Safety analysis for BH009 vs docetaxel from a bioavailability study.

Authors

null

Qun Sun

Zhuhai Beihai Biotech Co, Ltd, Zhuhai, China

Qun Sun , Xiaohua Wei , Haihua Jiang

Organizations

Zhuhai Beihai Biotech Co, Ltd, Zhuhai, China

Research Funding

Zhuhai Beihai Biotech Co., Ltd

Background: BH009 is a novel polysorbate 80-free formulation of docetaxel (DXT) that could eliminate hypersensitivity reactions associated with polysorbate 80. In a bioavailability study of BH009 vs docetaxel (Taxotere), we reported that the ratios for the total DXT and free-DXT fraction Cmax, AUC0-t, and AUC0-∞ of BH009 and docetaxel were within 80% to 125% (90% confidence intervals). Here, we report the safety analysis from the same study population. Methods: This multicenter, randomized, open-label, 2-way crossover study compared the pharmacokinetics and safety of BH009 and docetaxel (Winthrop docetaxel injection, an authorized generic of Taxotere). A total of 46 patients with breast, head and neck, lung, stomach, ovarian, or cervical cancers were randomized, of which 43 patients were treated with BH009 and 44 patients were treated with docetaxel. Patients received a single dose of 75 mg/m2 BH009 or Taxotere IV over 60 min, with ≥21-d washout between doses. Safety evaluation included treatment-emergent adverse events (TEAEs) and serious adverse events. Results: In all, 198 TEAEs were reported during the study: 94 after the administration of BH009 and 104 after the administration of docetaxel. No serious adverse events or deaths occurred. The only grade 3/4 toxicities that occurred for both arms during this study were hematologic. Overall, the incidence of grade 3/4 hematologic toxicity was significantly lower in the BH009 group than in the docetaxel group (2.3% vs 15.9%). Only one patient in BH009 arm experienced grade 3 anemia; no additional grade 3/4 hematologic adverse events were seen in the BH009 group. The incidence of grade 3/4 leukopenia, neutropenia, and lymphopenia in the Taxotere group was 6.8%, 4.6%, and 2.3%, respectively. The overall safety profile in the BH009 group was better than that in the Taxotere group. Conclusions: A better safety profile was observed in the study when BH009 group was compared to docetaxel group in grade 3/4 hematologic toxicity. Clinical trial information: NCT04889599.

Summary of grade3/4 hematologic toxicity (BH009 vs docetaxel).

Adverse Event TermBH009 (n=43), n (%)Taxotere (n=44), n (%)
Grade 3Grade 4Grade 3/4TotalGrade 3Grade 4Grade 3/4Total
Anemia1 (2.3)0 (0)1 (2.3)1 (2.3)1 (2.3)0 (0)1 (2.3)7 (15.9)
Leukopenia0 (0)0 (0)0 (0)2 (4.6)1 (2.3)3(6.8)
Neutropenia0 (0)0 (0)0 (0)1 (2.3)1 (2.3)2 (4.6)
Lymphopenia0 (0)0 (0)0 (0)1 (2.3)0 (0)1 (2.3)

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Abstract Details

Meeting

2024 ASCO Annual Meeting

Session Type

Publication Only

Session Title

Publication Only: Breast Cancer—Metastatic

Track

Breast Cancer

Sub Track

Triple-Negative

Clinical Trial Registration Number

NCT04889599

Citation

J Clin Oncol 42, 2024 (suppl 16; abstr e13129)

DOI

10.1200/JCO.2024.42.16_suppl.e13129

Abstract #

e13129

Abstract Disclosures