Cargando…

PemBla: A Phase 1 study of intravesical pembrolizumab in recurrent non‐muscle‐invasive bladder cancer

OBJECTIVES: This study aimed to investigate the anti‐PD‐1 inhibitor pembrolizumab as a potential agent for use in non‐muscle‐invasive bladder cancer (NMIBC) by conducting a Phase 1 safety run‐in study to assess the safety and tolerability of intravesical pembrolizumab after transurethral resection o...

Descripción completa

Detalles Bibliográficos
Autores principales: Woodcock, Victoria K., Chen, Ji‐Li, Purshouse, Karin, Butcher, Chrissie, Collins, Linda, Haddon, Caroline, Verrall, Gillian, Elhussein, Leena, Roberts, Corran, Tarlton, Andrea, Rei, Margarida, Napolitani, Giorgio, Salio, Mariolina, Middleton, Mark R., Cerundolo, Vincenzo, Crew, Jeremy, Protheroe, Andrew S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071078/
https://www.ncbi.nlm.nih.gov/pubmed/37025470
http://dx.doi.org/10.1002/bco2.220
_version_ 1785019124366180352
author Woodcock, Victoria K.
Chen, Ji‐Li
Purshouse, Karin
Butcher, Chrissie
Collins, Linda
Haddon, Caroline
Verrall, Gillian
Elhussein, Leena
Roberts, Corran
Tarlton, Andrea
Rei, Margarida
Napolitani, Giorgio
Salio, Mariolina
Middleton, Mark R.
Cerundolo, Vincenzo
Crew, Jeremy
Protheroe, Andrew S.
author_facet Woodcock, Victoria K.
Chen, Ji‐Li
Purshouse, Karin
Butcher, Chrissie
Collins, Linda
Haddon, Caroline
Verrall, Gillian
Elhussein, Leena
Roberts, Corran
Tarlton, Andrea
Rei, Margarida
Napolitani, Giorgio
Salio, Mariolina
Middleton, Mark R.
Cerundolo, Vincenzo
Crew, Jeremy
Protheroe, Andrew S.
author_sort Woodcock, Victoria K.
collection PubMed
description OBJECTIVES: This study aimed to investigate the anti‐PD‐1 inhibitor pembrolizumab as a potential agent for use in non‐muscle‐invasive bladder cancer (NMIBC) by conducting a Phase 1 safety run‐in study to assess the safety and tolerability of intravesical pembrolizumab after transurethral resection of the bladder tumour (TURBT). PATIENTS AND METHODS: Eligible patients had recurrent NMIBC for which adjuvant treatment post TURBT was a reasonable treatment option, Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0–1 and adequate end‐organ function. Pembrolizumab was administered by intravesical instillation once weekly for a total of six doses. Intra‐patient dose escalation was performed in three paired patient cohorts with doses starting at 50 mg and increasing through 100 mg to a maximum of 200 mg. Adverse events (AEs) were assessed using Common Terminology Criteria for Adverse Events (CTCAE) v4.03 with dose limiting toxicity (DLT) defined as a clinically significant, drug‐related, Grade 4 haematological or Grade 3 or higher non‐haematological toxicity occurring within 7 days of administration of the first treatment at a given dose for that patient. RESULTS: Six patients were treated with no DLTs seen during dose escalation. Drug‐related AEs were of low grade and included dysuria and fatigue. All patients completed six doses of treatment as planned. Pharmacokinetic and pharmacodynamic assays did not detect any pembrolizumab in the serum following repeated intravesical administration, and no changes in peripheral immune cell populations were observed. CONCLUSIONS: Administration of intravesical pembrolizumab was well tolerated and did not raise any safety concerns in patients with NMIBC following TURBT. There was no evidence of systemic absorption or systemic immune effects following intravesical administration. Further studies are required to assess whether intravesical administration has anti‐tumour activity.
format Online
Article
Text
id pubmed-10071078
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-100710782023-04-05 PemBla: A Phase 1 study of intravesical pembrolizumab in recurrent non‐muscle‐invasive bladder cancer Woodcock, Victoria K. Chen, Ji‐Li Purshouse, Karin Butcher, Chrissie Collins, Linda Haddon, Caroline Verrall, Gillian Elhussein, Leena Roberts, Corran Tarlton, Andrea Rei, Margarida Napolitani, Giorgio Salio, Mariolina Middleton, Mark R. Cerundolo, Vincenzo Crew, Jeremy Protheroe, Andrew S. BJUI Compass Original Articles OBJECTIVES: This study aimed to investigate the anti‐PD‐1 inhibitor pembrolizumab as a potential agent for use in non‐muscle‐invasive bladder cancer (NMIBC) by conducting a Phase 1 safety run‐in study to assess the safety and tolerability of intravesical pembrolizumab after transurethral