Patients with RAS wild-type right-sided unresectable liver-confined mCRC also benefit from cetuximab plus chemotherapy in first-line treatment

被引:1
|
作者
Zheng, Peng [1 ]
Ren, Li [1 ]
Feng, Qingyang [1 ]
Zhu, Dexiang [1 ]
Chang, Wenju [1 ]
He, Guodong [1 ]
Ji, Meiling [1 ]
Jian, Mi [1 ]
Lin, Qi [1 ]
Yi, Tuo [1 ]
Wei, Ye [1 ]
Xu, Jianmin [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Gen Surg, 180 Fenglin Rd, Shanghai 200032, Peoples R China
来源
AMERICAN JOURNAL OF CANCER RESEARCH | 2018年 / 8卷 / 11期
基金
中国国家自然科学基金;
关键词
Colorectal liver metastases; cetuximab; predictive marker; primary tumor location; METASTATIC COLORECTAL-CANCER; COLON-CANCER; TUMOR SITE; MUTATIONS; LOCATION; SURVIVAL; STAGE; KRAS; FLUOROURACIL; LEUCOVORIN;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Growing evidence indicates that primary tumor location of metastatic colorectal cancer (mCRC) can affect response to specific therapy. This study aimed to assess the impact of primary tumor location on efficacy of cetuximab in Chinese patients with mCRC. We included patients with RAS wild type liver-limited mCRC treated with first-line cetuximab plus chemotherapy or chemotherapy alone between June 2008 and December 2016. All patients were categorized as having left-sided tumors or right-sided tumors. Progression free survival (PFS), overall survival (OS), objective response rate (ORR) and conversion rate of surgery for liver metastases was analyzed according to tumor location and treatment. Right-sided tumors were characterized with larger primary tumor, poorer differentiation, more lymph node metastases and larger and more liver metastases. For patients with left-sided tumors (N=233), addition of cetuximab to chemotherapy significantly improved ORR (68.9% vs. 30.6%, OR=5.01, P < 0.001), conversion rate of liver surgery (33.5% vs. 10.8%, OR=4.18, P < 0.001), PFS (12.1 months vs. 6.1 months, HR=0.42, P < 0.001), and OS (not evaluable vs. 23.1 months, HR=0.31, P < 0.001). Among patients with right sided tumors (N=85), cetuximab plus chemotherapy, compared with chemotherapy alone, also significantly improved ORR (56.8% vs. 29.3%, OR=3.18, P=0.010), PFS (9.3 months vs. 5.1 months, OR=0.57, P=0.012) and OS (25.3 months vs. 16.8 months, HR=0.56, P=0.032) but conversion rate of liver surgery (20.5% vs. 9.8%, HR=2.38, P=0.171). Our results demonstrated differential effect of cetuximab on efficacy outcomes based on tumor sidedness. Also, we found that patients with right-sided tumors also benefit from cetuximab plus chemotherapy but not as great as left-sided tumors and in general, did worse. In conclusion, findings of previous studies about differential effect of anti-EGFR therapy based on tumor sidedness are applicable to an Asian population.
引用
收藏
页码:2337 / +
页数:14
相关论文
共 50 条
  • [31] A RANDOMIZED, CONTROLLED TRIAL OF CETUXIMAB PLUS CHEMOTHERAPY FOR PATIENTS WITH KRAS WILD-TYPE UNRESECTABLE COLORECTAL LIVER-LIMITED METASTASES
    Xu, J.
    Ye, L.
    Ren, L.
    Wei, Y.
    ANNALS OF ONCOLOGY, 2012, 23 : 190 - 190
  • [32] Phase II study of third-line cetuximab rechallenge in patients with metastatic wild-type K-RAS colorectal cancer who achieved a clinical benefit in response to first-line cetuximab plus chemotherapy (JACCRO CC-08)
    Tsuji, A.
    Eto, T.
    Masuishi, T.
    Satake, H.
    Segawa, Y.
    Tanioka, H.
    Hara, H.
    Kotaka, M.
    Sagawa, T.
    Watanabe, T.
    Nakamura, M.
    Takahashi, T.
