Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Department of Gynecologic Oncology, Saitama Medical University International Medical Center, Saitama, Japan.
J Clin Oncol. 2023 May 20;41(15):2789-2799. doi: 10.1200/JCO.22.02558. Epub 2023 Mar 28.
To investigate the efficacy and safety of trastuzumab deruxtecan, an antibody-drug conjugate targeting human epidermal growth factor receptor 2 (HER2) with a topoisomerase I inhibitor payload, in patients with uterine carcinosarcoma (UCS) expressing HER2.
Patients with recurrent UCS with HER2 immunohistochemistry scores ≥1+ previously treated with chemotherapy were included. Patients were assigned to the HER2-high (immunohistochemistry score ≥2+; n = 22) or low (immunohistochemistry score of 1+; n = 10) groups for primary and exploratory analyses, respectively. Trastuzumab deruxtecan 6.4 or 5.4 mg/kg was administered intravenously once every 3 weeks until unacceptable toxicity or disease progression. Dose modification was based on the updated recommended phase II dose for breast cancer to be 5.4 mg/kg. The primary end point was the objective response rate by central review in the HER2-high group. Secondary end points included the overall response rate (ORR) in the HER2-high group by investigator assessment, ORR in the HER2-low group, progression-free survival (PFS), overall survival (OS), and safety.
The ORR by central review in the HER2-high and HER2-low groups were 54.5% (95% CI, 32.2 to 75.6) and 70.0% (95% CI, 34.8 to 93.3) and those by investigator assessments were 68.2% and 60.0%, respectively. The median PFS and OS in the HER2-high and HER2-low groups were 6.2 and 13.3 months and 6.7 months and not reached, respectively. Grade ≥ 3 adverse events occurred in 20 patients (61%). Grades 1-2 and 3 pneumonitis/interstitial lung disease occurred in eight (24%) and one (3%) patient, respectively.
Trastuzumab deruxtecan has efficacy in patients with UCS, regardless of HER2 status. The safety profile was generally consistent with that previously reported. Toxicities were manageable with appropriate monitoring and treatment.
研究靶向人表皮生长因子受体 2(HER2)的抗体药物偶联物曲妥珠单抗 deruxtecan(一种拓扑异构酶 I 抑制剂有效载荷)在表达 HER2 的子宫癌肉瘤(UCS)患者中的疗效和安全性。
纳入先前接受过化疗且 HER2 免疫组织化学评分≥1+的复发性 UCS 患者。患者被分配到 HER2 高(免疫组化评分≥2+;n=22)或低(免疫组化评分 1+;n=10)组进行主要和探索性分析。曲妥珠单抗 deruxtecan 6.4 或 5.4 mg/kg 静脉输注,每 3 周一次,直至出现不可接受的毒性或疾病进展。剂量调整基于乳腺癌更新的推荐 II 期剂量为 5.4 mg/kg。主要终点是中心评估的 HER2 高组的客观缓解率。次要终点包括研究者评估的 HER2 高组的总缓解率(ORR)、HER2 低组的 ORR、无进展生存期(PFS)、总生存期(OS)和安全性。
中心评估的 HER2 高组和 HER2 低组的 ORR 分别为 54.5%(95%CI,32.2 至 75.6)和 70.0%(95%CI,34.8 至 93.3),研究者评估的 ORR 分别为 68.2%和 60.0%。HER2 高组和 HER2 低组的中位 PFS 和 OS 分别为 6.2 和 13.3 个月和 6.7 个月和未达到。20 名患者(61%)发生≥3 级不良事件。8 名(24%)和 1 名(3%)患者分别发生 1-2 级和 3 级肺炎/间质性肺病。
曲妥珠单抗 deruxtecan 对 UCS 患者有效,与 HER2 状态无关。安全性概况与先前报道的基本一致。通过适当的监测和治疗,可以控制毒性。