Abstract 1369P
Background
Intraventricular injection chemotherapy of pemetrexed is found to be effective in the treatment of non-small cell lung cancer (NSCLC) patients with leptomeningeal metastasis(LM),but chemotherapy-induced myelosuppression (CIM) greatly affects the quality of life and survival of patients. Trilaciclib has been approved for the use of SCLC before chemotherapy to reduce the incidence of CIM. This study aimed to evaluate the myeloprotective effect and safety of trilaciclib combined with intraventricular injection chemotherapy in the treatment of advanced NSCLC with LM.
Methods
This was a prospective, single-arm,phase Ⅱ clinical study (NCT 06332287). All patients underwent stereotactic installation of an Ommaya reservoir. IVC via the Ommaya reservoir was started the day after surgery. Patients received 30 mg pemetrexed and 240 mg/m2 trilaciclib twice weekly for 2 weeks as consolidation therapy, and then repeated every 3 to 4 weeks until disease progression or unacceptable toxicity, or patient refusal occurred.The primary endpoint was the incidence of severe neutropenia (SN) in the first cycle. The secondary endpoints were myeloprotective effect and safety of trilaciclib.
Results
All 28 enrolled NSCLC patients received trilaciclib before chemotherapy by December 2023. There were 13 males and 15 females patients, with a median age of 58 years (range:32-72). 96.4% patients received at least 2 lines of prior treatment. Nine patients received 4 cycles of trilaciclib combined with chemotherapy, with a median of 2 cycles (range:1-4). None of the 28 patients developed SN or febrile neutropenia (FN) in the first cycle. During treatment, only 1 patient (4%) developed grade 3/4 neutropenia, and no grade 3/4 anemia and ≥ grade 3 thrombocytopenia were observed. No dose reduction of chemotherapy drugs was observed. In terms of safety, most common adverse events were grade 1/2, and no treatment-related deaths occurred.
Conclusions
Trilaciclib yielded good myeloprotective effect and safety in advanced NSCLC with leptomeningeal metastasis who received intraventricular injection chemotherapy.
Clinical trial identification
NCT 06332287.
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1763P - Initial tumour size and residual mitotic count post-neoadjuvant imatinib linked to shorter relapse-free survival in GIST patients
Presenter: Javier Pozas Perez
Session: Poster session 06
1764P - Role of PIK3CA as a predictive biomarker in metastatic, imatinib-resistant GIST: A ct-DNA substudy of the VOYAGER trial
Presenter: Lennart Schardt
Session: Poster session 06
1765P - Second-line targeted therapy patterns and outcomes of advanced gastrointestinal stromal tumor: A prospective, multicentered real-world study
Presenter: Xinhua Zhang
Session: Poster session 06
1766P - Updated results of the RINGSIDE phase II trial and open-label extension of AL102 for treatment of desmoid tumors
Presenter: Bernd Kasper
Session: Poster session 06
1767P - Pegylated liposomal doxorubicin in symptomatic desmoid tumor
Presenter: Kjetil Boye
Session: Poster session 06
1768P - Desmoid tumors: Experience of a Spanish reference center
Presenter: Ana Gutierrez Ortiz
Session: Poster session 06
1769P - Safety and efficacy with vimseltinib in patients (pts) with tenosynovial giant cell tumor (TGCT) who received no prior anti–colony-stimulating factor 1 (CSF1) therapy: Ongoing phase II study
Presenter: Cesar Serrano
Session: Poster session 06
1771P - Blessed: Expanded yccess for DeltaRex-G in vivo gene therapy for sarcoma, pancreas and breast cancer (NCT04091295) and other solid malignancies (IND# 19130)
Presenter: Sant Chawla
Session: Poster session 06
1772P - Phosphoproteomic biomarker for afatinib response stratification in advanced chordoma
Presenter: Christoph Stange
Session: Poster session 06