Wenbin Zhou, Mengyao Zha, Hehui Fang, Kai Cao, Jiaqi Yong, Yue Sun, Yuan Yuan, Jian Zhang, Shencun Fang, Qiang Ding, Wei Li
Leptomeningeal metastasis (LM), an uncommon yet highly fatal condition, involves malignant tumor infiltration of the meninges resulting in progressive neurological deterioration and severe quality-of-life impairment. LM remains largely refractory to treatment and lacks standardized treatment consensus, with a low intracranial objective response rate (iORR) of 20% and a short median intracranial progression-free survival (iPFS) of 2.2 months. In this study, adult patients with breast cancer-related LM received intraventricular thiotepa combined with methotrexate. The primary endpoint was achieved with an iORR of 45.8% (11 out of 24, 95% CI: 25.55-67.18%), and the intracranial disease control rate was 58.3% (14 out of 24, 95% CI: 36.64-77.89%). From treatment initiation, the median iPFS and overall survival were 7.9 months (95% CI: 5.3-not estimable) and 11.7 months (95% CI: 5.7-not estimable), respectively. Grade 3-4 treatment-related adverse events occurred in 62.5% (15 out of 24) of patients, most commonly thrombocytopenia (37.5%) and leukopenia (33.3%), with no Grade 5 toxicities. The exploratory study indicated that two proteins in CSF and four plasma proteins were significantly associated with iORR. Overall, the regimen was feasible and demonstrated a manageable safety profile, with a preliminary signal of clinical benefit warranting further investigation.