European urology open science · 2026
Expression of NECTIN-4 and TROP-2 in Resected Upper Tract Urothelial Carcinoma with and Without Preoperative Chemotherapy.
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Clemente Leticia C, Igel Daniel A, Spooner Jesse T R, Pretzsch Shanna M, Zacharias Niki M, Guo Charles C, Matin Surena F
Аннотация
BACKGROUND: Antibody-drug conjugates (ADCs) have transformed the treatment of urothelial carcinoma, yet upper tract urothelial cancer (UTUC) data remain limited.
OBJECTIVE: We compared NECTIN-4 and trophoblast cell-surface antigen 2 (TROP-2) expression in UTUC specimens from treatment-naive (TN) and chemotherapy (CTX)-exposed patients.
DESIGN SETTING AND PARTICIPANTS: A retrospective cohort of 141 consecutive patients with UTUC who underwent resection from 1991 to 2021 was stratified into TN and CTX-exposed cohorts.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Tissue microarrays were stained for NECTIN-4 and TROP-2 and quantified using the H-score method, with H-score ≥15 and ≥10 defining positivity, respectively. Group comparisons were performed using Wilcoxon rank-sum and Fisher exact tests.
RESULTS AND LIMITATIONS: NECTIN-4 membrane positivity was observed in 47% (25/53) and 9.3% (8/86) of TN and CTX-exposed specimens, respectively (p < 0.001), with median H-scores of 8 (interquartile range [IQR] = 0-45) and 0 (IQR = 0-0), respectively (p < 0.001). TROP-2 membrane positivity was near universal in 100% (52/52) and 97% (83/86) of TN and CTX-exposed specimens, respectively (p = 0.3), with median H-scores of 280 (IQR = 229-300) and 141 (IQR = 100-197), respectively (p < 0.001). In patients with distant or local nonurothelial recurrence, membranous TROP-2 and NECTIN-4 were seen in 91% (21/23) and 17% (4/23), respectively. Limitations include a retrospective single-institution design and lack of paired specimens.
CONCLUSIONS: TROP-2 expression was near universal regardless of CTX exposure, including patients who developed recurrence, whereas NECTIN-4 expression was significantly lower in CTX-exposed cohorts. These findings support TROP-2 as a more durable ADC target in UTUC, warranting further investigation of TROP-2-directed ADCs, particularly with prior CTX exposure.
OBJECTIVE: We compared NECTIN-4 and trophoblast cell-surface antigen 2 (TROP-2) expression in UTUC specimens from treatment-naive (TN) and chemotherapy (CTX)-exposed patients.
DESIGN SETTING AND PARTICIPANTS: A retrospective cohort of 141 consecutive patients with UTUC who underwent resection from 1991 to 2021 was stratified into TN and CTX-exposed cohorts.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Tissue microarrays were stained for NECTIN-4 and TROP-2 and quantified using the H-score method, with H-score ≥15 and ≥10 defining positivity, respectively. Group comparisons were performed using Wilcoxon rank-sum and Fisher exact tests.
RESULTS AND LIMITATIONS: NECTIN-4 membrane positivity was observed in 47% (25/53) and 9.3% (8/86) of TN and CTX-exposed specimens, respectively (p < 0.001), with median H-scores of 8 (interquartile range [IQR] = 0-45) and 0 (IQR = 0-0), respectively (p < 0.001). TROP-2 membrane positivity was near universal in 100% (52/52) and 97% (83/86) of TN and CTX-exposed specimens, respectively (p = 0.3), with median H-scores of 280 (IQR = 229-300) and 141 (IQR = 100-197), respectively (p < 0.001). In patients with distant or local nonurothelial recurrence, membranous TROP-2 and NECTIN-4 were seen in 91% (21/23) and 17% (4/23), respectively. Limitations include a retrospective single-institution design and lack of paired specimens.
CONCLUSIONS: TROP-2 expression was near universal regardless of CTX exposure, including patients who developed recurrence, whereas NECTIN-4 expression was significantly lower in CTX-exposed cohorts. These findings support TROP-2 as a more durable ADC target in UTUC, warranting further investigation of TROP-2-directed ADCs, particularly with prior CTX exposure.