Abstract 523P
Background
Chemo-immunotherapy is the standard first-line (1L) therapy for patients (pts) with extensive-stage small cell lung cancer (ES-SCLC). However, not all ES-SCLC pts benefit from chemo-immunotherapy. We aimed to assess the efficacy and safety of camrelizumab + apatinib as maintenance treatment for ES-SCLC pts who had disease control after standard 1L chemotherapy.
Methods
Key inclusion criteria were age 18-75 years, histologically or cytologically confirmed ES-SCLC, ECOG PS 0-1, no disease progression after 4∼6 cycles of standard 1L chemotherapy. Eligible pts received camrelizumab (200mg, iv, d1, q3w) + apatinib (250mg, po, qd) until disease progression or intolerable toxicity. The primary endpoint was progression free survival (PFS); key secondary endpoints included overall response rate (ORR), disease control rate (DCR) and safety.
Results
From July 2021 to July 2023, 18 pts who received at least 1 dose of camrelizumab + apatinib were analyzed. The median age was 59 years (range: 45-75) with 16 (88.9%) males, 11 (61.1%) former smokers, 4 (22.2%) current smokers and 13 (72.2%) with ECOG PS 1. One patient (5.6%) had brain metastasis, 3 (16.7%) had liver metastasis, and 4 (22.2%) had bone metastasis. At data cutoff, 5 pts remained on treatment, and 16 pts had at least 1 post-treatment tumor assessment. The median PFS was 6.4 months (3.0-NR), the confirmed ORR and DCR were 12.5% (2/16) and 100% (16/16), respectively. Treatment-related adverse events (TRAEs) were reported in 17 pts (94.4%). Among them, 10 (55.6%) pts experienced grade 3 or 4 TRAEs. This included 2 pts (11.1%) with diarrhea, 2 (11.1%) with hyperglycemia, and 1 patient each (5.6%) with increased aspartate aminotransferase, increased alanine aminotransferase, decreased lymphocyte count, pancreatitis, hyponatremia, asthenia, elevated γ-glutamyl transferase and nerve injury. No grade 5 adverse events occurred.
Conclusions
Camrelizumab plus apatinib had promising efficacy and acceptable safety as maintenance treatment in ES-SCLC pts who responded or had stable disease after standard 1L chemotherapy. Further validation is warranted.
Clinical trial identification
NCT04901754.
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
571P - Dacomitinib in treatment-naïve EGFR-mutant NSCLC patients with multiple brain metastases: Initial efficacy and safety data from a phase II study
Presenter: Yongfeng Yu
Session: Poster Display
Resources:
Abstract
572P - Multivariable five-year survival prediction model for prognosing patients with EGFR-mutated NSCLC treated with EGFR-TKIs
Presenter: Qi-An Wang
Session: Poster Display
Resources:
Abstract
573P - LUMINATE-103: Real-world treatment patterns and outcomes of patients (pts) with epidermal growth factor receptor mutant (EGFR MU), non-squamous (NSQ) locally advanced/metastatic non-small cell lung cancer (a/mNSCLC): Pooled analysis of large US electronic health record (EHR) datasets
Presenter: Byoung Chul Cho
Session: Poster Display
Resources:
Abstract
574P - Efficacy and safety of dacomitinib in treatment-naïve patients with advanced NSCLC harboring uncommon EGFR mutations
Presenter: Lin Wu
Session: Poster Display
Resources:
Abstract
575P - Efficacy and safety of dacomitinib in treatment-naïve patients with advanced NSCLC and brain metastasis: A multicenter cohort study
Presenter: Puyuan Xing
Session: Poster Display
Resources:
Abstract
576P - Clonality of both EGFR and co-occurring TP53 mutations affect the treatment efficacy of the third-generation EGFR-TKIs in advanced-stage EGFR-mutant non-small cell lung cancer
Presenter: Wen Feng Fang
Session: Poster Display
Resources:
Abstract
577P - A study of the efficacy and safety of amivantamab in EGFR exon 20 insertion (E20I) mutations in NSCLC
Presenter: Daeho Choi
Session: Poster Display
Resources:
Abstract
578P - Tyrosine kinase inhibitor treatment of elderly patients with epidermal growth factor receptor mutated advanced non-small cell lung cancer: A multi-institute retrospective study
Presenter: Ling-Jen Hung
Session: Poster Display
Resources:
Abstract
579P - Real-world study of dacomitinib as first-line treatment for patients with EGFR-mutant non-small cell lung cancer
Presenter: Ji Eun Shin
Session: Poster Display
Resources:
Abstract
580P - Efficacy and safety of dacomitinib as first-line treatment for advanced non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor <italic>(EGFR)</italic> 21L858R mutation: A multicenter, ambispective, consecutive case-series study
Presenter: Shouzheng Wang
Session: Poster Display
Resources:
Abstract