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PD1/PD-L1 Expression in Blastic Plasmacytoid Dendritic Cell Neoplasm.
Aung, Phyu P; Sukswai, Narittee; Nejati, Reza; Loghavi, Sanam; Chen, Weina; Torres-Cabala, Carlos A; Yin, C Cameron; Konopleva, Marina; Zheng, Xiaofeng; Wang, Jing; Tang, Zhenya; Medeiros, L Jeffrey; Prieto, Victor G; Pemmaraju, Naveen; Khoury, Joseph D.
Afiliación
  • Aung PP; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. PAung@mdanderson.org.
  • Sukswai N; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. NSukswai@mdanderson.org.
  • Nejati R; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. reza.nejati@fccc.edu.
  • Loghavi S; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. sloghavi@mdanderson.org.
  • Chen W; Department of Pathology and Laboratory Medicine, The University of Texas at Southwestern, Dallas, TX 77030, USA. Weina.Chen@UTSouthwestern.edu.
  • Torres-Cabala CA; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. ctcabala@mdanderson.org.
  • Yin CC; Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. ctcabala@mdanderson.org.
  • Konopleva M; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. cyin@mdanderson.org.
  • Zheng X; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. mkonople@mdanderson.org.
  • Wang J; Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. XZheng2@mdanderson.org.
  • Tang Z; Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. jingwang@mdanderson.org.
  • Medeiros LJ; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. ZTang@mdanderson.org.
  • Prieto VG; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. ljmedeiros@mdanderson.org.
  • Pemmaraju N; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. vprieto@mdanderson.org.
  • Khoury JD; Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. vprieto@mdanderson.org.
Cancers (Basel) ; 11(5)2019 May 19.
Article en En | MEDLINE | ID: mdl-31109153
ABSTRACT
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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos