Ho Carrie, Zhu Songli, Gooley Ted, Gujral Taranjit S, Lynch Ryan C, Poh Christina, Shadman Mazyar, Smith Stephen D, Tseng Yolanda, Gopal Ajay K
Division of Hematology and Oncology, Department of Medicine University of Washington Seattle Washington USA.
Clinical Research Division Fred Hutchinson Cancer Center Seattle Washington USA.
EJHaem. 2024 Oct 10;5(6):1173-1181. doi: 10.1002/jha2.1029. eCollection 2024 Dec.
The tumor microenvironment (TME), including infiltrating T-cells, is thought to play a major role in the pathogenesis and prognosis of follicular lymphoma (FL) and may contribute to its widely varied disease course. We hypothesized that programmed death-1 inhibition may be most effective in untreated, immunocompetent FL patients. Thus, we developed a phase 2 study to evaluate the efficacy of pembrolizumab as the initial treatment for indolent B-cell lymphoma.
Adults with FL or marginal zone lymphoma and an indication for treatment were eligible. Patients received pembrolizumab 200 mg IV in 21-day cycles for up to 18 cycles, until progression or unacceptable toxicity. Early response assessment was obtained after cycle 3 with computed tomography (CT), and a fluorodeoxyglucose (FDG)-positron emission tomography-computed tomography (PET-CT) was obtained after cycle 6 to determine candidacy for continuation in the study. Immunosecretome profiling was performed at baseline and on cycle 2 day 1.
Nine patients with FL were enrolled between February 2019 and April 2021, including eight (89%) with advanced stage, seven (78%) with intermediate/high Follicular Lymphoma International Prognostic Index, and six (67%) with high-tumor burden by Groupe d'Etude des Lymphomes Folliculaires. The best overall response rate by FDG PET-CT was 33% (three partial metabolic responses). Three patients (33%) had stable disease, and three (33%) had progressive disease (including one patient who only had a follow-up CT). By CT four (44%) experienced a reduction in target lesions, but all were less than partial responses. Grade 3 or higher immune-related adverse events (IRAEs) were seen in two (22%) patients, both with transaminitis and one of whom had concurrent hypophysitis. Another patient had grade 1 pneumonitis, requiring treatment with steroids. No associations between the immunosecretome profile and clinical outcomes could be detected.
Frontline pembrolizumab for FL is associated with limited responses and a clinically significant rate of IRAEs. Alternative strategies for targeting the TME in FL should be explored.
肿瘤微环境(TME),包括浸润的T细胞,被认为在滤泡性淋巴瘤(FL)的发病机制和预后中起主要作用,并且可能导致其广泛多样的病程。我们假设程序性死亡-1抑制在未经治疗的、免疫功能正常的FL患者中可能最有效。因此,我们开展了一项2期研究,以评估帕博利珠单抗作为惰性B细胞淋巴瘤初始治疗的疗效。
符合条件的为患有FL或边缘区淋巴瘤且有治疗指征的成年人。患者接受静脉注射帕博利珠单抗200mg,每21天为一个周期,最多18个周期,直至疾病进展或出现不可接受的毒性。在第3周期后通过计算机断层扫描(CT)进行早期反应评估,并在第6周期后进行氟脱氧葡萄糖(FDG)-正电子发射断层扫描-计算机断层扫描(PET-CT)以确定是否有资格继续参与研究。在基线和第2周期第1天进行免疫分泌组分析。
2019年2月至2021年4月期间共纳入9例FL患者,其中8例(89%)为晚期,7例(78%)为中/高滤泡性淋巴瘤国际预后指数,6例(67%)为高肿瘤负荷(根据滤泡性淋巴瘤研究组标准)。根据FDG PET-CT评估的最佳总体缓解率为33%(3例部分代谢缓解)。3例患者(33%)病情稳定,3例(33%)病情进展(包括1例仅进行了随访CT检查的患者)。根据CT检查,4例(44%)患者的靶病灶有所缩小,但均未达到部分缓解。2例(22%)患者出现3级或更高等级的免疫相关不良事件(IRAEs),均有转氨酶升高,其中1例同时患有垂体炎。另1例患者出现1级肺炎,需要使用类固醇治疗。未发现免疫分泌组分析结果与临床结局之间存在关联。
FL一线使用帕博利珠单抗缓解有限,且IRAEs发生率具有临床意义。应探索针对FL中TME的替代策略。