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  3. Adverse prognostic value of PD-L1 expression in primary resected pulmonary squamous cell carcinomas and paired mediastinal lymph node metastases.

Adverse prognostic value of PD-L1 expression in primary resected pulmonary squamous cell carcinomas and paired mediastinal lymph node metastases.

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DOI
10.7892/boris.106234
Publisher DOI
10.1038/modpathol.2017.111
PubMed ID
28884747
Abstract
Immunohistochemical assessment of programmed cell death (PD)-ligand 1 (PD-L1) expression in lung cancer in the context of therapeutically targeting the PD1/PD-L1 axis is still controversially discussed. This includes the comparability of antibody clones, prognostic value, and discrepancies between primary tumors and metastases. We assessed tumoral PD-L1 expression using clones E1L3N and SP142 in 372 primary resected pulmonary squamous cell carcinomas, including 40 paired N2 lymph node metastases, in relation with clinico-pathological parameters. PD-L1 expression was negative (<1%) in 163/372 (44%, E1L3N) or 231/370 patients (62%, SP142). Positivity of 1-<50% was observed in 135 (36%, E1L3N) or 92 patients (25%, SP142) and ≥50% in 74 (20%, E1L3N) or 47 patients (13%, SP142). PD-L1 staining correlated significantly between both antibodies (r=0.781; P<0.001). Scores correlated significantly between full-slide sections (N=40) and tissue microarrays, and between primaries and N2 metastases (P<0.001 all). CD8(+) tumor infiltrating lymphocyte counts positively correlated with PD-L1 expression (P<0.001). PD-L1 ≥50% showed the best prognostic discrimination using the split-sample validation method. It was associated with shorter disease-specific survival in the observation group (E1L3N: P=0.035, SP142: P=0.002) and validation group (E1L3N: P=0.024, SP142: P=0.101) and shorter time to recurrence (observation group: E1L3N: P=0.056, SP142: P<0.001; validation group: E1L3N: P=0.036, SP142: P=0.247). Multivariate analysis showed that PD-L1 expression ≥50% determined by clone E1L3N was an independent prognostic factor in the observation group regarding disease-specific survival (HR=2.768; 95% CI=1.149-6.666; P=0.023) and time to recurrence (HR=2.164; 95% CI=1.056-4.436; P=0.035) and in the validation group (disease-specific survival: HR=1.978; 95% CI=0.928-4.214; P=0.077 and time to recurrence: HR=1.571; 95% CI=0.838-2.944; P=0.159). High PD-L1 expression was associated with adverse prognosis in pulmonary squamous cell carcinoma. Clone E1L3N was more sensitive than SP142 and superior regarding prognostication. PD-L1 expression correlated significantly between primary tumor and N2 metastases, rendering mediastinal lymph node metastases adequate for immunohistochemical assessment.Modern Pathology advance online publication, 8 September 2017; doi:10.1038/modpathol.2017.111.
Date Issued
2018-01
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
500 Science > 570 Life sciences; biology
Language(s)
en
Author(s)
Keller, Manuel D
Neppl, Christina  
Institut für Pathologie, Klinische Pathologie  
Irmak, Yasin  
Dekanat der Medizinischen Fakultät, Studiendekanat  
Hall, Sean  
Universitätsklinik für Thoraxchirurgie  
Department for BioMedical Research, Forschungsgruppe Thoraxchirurgie  
Schmid, Ralph  
Universitätsklinik für Thoraxchirurgie  
Department for BioMedical Research, Forschungsgruppe Thoraxchirurgie  
Universitätsklinik für Thoraxchirurgie  
Langer, Rupert  
Institut für Pathologie  
Berezowska, Sabina Anna  
Institut für Pathologie, Klinische Pathologie  
Additional Credits
Institut für Pathologie  
Universitätsklinik für Thoraxchirurgie  
Institut für Pathologie, Klinische Pathologie  
Department for BioMedical Research, Forschungsgruppe Thoraxchirurgie  
Dekanat der Medizinischen Fakultät, Studiendekanat  
Journal
Modern pathology
Publisher
Nature Publishing Group
ISSN
0893-3952
Access(Rights)
restricted
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