Analysis of expression of programmed cell death 1 ligand 1 (PD-L1) in malignant pleural mesothelioma (MPM).
Analysis of expression of programmed cell death 1 ligand 1 (PD-L1) in malignant pleural mesothelioma (MPM).
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DOI:
10.1371/journal.pone.0121071
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发表时间:
2015
期刊:
影响因子:
3.7
通讯作者:
Felip E
中科院分区:
文献类型:
--
作者:
Cedrés S;Ponce-Aix S;Zugazagoitia J;Sansano I;Enguita A;Navarro-Mendivil A;Martinez-Marti A;Martinez P;Felip E
The increasing incidence and poor outcome associated with MPM requires finding effective treatment for this disease. PD1/PD-L1 pathway plays a central role in tumor immune evasion and appears to be predictive and prognostic marker. PD-L1 is expressed in many different human cancers but its role in MPM has yet to be established. The aim of this study is to evaluate the expression of PD-L1 in MPM. 119 MPM patients (p) from two institutions between November 2002 and February 2014 were reviewed. Formalin-fixed, paraffin-embedded tissue was stained with anti-PD-L1 (clone E1L3N). Cases showing more than 1% of tumor cells expression of PD-L1 were considered positive. PD-L1 was analyzed in 77 p with tumor tissue available and was positive in 20.7% p (14 samples in membrane, 16 in cytoplasm and 4 in immune infiltrate). PD-L1 intensity was weak in 56.2%, moderate in 25% and strong in 18.7% p. There was a significant relationship between PD-L1 expression and histology (PD-L1 expression 37.5% in no-epithelioid tumor and 13.2% in epithelioid; p=0.033). The median survival in p PD-L1 positive was 4.79 vs 16.3 months in p PD-L1 negative (p=0.012). We have shown PD-L1 is expressed in 20% of patients, associated with no epithelioid histology and poor prognostic in MPM. Our results suggest PD-L1 warrants further exploration in selecting p for immunotherapy.
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影响因子:
11.5
作者:
Konishi, J;Yamazaki, K;Nishimura, M
通讯作者:
Nishimura, M
影响因子:
11.5
作者:
Ohigashi, Y;Sho, M;Nakajima, Y
通讯作者:
Nakajima, Y
DOI:
10.1097/jto.0000000000000177
发表时间:
2014-07
期刊:
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
影响因子:
--
作者:
Mansfield AS;Roden AC;Peikert T;Sheinin YM;Harrington SM;Krco CJ;Dong H;Kwon ED
通讯作者:
Kwon ED
影响因子:
3.4
作者:
Opitz, Isabelle;Soltermann, Alex;Weder, Walter
通讯作者:
Weder, Walter
DOI:
10.1056/nejmoa1200694
发表时间:
2012-06-28
期刊:
The New England journal of medicine
影响因子:
--
作者:
Brahmer JR;Tykodi SS;Chow LQ;Hwu WJ;Topalian SL;Hwu P;Drake CG;Camacho LH;Kauh J;Odunsi K;Pitot HC;Hamid O;Bhatia S;Martins R;Eaton K;Chen S;Salay TM;Alaparthy S;Grosso JF;Korman AJ;Parker SM;Agrawal S;Goldberg SM;Pardoll DM;Gupta A;Wigginton JM
通讯作者:
Wigginton JM