Division of Oncology, Rambam Health Care Campus, Haifa, Israel.
Davidoff Center, Rabin Medical Center, Petah Tikva, Israel.
Ann Oncol. 2022 Jul;33(7):720-727. doi: 10.1016/j.annonc.2022.03.012. Epub 2022 Mar 23.
Classical Kaposi sarcoma (cKS) is a rare human herpesvirus 8-associated sarcoma with limited treatment options. We evaluated the efficacy and safety of nivolumab in combination with ipilimumab in patients with previously treated progressive cKS.
cKS patients with progressive disease after one or more lines of systemic therapy and measurable disease by positron emission tomography/computed tomography and/or physical examination received nivolumab 240 mg every 2 weeks and ipilimumab 1 mg/kg every 6 weeks until progression or toxicity for a maximum of 24 months. The primary endpoint was overall response rate; secondary endpoints included 6-month progression-free survival (PFS) rate and safety. Immune correlates were explored using immunohistochemistry, DNA sequencing (596/648 genes) and RNA sequencing (whole transcriptome hybrid capture) of tumor specimens and matched blood.
Eighteen male patients (median age 76.5 years) were enrolled between April 2018 and December 2020. At a median follow up of 24.4 months, overall response rate by RECIST v1.1 was 87%. Metabolic complete response as assessed by positron emission tomography/computed tomography was observed in 8 of 13 (62%) assessable patients. Some 6/13 achieved pathological complete response after treatment. In two patients, palliative limb amputation was prevented. Median PFS was not reached. The 6- month and 12-month PFS rate was 76.5% and 58.8%, respectively. Only four patients (22%) experienced grade 3-4 adverse events. The most frequent genomic alteration was biallelic copy number loss of the FOX1A gene. The majority of tumors carried a low tumor mutational burden, were microsatellite stable, mismatch repair proficient, did not express programmed death-ligand 1, and displayed only low lymphocytic infiltrates, rendering them immunologically 'cold'.
This prospectively designed phase II study of nivolumab and ipilimumab demonstrates promising activity of this combination in progressive cKS representing a new treatment option in this population.
经典型卡波西肉瘤(cKS)是一种罕见的人类疱疹病毒 8 相关肉瘤,治疗选择有限。我们评估了纳武利尤单抗联合伊匹单抗在既往接受过治疗且疾病进展的 cKS 患者中的疗效和安全性。
接受过一种或多种全身治疗且正电子发射断层扫描/计算机断层扫描和/或体格检查可测量疾病的 cKS 患者,每 2 周接受 240mg 纳武利尤单抗和每 6 周 1mg/kg 伊匹单抗治疗,最长 24 个月,直至疾病进展或出现毒性。主要终点为总缓解率;次要终点包括 6 个月无进展生存率(PFS)和安全性。使用肿瘤标本和匹配血液的免疫组化、DNA 测序(596/648 个基因)和 RNA 测序(全转录本杂交捕获)探索免疫相关性。
18 名男性患者(中位年龄 76.5 岁)于 2018 年 4 月至 2020 年 12 月入组。在中位随访 24.4 个月时,根据 RECIST v1.1 评估的总缓解率为 87%。13 例可评估患者中有 8 例(62%)根据正电子发射断层扫描/计算机断层扫描评估为代谢完全缓解。治疗后有 6 例患者获得病理完全缓解。有 2 例患者避免了姑息性肢体截肢。中位 PFS 未达到。6 个月和 12 个月的 PFS 率分别为 76.5%和 58.8%。仅 4 名患者(22%)发生 3-4 级不良事件。最常见的基因组改变是 FOX1A 基因的双等位基因拷贝数缺失。大多数肿瘤具有低肿瘤突变负担、微卫星稳定、错配修复功能正常、不表达程序性死亡配体 1,并且仅显示低淋巴细胞浸润,使其具有免疫“冷”性。
这项前瞻性设计的纳武利尤单抗联合伊匹单抗的 II 期研究显示,该联合方案在进展期 cKS 中具有有前景的活性,为该人群提供了一种新的治疗选择。