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
193P - Impact of coronavirus disease 2019 on patients with unresectable hepatocellular carcinoma treated with atezolizumab/bevacizumab
Presenter: Hongjae Chon
Session: Poster Display
Resources:
Abstract
194P - Real-world outcomes of cadonilimab (PD-1/CTLA-4 bispecific antibody) plus chemotherapy as first-line treatment in advanced gastric (G) or gastroesophageal junction (GEJ) cancer with PD-L1 CPS≤5
Presenter: Qi Xu
Session: Poster Display
Resources:
Abstract
195P - Ferroptosis signatures in pancreatic ductal adenocarcinomas and their role in patient survival: A translational unsupervised clustering analysis
Presenter: Quoc-Huy Trinh
Session: Poster Display
Resources:
Abstract
196P - Clinical significance of circulating CD8+ and CD4+ T cell proliferation in advanced gastric cancer receiving first-line chemotherapy
Presenter: In-Ho Kim
Session: Poster Display
Resources:
Abstract
197P - Treatment patterns and clinical outcomes of patients with unresectable advanced or metastatic (UAM) gastric/gastroesophageal junction adenocarcinoma (GA/GEJA) in China: A multicenter real-world study
Presenter: Yanqiao Zhang
Session: Poster Display
Resources:
Abstract
198P - Effectiveness of lenvatinib in patients with unresectable hepatocellular carcinoma: A multicenter observational study in Japan
Presenter: Namiki Izumi
Session: Poster Display
Resources:
Abstract
199P - Efficacy of endostar in combination with concurrent chemoradiotherapy in patients with locally advanced squamous cell carcinoma of esophagus: A randomized, open-label, phase II trial
Presenter: Yuexiao Qi
Session: Poster Display
Resources:
Abstract
200P - Prognosis of patients with hepatocellular carcinoma treated with transarterial chemoembolization: Development and validation of the ALFP score
Presenter: Baocuo Gong
Session: Poster Display
Resources:
Abstract
201P - A phase II study of serplulimab (a programmed death-1 inhibitor) with or without HLX04 (a bevacizumab biosimilar) for the treatment of advanced hepatocellular carcinoma
Presenter: Zhenggang Ren
Session: Poster Display
Resources:
Abstract
202P - Comparison of liver injury after transcatheter arterial chemoembolization and hepatic arterial infusion chemotherapy for intermediate and advanced hepatocellular carcinoma
Presenter: Yongru Chen
Session: Poster Display
Resources:
Abstract