Survival with <i>EGFR</i> , <i>HER2</i> alterations in aUC: A multi-institution, real-world cohort.
Abstract
e16552 Background: Although overexpression of EGFR occurs in up to 74% of advanced urothelial carcinoma (aUC), alterations are rarer, present in only ~4% of cases. While overexpression is associated with inferior survival, the impact of EGFR rearrangements ( EGFR -alt) on survival remains unknown. Likewise, rearrangements in ERBB2 (HER2-alt) are of unclear significance in aUC. Methods: Utilizing Flatiron Health’s nationwide, de-identified electronic health record derived database, aUC patients (pts) with EGFR -alt or HER2 -alt on NGS testing were identified (2016-2024). Baseline characteristics, treatment history, and clinical outcomes were abstracted. Chi-square and t-tests were used for used for univariate analysis. Progression free survival (PFS) and overall survival (OS) on chemotherapy vs immunotherapy (IO) were compared between EGFR -alt, HER2 -alt, wild-type (WT) pts via Kaplan Meier log-rank analysis. Results: Of 11,944 pts with NGS results, 13 pts with EGFR -alt (0.1%) and 26 pts with HER2-alt (0.2%) were identified. Of the EGFR -alt, 11 pts had rearrangements, one duplication, and one deletion. Of HER2 -alt, 25 had rearrangements and one truncation. For EGFR -alt, six pts were female (47%), compared to 28% for the entire cohort (p<0.01). Seven (54%) were White, three (23%) Asian, and one (8%) Hispanic (compared to 1.4% Asian in overall cohort; p<0.01). Median age at diagnosis was 69. For HER2 -alt, six pts were female (23%), and 23 (89%) were White. Median age was also 69. There was no difference between EGFR, HER2 and WT pts in ECOG PS (p=0.42; Table 1). For EGFR -alt pts, four received platinum chemo (31%) and seven received IO (54%) in 1L. For HER2 -alt pts, 11 (42%) received chemo, nine (35%) received IO, and one (4%) received EVP in 1L. mPFS was 4.9m [95% CI:2.9-7.0] for EGFR -alt, 5.4 [4.2-5.8] for HER2 -alt, compared to 8.8 [8.7-8.9] for WT (p=0.02). For EGFR -alt pts, mPFS was 4.1m [2.9-5.1] on 1L IO and 5.2m [3.0-12.2] on chemo (p=0.41). For HER2 -alt pts, mPFS was 4.3m [2.6-5.4] on 1L IO, 5.6m [3.5-6.5] on chemo, and 7.1 [NR] on EVP (p=0.20). mOS was 9.3m [5.4-12.4] for EGFR -alt pts, 9.7m [5.6-13.0] for HER2 -alt, and 13.4 [13.1-13.6] for WT (p<0.01). Conclusions: EGFR and HER2 rearrangements were rare and associated with inferior PFS and OS compared to wild-type. Women and Asian pts were more likely to harbor EGFR rearrangements. Both EGFR and HER 2 rearranged pts had superior PFS on 1L chemo vs IO, though results were not significant, likely due to small sample size. Baseline characteristics, front-line therapy, survival. EGFR -alt HER2 -alt WT Sig (p) Median Age 69 69 67 0.71 Female (%) 47 23 28 <0.01 ECOG (%) 0.64 0-1 69 64 63 ≥2 15 16 16 Race (%) 0.03 White 54 89 80 Asian 23 0 1 Black 0 4 5 Other 8 8 14 1L Therapy (%) 0.21 Chemo 31 42 64 IO 54 35 28 EVP 0 4 4 Median PFS 4.9 [2.9-7.0] 5.4 [4.2-5.8] 8.8 [8.7-8.9] 0.02 Median OS 9.3 [5.4-12.4] 9.7 [5.6-13.0] 13.4 [13.1-13.6] <0.01 Sig values in bold. PFS and OS in months.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (7)
Adam Barsouk
2Division of Hematology and Oncology, University of Pennsylvania, Philadelphia, PA
Jonathan Henry Sussman
Abramson Cancer Center, Penn Medicine, Philadelphia, PA
Austin Yang
7Division of Oncology, Children’s Hospital of Philadelphia, Philadelphia, PA
Jessica Xu
Department of Chemical Engineering
Omar Elghawy
2Division of Hematology and Oncology, University of Pennsylvania, Philadelphia, PA
Pearl Subramanian
Hospital of the University of Pennsylvania, Philadelphia, PA
Lin Mei