PD-L1 Expression in Paired Samples of Rectal Cancer

被引:1
作者
Coussement, Mina [1 ]
Fazio, Roberta [1 ]
Audisio, Alessandro [1 ]
El Khoury, Reem [1 ]
Abbassi, Fatima-Zahra [1 ]
Assaf, Irene [1 ]
Conti, Chiara [1 ]
Gallio, Chiara [1 ]
Benhima, Nada [1 ]
Bregni, Giacomo [1 ]
Gkolfakis, Paraskevas [1 ]
Spagnolo, Valentina [1 ]
Anthoine, Geraldine [1 ]
Liberale, Gabriel [1 ]
Moretti, Luigi [1 ]
Martinive, Philippe [1 ]
Hendlisz, Alain [1 ]
Demetter, Pieter [2 ,3 ]
Sclafani, Francesco [1 ]
机构
[1] Univ Libre Bruxelles ULB, Hop Univ Bruxelles HUB, Inst Jules Bordet, B-1070 Brussels, Belgium
[2] Div CMP, Cerba Path, B-1070 Brussels, Belgium
[3] Univ Libre Bruxelles ULB, Lab Expt Gastroenterol, B-1070 Brussels, Belgium
关键词
PD-L1; tumour proportion score (TPS); immune cell score (ICS); combined positive score (CPS); immune checkpoint inhibitors; radiotherapy; rectal cancer; DEATH-LIGAND; 1; TUMOR-INFILTRATING LYMPHOCYTES; NEOADJUVANT CHEMORADIOTHERAPY; COLORECTAL-CANCER; OPEN-LABEL; PLUS CHEMOTHERAPY; CHEMORADIATION; PEMBROLIZUMAB; RADIOTHERAPY; PROGNOSIS;
D O I
10.3390/cancers16142606
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary There is an increased interest for the investigation of immunotherapy and immune-related biomarkers in rectal cancer. We retrospectively analysed the expression of the programmed death-ligand 1 (PD-L1) in diagnostic biopsies and resection samples from a cohort of 83 rectal cancer patients. Using three different methods for the analysis of PD-L1, we found that the expression of this biomarker was lower in resection samples than in diagnostic biopsies. Also, we observed that higher levels of PD-L1 in resection specimens were associated with better survival outcomes. The results of our study contribute to the knowledge of PD-L1 expression in rectal cancer, having the potential to inform the design of future immunotherapy trials in this setting.Abstract Immune checkpoint inhibitors and immune-related biomarkers are increasingly investigated in rectal cancer (RC). We retrospectively analysed PD-L1 expression in diagnostic biopsy and resection samples from RC patients treated at our centre between 2000 and 2020. PD-L1 immunostaining (22C3 clone) was evaluated according to tumour proportion (TPS), immune cell (ICS), and the combined positive score (CPS). Eighty-three patients were included. At diagnosis, PD-L1 expression >= 1%/>= 5% was observed in 15.4%/0%, 80.7%/37.4%, and 69.2%/25.6% of patients based on TPS, ICS, and CPS, respectively. At surgery, the respective figures were 4.6%/1.5%, 60.2%/32.5%, and 50.7%/26.2%. Using the 1% cut-off and regardless of the scoring system, PD-L1 was less expressed in surgery than biopsy samples (p <= 0.04). In paired specimens, PD-L1-ICS reduction was especially observed following neoadjuvant long-course (chemo)radiotherapy (p = 0.03). PD-L1-ICS of >= 5% in surgical samples (HR: 0.17; p = 0.02), and a biopsy-to-surgery increase in PD-L1-ICS (HR: 0.19; p = 0.04) was predictive for longer disease-free survival, while the PD-L1-ICS of either >= 1% (HR 0.28; p = 0.04) or >= 5% (HR 0.19; p = 0.03) in surgical samples and the biopsy-to-surgery increase in PD-L1-ICS (HR: 0.20; p = 0.04) were associated with better overall survival. Our study suggests that PD-L1 expression in RC is largely reflective of immune cell infiltration, and its presence/increase in surgical samples predicts better outcomes.
