Avelumab first-line (1L) maintenance therapy in advanced urothelial carcinoma: Final analysis from a real-world study in the UK.

R Robert Jones Jones (School of Cancer Sciences, University of Glasgow, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom) Y Yatri Shah (Merck Serono, Feltham, United Kingdom) A Alison Jane Birtle (University of Manchester, Manchester, University of Lancashire and Lancashire Teaching Hospitals NHS Foundation Trust, Preston, United Kingdom) A Amarnath Challapalli (Bristol Cancer Institute, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, United Kingdom) J Joachim Chan (Clatterbridge Cancer Centre NHS Foundation Trust, Wirral, United Kingdom) D Deborah Enting A Andrew Hudson (Duke School of Medicine) M Mark David Linch (University College London (UCL) Hospital and UCL Cancer Institute, London, United Kingdom) S Sophie Otter (Royal Surrey County Hospital NHS Foundation Trust, Guildford, United Kingdom) A Andrew Protheroe (Oxford University Hospitals NHS Trust, Oxford, United Kingdom) A Anand Sharma R Rufus Turner (The Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom) B Bhagyalakshmi Chengat Prakashbabu (IQVIA, London, United Kingdom) W Wendy Rice (IQVIA Ltd, London, United Kingdom) E Elima Enaji Jedy-Agba (Institute of Human Virology, Abuja, Nigeria)

Abstract

723 Background: In the JAVELIN Bladder 100 phase 3 trial, avelumab 1L maintenance therapy plus best supportive care (BSC) significantly improved overall survival (OS) and progression-free survival (PFS) vs BSC alone in patients with locally advanced or metastatic urothelial carcinoma (la/mUC) that had not progressed with 1L platinum-based chemotherapy (PBC). In the UK, initial access to avelumab was provided via the Early Access to Medicines Scheme (EAMS) from September 2020. This study reports 24-month real-world outcomes in patients treated with avelumab 1L maintenance via the EAMS in the UK. Methods: Patients aged ≥18 years who had been diagnosed with la/mUC, demonstrated at least stable disease following 1L PBC, and initiated avelumab since October 2020 were recruited consecutively from 10 UK hospitals. Primary outcomes included real-world OS, real-world PFS, and treatment patterns by 24 months. Recruitment was completed in June 2022, and all patients had completed 24 months of follow-up from avelumab initiation by June 2024. Results: Of 106 patients recruited, 78 (73.6%) were male. Median age at diagnosis of la/mUC was 72 years. Primary tumor site was bladder in 40 (78%), and the most common metastatic sites were lymph node in 64 (60.4%), lung in 31 (33%), and bone in 20 (21.3%). ECOG performance status was 0 in 35 (33.0%),1 in 36 (34%), 2-4 in 5 (4.7%), and not recorded in 30 (28.3%). 1L PBC was carboplatin/gemcitabine in 55 (51.9%) and cisplatin/gemcitabine in 49 (46.2%). Response to 1L PBC was partial or complete response in 63 (60.0%). From avelumab initiation, median OS was 16.8 months (95% CI, 11.6-23.4) and median PFS was 8.7 months (95% CI, 7.1-14.2). Median OS from the start of 1L PBC in this population without disease progression after 1L PBC was 21.8 months (95% CI, 17.0-28.9). In subgroup analyses of patients who had received 1L carboplatin/gemcitabine or cisplatin/gemcitabine, median OS from avelumab initiation was 14.4 months (95% CI, 10.1-not estimable [NE]) and 21.4 months (95% CI, 15.4-NE), and median OS from start of 1L PBC was 19.5 months (95% CI, 14.8-NE) and 26.7 months (95% CI, 20.5-NE), respectively. Conclusions: These results provide evidence of the clinical effectiveness of avelumab 1L maintenance therapy in patients who were progression free following 1L PBC in a UK real-world setting. Median OS was shorter than previously observed in the JAVELIN Bladder 100 trial, which may be due to the worse ECOG performance status and higher proportion of patients who had received 1L carboplatin-based chemotherapy in this real-world population.

Article Details

Volume / Issue Vol. 43, Issue 5_suppl
Published February 10, 2025
Pages 723-723
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (15)

R

Robert Jones Jones

School of Cancer Sciences, University of Glasgow, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom

Y

Yatri Shah

Merck Serono, Feltham, United Kingdom

A

Alison Jane Birtle

University of Manchester, Manchester, University of Lancashire and Lancashire Teaching Hospitals NHS Foundation Trust, Preston, United Kingdom

A

Amarnath Challapalli

Bristol Cancer Institute, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, United Kingdom

J

Joachim Chan

Clatterbridge Cancer Centre NHS Foundation Trust, Wirral, United Kingdom

D

Deborah Enting

A

Andrew Hudson

Duke School of Medicine

M

Mark David Linch

University College London (UCL) Hospital and UCL Cancer Institute, London, United Kingdom

S

Sophie Otter

Royal Surrey County Hospital NHS Foundation Trust, Guildford, United Kingdom

A

Andrew Protheroe

Oxford University Hospitals NHS Trust, Oxford, United Kingdom

A

Anand Sharma

R

Rufus Turner

The Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom

B

Bhagyalakshmi Chengat Prakashbabu

IQVIA, London, United Kingdom

W

Wendy Rice

IQVIA Ltd, London, United Kingdom

E

Elima Enaji Jedy-Agba

Institute of Human Virology, Abuja, Nigeria