Updated efficacy results from the phase I cervical cancer cohort of BAT8008, a TROP-2–directed antibody-drug conjugate, in patients with advanced cervical cancer.

5507 Background: BAT8008 is a novel antibody-drug conjugate comprising a TROP-2 antibody and an exatecan payload. Patients with recurrent or metastatic cervical cancer (r/m CC) who have progressed on platinum-based chemotherapy have limited treatment options and poor prognosis. This study reports the safety and efficacy of BAT8008 in a cohort of r/m CC patients from a phase 1 trial. Methods: This analysis is part of BAT-8008-001-CR, a multi-center, open-label phase 1 study with dose escalation and expansion cohorts. Patients with r/m CC who had failed prior systemic treatments were enrolled. BAT8008 was administered 2.4 mg/kg or 2.1mg/kg intravenously every two weeks (Q2W) 2.4 mg/kg. Results: As of Jan 5, 2026, 68 evaluable patients with r/m CC were enrolled (27 at 2.1 mg/kg, 41 at the 2.4 mg/kg). Patients were heavily pre-treated, with 55.9% having received ≥2 prior lines of therapy. 64.7% had prior anti-angiogenic therapy and 38.2% had prior immunotherapy. At the 2.4 mg/kg dose (n=44), the most common TRAEs (any grade/≥G3) were anemia (63.6%/15.9%), WBC decreased (68.2%/25.0%), stomatitis (54.5%/6.8%), and neutrophil count decreased (45.5%/20.5%). No treatment-related deaths occurred. For the RP2D cohort (n=41), the confirmed objective response rate (cORR) was 29.3% and disease control rate (DCR) was 78.0%. The median progression-free survival (mPFS) was 6.7 months (95% CI: 3.5-12.1) and median duration of response (mDoR) was 9.0 months (95% CI: 4.2-12.3). Efficacy was observed across subgroups and was independent of TROP-2 expression level. Conclusions: BAT8008 demonstrated promising and durable anti-tumor activity with a manageable safety profile in heavily pre-treated patients with r/m cervical cancer. These findings support the continued development of BAT8008 in this patient population. Clinical trial information: NCT05620017 . Efficacy Endpoint 2.1 mg/kg (n=27) 2.4 mg/kg (n=41) Overall (n=68) cORR, % (95% CI) 22.2 (10.6-40.8) 29.3 (17.6-44.5) 26.5 (17.4-38.0) DCR, % (95% CI) 81.5 (63.3-91.8) 78.0 (63.3-88.0) 79.4 (68.4-87.3) mPFS, months (95% CI) 5.3 (3.3-8.3) 6.7 (3.5-12.1) 6.5 (3.5-8.3) mDoR, months (95% CI) Not Reached 9.0 (4.2-12.3) 9.0 (5.3-12.3)

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Journal
Journal of Clinical Oncology
Published
2026-05-27
DOI
https://doi.org/10.1200/jco.2026.44.16_suppl.5507
Primary Topic
HER2/EGFR in Cancer Research
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article
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article

Updated efficacy results from the phase I cervical cancer cohort of BAT8008, a TROP-2–directed antibody-drug conjugate, in patients with advanced cervical cancer.

Hao Wang, M Zhang, Y Li, Zhiguo Luo et al.
Journal of Clinical Oncology
HER2/EGFR in Cancer Research
article

Updated efficacy results from the phase I cervical cancer cohort of BAT8008, a TROP-2–directed antibody-drug conjugate, in patients with advanced cervical cancer.

Hao Wang, M Zhang, Y Li, Zhiguo Luo, Shengfeng Li, J F, Hongrui Niu, J S Zhao, Q I N G Wen, Y Zhuo, Erwei Song, Jin Yang, Hong Wang, Meili Sun, Wenjuan Chen, Xiumin Li, Tienan Yi, Zhengbo Song
article en

Abstract

5507 Background: BAT8008 is a novel antibody-drug conjugate comprising a TROP-2 antibody and an exatecan payload. Patients with recurrent or metastatic cervical cancer (r/m CC) who have progressed on platinum-based chemotherapy have limited treatment options and poor prognosis. This study reports the safety and efficacy of BAT8008 in a cohort of r/m CC patients from a phase 1 trial. Methods: This analysis is part of BAT-8008-001-CR, a multi-center, open-label phase 1 study with dose escalation and expansion cohorts. Patients with r/m CC who had failed prior systemic treatments were enrolled. BAT8008 was administered 2.4 mg/kg or 2.1mg/kg intravenously every two weeks (Q2W) 2.4 mg/kg. Results: As of Jan 5, 2026, 68 evaluable patients with r/m CC were enrolled (27 at 2.1 mg/kg, 41 at the 2.4 mg/kg). Patients were heavily pre-treated, with 55.9% having received ≥2 prior lines of therapy. 64.7% had prior anti-angiogenic therapy and 38.2% had prior immunotherapy. At the 2.4 mg/kg dose (n=44), the most common TRAEs (any grade/≥G3) were anemia (63.6%/15.9%), WBC decreased (68.2%/25.0%), stomatitis (54.5%/6.8%), and neutrophil count decreased (45.5%/20.5%). No treatment-related deaths occurred. For the RP2D cohort (n=41), the confirmed objective response rate (cORR) was 29.3% and disease control rate (DCR) was 78.0%. The median progression-free survival (mPFS) was 6.7 months (95% CI: 3.5-12.1) and median duration of response (mDoR) was 9.0 months (95% CI: 4.2-12.3). Efficacy was observed across subgroups and was independent of TROP-2 expression level. Conclusions: BAT8008 demonstrated promising and durable anti-tumor activity with a manageable safety profile in heavily pre-treated patients with r/m cervical cancer. These findings support the continued development of BAT8008 in this patient population. Clinical trial information: NCT05620017 . Efficacy Endpoint 2.1 mg/kg (n=27) 2.4 mg/kg (n=41) Overall (n=68) cORR, % (95% CI) 22.2 (10.6-40.8) 29.3 (17.6-44.5) 26.5 (17.4-38.0) DCR, % (95% CI) 81.5 (63.3-91.8) 78.0 (63.3-88.0) 79.4 (68.4-87.3) mPFS, months (95% CI) 5.3 (3.3-8.3) 6.7 (3.5-12.1) 6.5 (3.5-8.3) mDoR, months (95% CI) Not Reached 9.0 (4.2-12.3) 9.0 (5.3-12.3)

Journal of Clinical OncologyVol. 44(16_suppl)
Hubei University of Medicine (CN), Fujian Medical University (CN), Sun Yat-sen University (CN), Chongqing University (CN), Anhui Medical University (CN), Ta Solutions (China) (CN), Sun Yat-sen Memorial Hospital (CN), Zhejiang Cancer Hospital (CN), Shanxi Provincial Cancer Hospital (CN), Zhangzhou Municipal Hospital of Fujian Province (CN), Jinan Central Hospital (CN), Third Hospital of Nanchang (CN), First Affiliated Hospital of Xinxiang Medical University (CN), Taihe Hospital (CN), Xiangyang Central Hospital (CN), First Affiliated Hospital of Xi'an Jiaotong University (CN), Fujian Provincial Cancer Hospital (CN), Second Affiliated Hospital of Anhui Medical University (CN), Chongqing Cancer Hospital (CN), Shandong First Medical University (CN), First Hospital of Xi'an (CN), Henan Medical University (CN)
Good health and well-being
Openalex Percentile: Top 11%
HER2/EGFR in Cancer Research
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