Panitumumab versus cetuximab in combination with irinotecan in refractory metastatic colorectal cancer

被引:0
|
作者
Braghiroli, Maria Ignez Freitas Melro [1 ,2 ]
Filho, Daniel Santos Rocha Sobral [1 ]
Fagundes, Juliana Goes Martins [1 ]
Mendoza, Elizabeth Zambrano [1 ]
Neffa, Maria Fernanda Batistuzzo Vicentini [1 ]
Campos, Karla Souza [1 ]
da Fonseca, Leonardo Gomes [1 ,2 ]
Bonadio, Renata Colombo [1 ,2 ]
Talans, Aley [1 ]
Braghiroli, Oddone Freitas Melro [1 ,2 ]
Mathias-Machado, Maria Cecilia [1 ]
Sabbaga, Jorge [1 ,2 ]
Venchiarutti, Camila Motta [1 ,2 ]
Hoff, Paulo Marcelo Gehm [1 ,2 ]
机构
[1] Univ Sao Paulo, Inst Canc Estado Sao Paulo, Av Dr Arnaldo 251, BR-02146000 Sao Paulo, SP, Brazil
[2] Inst DOr Pesquisa & Ensino, Av Brigadeiro Luis Antonio 5001, BR-01401002 Sao Paulo, SP, Brazil
关键词
Colorectal cancer; Panitumumab; Cetuximab; Third-line; Refractoriness; WILD-TYPE KRAS; PHASE-III TRIAL; PLUS IRINOTECAN; RAS MUTATIONS; 1ST-LINE TREATMENT; OPEN-LABEL; CHEMOTHERAPY; FLUOROURACIL; LEUCOVORIN; CARE;
D O I
10.1016/j.ctarc.2025.100867
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: There is evidence that adding cetuximab can overcome resistance to irinotecan, but a similar analysis with Panitumumab isn't readily available. This study evaluated the activity of each anti-EGFR plus irinotecan as a salvage third-line treatment for metastatic colorectal cancer. Methods: This is a retrospective cohort of metastatic colorectal cancer patients who progressed to irinotecan monotherapy and were exposed to an anti-EGFR antibody as a third line of treatment. This study was conducted at a single cancer center in Brazil. The primary outcome was overall survival. The secondary outcomes were objective response rate, stratified by primary tumor sidedness, progression-free survival, and toxicity. Results: This analysis included 412 patients who had progressed on irinotecan and were KRAS wild-type. One hundred eighty-two received Irinotecan plus Cetuximab (I + C group) and 230 Irinotecan plus Panitumumab (I + P group). There was no significant difference in median overall survival between treatment groups (9.1 months [I + C] vs 10.1 months [I + P]; p = 0.76). There was also no difference in progression-free survival (3.63 months [I + C] vs 3.73 months [I + P]; p = 0.19) and objective response rate (23.0 % [I + C] vs 22.3 % [I + P]; p = 0.97). Patients with right-sided tumors had worse overall survival than left-sided (6.2 months vs 10.1 months; p = 0.003) but presented a better objective response rate with panitumumab (8.3 % [I + P] vs 3.3 % [I + C]). There were more infusion reactions with cetuximab. Conclusions: Panitumumab and cetuximab have similar activity when combined with irinotecan as treatment for patients with disease progression with an irinotecan regimen, potentially rescuing the irinotecan activity.
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页数:7
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