CLIN CANCER RES:Patritumab联合西妥昔单抗和铂类治疗头颈部鳞状细胞癌

2019-01-26 MedSci MedSci原创

CLIN CANCER RES近期发表了一篇文章,研究Patritumab联合西妥昔单抗和铂类治疗头颈部复发和/或转移性(R / M)鳞状细胞癌(SCCHN)患者的的安全性并确定推荐II期联合剂量。

CLIN CANCER RES近期发表了一篇文章,研究Patritumab联合西妥昔单抗和铂类治疗头颈部复发和/或转移性(R / M)鳞状细胞癌(SCCHN)患者的的安全性并确定推荐II期联合剂量。

研究纳入年龄≥18岁且确诊R / M SCCHN的患者,患者接受静脉注射patritumab(18 mg / kg负荷剂量;每3周9 mg / kg维持剂量)+西妥昔单抗(400 mg / m 2负荷剂量; 250 mg / 每周m 2维持剂量)+顺铂(每3周100 mg / m 2)或卡铂(AUC为5)六个周期治疗或直至毒性,疾病进展或退出。主要终点是剂量限制性毒性和治疗出现的不良事件(TEAE)。研究还评估了药代动力学,人抗人抗体(HAHA),肿瘤反应,无进展生存(PFS)和总生存(OS)情况。最终共15名患者完成了治疗,patritumab治疗周期的中位数为8.7。未出现DLT。9名患者出现了严重不良事件(patritumab相关n = 4)。TEAE导致7名患者的patritumab治疗中断。1名患者出现Patritumab相关的剂量减低。所有患者在研究结束时均为HAHA阴性。肿瘤反应率为47%。中位PFS和OS分别为7.9和13.5个月。

文章最后认为,Patritumab(18mg / kg负荷剂量,9mg / kg维持剂量)联合西妥昔单抗/铂类是可耐受的,在SCCHN中有抗肿瘤活性,并推荐作为II期临床试验剂量。

原始出处:

Magnus T. Dillon, Lorna Grove, et al. Patritumab with Cetuximab plus Platinum-Containing Therapy in Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck: An Open-Label, Phase Ib Study. CLIN CANCER RES. January 2019 doi: 10.1158/1078-0432.CCR-18-1539

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    2019-09-08 chengjn
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10:21:00 CST 2019, time=2019-01-28, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1589793, encodeId=22321589e937d, content=<a href='/topic/show?id=124d10065220' target=_blank style='color:#2F92EE;'>#颈部#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=18, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=100652, encryptionId=124d10065220, topicName=颈部)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=c46a17776631, createdName=木头人519, createdTime=Mon Jan 28 10:21:00 CST 2019, time=2019-01-28, status=1, ipAttribution=)]
    2019-04-29 snf701207
  5. 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  6. 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  7. 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  8. 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    2019-01-28 wshxjq
  9. 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    2019-01-28 fengxx
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目前尚没有研究评估碳水化合物摄入量与头颈部鳞状细胞癌(HNSCC)预后之间的关系。本文前瞻性的研究了414例新诊断HNSCC患者的治疗前和治疗后碳水化合物摄入量和复发率,全因死亡率和HNSCC特异性死亡率之间的关系。数据表明治疗前高碳水化合物摄入量可能与头颈部鳞癌患者的不良预后相关,但还需要临床干预试验来进一步验证这一假设。

JAMA ONCOL:PD-L低表达的复发或转移头颈部鳞状细胞癌患者接受Durvalumab联合Tremelimumab治疗的安全性和有效性

程序性死亡配体1(PD-L1)和细胞毒性T淋巴细胞相关蛋白4(CTLA-4)的双重阻断可以克服免疫检查点抑制。复发或转移性头颈部鳞状细胞癌(R / M HNSCC)且肿瘤PD-L1低表达的患者进行双重阻断是否可以增强抗肿瘤活性且不损害安全性尚不清楚。JAMAONCOL近期发表了一篇文章,研究durvalumab联合tremelimumab的安全性和客观缓解率。