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摘要:
K-ras wild-type carcinoma is a tumour that is sensitive to treatment with anti-cancer and anti-EGFR drugs: the combination of Cetuximab and Panitumumab with chemotherapy (Cetuximab) or as a single therapy (Panitumumab). Case Report: The clinical case presented here refers to a 68-year-old patient who had been diagnosed with adenocarcinoma of the recto sigmoid with pelvic recurrence three years after surgery. The patient had a severe co-morbidity: correlated B-type liver cirrhosis. First-line chemotherapy was begun with Oxaliplatin plus Capecitabine (CAPOXI) following a relapse, and this continued for six months (six cycles), when the treatment was interrupted because of the disease’s progression and hematological and gastrointestinal toxicity. Following an assessment of the K-ras, diagnosed as wild type, the patient was excluded from second-line chemotherapy treatment because of decompensated cirrhosis and the persistence of thrombocytopenia and leukopenia. The patient was put forward for biological treatment with an anti-EGFR monoclonal antibody (Panitumumab). Panitumumab was administered at a dosage of 6 mg/kg every 2 weeks for 17 months;the treatment was well tolerated, despite the cirrhosis, and the main toxicity was the skin rash. Conclusion: In patients with severe comorbidities such as cirrhosis of the liver and K-ras wild-type carcinomas, therapy with a monoclonal antibody such as Panitumumab is a treatment that is well tolerated, with few serious toxic side-effects;it also offers advantages in terms of survival and clinical benefits.
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篇名 Case Report: Long-Term Survival in Patient with Cirrhosis of the Liver and Colon Cancer K-ras Wild-Type
来源期刊 临床医学病理报告(英文) 学科 医学
关键词 K-RAS WILD-TYPE Carcinoma Metastatic Colorectal Cancer PANITUMUMAB ANTI-EGFR Treatment CIRRHOSIS
年,卷(期) 2014,(6) 所属期刊栏目
研究方向 页码范围 373-377
页数 5页 分类号 R73
字数 语种
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K-RAS
WILD-TYPE
Carcinoma
Metastatic
Colorectal
Cancer
PANITUMUMAB
ANTI-EGFR
Treatment
CIRRHOSIS
研究起点
研究来源
研究分支
研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
临床医学病理报告(英文)
月刊
2325-7075
武汉市江夏区汤逊湖北路38号光谷总部空间
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569
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0
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