Cancers (May 2019)

PD1/PD-L1 Expression in Blastic Plasmacytoid Dendritic Cell Neoplasm

  • Phyu P. Aung,
  • Narittee Sukswai,
  • Reza Nejati,
  • Sanam Loghavi,
  • Weina Chen,
  • Carlos A. Torres-Cabala,
  • C. Cameron Yin,
  • Marina Konopleva,
  • Xiaofeng Zheng,
  • Jing Wang,
  • Zhenya Tang,
  • L. Jeffrey Medeiros,
  • Victor G. Prieto,
  • Naveen Pemmaraju,
  • Joseph D. Khoury

DOI
https://doi.org/10.3390/cancers11050695
Journal volume & issue
Vol. 11, no. 5
p. 695

Abstract

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Patients with blastic plasmacytoid dendritic cell neoplasm (BPDCN) have poor outcomes despite intensive chemotherapy, underscoring the need for novel therapeutic approaches. The expression status of PD1/PD-L1 in BPDCN remains unknown. We evaluated PD1/PD-L1 by immunohistochemistry and RNAseq expression profiling in a cohort of BPDCN patients. The study group included 28 patients with a median age of 66.8 years (range, 22.8−86.7), 22 men and 6 women. PD-L1 expression was detected by immunohistochemistry in 10/21 (47.6%) cases. PD-L1 expression had a median H-score of 157. The H-score was ≥60 in 7 patients. PD-L1 protein levels (H-score) were proportional to normalized PD-L1 mRNA transcript levels (CD274 mRNA). In addition, high-level PD-L1 expression correlated with higher numbers of PD1-positive cells within BPDCN tumors. There was no correlation between clinicopathologic characteristics and PD-L1 expression status. Similarly, there was no significant difference in overall survival between patients with PD-L1-positive and PD-L1-negative BPDCN (median 12 vs. 23 month, respectively; p = 0.743). In conclusion, PD-L1 expression by tumor cells is detectable in a sizeable subset of patients with BPDCN, suggesting that exploration of the effectiveness of therapeutic inhibition of the PD1/PD-L1 axis in patients with refractory or progressive BPDCN is warranted.

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