Phase II study of izalontamab (SI-B001) in combination with paclitaxel or docetaxel in patients with recurrent/metastatic (R/M) head and neck squamous cell carcinoma (HNSCC).

6019 Background: Izalontamab is a bispecific antibody targeting EGFR and HER3. Here we present safety and efficacy results from a phase II study on izalontamab in combination with paclitaxel/docetaxel in patients with R/M HNSCC. Methods: Patients with R/M HNSCC who had progressed on prior anti-PD-(L)1 therapy, with or without platinum-based chemotherapy, and received no more than two prior lines of treatment were enrolled. Izalontamab was administered at 12mg/kg QW in combination with paclitaxel (80mg/m 2 IV QW) (for patients without prior exposure to paclitaxel) or docetaxel (35mg/m 2 IV D1D8D15 Q4W) (for patients with prior exposure to paclitaxel). Primary endpoint was investigator-assessed ORR. Secondary endpoints included PFS, OS, DCR, and DoR. Results: As of Nov 7, 2025, a total of 45 patients (44 HNSCC and 1 sinnonasal) were enrolled, of whom 35 (77.8%) received one prior line of therapy and 10 (22.2%) received two prior lines of therapy. HNSCC patients who received at least one dose of study drug were included in the analysis. Median follow-up was 15.0 months. Overall, ORR was 43.2%, confirmed ORR was 31.8%, median PFS was 4.0 months, and median OS was 10.0 months. In patients treated with izalontamab combo with paclitaxel (n = 34), ORR was 52.9%, confirmed ORR was 41.2%, median PFS was 5.4 months, and median OS was 11.2 months. Grade≥3 TRAEs occurred in 57.8% of patients. The most common grade≥3 TRAE was leukopenia (20.0%), followed by neutropenia (15.6%), rash (13.3%), and anemia (8.9%). One (2.1%) patient discontinued study treatment due to TRAE. No treatment-related death was observed. Conclusions: Izalontamab in combination with paclitaxel showed encouraging antitumor activity and a manageable safety profile in patients with R/M HNSCC who were previously treated with anti-PD-(L)1 therapy. Clinical trial information: NCT05054439 . Izalontamab+Paclitaxel(N=34) Izalontamab+ Docetaxel(N=10) Total(N=44) ORR, % (95% CI) 52.9 (35.1, 70.2) 10.0 (0.3, 44.5) 43.2 (28.3, 59.0) cORR, % (95% CI) 41.2 (24.6, 59.3) 0 31.8 (18.6, 47.6) DCR, % (95% CI) 73.5 (55.6, 87.1) 30.0 (6.7, 65.2) 63.6 (47.8, 77.6) Median DOR (mo) (95% CI) 5.0 (3.7, 11.0) NR (NR, NR) 5.0 (3.7, 11.0) Median PFS (mo) (95% CI) 5.4 (3.9, 6.6) 1.5 (0.4, 3.6) 4.0 (2.8, 5.5) Median OS (mo) (95% CI) 11.2 (6.6, 19.3) 6.6 (0.4, 13.8) 10.0 (6.6, 13.8)

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Publication Details

Journal
Journal of Clinical Oncology
Published
2026-05-27
DOI
https://doi.org/10.1200/jco.2026.44.16_suppl.6019
Primary Topic
Head and Neck Cancer Studies
Type
article
Field-Weighted Citation Impact
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article

Phase II study of izalontamab (SI-B001) in combination with paclitaxel or docetaxel in patients with recurrent/metastatic (R/M) head and neck squamous cell carcinoma (HNSCC).

Jinguan Lin, Bihui Li, L. Xue, X F Ma et al.
Journal of Clinical Oncology
Head and Neck Cancer Studies
article

Phase II study of izalontamab (SI-B001) in combination with paclitaxel or docetaxel in patients with recurrent/metastatic (R/M) head and neck squamous cell carcinoma (HNSCC).

Jinguan Lin, Bihui Li, L. Xue, X F Ma, Ye Guo, Kunyu Yang, Sa Xiao, Yi Zhu, Hai Zhu, Meiyu Fang
article en

Abstract

6019 Background: Izalontamab is a bispecific antibody targeting EGFR and HER3. Here we present safety and efficacy results from a phase II study on izalontamab in combination with paclitaxel/docetaxel in patients with R/M HNSCC. Methods: Patients with R/M HNSCC who had progressed on prior anti-PD-(L)1 therapy, with or without platinum-based chemotherapy, and received no more than two prior lines of treatment were enrolled. Izalontamab was administered at 12mg/kg QW in combination with paclitaxel (80mg/m 2 IV QW) (for patients without prior exposure to paclitaxel) or docetaxel (35mg/m 2 IV D1D8D15 Q4W) (for patients with prior exposure to paclitaxel). Primary endpoint was investigator-assessed ORR. Secondary endpoints included PFS, OS, DCR, and DoR. Results: As of Nov 7, 2025, a total of 45 patients (44 HNSCC and 1 sinnonasal) were enrolled, of whom 35 (77.8%) received one prior line of therapy and 10 (22.2%) received two prior lines of therapy. HNSCC patients who received at least one dose of study drug were included in the analysis. Median follow-up was 15.0 months. Overall, ORR was 43.2%, confirmed ORR was 31.8%, median PFS was 4.0 months, and median OS was 10.0 months. In patients treated with izalontamab combo with paclitaxel (n = 34), ORR was 52.9%, confirmed ORR was 41.2%, median PFS was 5.4 months, and median OS was 11.2 months. Grade≥3 TRAEs occurred in 57.8% of patients. The most common grade≥3 TRAE was leukopenia (20.0%), followed by neutropenia (15.6%), rash (13.3%), and anemia (8.9%). One (2.1%) patient discontinued study treatment due to TRAE. No treatment-related death was observed. Conclusions: Izalontamab in combination with paclitaxel showed encouraging antitumor activity and a manageable safety profile in patients with R/M HNSCC who were previously treated with anti-PD-(L)1 therapy. Clinical trial information: NCT05054439 . Izalontamab+Paclitaxel(N=34) Izalontamab+ Docetaxel(N=10) Total(N=44) ORR, % (95% CI) 52.9 (35.1, 70.2) 10.0 (0.3, 44.5) 43.2 (28.3, 59.0) cORR, % (95% CI) 41.2 (24.6, 59.3) 0 31.8 (18.6, 47.6) DCR, % (95% CI) 73.5 (55.6, 87.1) 30.0 (6.7, 65.2) 63.6 (47.8, 77.6) Median DOR (mo) (95% CI) 5.0 (3.7, 11.0) NR (NR, NR) 5.0 (3.7, 11.0) Median PFS (mo) (95% CI) 5.4 (3.9, 6.6) 1.5 (0.4, 3.6) 4.0 (2.8, 5.5) Median OS (mo) (95% CI) 11.2 (6.6, 19.3) 6.6 (0.4, 13.8) 10.0 (6.6, 13.8)

Journal of Clinical OncologyVol. 44(16_suppl)
Guilin Medical University (CN), Sichuan University (CN), West China Hospital of Sichuan University (CN), Zhejiang Cancer Hospital (CN), Chengdu Organic Chemicals (China) (CN), Hunan Cancer Hospital (CN), Shanghai East Hospital (CN), Wuhan Union Hospital (CN)
Good health and well-being
Openalex Percentile: Top 7%
Head and Neck Cancer Studies
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