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回顧了在2024年聖安東尼奧乳腺癌研討會上呈現的ReSPECt-Lm一期中期數據
Key Highlights from the Presentation:
演示文稿的主要亮點:
- 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名乳腺癌原發癌患者中,有9名接受了治療並經過評估,五個劑量遞增隊列中尚未達到最大耐受劑量
- 9名患者的乳腺癌生物標誌物狀態爲:
- 雌激素受體陽性/HER2陰性:n=3
- HER2陽性:n=2
- 三陰性:n=4
- 患者接受了一劑6.6到66.14毫克錸(186Re)Obisbemeda的單次鞘內注射,輻射劑量爲
- 僅報告了一例劑量限制性毒性(血小板減少症)(隊列5)
- 從第1組到第5組觀察到吸收劑量線性增加,第5組的平均吸收劑量爲253 Gy,作用於顱內蛛網膜下腔。
- 循環境腫瘤細胞(CTC)和影像學(MRI)反應數據可用於9名患有Lm的乳腺癌患者中的8位,臨牀反應數據可用於9名患者中的7位。
- 最佳反應率(僅反應)爲:
- CTC: 88% (7/8)
- MRI成像: 25% (2/8)
- 臨牀: 29% (2/7)
- 臨牀獲益率(反應和穩定疾病)爲:
- CTC: 100% (8/8)
- MRI成像:75% (6/8)
- 臨牀:71% (5/7)
- 最佳反應率(僅反應)爲:
- 9名乳腺癌患者的中位生存時間爲9個月,其中2名患者在治療後存活超過600天。