TROP-2 expression in germ cell tumors (GCT).

N Noah Richardson (Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN) T Tareq Salous (Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN) J Jennifer King (Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN) N Nasser H. Hanna (Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN) M Muhammad T. Idrees (Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN) T Thomas M. Ulbright (Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN) L Lawrence H. Einhorn (Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN) A Andrew Acosta (Indiana University, Indianapolis, IN) N Nabil Adra (Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN)

Abstract

5031 Background: Trophoblast cell surface antigen 2 (TROP-2) is a tumor associated antigen overexpressed in several malignancies including breast and urothelial cancer. The TROP-2 antibody-drug conjugate (ADC) Sacituzumab govitecan is approved for treatment of metastatic breast cancer. The expression of TROP-2 in GCT is unknown. We present immunohistochemistry results of TROP-2 expression in GCT. Methods: Patients who underwent resection for GCT at Indiana University were included. Sixty formalin-fixed paraffin-embedded (FFPE) GCT samples were available. FFPE slides were selected from differing GCT histology and surgical sites including primary tumor, retroperitoneal lymph node, and distant metastases. Immunohistochemical (IHC) staining for TROP-2 (clone 1, mouse monoclonal, Enzo Life Sciences) was conducted and scored by intensity on a 0-3 scale by an experienced pathologist. Results: Samples from 60 individual specimens were available for IHC analysis. TROP2 expression was detected in 29 (48%) of these samples. Intensity expression differed from pure seminoma, mixed non-seminoma (NSGCT), teratoma, yolk sac tumor, and choriocarcinoma samples. Both primary and metastatic samples had TROP-2 expression of varying degrees. Conclusions: TROP-2 expression varies across histology in GCT. Seminoma appears to have the lowest expression of TROP-2. Higher TROP-2 expression was noted in choriocarcinoma and yolk sac tumor samples indicating potential as a target in these histologic subtypes in future clinical trials. Detectable TROP-2 by histology. Sample histology (N) Total detectable TROP-2 expression (%) 3+ 2+ 1+ Seminoma (20) 3 (15) 2 1 NSGCT (19) 12 (63) 9 (6*) 2* 1* Teratoma (9**) 6 (66) 3* 3* Yolk sac (9) 5 (56) 2 3 Choriocarcinoma (3) 3 (100) 1 1 1 *In epithelial elements of teratoma. **Three negative samples with only small fragments of teratoma and false negative may be present.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 5031-5031
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (9)

N

Noah Richardson

Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN

T

Tareq Salous

Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN

J

Jennifer King

Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN

N

Nasser H. Hanna

Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN

M

Muhammad T. Idrees

Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN

T

Thomas M. Ulbright

Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN

L

Lawrence H. Einhorn

Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN

A

Andrew Acosta

Indiana University, Indianapolis, IN

N

Nabil Adra

Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN