TY - JOUR
T1 - A phase II study of monalizumab in patients with recurrent/metastatic squamous cell carcinoma of the head and neck
T2 - The I1 cohort of the EORTC-HNCG-1559 UPSTREAM trial
AU - Galot, Rachel
AU - Le Tourneau, Christophe
AU - Saada-Bouzid, Esma
AU - Daste, Amaury
AU - Even, Caroline
AU - Debruyne, Philip
AU - Henry, Stéphanie
AU - Zanetta, Sylvie
AU - Rutten, Anemie
AU - Licitra, Lisa
AU - Canon, Jean Luc
AU - Kaminsky, Marie Christine
AU - Specenier, Pol
AU - Rottey, Sylvie
AU - Guigay, Joël
AU - Kong, Anthony
AU - Tinhofer, Inge
AU - Borcoman, Edith
AU - Dirix, Lieve
AU - Raveloarivahy, Tiana
AU - Fortpied, Catherine
AU - Vanlancker, Maureen
AU - Morfouace, Marie
AU - Govaerts, Anne Sophie
AU - Machiels, Jean Pascal
N1 - Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/11/1
Y1 - 2021/11/1
N2 - Purpose: Monalizumab is a monoclonal antibody targeting the inhibitory natural killer group 2A (NKG2A) receptor localised on natural killer (NK) and T cells. Its ligand, the human leukocyte antigen E (HLA-E), is overexpressed in squamous cell carcinoma of the head and neck (SCCHN). By targeting the HLA-E-NKG2A pathway, monalizumab may enhance NK and T cell activity. Experimental design: The UPSTREAM trial is a biomarker-driven umbrella trial studying targeted therapies and immunotherapies in patients with recurrent/metastatic (R/M) SCCHN progressing after platinum therapy. The immunotherapy 1 (I1) cohort was a phase II, single-arm substudy evaluating monalizumab (10 mg/kg intravenously on day 1 of a 14-day cycle). The primary end-point was the objective response (OR) rate (Response Evaluation Criteria in Solid Tumours 1.1) over the first 16 weeks. A two-stage Simon design was used (H1 15%, H0 3%, α 8%, power 90%) with pre-planned interruption of accrual if no OR was observed after the first 25 patients. Results: Twenty-six eligible patients were enrolled. Seventeen (65%) patients had received ≥2 previous lines of systemic treatment, and 15 (58%) patients were PD(-L)1 inhibitor pretreated. No OR was observed. Stable disease was observed in 6 patients (23%) with a median duration of 3.8 months (95% confidence interval [CI]: 2.7–NE). The median progression-free survival and overall survival were 1.7 months (95% CI: 1.5–1.8) and 6.7 months (95% CI: 3.0–9.6), respectively. The most frequent treatment-related adverse event was grade I/II fatigue (19%). Conclusions: Monalizumab monotherapy has limited activity in R/M SCCHN. The I1 cohort did not meet its primary objective. Monalizumab combined with durvalumab is under investigation within UPSTREAM.
AB - Purpose: Monalizumab is a monoclonal antibody targeting the inhibitory natural killer group 2A (NKG2A) receptor localised on natural killer (NK) and T cells. Its ligand, the human leukocyte antigen E (HLA-E), is overexpressed in squamous cell carcinoma of the head and neck (SCCHN). By targeting the HLA-E-NKG2A pathway, monalizumab may enhance NK and T cell activity. Experimental design: The UPSTREAM trial is a biomarker-driven umbrella trial studying targeted therapies and immunotherapies in patients with recurrent/metastatic (R/M) SCCHN progressing after platinum therapy. The immunotherapy 1 (I1) cohort was a phase II, single-arm substudy evaluating monalizumab (10 mg/kg intravenously on day 1 of a 14-day cycle). The primary end-point was the objective response (OR) rate (Response Evaluation Criteria in Solid Tumours 1.1) over the first 16 weeks. A two-stage Simon design was used (H1 15%, H0 3%, α 8%, power 90%) with pre-planned interruption of accrual if no OR was observed after the first 25 patients. Results: Twenty-six eligible patients were enrolled. Seventeen (65%) patients had received ≥2 previous lines of systemic treatment, and 15 (58%) patients were PD(-L)1 inhibitor pretreated. No OR was observed. Stable disease was observed in 6 patients (23%) with a median duration of 3.8 months (95% confidence interval [CI]: 2.7–NE). The median progression-free survival and overall survival were 1.7 months (95% CI: 1.5–1.8) and 6.7 months (95% CI: 3.0–9.6), respectively. The most frequent treatment-related adverse event was grade I/II fatigue (19%). Conclusions: Monalizumab monotherapy has limited activity in R/M SCCHN. The I1 cohort did not meet its primary objective. Monalizumab combined with durvalumab is under investigation within UPSTREAM.
KW - Immunotherapy
KW - NKG2A
KW - Precision medicine
KW - Squamous cell carcinoma of the head and neck
KW - Umbrella trial
UR - http://www.scopus.com/inward/record.url?scp=85116942347&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2021.09.003
DO - 10.1016/j.ejca.2021.09.003
M3 - Article
C2 - 34638090
AN - SCOPUS:85116942347
SN - 0959-8049
VL - 158
SP - 17
EP - 26
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -