Stage II embryonal predominant NSGCT: Minimizing treatment burden.

J Jiping Zeng P Parth Thakker (Indiana University School of Medicine, Department of Urology, Indianapolis, IN) T Timothy A. Masterson (Indiana University 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 Nabil Adra (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) C Clint Cary (Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN)

Abstract

634 Background: Embryonal carcinoma predominance (ECP) in the orchiectomy specimen is linked to a higher risk of retroperitoneal and systemic relapse. Both chemotherapy and primary retroperitoneal lymph node dissection (RPLND) are recommended options for stage II disease, but the approach that minimizes treatment burden remains unclear. Methods: We queried the Indiana University Testicular Cancer Database to identify patients with non-seminomatous germ cell tumors (NSGCT) and ECP >50% in the orchiectomy specimen, stage II with retroperitoneal adenopathy <5 cm, and normal serum tumor markers. Patients with malignant transformation (n=3) or bilateral cancer (n=3) or receiving 1-2 cycles of BEP after orchiectomy were excluded (n=14). Treatment courses and outcomes were compared. Results: Between 2005 and 2022, 142 patients met the criteria. Of 67 patients who underwent primary RPLND, 62 had active EC in final pathology. Adjuvant chemotherapy (2 cycles of EP or BEP) was given to 5 patients. After a median follow-up of 37.7 months, 10 recurred, with a recurrence-free survival (RFS) of 85.1%. Following induction chemotherapy for documented recurrence, 9 patients were disease-free, with 1 disease-related death. Disease-free survival (DFS) was 98.5%. There were no in-field recurrences in the primary RPLND group. Of the 75 patients who received chemotherapy, 25 required post-chemotherapy (PC) RPLND, which revealed either teratoma or necrosis, and no active cancer was found. One recurred and needed re-do RPLND. Five patients who achieved complete remission after chemotherapy recurred, requiring second-line and high-dose chemotherapy. The RFS was 92%, with a median follow-up of 34.1 months. DFS was 97.3%. Univariate analysis showed pre-orchiectomy AFP >100 ng/mL (OR 7.6, 95% CI 1.6–54.9) and teratoma >5% in the orchiectomy specimen (OR 4.1, 95% CI 1.3–13.2) were associated with the need for PC-RPLND, but no parameters were predictive in multivariate analysis. Conclusions: Primary RPLND achieved complete remission as a single treatment modality in 85% of patients, compared to 67% for chemotherapy. Primary RPLND may reduce treatment burden in early-stage II ECP NSGCT in well-selected patients.

Article Details

Volume / Issue Vol. 43, Issue 5_suppl
Published February 10, 2025
Pages 634-634
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (8)

J

Jiping Zeng

P

Parth Thakker

Indiana University School of Medicine, Department of Urology, Indianapolis, IN

T

Timothy A. Masterson

Indiana University 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

Nabil Adra

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

C

Clint Cary

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