Farooqi Hanzala Ahmed, Saffi Ullah Muhammad, Raza Ahmed, Sadiq Zain, Shaikh Wardah Ali, Muhammad Rahmah, Hussain Muhammad Shoaib
Islamic International Medical College Riphah International University, Islamabad, Islamabad Capital Territory, Pakistan.
Quaid-e-Azam Medical College, Bahawalpur, Punjab, Pakistan.
Crit Rev Oncol Hematol. 2025 Mar;207:104611. doi: 10.1016/j.critrevonc.2024.104611. Epub 2025 Jan 8.
Diffuse large B-cell lymphoma (DLBCL), the most common non-Hodgkin's lymphoma subtype, relapses or becomes refractory (R/R) in 40 % of cases after initial treatment. Among the second-line treatments for these patients is CAR T-cell therapy, which is considered the gold standard and treatment better than SCT. For these patients, polatuzumab vedotin in combination with bendamustine and rituximab (Pola-BR) is a novel treatment. The main goal of our research is to evaluate Pola-BR's efficacy in R/R DLBCL patients.
We followed PRISMA criteria for conducting this systematic review and meta-analysis. A search was conducted from the start until May 2024 using the Cochrane Library, PubMed, and clinicaltrials.gov. Studies included randomized-controlled trials, observational studies, and single-arm studies assessing Pola-BR efficacy in R/R DLBCL patients. The overall response rate (ORR), partial response (PR), and complete response (CR) were the main outcomes. Using random-effect models, statistical analysis was carried out on OpenMeta[Analyst] software leading to pooled risk ratios with 95 % confidence intervals (CIs).
Eight studies with 398 patients were present in our study. The studies were of high quality, with pooled analysis showing a significant ORR of 52.6 % (95 % CI: 43.6 - 61.6 %), CR of 34.3 % (95 % CI: 23.5 - 45.0 %), and PR of 15.5 % (95 % CI: 8.7 - 22.3 %). Significant hematologic toxicities were observed, the most common being, neutropenia, thrombocytopenia, neuropathy, and anemia.
Pola-BR is an effective option for advanced R/R DLBCL but poses significant hematologic toxicity, requiring careful management. Further high-quality randomized trials are needed to better understand and evaluate Pola-BR's success. To fully assess its effectiveness, comparisons with non-cell therapies are essential.
弥漫性大B细胞淋巴瘤(DLBCL)是最常见的非霍奇金淋巴瘤亚型,40%的患者在初始治疗后会复发或难治(R/R)。这些患者的二线治疗方法之一是CAR T细胞疗法,该疗法被视为金标准,且比自体造血干细胞移植(SCT)治疗效果更好。对于这些患者,泊洛妥珠单抗联合苯达莫司汀和利妥昔单抗(Pola-BR)是一种新型治疗方法。我们研究的主要目的是评估Pola-BR在R/R DLBCL患者中的疗效。
我们遵循PRISMA标准进行这项系统评价和荟萃分析。从开始到2024年5月,使用Cochrane图书馆、PubMed和clinicaltrials.gov进行检索。纳入的研究包括评估Pola-BR在R/R DLBCL患者中疗效的随机对照试验、观察性研究和单臂研究。主要结局指标为总缓解率(ORR)、部分缓解(PR)和完全缓解(CR)。使用随机效应模型,在OpenMeta[Analyst]软件上进行统计分析,得出合并风险比及95%置信区间(CI)。
我们的研究纳入了8项研究,共398例患者。这些研究质量较高,汇总分析显示ORR为52.6%(95%CI:43.6 - 61.6%),CR为34.3%(95%CI:23.5 - 45.0%),PR为15.5%(95%CI:8.7 - 22.3%)。观察到明显的血液学毒性,最常见的是中性粒细胞减少、血小板减少、神经病变和贫血。
Pola-BR是晚期R/R DLBCL的一种有效选择,但存在明显的血液学毒性,需要谨慎管理。需要进一步开展高质量的随机试验,以更好地理解和评估Pola-BR的成效。为全面评估其有效性,与非细胞疗法进行比较至关重要。