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Landscape of Immune Checkpoint Inhibition in Carcinosarcoma (MMMT): Analysis of IDO-1, PD-L1 and PD-1.
- Source :
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Pathology, research and practice [Pathol Res Pract] 2020 Apr; Vol. 216 (4), pp. 152847. Date of Electronic Publication: 2020 Jan 31. - Publication Year :
- 2020
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Abstract
- Background: Carcinosarcoma (CS) or malignant mixed Müllerian tumor (MMMT), is a rare malignant biphasic tumor, which contains both a malignant epithelial and mesenchymal component. That being said, they have an aggressive clinical course. Given that immune checkpoint inhibitors have mustered significant excitement in the oncology world - immunotherapy could offer significant promise to this poor prognostic cancer subtype. A total of 75 carcinosarcoma cases were identified in our institutional database from 2010 to 2019 and immunohistochemistry for PD-L1, PD-1 and IDO-1 was performed. Out of the 75 patients, 65(87 %) demonstrated >1 % PD-1 expression and 50(67 %) expressed >1 % PD-L1 in either the tumoral and immune stromal components. 29 (39 %) cases demonstrated >20 % PD-1 expression and 14 (19 %) cases expressed >20 % PD-L1. 41(55 %) cases demonstrating co-expression of PD-1 and PD-L1. For IDO-1 64 (85 %) patients showed at least >5 %, while 34 (45 %) showed staining above 20 %. 45 patients (60 %) showed co-expression of IDO-1 and PD-L1, while 59 (79 %) patients had co-expression of IDO and PD-1 above 5 and 1 % respectively. Regarding clinicopathologcial features; older patients (> 65) were more likely to express PD-L1 (>1 %) and IDO-1 (>20 %). For tumor size, IDO-1 expression (>5 %), along with PD-1/IDO-1 Co-expression (>1/5 %), was associated with larger tumor size (>5cm). For myometrial invasion, CSs with >50 % invasion were more likely to express IDO-1 (>20 %) and PD-1/IDO-1 (>1/5 %). Ultimately, the effect of IDO-1, PD-1 and PD-L1 on the clinical profile may be less important than its potential use as a immunotherapeutic, where safe and effective corresponding drugs could be used to treat particular patient populations. Future clinical trials are needed to decipher the association between immune check point inhibitor expression and therapeutic response. This is the only way to definitively prove immune checkpoint immunohistochemistry as predictive biomarkers in this cancer subtype.<br />Competing Interests: Declaration of Competing Interest The authors report no conflicts of interest in this work.<br /> (Copyright © 2020 Elsevier GmbH. All rights reserved.)
- Subjects :
- Aged
Female
Humans
Middle Aged
Ovarian Neoplasms metabolism
Ovarian Neoplasms pathology
Peritoneal Neoplasms metabolism
Peritoneal Neoplasms pathology
Transcriptome
Uterine Cervical Neoplasms metabolism
Uterine Cervical Neoplasms pathology
Uterine Neoplasms metabolism
Uterine Neoplasms pathology
B7-H1 Antigen biosynthesis
Biomarkers, Tumor analysis
Carcinosarcoma metabolism
Indoleamine-Pyrrole 2,3,-Dioxygenase biosynthesis
Programmed Cell Death 1 Receptor biosynthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1618-0631
- Volume :
- 216
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Pathology, research and practice
- Publication Type :
- Academic Journal
- Accession number :
- 32085927
- Full Text :
- https://doi.org/10.1016/j.prp.2020.152847