Abstract CT301: SHR-A1811 ± adebrelimab as first-line (1L) treatment for advanced HER2-mutant NSCLC: A randomized phase 2 cohort from a phase 1b/2 study

Abstract Background: Trastuzumab rezetecan (SHR-A1811) is a novel HER2-directed ADC approved for pretreated HER2-mutant NSCLC (Lancet Oncol, 2025). ADCs may enhance antitumor immunity and synergize with immunotherapy. We conducted an open-label, phase 1/2 (dose-escalation/efficacy-exploration) study (NCT05482568) to evaluate SHR-A1811 in combination therapy for HER2-altered NSCLC and here report data from phase 2 Cohort D of 1L SHR-A1811 ± adebrelimab (anti-PD-L1 mAb) for HER2-mutant NSCLC. Methods: Patients (pts) were randomized (1:1) to receive SHR-A1811 (4.8 mg/kg, iv, Q3W) + adebrelimab (1200 mg, iv, Q3W) or SHR-A1811 (4.8 mg/kg, iv, Q3W) alone, stratified by PD-L1 expression (TPS, <1% vs ≥1%). The primary endpoint was ORR per investigator. Results: 68 pts (PD-L1 TPS <1%/1-49%/≥50%, 50.0%/41.2%/8.8%; exon 20 insertions/A775_G776insYVMA, 89.7%/55.9%) were treated. At data cutoff (Oct 20, 2025), median follow-up was 16.7 mo. Confirmed ORR was 69.4% (95% CI 51.9-83.7) with SHR-A1811 + adebrelimab (combo) vs 81.3% (95% CI 63.6-92.8) with SHR-A1811; median DoR was not reached (NR) and 16.6 mo (95% CI 8.5-NR), respectively. PFS events occurred in 10 pts (27.8%) with combo vs 13 (40.6%) with SHR-A1811; median PFS was NR (95% CI 15.3-NR) vs 17.9 mo (95% CI 9.7-NR; HR 0.65, 95% CI 0.28-1.47). Efficacy by PD-L1 TPS is shown in Table 1. A trend toward improved PFS with addition of adebrelimab was seen across subgroups. All grade ≥3 TRAEs occurring in ≥10% were hematologic in both arms. ILD occurred in 2 (5.6%) pts with combo and 1 (1.3%) with SHR-A1811. TRAEs led to discontinuation of SHR-A1811 in 2 (5.6%) and adebrelimab in 4 (11.1%) in combo arm and SHR-A1811 in 2 (6.3%) in monotherapy arm. Conclusions: SHR-A1811 ± adebrelimab as 1L therapy showed robust activity with manageable safety in HER2-mutant NSCLC. Early data suggest clinical benefits with addition of adebrelimab, regardless of PD-L1 expression, driven by durablity of disease control. Citation Format: Shun Lu, Zhengbo Song, Ziming Li, Haiyong Wang, Yan Yu, Qitao Yu, Shaozhang Zhou, Zhiyong He, Yan Wang, Yiping Zhang, Songyan Han, Rui Meng, Guoqun Zhang, Longhua Sun, Xueqin Chen, Yong Mao, Yongsheng Li, Yongzhong Luo, Kangsheng Gu, Xuhong Min, Bo Jin, Runxiang Yang, Yanqiu Zhao, Liqiang Zhong, Jun Wang, Zhiguo Zhou, Chengzhi Zhou, Kaijun Zhang, Xiaotong Li, Xinjing Ma, Liju Zong, You Li. SHR-A1811 ± adebrelimab as first-line (1L) treatment for advanced HER2-mutant NSCLC: A randomized phase 2 cohort from a phase 1b/2 study [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(8_Suppl):Abstract nr CT301.

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Cancer Research
Published
2026-04-17
DOI
https://doi.org/10.1158/1538-7445.am2026-ct301
Primary Topic
HER2/EGFR in Cancer Research
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article
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Abstract CT301: SHR-A1811 ± adebrelimab as first-line (1L) treatment for advanced HER2-mutant NSCLC: A randomized phase 2 cohort from a phase 1b/2 study

Shaozhang Zhou, Liqiang Zhong, Guoqun Zhang, Liju Zong et al.
Cancer Research
HER2/EGFR in Cancer Research
article

Abstract CT301: SHR-A1811 ± adebrelimab as first-line (1L) treatment for advanced HER2-mutant NSCLC: A randomized phase 2 cohort from a phase 1b/2 study

Shaozhang Zhou, Liqiang Zhong, Guoqun Zhang, Liju Zong, Y Li, Yi Luo, X Chen, Xinjing Ma, Bo Jin, Kaijun Zhang, Yi-Xiang Wang, Yuxing Wang, Y W Zhao, L G Sun, Xiaotong Li, Xuhong Min, Yan Yu, Runxiang Yang, Haiyong Wang, Kangsheng Gu, Zhiyong He, Yong Mao, Ziming Li, Songyan Han, Chengzhi Zhou, Zhengbo Song, Yiping Zhang, Shun Lu, Rui Meng, Qitao Yu, Zhiguo Zhou
article en

