Ng Raymond A, Barratt Susanna, Parisian Alison, Palanisamy Gopinath S, Phukan Samiron, Sun Richard, Robello Brandon, Peña Guadalupe, Sapugay Judevin, Yeghikyan David, Wang Chenbo, Satish Kher Samir, Thangathirupathy Srinivasan, Millikin Robert, Yu Guijun, Watanabe Teruki, Zhou Fei, Rich Brian, Duncan Alexis, Andersen Samuel E, Chawla Reena, Zak David R, Heerding Dirk A, Hearn Brian R, Greene Geoffrey, Harmon Cyrus L, Hodges-Gallagher Leslie, Kushner Peter J, Fanning Sean W, Myles David C
Olema Oncology, 780 Brannan Street, San Francisco 94107, California, United States.
Aragen Life Sciences Private Ltd., Hyderabad 500076, India.
ACS Omega. 2025 May 29;10(22):22685-22700. doi: 10.1021/acsomega.4c11023. eCollection 2025 Jun 10.
Metastatic breast cancer (mBC) is a leading cause of cancer death in women. Most breast cancer patients are administered estrogen-receptor-targeted endocrine therapies to treat or prevent progressive metastatic disease. Development of endocrine resistance through acquisition of mutations in the estrogen receptor gene, , that constitutively activate the estrogen receptor leads to relapse. Complete antagonism of both WT and mutant () with an oral therapeutic that persistently antagonizes ER-driven oncogenic transcriptional activities is a requirement for efficacy. Here, we describe our discovery of the investigational drug OP-1250 (palazestrant). OP-1250 is a potent complete estrogen receptor antagonist (CERAN) and selective estrogen receptor degrader (SERD) that is active in both WT and breast cancer tumors. OP-1250's effective induction of tumor regression either as a single agent or in combination with a CDK4/6 inhibitor has led to the rapid advancement of this compound into a Phase 3 clinical trial (OPERA-01).
转移性乳腺癌(mBC)是女性癌症死亡的主要原因。大多数乳腺癌患者接受靶向雌激素受体的内分泌疗法来治疗或预防进展性转移性疾病。通过在雌激素受体基因中获得突变而产生的内分泌抵抗,即组成性激活雌激素受体,会导致复发。使用一种持续拮抗雌激素受体驱动的致癌转录活性的口服治疗药物对野生型和突变型()进行完全拮抗是疗效的必要条件。在此,我们描述了我们对研究药物OP-1250(帕拉泽司琼)的发现。OP-1250是一种强效的完全雌激素受体拮抗剂(CERAN)和选择性雌激素受体降解剂(SERD),在野生型和乳腺癌肿瘤中均有活性。OP-1250作为单一药物或与CDK4/6抑制剂联合使用时有效诱导肿瘤消退,这使得该化合物迅速进入3期临床试验(OPERA-01)。