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本页为公开参考信息,不构成医疗建议、处方或药品供应要约。请向持证专业人士确认当前批准情况、可获得性及适用性。

其他

商品名
Keytruda
企业
Merck & Co., Inc.
药品类型
生物药Biologic
治疗领域
肿瘤科Oncology
公开来源记录的适应症
美国部分适应症包括不可切除或转移性黑色素瘤;成人及12岁及以上儿童完全切除IIB、IIC或III期黑色素瘤后的治疗;以及多种非小细胞肺癌(NSCLC)情形。对于无EGFR或ALK改变的转移性非鳞状NSCLC,一线与培美曲塞及铂类化疗联合使用。NSCLC一线单药治疗要求PD-L1 TPS至少为1%、无EGFR或ALK改变,且为转移性疾病或不适合手术或根治性放化疗的III期疾病。其他适应症及联合用药要求见所链接的美国说明书。Selected US indications include unresectable or metastatic melanoma; postoperative treatment of completely resected stage IIB, IIC or III melanoma in adults and children aged 12 or older; and several NSCLC settings. For metastatic nonsquamous NSCLC without EGFR or ALK alterations, it is used first line with pemetrexed and platinum chemotherapy. Single-agent first-line NSCLC requires PD-L1 TPS at least 1%, no EGFR or ALK alterations, and metastatic disease or stage III disease unsuitable for surgery or definitive chemoradiation. Other indications and combination requirements appear in the linked US label.
适应症来源与口径
美国说明书; 适应症更新于 2026年10月. 部分境外适应症;不确立中国批准范围。US label; indications updated October 2026. Selected overseas indications; does not establish the Chinese approved scope.
说明书信息局限
已链接境外官方处方资料;尚未核实完整的现行中国说明书。Overseas official prescribing information linked; a complete current Chinese label has not been verified.
中国可获得性状态
本次英文来源核查未独立核实中国批准详情及当前供应情况。Chinese approval details and current availability have not been independently verified in this English-source review.
海外状态
请参阅所链接的境外监管机构或厂商证据。批准及适应症因司法辖区而异;尚未确认当前供应情况。See the linked overseas regulator / manufacturer evidence. Approval and indications are jurisdiction-specific; current supply is not established.
医保分类
尚未核实Not yet verified
医保版本
中国国家医保信息待核实Chinese national insurance review pending
医保核查说明
本次新增记录尚未确定报销资格;缺少信息不代表未被纳入。No reimbursement determination was made for this addition; missing information is not proof of exclusion.

来源

证据核查日期:

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