Real-world outcomes of diffuse large B-cell lymphoma treated with frontline R-CHOP(-like) regimens in an Asian multi-ethnic population.

IF 3 3区 医学 Q2 HEMATOLOGY
Ryan Mao Heng Lim, Jing Yuan Tan, Ya Hwee Tan, Zane En Qi Heng, Lawrence Cheng Kiat Ng, Francesca Lorraine Wei Inng Lim, Yeow Tee Goh, Soon Thye Lim, Jason Yongsheng Chan
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引用次数: 0

Abstract

Background: Recent breakthrough advances in the treatment of DLBCL, such as the antibody-drug conjugate polatuzumab vedotin, have yielded clinical survival benefit over rituximab, cyclophosphamide, doxorubicin, vincristine and prednisolone (R-CHOP) for the first time in 20 years since the advent of the rituximab era. We thus examine the outcomes of standard immunochemotherapy for DLBCL in our multi-ethnic Asian population, so as to determine the real-world clinical need to adopt new therapeutics in this disease entity.

Methods: We conducted a retrospective study involving patients (n = 1071) diagnosed with DLBCL at the National Cancer Centre Singapore from 2010 to 2022, and treated with first-line rituximab-based regimens. The median follow-up duration was 48 months. Survival analyses were performed using the Kaplan-Meier method and multivariate Cox proportional models.

Results: The cohort consisted of 590 male and 481 female patients with a median age of 63.8 years (range, 19.3-93.6). Most were stage III-IV at diagnosis (60.9%) and of non-germinal center B-cell like (non-GCB) subtype by Han's criteria (56.5%). The vast majority received R-CHOP(-like) regimens (n = 997, 93.1%), including rituximab, etoposide, prednisone, vincristine, cyclophosphamide and doxorubicin (EPOCH-R) (n = 95), achieving a 5-year progression-free survival (PFS) and overall survival (OS) of 64.5% and 74.7% respectively. Male sex (p = 0.0294), age > 60 years (p < 0.0001), poor ECOG scores (2-4) (p < 0.0001), advanced stage (III-IV) (p < 0.0001), presence of B-symptoms (p = 0.0305), and raised LDH (p = 0.0161) were independent predictors of OS, 4 of which are risk factors in the International Prognostic Index (IPI). In the intermediate to high-risk subgroup (IPI scores 2-5; n = 752), the 5-year PFS and OS were only 59.0% and 69.8% respectively. EBV status, MYC and/or BCL2/BCL6 rearrangements, were not significantly associated with survival outcomes. EPOCH-R was used more frequently than R-CHOP in patients with MYC rearrangements (n = 82, p < 0.0001), including those with MYC/BCL2 double-hit genetics (n = 31, p < 0.0001). Notably, neither regimen significantly affected survival outcomes, both in MYC-rearranged (PFS: HR 0.60, p = 0.1704; OS: HR 0.49, p = 0.0852), and in MYC/BCL2 double-hit DLBCL (PFS: HR 1.30, p = 0.6433; OS: HR 1.02, p = 0.9803).

Conclusion: Our study demonstrates that our local population has similar clinicopathological and prognostic characteristics of DLBCL as compared to global findings. It also highlights the limitations of R-CHOP(-like) regimens in contemporary DLBCL management and therefore an ongoing need for improved therapeutic strategies.

亚洲多种族人群中弥漫大B细胞淋巴瘤接受前线R-CHOP(类)方案治疗的实际效果。
背景:最近在治疗DLBCL方面取得了突破性进展,如抗体药物结合体泊拉珠单抗维多汀(polatuzumab vedotin),与利妥昔单抗、环磷酰胺、多柔比星、长春新碱和泼尼松龙(R-CHOP)相比,在利妥昔单抗时代到来后的20年里首次获得了临床生存获益。因此,我们研究了多种族亚洲人群中DLBCL标准免疫化疗的疗效,以确定该疾病实体采用新疗法的实际临床需求:我们开展了一项回顾性研究,涉及2010年至2022年期间在新加坡国立癌症中心确诊的DLBCL患者(n = 1071),这些患者接受了以利妥昔单抗为基础的一线治疗方案。中位随访时间为48个月。采用卡普兰-梅耶法和多变量考克斯比例模型进行生存分析:队列中有 590 名男性患者和 481 名女性患者,中位年龄为 63.8 岁(19.3-93.6 岁)。大多数患者在确诊时处于 III-IV 期(60.9%),根据 Han 的标准属于非生殖中心 B 细胞(non-GCB)亚型(56.5%)。绝大多数患者接受了R-CHOP(类)方案治疗(997人,93.1%),包括利妥昔单抗、依托泊苷、泼尼松、长春新碱、环磷酰胺和多柔比星(EPOCH-R)(95人),5年无进展生存期(PFS)和总生存期(OS)分别为64.5%和74.7%。男性(p = 0.0294),年龄大于 60 岁(p 结论:我们的研究表明,我们的本地人群中存在着更多的癌症患者:我们的研究表明,与全球调查结果相比,我们当地的 DLBCL 患者具有相似的临床病理和预后特征。研究还强调了 R-CHOP(类似)方案在当代 DLBCL 治疗中的局限性,因此需要不断改进治疗策略。
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来源期刊
Annals of Hematology
Annals of Hematology 医学-血液学
CiteScore
5.60
自引率
2.90%
发文量
304
审稿时长
2 months
期刊介绍: Annals of Hematology covers the whole spectrum of clinical and experimental hematology, hemostaseology, blood transfusion, and related aspects of medical oncology, including diagnosis and treatment of leukemias, lymphatic neoplasias and solid tumors, and transplantation of hematopoietic stem cells. Coverage includes general aspects of oncology, molecular biology and immunology as pertinent to problems of human blood disease. The journal is associated with the German Society for Hematology and Medical Oncology, and the Austrian Society for Hematology and Oncology.
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