
KW - SCLC
KW - ipilimumab
KW - limited disease
KW - nivolumab
KW - randomised clinical trial
KW - small-cell lung cancer
UR - http://www.scopus.com/inward/record.url?scp=85118330783&partnerID=8YFLogxK
U2 - 10.1016/j.annonc.2021.09.011
DO - 10.1016/j.annonc.2021.09.011
M3 - Article
C2 - 34562610
AN - SCOPUS:85118330783
SN - 0923-7534
VL - 33
SP - 67
EP - 79
JO - Annals of Oncology
JF - Annals of Oncology
IS - 1
ER -