Abstract

Abstract Background: Trastuzumab rezetecan (SHR-A1811) is a novel HER2-directed ADC approved for pretreated HER2-mutant NSCLC (Lancet Oncol, 2025). ADCs may enhance antitumor immunity and synergize with immunotherapy. We conducted an open-label, phase 1/2 (dose-escalation/efficacy-exploration) study (NCT05482568) to evaluate SHR-A1811 in combination therapy for HER2-altered NSCLC and here report data from phase 2 Cohort D of 1L SHR-A1811 ± adebrelimab (anti-PD-L1 mAb) for HER2-mutant NSCLC. Methods: Patients (pts) were randomized (1:1) to receive SHR-A1811 (4.8 mg/kg, iv, Q3W) + adebrelimab (1200 mg, iv, Q3W) or SHR-A1811 (4.8 mg/kg, iv, Q3W) alone, stratified by PD-L1 expression (TPS, <1% vs ≥1%). The primary endpoint was ORR per investigator. Results: 68 pts (PD-L1 TPS <1%/1-49%/≥50%, 50.0%/41.2%/8.8%; exon 20 insertions/A775_G776insYVMA, 89.7%/55.9%) were treated. At data cutoff (Oct 20, 2025), median follow-up was 16.7 mo. Confirmed ORR was 69.4% (95% CI 51.9-83.7) with SHR-A1811 + adebrelimab (combo) vs 81.3% (95% CI 63.6-92.8) with SHR-A1811; median DoR was not reached (NR) and 16.6 mo (95% CI 8.5-NR), respectively. PFS events occurred in 10 pts (27.8%) with combo vs 13 (40.6%) with SHR-A1811; median PFS was NR (95% CI 15.3-NR) vs 17.9 mo (95% CI 9.7-NR; HR 0.65, 95% CI 0.28-1.47). Efficacy by PD-L1 TPS is shown in Table 1. A trend toward improved PFS with addition of adebrelimab was seen across subgroups. All grade ≥3 TRAEs occurring in ≥10% were hematologic in both arms. ILD occurred in 2 (5.6%) pts with combo and 1 (1.3%) with SHR-A1811. TRAEs led to discontinuation of SHR-A1811 in 2 (5.6%) and adebrelimab in 4 (11.1%) in combo arm and SHR-A1811 in 2 (6.3%) in monotherapy arm. Conclusions: SHR-A1811 ± adebrelimab as 1L therapy showed robust activity with manageable safety in HER2-mutant NSCLC. Early data suggest clinical benefits with addition of adebrelimab, regardless of PD-L1 expression, driven by durablity of disease control. Citation Format: Shun Lu, Zhengbo Song, Ziming Li, Haiyong Wang, Yan Yu, Qitao Yu, Shaozhang Zhou, Zhiyong He, Yan Wang, Yiping Zhang, Songyan Han, Rui Meng, Guoqun Zhang, Longhua Sun, Xueqin Chen, Yong Mao, Yongsheng Li, Yongzhong Luo, Kangsheng Gu, Xuhong Min, Bo Jin, Runxiang Yang, Yanqiu Zhao, Liqiang Zhong, Jun Wang, Zhiguo Zhou, Chengzhi Zhou, Kaijun Zhang, Xiaotong Li, Xinjing Ma, Liju Zong, You Li. SHR-A1811 ± adebrelimab as first-line (1L) treatment for advanced HER2-mutant NSCLC: A randomized phase 2 cohort from a phase 1b/2 study [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(8_Suppl):Abstract nr CT301.

Cancer ResearchVol. 86(8_Supplement)
Hebei Medical University (CN), Jiangnan University (CN), Central South University (CN), Nanchang University (CN), Harbin Medical University (CN), Anhui Medical University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Kunming Medical University (CN), Shanghai Chest Hospital (CN), First Affiliated Hospital of Guangzhou Medical University (CN), Zhejiang Cancer Hospital (CN), Shandong Tumor Hospital (CN), Shanxi Provincial Cancer Hospital (CN), Third Affiliated Hospital of Harbin Medical University (CN), Fourth Hospital of Hebei Medical University (CN), Zhongshan People's Hospital (CN), Hunan Cancer Hospital (CN), Anhui Provincial Hospital (CN), First Affiliated Hospital of Anhui Medical University (CN), First Hospital of China Medical University (CN), Henan Cancer Hospital (CN), Jiangsu Hengrui Medicine (China) (CN), Fujian Provincial Cancer Hospital (CN), Chongqing Cancer Hospital (CN), Tumor Hospital of Guangxi Medical University (CN), First Affiliated Hospital of Zhengzhou University (CN), Second People’s Hospital of Yibin (CN), Xiangya Hospital Central South University (CN), Shandong First Medical University (CN), First Affiliated Hospital of Nanchang University (CN), Hangzhou Cancer Hospital (CN), Huazhong University of Science and Technology (CN), China Medical University (CN), Guangzhou Medical University (CN)
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HER2/EGFR in Cancer Research
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