resection of the bladder tumour (TURBT). PATIENTS AND METHODS: Eligible patients had recurrent NMIBC for which adjuvant treatment post TURBT was a reasonable treatment option, Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0–1 and adequate end‐organ function. Pembrolizumab was administered by intravesical instillation once weekly for a total of six doses. Intra‐patient dose escalation was performed in three paired patient cohorts with doses starting at 50 mg and increasing through 100 mg to a maximum of 200 mg. Adverse events (AEs) were assessed using Common Terminology Criteria for Adverse Events (CTCAE) v4.03 with dose limiting toxicity (DLT) defined as a clinically significant, drug‐related, Grade 4 haematological or Grade 3 or higher non‐haematological toxicity occurring within 7 days of administration of the first treatment at a given dose for that patient. RESULTS: Six patients were treated with no DLTs seen during dose escalation. Drug‐related AEs were of low grade and included dysuria and fatigue. All patients completed six doses of treatment as planned. Pharmacokinetic and pharmacodynamic assays did not detect any pembrolizumab in the serum following repeated intravesical administration, and no changes in peripheral immune cell populations were observed. CONCLUSIONS: Administration of intravesical pembrolizumab was well tolerated and did not raise any safety concerns in patients with NMIBC following TURBT. There was no evidence of systemic absorption or systemic immune effects following intravesical administration. Further studies are required to assess whether intravesical administration has anti‐tumour activity. John Wiley and Sons Inc. 2023-01-13 /pmc/articles/PMC10071078/ /pubmed/37025470 http://dx.doi.org/10.1002/bco2.220 Text en © 2023 The Authors. BJUI Compass published by John Wiley & Sons Ltd on behalf of BJU International Company. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Woodcock, Victoria K.
Chen, Ji‐Li
Purshouse, Karin
Butcher, Chrissie
Collins, Linda
Haddon, Caroline
Verrall, Gillian
Elhussein, Leena
Roberts, Corran
Tarlton, Andrea
Rei, Margarida
Napolitani, Giorgio
Salio, Mariolina
Middleton, Mark R.
Cerundolo, Vincenzo
Crew, Jeremy
Protheroe, Andrew S.
PemBla: A Phase 1 study of intravesical pembrolizumab in recurrent non‐muscle‐invasive bladder cancer
title PemBla: A Phase 1 study of intravesical pembrolizumab in recurrent non‐muscle‐invasive bladder cancer
title_full PemBla: A Phase 1 study of intravesical pembrolizumab in recurrent non‐muscle‐invasive bladder cancer
title_fullStr PemBla: A Phase 1 study of intravesical pembrolizumab in recurrent non‐muscle‐invasive bladder cancer
title_full_unstemmed PemBla: A Phase 1 study of intravesical pembrolizumab in recurrent non‐muscle‐invasive bladder cancer
title_short PemBla: A Phase 1 study of intravesical pembrolizumab in recurrent non‐muscle‐invasive bladder cancer
title_sort pembla: a phase 1 study of intravesical pembrolizumab in recurrent non‐muscle‐invasive bladder cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071078/
https://www.ncbi.nlm.nih.gov/pubmed/37025470
http://dx.doi.org/10.1002/bco2.220
work_keys_str_mv AT woodcockvictoriak pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT chenjili pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT purshousekarin pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT butcherchrissie pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT collinslinda pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT haddoncaroline pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT verrallgillian pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT elhusseinleena pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT robertscorran pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT tarltonandrea pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT reimargarida pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT napolitanigiorgio pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT saliomariolina pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT middletonmarkr pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT cerundolovincenzo pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT crewjeremy pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer
AT protheroeandrews pemblaaphase1studyofintravesicalpembrolizumabinrecurrentnonmuscleinvasivebladdercancer