Cited by 210Endometrial and Cervical Cancer TreatmentsCancer Immunotherapy and BiomarkersCervical Cancer and HPV Research

Camrelizumab Plus Apatinib in Patients With Advanced Cervical Cancer (CLAP): A Multicenter, Open-Label, Single-Arm, Phase II Trial

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Lan, Chunyan, Shen, Jingxian, Wang, Yin, Li, Jundong, Liu, Zhimin, He, Mian, Cao, Xinping, Ling, Jiayu +10 more·2020·Journal of Clinical Oncology

Abstract

PURPOSE: Camrelizumab is an antibody against programmed death protein 1. We assessed the activity and safety of camrelizumab plus apatinib, a tyrosine kinase inhibitor of vascular endothelial growth factor receptor-2, in patients with advanced cervical cancer. METHODS: This multicenter, open-label, single-arm, phase II study enrolled patients with advanced cervical cancer who progressed after at least one line of systemic therapy. Patients received camrelizumab 200 mg every 2 weeks and apatinib 250 mg once per day. The primary end point was objective response rate (ORR) assessed by investigators per RECIST version 1.1. Key secondary end points were progression-free survival (PFS), overall survival (OS), duration of response, and safety. RESULTS: Forty-five patients were enrolled and received treatment. Median age was 51.0 years (range, 33-67 years), and 57.8% of patients had previously received two or more lines of chemotherapy for recurrent or metastatic disease. Ten patients (22.2%) had received bevacizumab. Median follow-up was 11.3 months (range, 1.0-15.5 months). ORR was 55.6% (95% CI, 40.0% to 70.4%), with two complete and 23 partial responses. Median PFS was 8.8 months (95% CI, 5.6 months to not estimable). Median duration of response and median OS were not reached. Treatment-related grade 3 or 4 adverse events (AEs) occurred in 71.1% of patients, and the most common AEs were hypertension (24.4%), anemia (20.0%), and fatigue (15.6%). The most common potential immune-related AEs included grade 1-2 hypothyroidism (22.2%) and reactive cutaneous capillary endothelial proliferation (8.9%). CONCLUSION: Camrelizumab plus apatinib had promising antitumor activity and manageable toxicities in patients with advanced cervical cancer. Larger randomized controlled trials are warranted to validate our findings.

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  • Combination therapies such as sintilimab plus anlotinib, sintilimab plus IBI305, camrelizumab plus apatinib, and toripalimab plus axitinib demonstrated potent antitumor effects in multiple types of cancers.

    “Combination therapies such as sintilimab plus anlotinib, sintilimab plus IBI305 (bevacizumab biosimilar), camrelizumab plus apatinib, and toripalimab plus axitinib demonstrated potent antitumor effects in multiple types of cancers [22, 114–120].”

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Authors
Lan, C., Shen, J., Wang, Y., Li, J., Liu, Z., He, M., Cao, X., Ling, J., Huang, J., Zheng, M., Zou, G., Yan, H., Liu, Q., Yang, F., Wei, W., Deng, Y., Xiong, Y., & Huang, X.
Affiliations
  • Sun Yat-sen University (CN)
  • Panyu District Central Hospital (CN)
Corresponding author
Huang, Xin
Venue
Journal of Clinical Oncology
Published
2020-12-01
Volume
38
Issue
34
Pages
4095-4106
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W3032571309
Cited by
210
References
30
Citations by year
2026: 20 · 2025: 34 · 2024: 41 · 2023: 41 · 2022: 50 · 2021: 24
FWCI
17.59
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Journal of Clinical Oncology (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
Jiangsu Hengrui Medicine
Topics
  • Health Sciences › Medicine › Obstetrics and Gynecology › Endometrial and Cervical Cancer Treatments
  • Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
  • Health Sciences › Medicine › Epidemiology › Cervical Cancer and HPV Research
Keywords
camrelizumab, apatinib, advanced cervical cancer, PD-1 inhibitors, VEGFR-2 inhibitors, combination immunotherapy, objective response rate, progression-free survival, immune-related adverse events
MeSH terms
Progression-Free Survival, Adult, Aged, Antineoplastic Combined Chemotherapy Protocols, Uterine Cervical Neoplasms, Female, Humans, Middle Aged, Pyridines, Survival Rate, Protein Kinase Inhibitors, Kaplan-Meier Estimate, Antibodies, Monoclonal, Humanized

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