Plus Therapeutics Recaps Presentation Of ReSPECT-LM Phase 1 Interim Data At 2024 San Antonio Breast Cancer Symposium
Plus Therapeutics Recaps Presentation Of ReSPECT-LM Phase 1 Interim Data At 2024 San Antonio Breast Cancer Symposium
Plus Therapeutics回顾了在2024年圣安东尼奥乳腺癌研讨会上呈现的ReSPECt-Lm一期中期数据
Key Highlights from the Presentation:
演示文稿的主要亮点:
- Nine of 20 patients with LM primary breast cancer were treated and evaluable through five dose escalation cohorts, with the maximum tolerated dose yet to be reached
- Primary breast cancer biomarker status across the 9 patients were:
- ER positive/HER2 negative: n=3
- HER2 positive: n=2
- Triple negative: n=4
- Patients received a single intrathecal dose of Rhenium (186Re) Obisbemeda, ranging from 6.6 to 66.14 mCi of radiation
- Only one dose-limiting toxicity (thrombocytopenia) was reported (Cohort 5)
- A linear increase in absorbed dose was observed from Cohorts 1 through 5, with an average absorbed dose of 253 Gy to the cranial subarachnoid space in Cohort 5
- Circulating tumor cell (CTC) and radiographic (MRI) response data were available for 8 of the 9 breast cancer patients with LM, and clinical response data were available for 7 of the 9 patients
- Best response rates (response only) were:
- CTC: 88% (7/8)
- MRI imaging: 25% (2/8)
- Clinical: 29% (2/7)
- Clinical benefit rates (response and stable disease) were:
- CTC: 100% (8/8)
- MRI imaging: 75% (6/8)
- Clinical: 71 % (5/7)
- Best response rates (response only) were:
- Median overall survival for 9 breast cancer patients was 9 months, with 2 patients surviving beyond 600 days post-treatment
- 20名乳腺癌原发癌患者中,有9名接受了治疗并经过评估,五个剂量递增队列中尚未达到最大耐受剂量
- 9名患者的乳腺癌生物标志物状态为:
- 雌激素受体阳性/HER2阴性:n=3
- HER2阳性:n=2
- 三阴性:n=4
- 患者接受了一剂6.6到66.14毫克铼(186Re)Obisbemeda的单次鞘内注射,辐射剂量为
- 仅报告了一例剂量限制性毒性(血小板减少症)(队列5)
- 从第1组到第5组观察到吸收剂量线性增加,第5组的平均吸收剂量为253 Gy,作用于颅内蛛网膜下腔。
- 循环境肿瘤细胞(CTC)和影像学(MRI)反应数据可用于9名患有Lm的乳腺癌患者中的8位,临床反应数据可用于9名患者中的7位。
- 最佳反应率(仅反应)为:
- CTC: 88% (7/8)
- MRI成像: 25% (2/8)
- 临床: 29% (2/7)
- 临床获益率(反应和稳定疾病)为:
- CTC: 100% (8/8)
- MRI成像:75% (6/8)
- 临床:71% (5/7)
- 最佳反应率(仅反应)为:
- 9名乳腺癌患者的中位生存时间为9个月,其中2名患者在治疗后存活超过600天。