    Negoro, Y.
    Manaka, D.
    Fujita, H.
    Suto, T.
    Ichikawa, W.
    Fujii, M.
    Takeuchi, M.
    Nakajima, T.
    ANNALS OF ONCOLOGY, 2016, 27
  • [33] The impact of toxicity and efficacy on quality of life in KRAS wild-type metastatic colorectal cancer patients treated with first-line chemotherapy plus cetuximab
    Yamaguchi, K.
    Ando, M.
    Ooki, A.
    Beier, F.
    Von Hohnhorst, P.
    Esser, R.
    Van Cutsem, E.
    EUROPEAN JOURNAL OF CANCER, 2013, 49 : S518 - S518
  • [34] Cost-effectiveness of cetuximab plus FOLFIRI versus bevacizumab plus FOLFIRI in the first-line treatment of RAS wild-type metastatic colorectal cancer in China.
    Van Oostrum, Ilse
    Hu Yannan
    Yuan Zijiao
    Schlichting, Michael
    Tao Libo
    Pescott, Chris P.
    JOURNAL OF CLINICAL ONCOLOGY, 2021, 39 (03)
  • [35] Overall survival with cetuximab every 2 weeks vs standard once-weekly administration schedule for first-line treatment of RAS wild-type metastatic colorectal cancer in patients with left- and right-sided primary tumor location
    Kasper, S.
    Cheng, A.
    Rouyer, M.
    Foch, C.
    Lamy, F.
    Esser, R.
    Batech, M.
    Wong, C.
    Zhang, A.
    Brodowicz, T.
    Zielinski, C.
    ANNALS OF ONCOLOGY, 2021, 32 : S114 - S114
  • [36] COST-EFFECTIVENESS OF CETUXIMAB AND BEVACIZUMAB IN THE FIRST-LINE TREATMENT OF METASTATIC COLORECTAL CANCER (MCRC) FOR PATIENTS WITH KRAS WILD-TYPE TUMOURS IN THE UNITED KINGDOM
    Samyshkin, Y.
    Hertel, N.
    Griebsch, I
    VALUE IN HEALTH, 2011, 14 (07) : A446 - A447
  • [37] Cost-Effectiveness of Cetuximab and Bevacizumab in the First-Line Treatment of Metastatic Colorectal Cancer (mCRC) for Patients With KRas Wild-Type Tumours in the United Kingdom
    Samyshkin, Y.
    Hertel, N.
    Griebsch, I.
    EUROPEAN JOURNAL OF CANCER, 2011, 47 : S264 - S264
  • [38] Cost-Effectiveness Analysis of First-Line FOLFIRI Combined With Cetuximab or Bevacizumab in Patients With RAS Wild-Type Left-Sided Metastatic Colorectal Cancer
    Han, Jiaqi
    Xiao, Desheng
    Tan, Chongqing
    Zeng, Xiaohui
    Hu, Huabin
    Zeng, Shan
    Jiang, Qin
    She, Longjiang
    Yao, Linli
    Li, Li
    Tang, Lanhua
    Ma, Jian
    Huang, Jin
    Shen, Liangfang
    CANCER CONTROL, 2020, 27 (01)
  • [39] A SYSTEMATIC LITERATURE REVIEW TO IDENTIFY TRIALS IN FIRST-LINE RAS WILD-TYPE (WT) METASTATIC COLORECTAL CANCER (MCRC) PATIENTS
    Jarrett, J.
    Weijers, L.
    Hnoosh, A.
    Harty, G.
    von Hohnhorst, P.
    VALUE IN HEALTH, 2014, 17 (07) : A617 - A617
  • [40] Dynamic ctDNA-based analysis of drug-resistant gene alterations at RAS/ BRAF wild-type metastatic colorectal cancer patients after cetuximab plus chemotherapy as the first-line treatment
    Zhou, Yu-Wen
    Zhao, Xin
    Ni, Lu
    Cao, Peng
    Leng, Wei-Bing
    Zhu, Qing
    Gou, Hong-Feng
    Zhang, Jiao
    Li, Xiao-Fen
    Qiu, Meng
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2024, 131