信迪利单抗注射液 | China Drugs ListSintilimab injection | China Drugs List
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。
- 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
- 经典型霍奇金淋巴瘤本品适用于至少经过二线系统化疗的复发或难治性经典型霍奇金淋巴瘤的治疗。 非小细胞肺癌非鳞状非小细胞肺癌本品联合培美曲塞和铂类化疗,用于表皮生长因子受体( EGFR )基因突变阴性和间变性淋巴瘤激酶( ALK )阴性、不可手术切除的局部晚期或转移性非鳞状非小细胞肺癌( NSCLC )患者的一线治疗。 本品联合贝伐珠单抗、培美曲塞和顺铂,用于经表皮生长因子受体酪氨酸激酶抑制剂( EGFR-TKI )治疗失败的 EGFR 基因突变阳性的局部晚期或转移性非鳞状非小细胞肺癌( NSCLC )患者的治疗。 鳞状非小细胞肺癌本品联合吉西他滨和铂类化疗,用于不可手术切除的局部晚期或转移性鳞状非小细胞肺癌( NSCLC )的一线治疗。 肝细胞癌本品联合贝伐珠单抗,用于既往未接受过系统治疗的不可切除或转移性肝细胞癌的一线治疗。 食管鳞癌本品联合紫杉醇和铂类药物或氟尿嘧啶类和铂类药物用于不可切除的局部晚期、复发或转移性食管鳞癌的一线治疗。 胃及胃食管交界处腺癌本品联合含氟尿嘧啶类和铂类药物化疗用于不可切除的局部晚期、复发或转移性胃及胃食管交界处腺癌的一线治疗。 子宫内膜癌本品联合呋喹替尼胶囊用于既往系统性抗肿瘤治疗后失败且不适合进行根治性手术治疗或根治性放疗的晚期错配修复完整 ( pMMR )子宫内膜癌患者。 基于替代终点获得附条件批准上市,暂未获得临床终点数据,有效性和安全性尚待上市后进一步确证。本适应症的完全批准将取决于正在开展的确证性随机对照临床试验能否证实信迪利单抗联合呋喹替尼胶囊治疗临床获益。 结肠癌本品联合伊匹木单抗 N01 用于可手术切除的 IIB-III 期微卫星高度不稳定型( MSI-H )或错配修复缺陷型( dMMR )结肠癌患者的新辅助治疗。 本适应症为基于替代终点获得附条件批准上市,暂未获得临床终点数据,有效性和安全性尚待上市后进一步确证。本适应症的完全批准将取决于正在开展的确证性临床试验能否证实信迪利单抗联合伊匹木单抗 N01 新辅助治疗相对于标准治疗的显著临床获益。 肾细胞癌本品联合呋喹替尼胶囊用于既往接受血管内皮生长因子受体 - 酪氨酸激酶抑制剂( VEGFR-TKI )治疗失败且一线未接受程序性死亡受体 -1 ( PD-1 )或程序性死亡配体 -1 ( PD-L1 )抑制剂的局部晚期或转移性肾细胞癌患者。Classical Hodgkin lymphoma: for relapsed or refractory disease after at least two lines of systemic chemotherapy. Nonsquamous NSCLC: (1) with pemetrexed and platinum-based chemotherapy as first-line treatment of unresectable locally advanced or metastatic disease with negative EGFR mutation and ALK status; (2) with bevacizumab, pemetrexed and cisplatin for EGFR mutation-positive locally advanced or metastatic disease after failure of an EGFR TKI. Squamous NSCLC: with gemcitabine and platinum-based chemotherapy as first-line treatment of unresectable locally advanced or metastatic disease. Hepatocellular carcinoma: with bevacizumab as first-line treatment of unresectable or metastatic disease without prior systemic treatment. Esophageal squamous cell carcinoma: with paclitaxel and a platinum agent, or a fluoropyrimidine and a platinum agent, as first-line treatment of unresectable locally advanced, recurrent or metastatic disease. Gastric or gastroesophageal junction adenocarcinoma: with fluoropyrimidine- and platinum-based chemotherapy as first-line treatment of unresectable locally advanced, recurrent or metastatic disease. Endometrial cancer: with fruquintinib for advanced mismatch repair-proficient (pMMR) disease after failure of systemic anticancer therapy, when curative surgery or radiotherapy is unsuitable. This endometrial indication has conditional approval based on a surrogate endpoint; clinical endpoint data are not yet available, and efficacy and safety require further post-approval confirmation. Full approval depends on an ongoing confirmatory randomized controlled trial establishing clinical benefit with sintilimab plus fruquintinib. Colon cancer: with ipilimumab N01 as neoadjuvant treatment of resectable stage IIB-III MSI-H or dMMR colon cancer. This indication has conditional approval based on a surrogate endpoint; clinical endpoint data are not yet available, and efficacy and safety require further confirmation. Full approval depends on ongoing confirmatory trials establishing a significant clinical benefit over standard treatment. Renal cell carcinoma: with fruquintinib for locally advanced or metastatic disease after failure of a VEGFR TKI, provided that a PD-1 or PD-L1 inhibitor was not used as first-line treatment.
