Adjuvant pembrolizumab in genomically selected high-risk patients with muscle-invasive bladder cancer.
Antibodies, Monoclonal, Humanized
Antineoplastic Combined Chemotherapy Protocols
Carcinoma, Transitional Cell
/ drug therapy
Chemotherapy, Adjuvant
Cisplatin
/ therapeutic use
Humans
Muscles
Neoplasm Invasiveness
Neoplasm Recurrence, Local
/ drug therapy
Treatment Outcome
Urinary Bladder Neoplasms
/ drug therapy
PD-L1
Urothelial carcinoma
adjuvant therapy
pembrolizumab
tumor mutational burden
Journal
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372
Informations de publication
Date de publication:
Dec 2021
Dec 2021
Historique:
pubmed:
21
5
2021
medline:
9
2
2022
entrez:
20
5
2021
Statut:
ppublish
Résumé
Patients with muscle-invasive urothelial bladder cancer post neoadjuvant cisplatin-based chemotherapy with pathologic advanced disease (ypT3, ypT4, ypN+) at radical cystectomy have a significantly worse five-year overall survival. There is currently no preferred adjuvant therapy to reduce risk of cancer recurrence in this high-risk patient cohort and surveillance remains the standard-of-care. We present a case series of two patients who received cisplatin-based neoadjuvant chemotherapy and had pathologic node-positive urothelial carcinoma at the time of radical cystectomy. Tumor next generation sequencing revealed high mutational burden in both patients and positive PD-L1 in one patient.Management and outcome: Patients were treated with adjuvant pembrolizumab and experienced long-term disease free intervals. Use of adjuvant checkpoint inhibitors in patients post neoadjuvant cisplatin-based chemotherapy with pathologic advanced disease at the time of radical cystectomy at high-risk of cancer recurrence sounds appealing. Careful patient selection based on tumor-specific genomic alterations may be key. Large trials addressing this question are ongoing.
Identifiants
pubmed: 34013824
doi: 10.1177/10781552211016526
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
pembrolizumab
DPT0O3T46P
Cisplatin
Q20Q21Q62J
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM