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
1773P - Genomic and transcriptomic analysis of chondrosarcomas to explore new potential treatment options
Presenter: Konstantin Zirov
Session: Poster session 06
1774P - Immunological-molecular profiling of chondrosarcoma (ChS)
Presenter: Piotr Rutkowski
Session: Poster session 06
1775P - Peripheral blood (PB) T cell phenotype and tumor microenvironment (TME) subtype are independently associated with immune checkpoint blockade (ICB) outcomes in sarcomas
Presenter: Evan Rosenbaum
Session: Poster session 06
1776P - Targeting B7H3 biomimetic nanoparticles for strengthening osteosarcoma photodynamic therapy through aggravating DNA damage
Presenter: Tianqi Luo
Session: Poster session 06
1777P - Molecular profiling from next-generation sequencing (NGS) reveals new potential therapeutic targets in patients with pediatric-type sarcomas
Presenter: Anthony Conley
Session: Poster session 06
1778P - Clear cell sarcomas (CCS) express Gp100: A novel immune target for a bispecific T cell engager
Presenter: Elise Nassif Haddad
Session: Poster session 06
1779P - Deep learning tertiary lymphoid structures detection on HES/H&E slides and association to survival outcome in sarcoma
Presenter: Lucile Vanhersecke
Session: Poster session 06
1780P - Homologous recombination pathway in sarcomas: A novel opportunity of therapy?
Presenter: María del Carmen Garijo Martínez
Session: Poster session 06