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Inetetamab combined with S-1 and oxaliplatin as first-line treatment for human epidermal growth factor receptor 2-positive gastric cancer

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摘要 BACKGROUND Patients with human epidermal growth factor receptor 2(HER2)-positive advanced gastric cancer have poor outcomes.Trastuzumab combined with chemotherapy is the first-line standard treatment for HER2-positive advanced gastric cancer.Inetetamab is a novel anti-HER2 drug,and its efficacy and safety in gastric cancer have not yet been reported.AIM To evaluate the efficacy and safety of the S-1 plus oxaliplatin(SOX)regimen combined with inetetamab as a first-line treatment for HER2-positive advanced gastric cancer.METHODS Thirty-eight patients with HER2-positive advanced gastric cancer or gastroeso-phageal junction adenocarcinoma were randomly divided into two groups:One group received inetetamab combined with the SOX regimen,and the other group received trastuzumab combined with the SOX regimen.After 4-6 cycles,patients with stable disease received maintenance therapy.The primary endpoints were progression-free survival(PFS)and overall survival(OS),and the secondary endpoints were the objective response rate,disease control rate,and adverse events(AEs).RESULTS Thirty-seven patients completed the trial,with 18 patients in the inetetamab group and 19 patients in the trastuzumab group.In the inetetamab group,the median PFS was 8.5 months,whereas it was 7.3 months in the trastuzumab group(P=0.046);this difference was significant.The median OS in the inetetamab group vs the trastuzumab group was 15.4 months vs 14.3 months(P=0.33),and the objective response rate was 50%vs 42%(P=0.63),respectively;these differences were not significant.Common AEs included leukopenia,thrombocytopenia,nausea,and vomiting.The incidence rates of grade≥3 AEs were 56%in the inetetamab group and 47%in the trastuzumab group(P=0.63),with no significant difference.CONCLUSION In the first-line treatment of HER2-positive advanced gastric cancer,inetetamab and trastuzumab showed comparable efficacy.The inetetamab group showed superior PFS,and both groups had good safety.
出处 《World Journal of Gastroenterology》 SCIE CAS 2024年第40期4367-4375,共9页 世界胃肠病学杂志(英文)
基金 Supported by China Scientific Research Fund for HER2 Target from China Anti-Cancer Association,No.CORP-239-M9.
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  • 1WHO. The global burden of disease: 2004 update. [ EB/OL] ht- tp ://who. int/healthinfo/global _ burden_ disease/GBD _ report _ 2004update_full. pdf.
  • 2ZHENG S, BAI J Q, LI J, et al. The pathologic characteristics of breast cancer in China and its shift during 1999-2008 : A na- tional-wide muhicenter cross-sectional image over 10 years [ J]. Int J Cancer, 2012, 131 ( 11 ) :2622-2631.
  • 3JIANG Z F, SONG S T, YAO K T. New strategies and clinical practices for medical treatment of breast cancer[ J]. 临床药物治疗杂志,2005,1:1-4.
  • 4WANG Y, SUN Y. The present situation and prospects of neo-plasmtargetedtherapy[J].中华肿瘤杂志,2005,27(10):638-640.
  • 5MA P Q. The present and prospects of therapeutic monoclonal an-tibodymarket[J].药学进展,2005,29(1):46-47.
  • 6HER2 Test Guideline Recommendations editing group. HER2 Test GuidelineRecommendations[J].中华病理学杂志,2006,35(10):631-633.
  • 7TAN Q Q,GUO Q C,FANG C, et al. Characterization and com- parison of commereiallyavailable TNF receptor 2-Fc fusion pro- teinproducts [ J ]. MAbs,2012, 4 ( 6 ) : 761-774.
  • 8JEFFERIS R. Isotype and glycoform selection for antibody thera- peutics [ J ]. Arch Biochem Biophys, 2012,526 ( 2 ) : 159-166.
  • 9JEFFERIS R. Recombinant antibody therapeutics: The impact of glycosylation on mechanisms of action [ J ] . Trends Pharmacol Sci, 2009,30(7 ): 356-362.
  • 10FRADKIN A H, CARPENTER J F, RANDOLFH T W. Immuno- genicity of aggregates of recombinant human growth hormone in mouse models[ J]. J Pharm Sci, 2009, 98 (9) :3247-3264.

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