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Patterns of response with talimogene laherparepvec in combination with ipilimumab or ipilimumab alone in metastatic unresectable melanoma

机译:talimogene laherparepvec联合ipilimumab或ipilimumab单独治疗转移性不可切除黑色素瘤的反应模式

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摘要

Talimogene laherparepvec (T-VEC) has demonstrated efficacy for unresectable melanoma. We explored response patterns from a phase 2 study evaluating patients with unresectable stage IIIB–IVM1c malignant melanoma who received T-VEC plus ipilimumab or ipilimumab alone. Patients with objective response per modified irRC were evaluated for pseudo-progression (single ≥25% increase in tumour burden before response). Patients without pseudo-progression were classified by whether they responded within or after 6 months of treatment start; those with pseudo-progression were classified by whether pseudo-progression was due to increase in existing lesions or development of new lesions. Overall, 39% (n = 38/98) in the combination arm and 18% (n = 18/100) in the ipilimumab arm had an objective response. Eight responders (combination, n = 7 [18.4%]; ipilimumab, n = 1 [5.6%]) had pseudo-progression; most occurred by week 12 and were caused by an increase in existing lesions. These data reinforce use of T-VEC through initial progression when combined with checkpoint inhibitors.>Trial Registration (ClinicalTrials.gov; date of registration, December 4, 2012); 2012-000307-32 (ClinicalTrialsRegister.eu; date of registration, May 13, 2014).
机译:Talimogene laherparepvec(T-VEC)已证明对不可切除的黑色素瘤有效。我们探讨了一项2期研究的反应模式,该研究评估了接受T-VEC加伊匹木单抗或伊匹木单抗治疗的不可切除的IIIB-IVM1c期恶性黑色素瘤患者。对经过改良的irRC客观应答的患者进行假进展评估(应答前肿瘤负荷增加≥25%)。没有假进展的患者根据在治疗开始后6个月内或治疗后是否有反应进行分类。具有假进展的患者按假进展是由于现有病变的增加还是新病变的发展进行分类。总体而言,联合用药组中有39%(n = 38/98),伊立木单抗组中有18%(n = 18/100)有客观反应。八名反应者(组合,n = 7,占[18.4%]; ipilimumab,n = 1,[5.6%])具有假进展。大多数发生在第12周,并且是由现有病变的增加引起的。这些数据在与检查点抑制剂联合使用时可增强T-VEC在初始过程中的使用。>试验注册(ClinicalTrials.gov;注册日期,2012年12月4日); 2012-000307-32(ClinicalTrialsRegister.eu;注册日期,2014年5月13日)。

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