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Poster Display session

43P - Update on long term outcome of a multicentre, prospective, real-world study of camrelizumab in the treatment of patients with advanced lung cancer

Date

03 Apr 2022

Session

Poster Display session

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Yongqian Shu

Citation

Annals of Oncology (2022) 33 (suppl_2): S27-S70. 10.1016/annonc/annonc856

Authors

Y. Shu1, R. Wang2, M. Ji3, M. Shi1, X. Zhang4

Author affiliations

  • 1 Jiangsu Province People's Hospital, Nanjing/CN
  • 2 Nanjing University, Nanjing/CN
  • 3 The First People's Hospital of Changzhou, Changzhou/CN
  • 4 Subei People's Hospital of Jiangsu province, Yangzhou/CN

Resources

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Abstract 43P

Background

Camrelizumab is a humanized PD-1 monoclonal antibody. We sought to analyse the antitumour activity and toxicity of camrelizumab in advanced lung cancer to explore benefit subgroups and optimal treatments. Preliminary data had been previously presented.

Methods

This is a multicentre, prospective cohort study of advanced lung cancer in Jiangsu province, China. Patients with advanced lung cancer received at least one course of camrelizumab-based treatment regimens. Tumor responses were assessed by RECIST 1.1 after every 2 or 3 months by CT or MRI. Primary endpoint is progression-free survival (PFS).

Results

Between August 7, 2019 to February 2, 2021, we screened 480 pts with advanced lung cancer, of whom 468 eligible pts were enrolled and received study treatment. 400 pts (85.5%) had at least one post-treatment tumor assessment. As of data cutoff (June 30, 2021), the median follow-up was 8.2 months. In the ITT population (n=468), 138 (29.5%), 229(48.9%), and 33(7.1%) pts showed partial response (PR), stable disease (SD), and progression disease (PD), respectively. The ORR, DCR was 29.5%, 78.4%. The median PFS was 8.8 months (95% CI, 7.6-10.3), the median OS was 22.0 months ( 95% CL 19.0-not reached). The ≥3 grade AEs included anemia (5.8%, 27/468), neutropenia (3.0%, 14/468), leucopenia (3.0%, 14/468), thrombocytopenia (1.7%, 8/468), reactive cutaneous capillary hyperplasia (RCCEP) (1.5%, 7/468), checkpoint inhibitor pneumonitis (0.85%, 4/468). No treatment-related deaths occurred.

Table: 43P

Baseline characteristics of all enrolled patients

Characteristic Patients (N=468)
Median age 65.00 (57.00-71.00)
Gender, no. (%)
Male 357 (76.28%)
Female 111 (23.72%)
Age, no. (%)
<70yr 324 (69.23%)
≥70yr 144 (30.77%)
Pathological type, no. (%)
Adenocarcinoma 259 (55.34%)
Squamous 140 (29.91%)
SCLC 45 (9.62%)
Others 24 (5.13%)
Previous treatment lines, no. (%)
No previous treatment 139 (29.7%)
First-line 197 (42.09%)
≥Second-line 132 (28.21%)
Combination therapy with camrelizumab, no. (%)
Monotherapy 50 (10.68%)
Combined chemotherapy 316 (67.52%)
Combined with antiangiogenesis 100 (21.36%)
Others 2 (0.43%)

Conclusions

This Real-world study showed current clinical practice of advanced lung cancer in China, and camrelizumab showed consistent efficacy in the treatment of advanced lung cancer as previous trials. [ChiCTR1900026089].

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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