Lin Nancy U, Parker Leroy M, Come Steven E, Burstein Harold J, Haldoupis Margaret, Ryabin Nicole, Gelman Rebecca, Winer Eric P, Shulman Lawrence N
Department of Medical Oncology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.
Invest New Drugs. 2007 Aug;25(4):369-75. doi: 10.1007/s10637-007-9034-y. Epub 2007 Mar 8.
This study evaluated the safety and efficacy of CT-2103, a novel conjugate of paclitaxel and poly-L-glutamate, in patients with HER2-negative, metastatic breast cancer who had received 0 or 1 prior lines of chemotherapy. Although CT-2103 had activity in this small study, neurotoxicity and hypersensitivity reactions were more frequent in this patient population than expected, and led to early termination of the trial.
To evaluate the safety and efficacy of CT-2103, a novel conjugate of paclitaxel and poly-L-glutamate, in patients with metastatic breast cancer who had received 0 or 1 prior lines of chemotherapy.
Eighteen women with HER2-negative breast cancer were enrolled. Patients received intravenous CT-2103 at a dose of 175 mg/m2 of conjugated paclitaxel over 10 min every 3 weeks, without routine premedication. Eighty-three percent of women had received prior chemotherapy as part of adjuvant (39%), metastatic (17%), or both adjuvant and metastatic (28%) treatment. Three patients (17%) had previously received a taxane in the adjuvant setting.
Objective responses were observed in 4 of 18 patients (overall response rate, 22%, 95% confidence interval, 6 to 48%). Grade 3 or 4 neuropathy was observed in four patients. Grade 3 or 4 hypersensitivity reactions (HSR) were observed in four patients; none occurred prior to cycle 4 of therapy. Because of the higher-than-expected rate of HSR, the study was terminated early.
Although CT-2103 had activity in this small study of women with HER2-negative metastatic breast cancer, neurotoxicity and hypersensitivity reactions were more frequent in this patient population than expected. Hypersensitivity reactions were most likely to occur in later cycles of treatment, suggesting a true drug allergy, distinct from the HSR typically seen with standard paclitaxel.
本研究评估了CT - 2103(一种新型的紫杉醇与聚 - L - 谷氨酸偶联物)在接受过0或1线既往化疗的HER2阴性转移性乳腺癌患者中的安全性和疗效。尽管CT - 2103在这项小型研究中有活性,但该患者群体中神经毒性和超敏反应比预期更频繁,导致试验提前终止。
评估CT - 2103(一种新型的紫杉醇与聚 - L - 谷氨酸偶联物)在接受过0或1线既往化疗的转移性乳腺癌患者中的安全性和疗效。
纳入18例HER2阴性乳腺癌女性患者。患者每3周静脉注射CT - 2103,剂量为175 mg/m²的偶联紫杉醇,持续10分钟,不进行常规预处理。83%的女性曾接受过化疗,作为辅助治疗(39%)、转移性治疗(17%)或辅助和转移性治疗(28%)的一部分。3例患者(1%)曾在辅助治疗中接受过紫杉烷类药物。
18例患者中有4例观察到客观缓解(总缓解率22%,95%置信区间,6%至48%)。4例患者观察到3级或4级神经病变。4例患者观察到3级或4级超敏反应(HSR);在治疗第4周期之前均未发生。由于HSR发生率高于预期,该研究提前终止。
尽管CT - 2103在这项针对HER2阴性转移性乳腺癌女性的小型研究中有活性,但该患者群体中神经毒性和超敏反应比预期更频繁。超敏反应最有可能发生在治疗的后期周期,提示这是一种真正的药物过敏,与标准紫杉醇通常所见的HSR不同。