- 适应症来源与口径
- 2026-05-25
- 说明书信息局限
- 已取得完整官方药品说明书。 中国大陆说明书。Complete official prescribing information obtained. Mainland China label.
- 中国可获得性状态
- 已核实中国历史批准记录；尚未逐项核查每个产品目前是否持续上市销售。Historical Chinese approval verified; current continuous market availability has not been checked for every product.
- 海外状态
- 待逐一核查各市场。Market-by-market verification pending.
- 医保分类
- 已纳入国家医保（乙类）Included in national insurance (Category B)
- 医保版本
- 2025版；2026年1月1日起执行2025 edition; effective 1 January 2026
- 医保限制
- 限：1.至少经过二线系统化疗的复发或难治性经典型霍奇金淋巴瘤的治疗；2.非鳞状非小细胞肺癌：(1)联合培美曲塞和铂类化疗，用于表皮生长因子受体(EGFR)基因突变阴性和间变性淋巴瘤激酶(ALK)阴性、不可手术切除的局部晚期或转移性非鳞状非小细胞肺癌(NSCLC)患者的一线治疗；(2)联合贝伐珠单抗、培美曲塞和顺铂，用于经表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗失败的EGFR基因突变阳性的局部晚期或转移性非鳞状非小细胞肺癌(NSCLC)患者的治疗；3.联合吉西他滨和铂类化疗，用于不可手术切除的局部晚期或转移性鳞状非小细胞肺癌(NSCLC)的一线治疗；4.联合贝伐珠单抗，用于既往未接受过系统治疗的不可切除或转移性肝细胞癌的一线治疗；5.联合紫杉醇和顺铂或氟尿嘧啶和顺铂用于不可切除的局部晚期、复发或转移性食管鳞癌的一线治疗；6.联合含氟尿嘧啶类和铂类药物化疗用于不可切除的局部晚期、复发或转移性胃及胃食管交界处腺癌的一线治疗；7.联合呋喹替尼胶囊用于既往系统性抗肿瘤治疗后失败且不适合进行根治性手术治疗或根治性放疗的晚期错配修复完整(pMMR)子宫内膜癌患者。Restricted to: Classical Hodgkin lymphoma: for relapsed or refractory disease after at least two lines of systemic chemotherapy. Nonsquamous NSCLC: (1) with pemetrexed and platinum-based chemotherapy as first-line treatment of unresectable locally advanced or metastatic disease with negative EGFR mutation and ALK status; (2) with bevacizumab, pemetrexed and cisplatin for EGFR mutation-positive locally advanced or metastatic disease after failure of an EGFR TKI. Squamous NSCLC: with gemcitabine and platinum-based chemotherapy as first-line treatment of unresectable locally advanced or metastatic disease. Hepatocellular carcinoma: with bevacizumab as first-line treatment of unresectable or metastatic disease without prior systemic treatment. Esophageal squamous cell carcinoma: with paclitaxel and cisplatin, or fluorouracil and cisplatin, as first-line treatment of unresectable locally advanced, recurrent or metastatic disease. Gastric or gastroesophageal junction adenocarcinoma: with fluoropyrimidine- and platinum-based chemotherapy as first-line treatment of unresectable locally advanced, recurrent or metastatic disease. Endometrial cancer: with fruquintinib for advanced mismatch repair-proficient (pMMR) disease after failure of systemic anticancer therapy, when curative surgery or radiotherapy is unsuitable.
- 医保期限
- 2026-01-01 至 2027-12-312026-01-01 to 2027-12-31
- 医保核查说明
- 按成分／剂型名称精确或标准化匹配。报销仍取决于剂型及目录所列支付限制。Matched by exact or normalized ingredient/formulation name. Reimbursement still depends on the dosage form and listed payment restrictions.