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.
引用
收藏
页数:7
相关论文
共 50 条
  • [21] Cetuximab plus irinotecan in refractory colorectal cancer patients
    Delgao, Marian Gil
    Spano, Jean-Philippe
    Khayat, David
    EXPERT REVIEW OF ANTICANCER THERAPY, 2007, 7 (04) : 407 - 413
  • [22] Randomised phase II study of panitumumab plus irinotecan versus cetuximab plus irinotecan in patients with KRAS wild-type metastatic colorectal cancer refractory to fluoropyrimidine, irinotecan and oxaliplatin (WJOG 6510G)
    Sakai, Daisuke
    Taniguchi, Hiroya
    Sugimoto, Naotoshi
    Tamura, Takao
    Nishina, Tomohiro
    Hara, Hiroki
    Esaki, Taito
    Denda, Tadamichi
    Sakamoto, Takeshi
    Okuda, Hiroyuki
    Satoh, Taroh
    Tsushima, Takahiro
    Makiyama, Akitaka
    Tsuda, Takashi
    Hosokawa, Ayumu
    Kuramochi, Hidekazu
    Tokunaga, Shinya
    Moriwaki, Toshikazu
    Yasui, Hisateru
    Ishida, Hiroyasu
    Tsuji, Akihito
    Otsu, Satoshi
    Shimokawa, Hozumi
    Baba, Eishi
    Sato, Mikio
    Matsumoto, Shigemi
    Ozaki, Yukinori
    Shinozaki, Katsunori
    Tamagawa, Hiroshi
    Goto, Masahiro
    Kadowaki, Shigenori
    Fujii, Hirofumi
    Koh, Yasuhiro
    Yamazaki, Kentaro
    Hironaka, Shuichi
    Kishimoto, Junji
    Boku, Narikazu
    Hyodo, Ichinosuke
    Muro, Kei
    EUROPEAN JOURNAL OF CANCER, 2020, 135 : 11 - 21
  • [23] Irinotecan associated with cetuximab given every 2 weeks versus cetuximab weekly in metastatic colorectal cancer
    Mrabti, Hind
    De la Fouchardiere, Christelle
    Desseigne, Francoise
    Dussart, Sophie
    Negrier, Sylvie
    Errihani, Hassan
    JOURNAL OF CANCER RESEARCH AND THERAPEUTICS, 2009, 5 (04) : 272 - 276
  • [24] COMPARATIVE EFFECTIVENESS OF PANITUMUMAB VERSUS CETUXIMAB IN PATIENTS WITH CHEMO-REFRACTORY WILD-TYPE KRAS METASTATIC COLORECTAL CANCER
    Xu, Y.
    Hay, J. W.
    Barzi, A.
    VALUE IN HEALTH, 2016, 19 (03) : A2 - A2
  • [25] Comparative Effectiveness of Cetuximab Versus Panitumumab in Patients With Metastatic Colorectal Cancer: A Nationwide Database Study
    Wu, Chih-chien
    Su, Chien-chou
    Chen, Yu-hsun
    Hsu, Chao-wen
    Hsieh, Meng-che
    Chang, Yu-ching
    Wang, Yung-chang
    Su, Yi-chia
    ANTICANCER RESEARCH, 2023, 43 (11) : 5127 - 5138
  • [26] Irinotecan, cetuximab, and bevacizumab (CBI) versus irinotecan, cetuximab, and placebo (CI) in irinotecan-refractory metastatic colorectal cancer (mCRC): Results from an ACCRU network randomized phase II trial
    Lipsyc-Sharf, Marla
    Ou, Fang-Shu
    Yurgelun, Matthew B.
    Rubinson, Douglas Adam
    Schrag, Deborah
    Dakhil, Shaker R.
    Stella, Philip J.
    Weckstein, Douglas Jay
    Wender, Donald B.
    Faggen, Meredith Gail
    Zemla, Tyler
    Heying, Erica N.
    Schuetz, Samantha R.
    Noble, Stephanie
    Meyerhardt, Jeffrey A.
    Bekaii-Saab, Tanios S.
    Fuchs, Charles S.
    Ng, Kimmie
    JOURNAL OF CLINICAL ONCOLOGY, 2020, 38 (04)
  • [27] Phase II study of combination chemotherapy with biweekly cetuximab and irinotecan for wild-type KRAS metastatic colorectal cancer refractory to irinotecan, oxaliplatin, and fluoropyrimidines
    Yuki, S.
    Shitara, K.
    Yoshida, M.
    Takahari, D.
    Utsunomiya, S.
    Yokota, T.
    Sato, Y.
    Tajika, M.
    Muro, K.
    JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (04)
  • [28] Phase II study of combination chemotherapy with biweekly cetuximab and irinotecan for wild-type KRAS metastatic colorectal cancer refractory to irinotecan, oxaliplatin, and fluoropyrimidines
    Kohei Shitara
    Satoshi Yuki
    Motoki Yoshida
    Daisuke Takahari
    Setsuo Utsunomiya
    Tomoya Yokota
    Yozo Sato
    Yoshitaka Inaba
    Masahiro Tajika
    Hiroki Kawai
    Hidekazu Yamaura
    Mina Kato
    Kentaro Yamazaki
    Yoshito Komatsu
    Kei Muro
    Investigational New Drugs, 2012, 30 : 787 - 793
  • [29] Phase II study of combination chemotherapy with biweekly cetuximab and irinotecan for wild-type KRAS metastatic colorectal cancer refractory to irinotecan, oxaliplatin, and fluoropyrimidines
    Shitara, Kohei
    Yuki, Satoshi
    Yoshida, Motoki
    Takahari, Daisuke
    Utsunomiya, Setsuo
    Yokota, Tomoya
    Sato, Yozo
    Inaba, Yoshitaka
    Tajika, Masahiro
    Kawai, Hiroki
    Yamaura, Hidekazu
    Kato, Mina
    Yamazaki, Kentaro
    Komatsu, Yoshito
    Muro, Kei
    INVESTIGATIONAL NEW DRUGS, 2012, 30 (02) : 787 - 793
  • [30] PHASE II STUDY OF COMBINATION CHEMOTHERAPY WITH BIWEEKLY CETUXIMAB AND IRINOTECAN FOR WILD-TYPE KRAS METASTATIC COLORECTAL CANCER REFRACTORY TO IRINOTECAN, OXALIPLATIN, AND FLUOROPYRIMIDINES
    Yuki, S.
    Shitara, K.
    Yoshida, M.
    Takahari, D.
    Utsunomiya, S.
    Yokota, T.
    Sato, Y.
    Tajika, M.
    Muro, K.
    ANNALS OF ONCOLOGY, 2010, 21 : 216 - 216