Abstract 346P
Background
In this prospective clinical study, we aimed to evaluate the efficacy and toxicities of intrathecal chemotherapy (IC) with pemetrexed via the Ommaya reservoir in lung adenocarcinoma (LUAD) with refractory leptomeningeal metastases (LM).
Methods
LUAD-LM patients who had failed at least two prior treatments were recruited. After the implantation of the Ommaya reservoir, 30 mg to 50 mg pemetrexed was administered on Days 1 and 8 every 3 weeks via the Ommaya reservoir. Serial samples of cerebrospinal fluid (CSF) and plasma were obtained for pharmacokinetic studies. The primary endpoint was progression-free survival (PFS), and the secondary endpoints included overall survival (OS), objective response rate (ORR), disease control rate (DCR) and therapeutic toxicities.
Results
Twenty-six patients were enrolled and analyzed. Clinical outcomes included response in 10 patients, stable disease in 9 patients and disease progression in 4 patients, revealing an ORR of 43.5% and DCR of 82.6%. The median PFS and OS were 6.3 and 9.2 months, respectively. Three patients without imaging evaluation or CSF cytology after treatment were not evaluable. Grade 1-2 myelosuppression (9/26, 34.6%), elevation of transaminase (6/26, 23.1%) and anaemia (4/26, 15.4%) were the three main adverse events. Dose-limiting toxicity was only observed in two patients (2/26, 7.7%), and 30 mg pemetrexed was considered as the recommended dose for IC. Pharmacokinetic analysis showed that using Ommaya reservoirs, higher pemetrexed concentrations and prolonged half-lives were achieved in the CSF compared with lumbar puncture (LP).
Conclusions
Intrathecal pemetrexed at a dose of 30 mg via the Ommaya reservoirs on Days 1 and 8 every 21 days achieved promising disease control and satisfactory survival with moderate toxicities in resistant LUAD-LM. Ommaya reservoirs may be a more convenient and safer route to implement IC, especially for the patients who cannot tolerate LP.
Clinical trial identification
ChiCTR2000028936.
Editorial acknowledgement
Legal entity responsible for the study
Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School.
Funding
Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
318P - EMPOWER-Lung 3: Cemiplimab in combination with platinum doublet chemotherapy for first-line (1L) treatment of advanced non-small cell lung cancer (NSCLC)
Presenter: Miranda Gogishvili
Session: Poster viewing 05.
323P - Development of a model to predict PD-L1 expression in pulmonary squamous cell carcinoma based on CT imaging features
Presenter: Yun Kyoung Shin
Session: Poster viewing 05.
324P - Efficacy and safety analysis of anlotinib combined with immunotherapy as second-line therapy for advanced non-small cell lung cancer (NSCLC)
Presenter: Qin Shi
Session: Poster viewing 05.
326P - Durvalumab (D) ± tremelimumab (T) + chemotherapy (CT) in 1L metastatic (m) NSCLC: Overall survival (OS) update from POSEIDON after median follow-up (mFU) of approximately 4 years (y)
Presenter: Byoung Chul Cho
Session: Poster viewing 05.
328P - Long-term follow-up of pembrolizumab plus chemotherapy in Chinese patients with metastatic squamous non-small cell lung cancer (NSCLC) from KEYNOTE-407
Presenter: Ying Cheng
Session: Poster viewing 05.
329P - ORCHARD: Osimertinib + necitumumab in patients (pts) with advanced NSCLC whose disease progressed on first-line (1L) osimertinib
Presenter: Jonathan Riess
Session: Poster viewing 05.
332P - A phase II, open-label, single-center study of QL1706 plus platinum doublet chemotherapy with bevacizumab as first-line treatment in patients with advanced NSCLC: Data from EGFR mutant cohort
Presenter: Wen Feng Fang
Session: Poster viewing 05.