TY - JOUR
T1 - The impact of HER2-Low expression in salivary duct carcinoma
T2 - Clinicopathologic features, survival outcomes, and association with androgen receptor-targeted therapy
AU - Multi-institutional Joint SDC Study Group in Japan
AU - Kano, Satoshi
AU - Kawakita, Daisuke
AU - Honma, Yoshitaka
AU - Takahashi, Hideaki
AU - Nakaguro, Masato
AU - Utsumi, Yoshitaka
AU - Saigusa, Natsuki
AU - Hanazawa, Toyoyuki
AU - Tsukahara, Kiyoaki
AU - Okada, Takuro
AU - Okami, Kenji
AU - Yamazaki, Keisuke
AU - Ueki, Yushi
AU - Saito, Yuki
AU - Ozawa, Hiroyuki
AU - Arai, Tomoyuki
AU - Shimizu, Akira
AU - Hanyu, Kenji
AU - Iwaki, Sho
AU - Imaizumi, Sae
AU - Sakai, Akihiro
AU - Yamauchi, Mayu
AU - Tanaka, Ryoko
AU - Sato, Yuichiro
AU - Yamamura, Koji
AU - Sekimizu, Mariko
AU - Imanishi, Yorihisa
AU - Hirai, Hideaki
AU - Sato, Yukiko
AU - Urano, Makoto
AU - Yamamoto, Hidetaka
AU - Fushimi, Chihiro
AU - Matsuki, Takashi
AU - Nagao, Toshitaka
AU - Tada, Yuichiro
N1 - Publisher Copyright:
© 2025 Elsevier Ltd
PY - 2025/6
Y1 - 2025/6
N2 - Objectives: Recent advances in systemic therapy for salivary duct carcinoma (SDC) have been driven by the development of HER2- and androgen receptor (AR)-targeted therapies. Trastuzumab deruxtecan has proven effective not only in HER2-positive but also HER2-low breast and gastro-esophageal cancers. However, the significance of HER2-low expression in SDC remains unknown. This study aimed to investigate the clinicopathologic characteristics, prognostic implications, and impact on efficacy to AR-targeted therapy in HER2-low SDC. Materials and Methods: This was a multi-center, observational study. HER2 status was reclassified as follows: HER2-positive (IHC3+ or 2+/ISH+ ), HER2-low (IHC1+ or 2+/ISH-), and HER2-zero (IHC0). The subjects were compared in three groups: total population, curative treatment cohort, and AR-targeted therapy cohort. Results: The total population consisted of 526 patients, of whom, 271 (52 %), 184 (35 %), and 71 (13 %) had HER2-positive, -low, and -zero tumors, respectively. Sex, M category, histological origin, Ki67, and p53 expression differed significantly between the HER2-low and HER2-positive cases. No differences in relapse-free or overall survival were observed for HER2 status in the curative treatment cohort; however, in the AR-targeted therapy cohort, the HER2-low group had significantly better response rates (41.6 % vs. 18.9 %, Odds ratio = 0.30, P = 0.012) and longer median progression-free survival (6.9 vs. 4.2 months, Hazard ratio = 1.61, P = 0.029) than those of the HER2-positive group. Conclusion: HER2-low showed different clinicopathologic features from HER2-positive cases, with no prognostic differences observed in patients who underwent curative treatment. Still, HER2-low may be associated with the efficacy of AR-targeted therapy.
AB - Objectives: Recent advances in systemic therapy for salivary duct carcinoma (SDC) have been driven by the development of HER2- and androgen receptor (AR)-targeted therapies. Trastuzumab deruxtecan has proven effective not only in HER2-positive but also HER2-low breast and gastro-esophageal cancers. However, the significance of HER2-low expression in SDC remains unknown. This study aimed to investigate the clinicopathologic characteristics, prognostic implications, and impact on efficacy to AR-targeted therapy in HER2-low SDC. Materials and Methods: This was a multi-center, observational study. HER2 status was reclassified as follows: HER2-positive (IHC3+ or 2+/ISH+ ), HER2-low (IHC1+ or 2+/ISH-), and HER2-zero (IHC0). The subjects were compared in three groups: total population, curative treatment cohort, and AR-targeted therapy cohort. Results: The total population consisted of 526 patients, of whom, 271 (52 %), 184 (35 %), and 71 (13 %) had HER2-positive, -low, and -zero tumors, respectively. Sex, M category, histological origin, Ki67, and p53 expression differed significantly between the HER2-low and HER2-positive cases. No differences in relapse-free or overall survival were observed for HER2 status in the curative treatment cohort; however, in the AR-targeted therapy cohort, the HER2-low group had significantly better response rates (41.6 % vs. 18.9 %, Odds ratio = 0.30, P = 0.012) and longer median progression-free survival (6.9 vs. 4.2 months, Hazard ratio = 1.61, P = 0.029) than those of the HER2-positive group. Conclusion: HER2-low showed different clinicopathologic features from HER2-positive cases, with no prognostic differences observed in patients who underwent curative treatment. Still, HER2-low may be associated with the efficacy of AR-targeted therapy.
KW - Androgen receptor
KW - Combined androgen blockade
KW - HER2
KW - HER2-low
KW - Head and neck cancer
KW - Salivary duct carcinoma
KW - Salivary gland cancer
UR - https://www.scopus.com/pages/publications/105002867977
UR - https://www.scopus.com/pages/publications/105002867977#tab=citedBy
U2 - 10.1016/j.oraloncology.2025.107280
DO - 10.1016/j.oraloncology.2025.107280
M3 - Article
C2 - 40252453
AN - SCOPUS:105002867977
SN - 1368-8375
VL - 165
JO - Oral Oncology
JF - Oral Oncology
M1 - 107280
ER -