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相关论文
共 78 条
[1]   A meta-analysis of CD274 (PD-L1) assessment and prognosis in colorectal cancer and its role in predicting response to anti-PD-1 therapy [J].
Alexander, Peter G. ;
McMillan, Donald C. ;
Park, James H. .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2021, 157
[2]  
[Anonymous], 2022, IRISH J MED SCI, V191, pS207, DOI 10.1007/s11845-022-03228-y
[3]   Overall Survival with Durvalumab after Chemoradiotherapy in Stage III NSCLC [J].
Antonia, S. J. ;
Villegas, A. ;
Daniel, D. ;
Vicente, D. ;
Murakami, S. ;
Hui, R. ;
Kurata, T. ;
Chiappori, A. ;
Lee, K. H. ;
de Wit, M. ;
Cho, B. C. ;
Bourhaba, M. ;
Quantin, X. ;
Tokito, T. ;
Mekhail, T. ;
Planchard, D. ;
Kim, Y. -C. ;
Karapetis, C. S. ;
Hiret, S. ;
Ostoros, G. ;
Kubota, K. ;
Gray, J. E. ;
Paz-Ares, L. ;
Carpeno, J. de Castro ;
Faivre-Finn, C. ;
Reck, M. ;
Vansteenkiste, J. ;
Spigel, D. R. ;
Wadsworth, C. ;
Melillo, G. ;
Taboada, M. ;
Dennis, P. A. ;
Ozguroglu, M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (24) :2342-2350
[4]  
Bae SU, 2019, ANN SURG ONCOL, V26, pS207
[5]   Preoperative Chemoradiotherapy plus Nivolumab before Surgery in Patients with Microsatellite Stable and Microsatellite Instability-High Locally Advanced Rectal Cancer [J].
Bando, Hideaki ;
Tsukada, Yuichiro ;
Inamori, Koji ;
Togashi, Yosuke ;
Koyama, Shohei ;
Kotani, Daisuke ;
Fukuoka, Shota ;
Yuki, Satoshi ;
Komatsu, Yoshito ;
Homma, Shigenori ;
Taketomi, Akinobu ;
Uemura, Mamoru ;
Kato, Takeshi ;
Fukui, Makoto ;
Wakabayashi, Masashi ;
Nakamura, Naoki ;
Kojima, Motohiro ;
Kawachi, Hiroshi ;
Kirsch, Richard ;
Yoshida, Tsutomu ;
Suzuki, Yutaka ;
Sato, Akihiro ;
Nishikawa, Hiroyoshi ;
Ito, Masaaki ;
Yoshino, Takayuki .
CLINICAL CANCER RESEARCH, 2022, 28 (06) :1136-1146
[6]   Novel Immunological Approaches in the Treatment of Locally Advanced Rectal Cancer [J].
Bando, Hideaki ;
Tsukada, Yuichiro ;
Ito, Masaaki ;
Yoshino, Takayuki .
CLINICAL COLORECTAL CANCER, 2022, 21 (01) :3-9
[7]  
Baretti Marina, 2022, Oncotarget, V13, P907, DOI 10.18632/oncotarget.28255
[8]  
Benson A B VA., Rectal cancer
[9]   Radiotherapy Scheme Effect on PD-L1 Expression for Locally Advanced Rectal Cancer [J].
Boustani, Jihane ;
Derangere, Valentin ;
Bertaut, Aurelie ;
Adotevi, Olivier ;
Morgand, Veronique ;
Charon-Barra, Celine ;
Ghiringhelli, Francois ;
Mirjolet, Celine .
CELLS, 2020, 9 (09) :1-20
[10]   Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries [J].
Bray, Freddie ;
Laversanne, Mathieu ;
Sung, Hyuna ;
Ferlay, Jacques ;
Siegel, Rebecca L. ;
Soerjomataram, Isabelle ;
Jemal, Ahmedin .
CA-A CANCER JOURNAL FOR CLINICIANS, 2024, 74 (03) :229-263