Condition: Breast Cancer · HR+/HER2- Breast Cancer · Sponsor: Henan Cancer Hospital
The goal of this clinical trial is to learn if QL1706 is effective in early HR+/HER2- breast cancer. It will also learn about the safety of QL1706. The main questions it aims to answer are: Does QL1706 combined with neoadjuvant chemotherapy improve the pCR rate of early HR+/HER2- breast cancer? What adverse events do participants have when receiving QL1706? Participants will: Receive QL1706 plus chemotherapy or chemotherapy every 3 weeks for 6 cycles; All patients will receive surgery, and the primary end point is pathological complete response at the time of definitive surgery; After definitive surgery, the participants will receive adjuvant QL1706 every 3 weeks for up to 6 months from the beginning of the treatment.
This description comes directly from the study's public registry record.
Zhenzhen Liu · 13603862755 · zlyyliuzhenzhen0800@zzu.edu.cn
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| Henan cancer hospital | Zhengzhou, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06967103