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PD1/PD-L1 targeting in advanced soft-tissue sarcomas: a pooled analysis of phase II trials

Authors :
Sandra P. D'Angelo
Antoine Italiano
Carine Bellera
Bordeaux population health (BPH)
Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Source :
Journal of Hematology & Oncology, Vol 13, Iss 1, Pp 1-4 (2020), Journal of Hematology and Oncology, Journal of Hematology and Oncology, BioMed Central, 2020, 13 (1), pp.55. ⟨10.1186/s13045-020-00891-5⟩, Journal of Hematology & Oncology
Publication Year :
2020
Publisher :
BMC, 2020.

Abstract

Immune checkpoint inhibitors, especially the programmed cell death receptor-1/ligand 1 (PD-1/L1) inhibitors, displayed promising efficacy in several solid tumor types and hematological malignancies. Data related to their activity in soft-tissue sarcomas (STS) are scarce.We performed a pooled analysis of clinical trials investigating a PD1 or PD-L1 antagonist in patients with advanced STS. Three hundred eighty-four patients were included in the pooled analysis; of those, 153 (39.8%) received a PD1/PD-L1 antagonist as a single agent. In patients treated with anti-PD1/PDL1 as a single agent, the overall response rate (ORR) and non-progression rate (NPR) were 15.1% and 58.5% respectively. In patients treated with a combination regimen, the ORR and NPR were 13.4% and 55.8% respectively. Analysis by histological subtype revealed that patients with alveolar soft part sarcoma and undifferentiated pleomorphic sarcoma exhibited the highest response rates and leiomyosarcoma the lowest. PD-L1 expression rate was low and inconsistently associated with objective response.PD-1/PD-L1 antagonists have limited activity in unselected STS. Future studies should implement histology and immune-based stratification of STS in their design as well as sequential blood and tissue sampling to better understand the mechanisms of resistance and response given sarcomas inherent heterogeneity.

Details

Language :
English
ISSN :
17568722
Volume :
13
Issue :
1
Database :
OpenAIRE
Journal :
Journal of Hematology & Oncology
Accession number :
edsair.doi.dedup.....a170282530b4fdec976f7cd48685df17
Full Text :
https://doi.org/10.1186/s13045-020-00891-5