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奥沙利铂治疗上消化道癌的经验。

The experience with oxaliplatin in the treatment of upper gastrointestinal carcinomas.

作者信息

Hoff Paulo M, Fuchs Charles S

机构信息

Center for Clinical Studies in Cancer, Albert Einstein Hospital, Sao Paulo, Brazil.

出版信息

Semin Oncol. 2003 Aug;30(4 Suppl 15):54-61. doi: 10.1016/s0093-7754(03)00406-8.

DOI:10.1016/s0093-7754(03)00406-8
PMID:14523796
Abstract

The treatment for advanced gastroesophageal tumors is still largely based on 5-fluorouracil and cisplatin combinations, and the treatment for advanced pancreatic tumors principally relies on gemcitabine. The need for more active agents is evident in light of the poor outcomes for patients with these tumors. Oxaliplatin is an important chemotherapeutic agent currently being investigated in the treatment of gastrointestinal carcinomas. This diaminocyclohexane-platinum compound has significant differences from cisplatin and carboplatin with respect to its activity and toxicity. It appears to have activity in tumors believed to be marginally sensitive to the other platinum agents, and it is neither ototoxic nor nephrotoxic. The main side effect of oxaliplatin is a sensory neuropathy exacerbated by cold exposure. After extensive clinical development, oxaliplatin has become an important option in the treatment of colorectal cancer. Its role in the treatment of upper gastrointestinal cancers is less well established, but is the focus of intense investigation. Much of what we currently know is based on small phase I and II studies, but knowledge is rapidly accumulating. The fact that cisplatin remains an important drug in the treatment of several upper gastrointestinal cancers raises the hope that oxaliplatin will contribute significantly to the treatment of those malignancies as well. Larger randomized phase III trials are being designed and conducted to fully define the role of oxaliplatin in the treatment of upper gastrointestinal tumors in the relatively near future.

摘要

晚期胃食管肿瘤的治疗仍主要基于5-氟尿嘧啶和顺铂联合用药,而晚期胰腺肿瘤的治疗主要依赖吉西他滨。鉴于这些肿瘤患者预后较差,显然需要更有效的药物。奥沙利铂是目前正在研究用于治疗胃肠道癌的一种重要化疗药物。这种二环己烷铂化合物在活性和毒性方面与顺铂和卡铂有显著差异。它似乎对被认为对其他铂类药物敏感性较低的肿瘤有活性,且无耳毒性和肾毒性。奥沙利铂的主要副作用是冷刺激会加重的感觉神经病变。经过广泛的临床研发,奥沙利铂已成为治疗结直肠癌的重要选择。其在上消化道癌治疗中的作用尚不明确,但已成为深入研究的重点。我们目前所了解的大部分内容基于小型I期和II期研究,但相关知识正在迅速积累。顺铂在几种上消化道癌的治疗中仍然是一种重要药物,这使得人们希望奥沙利铂也能对这些恶性肿瘤的治疗做出重大贡献。目前正在设计和开展更大规模的随机III期试验,以便在相对不久的将来全面确定奥沙利铂在上消化道肿瘤治疗中的作用。

相似文献

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The experience with oxaliplatin in the treatment of upper gastrointestinal carcinomas.奥沙利铂治疗上消化道癌的经验。
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Platinum compounds in the treatment of advanced breast cancer.铂类化合物在晚期乳腺癌治疗中的应用
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Can cisplatin and infused 5-fluorouracil be replaced by oxaliplatin and capecitabine in the treatment of advanced oesophagogastric cancer? The REAL 2 trial.在晚期食管胃癌的治疗中,顺铂和静脉输注的5-氟尿嘧啶能否被奥沙利铂和卡培他滨替代?REAL 2试验。
Clin Oncol (R Coll Radiol). 2005 Apr;17(2):79-80. doi: 10.1016/j.clon.2004.12.004.
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The integration of paclitaxel and new platinum compounds in the treatment of advanced ovarian cancer.紫杉醇与新型铂类化合物在晚期卵巢癌治疗中的联合应用。
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Semin Oncol. 2003 Aug;30(4 Suppl 15):62-7. doi: 10.1016/s0093-7754(03)00407-x.
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Current status of oxaliplatin in colorectal cancer.奥沙利铂在结直肠癌中的现状
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引用本文的文献

1
Comparison of the Efficacy of S-1 Plus Oxaliplatin or Capecitabine Plus Oxaliplatin for Six and Eight Chemotherapy Cycles as Adjuvant Chemotherapy in Patients With Stage II-III Gastric Cancer After D2 Resection.S-1联合奥沙利铂或卡培他滨联合奥沙利铂作为Ⅱ-Ⅲ期胃癌D2切除术后辅助化疗进行6个和8个化疗周期的疗效比较。
Front Oncol. 2021 May 24;11:684627. doi: 10.3389/fonc.2021.684627. eCollection 2021.
2
Inhibiting DNA Polymerases as a Therapeutic Intervention against Cancer.抑制DNA聚合酶作为一种抗癌治疗干预手段。
Front Mol Biosci. 2017 Nov 21;4:78. doi: 10.3389/fmolb.2017.00078. eCollection 2017.
3
A phase II study of capecitabine plus 3-weekly oxaliplatin as first-line therapy for patients with advanced gastric cancer.
卡培他滨联合每三周一次奥沙利铂作为晚期胃癌患者一线治疗的II期研究。
Br J Cancer. 2006 Apr 10;94(7):959-63. doi: 10.1038/sj.bjc.6603046.
4
Second-line treatment with oxaliplatin, leucovorin and 5-fluorouracil in gemcitabine-pretreated advanced pancreatic cancer: A phase II study.奥沙利铂、亚叶酸钙和5-氟尿嘧啶用于吉西他滨预处理的晚期胰腺癌的二线治疗:一项II期研究。
Invest New Drugs. 2005 Aug;23(4):369-75. doi: 10.1007/s10637-005-1446-y.