Arjun Pandey, Kim Roos, Yidi Jiang, Kathryn Mangoff, Gail Klein, Nick Forward, Douglas Stewart, Pierre Laneuville, Isabelle Bence-Bruckler, Joy Mangel, George Tomlinson, Neil L. Berinstein
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This regimen was designed to activate tumor-specific T cells by targeting the tumor-associated antigen survivin with MVP-S and reducing two important T cell inhibitory pathways: T cell exhaustion and regulatory T cells with pembrolizumab and metronomic cyclophosphamide, respectively.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>This was a single-arm Phase II clinical trial in 25 participants with R/R DLBCL-SPiReL trial (NCT03349450).</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The median overall survival was 10.1 months and a third of participants survived over 2 years. Enhanced long-term survival was associated with favorable clinical characteristics and enhanced immune reactivity, as assessed by ELISpot and ISR-immune reactive responses. The regimen was well-tolerated with minimal Grade 3–4 toxicities.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Combination immunotherapy regimens such as this could offer a promising alternative to other treatments with significant toxicities for select patients.</p>\n </section>\n </div>","PeriodicalId":72883,"journal":{"name":"EJHaem","volume":"6 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11756968/pdf/","citationCount":"0","resultStr":"{\"title\":\"Characteristics of relapsed/refractory diffuse large B-cell lymphoma patients with durable responses to maveropepimut-S, pembrolizumab, and cyclophosphamide: Long-term follow-up from the SPiReL trial\",\"authors\":\"Arjun Pandey, Kim Roos, Yidi Jiang, Kathryn Mangoff, Gail Klein, Nick Forward, Douglas Stewart, Pierre Laneuville, Isabelle Bence-Bruckler, Joy Mangel, George Tomlinson, Neil L. 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引用次数: 0
摘要
复发/难治性弥漫性大b细胞淋巴瘤(R/R DLBCL)患者的医疗需求未得到满足。该试验的目的是评估一种新型三联免疫治疗方案——派姆单抗、低剂量环磷酰胺和maveropepimot - s (MVP-S)的疗效和毒性。该方案旨在通过使用MVP-S靶向肿瘤相关抗原survivin来激活肿瘤特异性T细胞,并分别使用派姆单抗和节律环磷酰胺降低两个重要的T细胞抑制途径:T细胞衰竭和调节性T细胞。方法:这是一项单臂II期临床试验,25名参与者进行R/R DLBCL-SPiReL试验(NCT03349450)。结果:中位总生存期为10.1个月,三分之一的参与者存活超过2年。通过ELISpot和isr免疫反应性评估,延长的长期生存率与良好的临床特征和增强的免疫反应性相关。该方案耐受性良好,3-4级毒性最小。结论:像这样的联合免疫治疗方案可以为特定患者提供一种有希望的替代其他具有显著毒性的治疗方案。
Characteristics of relapsed/refractory diffuse large B-cell lymphoma patients with durable responses to maveropepimut-S, pembrolizumab, and cyclophosphamide: Long-term follow-up from the SPiReL trial
Introduction
Patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL) have an unmet medical need. The objective of this trial was to assess the efficacy and toxicities of a novel triple immunotherapy regimen—pembrolizumab, low-dose cyclophosphamide, and maveropepimut-S (MVP-S). This regimen was designed to activate tumor-specific T cells by targeting the tumor-associated antigen survivin with MVP-S and reducing two important T cell inhibitory pathways: T cell exhaustion and regulatory T cells with pembrolizumab and metronomic cyclophosphamide, respectively.
Methods
This was a single-arm Phase II clinical trial in 25 participants with R/R DLBCL-SPiReL trial (NCT03349450).
Results
The median overall survival was 10.1 months and a third of participants survived over 2 years. Enhanced long-term survival was associated with favorable clinical characteristics and enhanced immune reactivity, as assessed by ELISpot and ISR-immune reactive responses. The regimen was well-tolerated with minimal Grade 3–4 toxicities.
Conclusion
Combination immunotherapy regimens such as this could offer a promising alternative to other treatments with significant toxicities for select patients.