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Advances in Radiotherapy
            & Nuclear Medicine                                                     Chinese Expert Consensus for LACC










                                Adverse reactions/events  36.7% of patients experienced grade  ≥3 adverse events (26.5% with grade 3,   10.2% with grade 4)  Similar safety profiles  Higher incidence of neutropenia (68%  vs. 44%), hypertension (16% vs. 2%),  and infections (50% vs. 18%) noted in   the experimental group  Similar safety profiles  Well-tolerated by most patients  Similar safety profiles  Majority of drug-related adverse   reactions were Grades 1–2  Similar s









                                     3-year OS, DFS, and LRF of   81.3%, 68.7%, and 23.2%,   1-year PFS 91.4% vs. 82.1%;   2-year PFS 80.8% vs. 63.5%  2-year OS 83% vs. 87%;   2-year DFS 63% vs. 76%  5-year PFS rate and OS rate  57.5% and 58.5% respectively  ORR 86.3% vs. 76.3%  CRR 42.6%, PRR 45.0%  Significant improvements in   experimental group CRR,   ORR, and 3-year OS






                                Efficacy  respectively  CRR 83% vs. 65%


                                Follow‑up   (Mo.)  45  22  NA  31  NA  Ongoing  Ongoing  NA





                                RT   EBRT   IMRT  IMRT   EBRT,   IMRT  EFRT  IMRT,   VMAT  IMRT,   VMAT  IMRT
                                No. of   cases  60  116  91  78  21  291  122  393   Abbreviations: CRR: Complete response rate; DCR: Disease control rate; DFS: Disease-free survival; DMFS: Distant metastasis-free survival; EBRT: External beam radiotherapy;  EFRT: Extended-field radiotherapy; EGFR: Epidermal growth factor receptor; IMRT: Intensity-modulated radiotherapy; LACC: Locally advanced cervical cancer; LRF: Locoregional failure;  mOS: Median overall survival; NA:

                             Table 2. Clinical studies of targeted drugs in combination with CCRT for LACC



                                Study type  Phase II single-arm  Phase II randomized   controlled  Phase II randomized   controlled  Phase II randomized   controlled  Phase I study  Phase III study  Phase II study  Meta-analysis





                                Researcher  Schefter et al. 8  Lu et al. 9  Shu et al. 10  De la   Rochefordiere   et al. 11  Fracasso et al. 12  Wang et al. 13  Qu et al. 14  Yuan et al. 15  adverse events; VEGFR: Vascular endothelial growth factor; VMAT: Volumetric modulated arc therapy.




                                Drug name  Bevacizumab  Endostar  Endostar  Cetuximab  Cetuximab  Nimotuzumab  Nimotuzumab  Nimotuzumab




                                            Recombinant human endostatin  Recombinant human endostatin  Anti-EGFR monoclonal antibody  Anti-EGFR monoclonal antibody  Anti-EGFR monoclonal antibody  Anti-EGFR monoclonal antibody  Anti-EGFR monoclonal antibody





                                Classification  Anti-VEGFR







            Volume 3 Issue 1 (2025)                         20                             doi: 10.36922/arnm.4032
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