Surveillance after complete response (CR) to first-line chemotherapy (chemo) in non-seminomatous germ-cell tumor (NSGCT).
Abstract
599 Background: Management of NSGCT following CR after first-line chemo remains variable across institutions. Recent data indicates that patients (pts) with teratoma and/or yolk sac tumor (YST) in their orchiectomy specimen were associated with finding teratoma or viable non-teratomatous GCT at post-chemo retroperitoneal lymph node dissection (PCRPLND) specimen. It is not clear whether this finding impacts long-term survival outcomes. We sought to evaluate long-term outcomes of surveillance after CR at Indiana University (IU) specifically in this patient population. Methods: We retrospectively reviewed the IU GCT database (January 1990-June 2024). Eligible pts were diagnosed with metastatic testicular/retroperitoneal NSGCT who achieved CR after first-line chemo defined by no residual mass >1cm in the longitudinal axis. Pts who were treated with chemo outside IU were excluded to reduce referral bias. Pts were stratified according to orchiectomy specimen into two groups: Those with teratoma and/or YST and those without either component. Primary outcomes were to estimate progression-free survival (PFS) and overall survival (OS) in these subgroups using Kaplan-Meier methodology. Results: A total of 261 pts met the inclusion criteria. Of these, 21 (8.0%) had teratoma, 50 had YST (19.2%), and 65 had both (24.9%). IGCCCG risk was good in 85.1%, intermediate in 6.1%, and poor in 8.8%. Median follow-up was 4.97 years (range, 0.01-28.80). Pre-chemo retroperitoneal lymph node size was <1 cm in 19 (7.3%), 1-3cm in 102 (39.1%), >3cm in 67 (25.7%), and unknown in 73 (28.0%). Four-year PFS for pts with teratoma or YST in their orchiectomy specimen was 92.2% vs 95.3% in pts without teratoma/YST (P=0.37). Four-year OS for pts with teratoma/YST in orchiectomy specimen was 98.0% vs 98.1% in pts without teratoma/YST (P=0.59). Late relapse occurred in 3.7% (n=5) of those with teratoma/YST and 2.4% (n=3) for those with neither (P=0.72). Of the 16 pts who relapsed, 8 underwent delayed RPLND, 3 received salvage chemo, 2 were treated with salvage chemo and RPLND, and 3 underwent resection of other metastatic sites. At last follow-up, 12 pts who relapsed were without evidence of disease, 2 were alive with disease, and 2 died of NSGCT. Conclusions: In this large cohort, most pts with NSGCT who achieved CR after first-line chemo remained disease-free on surveillance, regardless of the presence of teratoma or YST in the orchiectomy specimen. Relapses were uncommon and most pts who relapsed were salvaged successfully with surgery and/or chemo. Group Progression Count Row N % Late Relapse Count Row N % Any Teratoma (86) 7 8.1 % 3 3.5 % Any YST (115) 10 8.7 % 5 4.3 % Both Present (65) 6 9.2 % 3 4.6 % Either Present (136) 11 8.1 % 5 3.7 % Neither Present (125) 5 4.0 % 3 2.4 % P-value a 0.17 P-value a 0.72 a P -values compare “Either Present” vs “Neither Present.”
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (9)
Towfik Sebai
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN
Clint Cary
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN
Timothy Masterson
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN
Sandra K. Althouse
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN
Tareq Salous
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN
Jennifer King
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN
Noah Richardson
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN
Lawrence H. Einhorn
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN
Nabil Adra
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN