| Literature DB >> 30665814 |
Nora Sundahl1, Gillian Vandekerkhove2, Karel Decaestecker3, Annabel Meireson4, Pieter De Visschere5, Valérie Fonteyne6, Daan De Maeseneer7, Dries Reynders8, Els Goetghebeur8, Jo Van Dorpe9, Sofie Verbeke9, Matti Annala2, Lieve Brochez4, Kim Van der Eecken10, Alexander W Wyatt2, Sylvie Rottey11, Piet Ost6.
Abstract
Preclinical data indicate that radiotherapy works synergistically with pembrolizumab, but the effect and toxicity of this combination may depend on radiotherapy timing. We conducted a randomized phase 1 trial combining pembrolizumab with either sequential (A) or concomitant (B) stereotactic body radiotherapy (SBRT) in metastatic urothelial carcinoma (mUC). No dose-limiting toxicity occurred. Treatment-related adverse events (trAEs; Common Terminology Criteria for Adverse Events v4.0) of grade 1-2 occurred in six of nine and all nine patients in arms A and B, respectively. One grade 3 trAE occurred in arm B. No grade 4-5 trAEs occurred. Overall response rates of 0% and 44.4% were noted in arms A and B, respectively, as per Response Evaluation Criteria in Solid Tumors v1.1. The trial was not powered to compare efficacy between arms. Targeted sequencing of tissue DNA and circulating tumor DNA (ctDNA) revealed high genomic concordance. Treatment response was associated with ctDNA fraction decline. We conclude that sequential and concomitant SBRT can be safely combined with pembrolizumab in mUC and that the effect of SBRT timing on efficacy is worth exploring further. PATIENTEntities:
Keywords: Checkpoint inhibitor; Circulating tumor DNA; Immunotherapy; Metastatic urothelial carcinoma; Precision oncology; Stereotactic body radiotherapy
Year: 2019 PMID: 30665814 DOI: 10.1016/j.eururo.2019.01.009
Source DB: PubMed Journal: Eur Urol ISSN: 0302-2838 Impact factor: 20.096