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A phase II open-label trial of avelumab plus axitinib in previously treated non-small-cell lung cancer or treatment-naïve, cisplatin-ineligible urothelial cancer

BACKGROUND: We hypothesized that avelumab plus axitinib could improve clinical outcomes in patients with advanced non-small-cell lung cancer (NSCLC) or urothelial carcinoma (UC). PATIENTS AND METHODS: We enrolled previously treated patients with advanced or metastatic NSCLC, or untreated, cisplatin-...

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Autores principales: Galffy, G., Lugowska, I., Poddubskaya, E.V., Cho, B.C., Ahn, M.-J., Han, J.-Y., Su, W.-C., Hauke, R.J., Dyar, S.H., Lee, D.H., Serwatowski, P., Estelles, D.L., Holden, V.R., Kim, Y.J., Vladimirov, V., Horvath, Z., Ghose, A., Goldman, A., di Pietro, A., Wang, J., Murphy, D.A., Alhadab, A., Laskov, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265612/
https://www.ncbi.nlm.nih.gov/pubmed/37141847
http://dx.doi.org/10.1016/j.esmoop.2023.101173
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author Galffy, G.
Lugowska, I.
Poddubskaya, E.V.
Cho, B.C.
Ahn, M.-J.
Han, J.-Y.
Su, W.-C.
Hauke, R.J.
Dyar, S.H.
Lee, D.H.
Serwatowski, P.
Estelles, D.L.
Holden, V.R.
Kim, Y.J.
Vladimirov, V.
Horvath, Z.
Ghose, A.
Goldman, A.
di Pietro, A.
Wang, J.
Murphy, D.A.
Alhadab, A.
Laskov, M.
author_facet Galffy, G.
Lugowska, I.
Poddubskaya, E.V.
Cho, B.C.
Ahn, M.-J.
Han, J.-Y.
Su, W.-C.
Hauke, R.J.
Dyar, S.H.
Lee, D.H.
Serwatowski, P.
Estelles, D.L.
Holden, V.R.
Kim, Y.J.
Vladimirov, V.
Horvath, Z.
Ghose, A.
Goldman, A.
di Pietro, A.
Wang, J.
Murphy, D.A.
Alhadab, A.
Laskov, M.
author_sort Galffy, G.
collection PubMed
description BACKGROUND: We hypothesized that avelumab plus axitinib could improve clinical outcomes in patients with advanced non-small-cell lung cancer (NSCLC) or urothelial carcinoma (UC). PATIENTS AND METHODS: We enrolled previously treated patients with advanced or metastatic NSCLC, or untreated, cisplatin-ineligible patients with advanced or metastatic UC. Patients received avelumab 800 mg every 2 weeks (Q2W) and axitinib 5 mg orally two times daily. The primary endpoint was objective response rate (ORR). Immunohistochemistry was used to assess programmed death-ligand 1 (PD-L1) expression (SP263 assay) and the presence of CD8+ T cells (clone C8/144B). Tumor mutational burden (TMB) was assessed by whole-exome sequencing. RESULTS: A total of 61 patients were enrolled and treated (NSCLC, n = 41; UC, n = 20); 5 remained on treatment at data cut-off (26 February 2021). The confirmed ORR was 31.7% in the NSCLC cohort and 10.0% in the UC cohort (all partial responses). Antitumor activity was observed irrespective of PD-L1 expression. In exploratory subgroups, ORRs were higher in patients with higher (≥median) CD8+ T cells in the tumor. ORRs were higher in patients with lower TMB (<median) in the NSCLC cohort and higher TMB (≥median) in the UC cohort. Treatment-related adverse events (TRAEs) occurred in 93.4% of patients, including grade ≥3 TRAEs in 55.7%. Avelumab exposures with 800 mg Q2W dosing were similar to those observed with 10 mg/kg Q2W dosing. CONCLUSIONS: In previously treated patients with advanced/metastatic NSCLC, ORR appeared to be superior to anti-PD-L1 or anti-programmed cell death protein 1 monotherapy, irrespective of PD-L1 status, whereas in untreated, cisplatin-ineligible patients with advanced/metastatic UC, ORR was lower than expected, potentially limited by small patient numbers. TRIAL REGISTRATION: Clinicaltrial.gov NCT03472560; https://clinicaltrials.gov/ct2/show/NCT03472560
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spelling pubmed-102656122023-06-15 A phase II open-label trial of avelumab plus axitinib in previously treated non-small-cell lung cancer or treatment-naïve, cisplatin-ineligible urothelial cancer Galffy, G. Lugowska, I. Poddubskaya, E.V. Cho, B.C. Ahn, M.-J. Han, J.-Y. Su, W.-C. Hauke, R.J. Dyar, S.H. Lee, D.H. Serwatowski, P. Estelles, D.L. Holden, V.R. Kim, Y.J. Vladimirov, V. Horvath, Z. Ghose, A. Goldman, A. di Pietro, A. Wang, J. Murphy, D.A. Alhadab, A. Laskov, M. ESMO Open Original Research BACKGROUND: We hypothesized that avelumab plus axitinib could improve clinical outcomes in patients with advanced non-small-cell lung cancer (NSCLC) or urothelial carcinoma (UC). PATIENTS AND METHODS: We enrolled previously treated patients with advanced or metastatic NSCLC, or untreated, cisplatin-ineligible patients with advanced or metastatic UC. Patients received avelumab 800 mg every 2 weeks (Q2W) and axitinib 5 mg orally two times daily. The primary endpoint was objective response rate (ORR). Immunohistochemistry was used to assess programmed death-ligand 1 (PD-L1) expression (SP263 assay) and the presence of CD8+ T cells (clone C8/144B). Tumor mutational burden (TMB) was assessed by whole-exome sequencing. RESULTS: A total of 61 patients were enrolled and treated (NSCLC, n = 41; UC, n = 20); 5 remained on treatment at data cut-off (26 February 2021). The confirmed ORR was 31.7% in the NSCLC cohort and 10.0% in the UC cohort (all partial responses). Antitumor activity was observed irrespective of PD-L1 expression. In exploratory subgroups, ORRs were higher in patients with higher (≥median) CD8+ T cells in the tumor. ORRs were higher in patients with lower TMB (<median) in the NSCLC cohort and higher TMB (≥median) in the UC cohort. Treatment-related adverse events (TRAEs) occurred in 93.4% of patients, including grade ≥3 TRAEs in 55.7%. Avelumab exposures with 800 mg Q2W dosing were similar to those observed with 10 mg/kg Q2W dosing. CONCLUSIONS: In previously treated patients with advanced/metastatic NSCLC, ORR appeared to be superior to anti-PD-L1 or anti-programmed cell death protein 1 monotherapy, irrespective of PD-L1 status, whereas in untreated, cisplatin-ineligible patients with advanced/metastatic UC, ORR was lower than expected, potentially limited by small patient numbers. TRIAL REGISTRATION: Clinicaltrial.gov NCT03472560; https://clinicaltrials.gov/ct2/show/NCT03472560 Elsevier 2023-05-02 /pmc/articles/PMC10265612/ /pubmed/37141847 http://dx.doi.org/10.1016/j.esmoop.2023.101173 Text en © 2023 Published by Elsevier Ltd on behalf of European Society for Medical Oncology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Galffy, G.
Lugowska, I.
Poddubskaya, E.V.
Cho, B.C.
Ahn, M.-J.
Han, J.-Y.
Su, W.-C.
Hauke, R.J.
Dyar, S.H.
Lee, D.H.
Serwatowski, P.
Estelles, D.L.
Holden, V.R.
Kim, Y.J.
Vladimirov, V.
Horvath, Z.
Ghose, A.
Goldman, A.
di Pietro, A.
Wang, J.
Murphy, D.A.
Alhadab, A.
Laskov, M.
A phase II open-label trial of avelumab plus axitinib in previously treated non-small-cell lung cancer or treatment-naïve, cisplatin-ineligible urothelial cancer
title A phase II open-label trial of avelumab plus axitinib in previously treated non-small-cell lung cancer or treatment-naïve, cisplatin-ineligible urothelial cancer
title_full A phase II open-label trial of avelumab plus axitinib in previously treated non-small-cell lung cancer or treatment-naïve, cisplatin-ineligible urothelial cancer
title_fullStr A phase II open-label trial of avelumab plus axitinib in previously treated non-small-cell lung cancer or treatment-naïve, cisplatin-ineligible urothelial cancer
title_full_unstemmed A phase II open-label trial of avelumab plus axitinib in previously treated non-small-cell lung cancer or treatment-naïve, cisplatin-ineligible urothelial cancer
title_short A phase II open-label trial of avelumab plus axitinib in previously treated non-small-cell lung cancer or treatment-naïve, cisplatin-ineligible urothelial cancer
title_sort phase ii open-label trial of avelumab plus axitinib in previously treated non-small-cell lung cancer or treatment-naïve, cisplatin-ineligible urothelial cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265612/
https://www.ncbi.nlm.nih.gov/pubmed/37141847
http://dx.doi.org/10.1016/j.esmoop.2023.101173
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