Phase I Study of Subcutaneous Rituximab Hyaluronidase Combined With CHOP Chemotherapy for the Treatment of Diffuse Large B-Cell Lymphoma in Uganda.

IF 3 Q2 ONCOLOGY JCO Global Oncology Pub Date : 2025-04-01 Epub Date: 2025-04-04 DOI:10.1200/GO-24-00489
Manoj P Menon, Henry Ddungu, Kelvin R Mubiru, Scott V Adams, Jacqueline Asea, Rosemary Namagembe, Prossy Namuli, Joyce Kambugu, Andrea M H Towlerton, Camille Puronen, Thomas S Uldrick, Jackson Orem, Edus H Warren
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Abstract

Purpose: Patients with diffuse large B-cell lymphoma (DLBCL) who are treated in low-resource settings have inferior outcomes compared with those in high-resource settings. Rituximab, an anti-CD20 monoclonal antibody, when combined with chemotherapy, improves overall survival (OS) for DLBCL. However, in part due to the limited availability of infusion centers in low-resource countries, rituximab is rarely used. Subcutaneous rituximab (sqR) is a potential solution; however, its safety and efficacy have not been tested in low-income countries.

Methods: This open-label phase I study enrolled patients 18 years or older with newly diagnosed DLBCL. The first cohort (n = 6) received intravenous rituximab plus CHOP. This cohort received sqR for subsequent cycles. The second cohort (n = 12) received sqR plus CHOP for all cycles. Safety and tolerability were evaluated; secondary outcomes included response rates and treatment completion.

Results: Between October 25, 2019, and October 7, 2022, 18 patients, with a median age of 36.5 years, were enrolled; 10 were male, and 10 presented with advanced-stage disease. The most common hematologic toxicity was neutropenia (n = 9, 50%). Fifteen of the 18 participants completed treatment; 14 (93.3%) patients achieved a complete response, and one patient (6.7%) had a partial response. The OS and progression-free survival (PFS) at 12 months were 83% (95% CI, 68 to 100) and 67% (95% CI, 48 to 92), respectively. The OS and PFS at 24 months were 66% (95% CI, 47 to 92) and 67% (95% CI, 48 to 92), respectively.

Conclusion: As demonstrated in other parts of the world, sqR together with CHOP was safe, well-tolerated, and efficacious among Ugandan patients with DLBCL. The very high OS rates are nearly double those of historical controls and comparable with outcomes expected in resource-rich settings. This study demonstrated the feasibility, safety, and efficacy of sqR-CHOP, increased the research infrastructure in Uganda, and will improve care in other resource-limited settings.

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皮下利妥昔单抗透明质酸酶联合CHOP化疗治疗乌干达弥漫性大b细胞淋巴瘤的I期研究
目的:在低资源环境中治疗弥漫性大b细胞淋巴瘤(DLBCL)的患者与在高资源环境中治疗的患者相比预后较差。抗cd20单克隆抗体利妥昔单抗联合化疗可提高DLBCL的总生存期(OS)。然而,部分由于资源匮乏国家输注中心的可用性有限,利妥昔单抗很少被使用。皮下美罗华(sqR)是一个潜在的解决方案;然而,其安全性和有效性尚未在低收入国家进行测试。方法:这项开放标签I期研究纳入了18岁或以上新诊断的DLBCL患者。第一组(n = 6)接受静脉利妥昔单抗加CHOP治疗。该队列在随后的周期中接受sqR。第二组(n = 12)在所有周期均接受sqR + CHOP治疗。评估安全性和耐受性;次要结局包括有效率和治疗完成率。结果:在2019年10月25日至2022年10月7日期间,入组了18例患者,中位年龄为36.5岁;10例为男性,10例为晚期疾病。最常见的血液学毒性是中性粒细胞减少(n = 9.50%)。18名参与者中有15人完成了治疗;14例(93.3%)患者达到完全缓解,1例(6.7%)患者达到部分缓解。12个月的OS和无进展生存期(PFS)分别为83% (95% CI, 68 - 100)和67% (95% CI, 48 - 92)。24个月时OS和PFS分别为66% (95% CI, 47 ~ 92)和67% (95% CI, 48 ~ 92)。结论:正如世界其他地区所证明的那样,在乌干达DLBCL患者中,sqR联合CHOP是安全、耐受性良好且有效的。非常高的OS率几乎是历史对照的两倍,与资源丰富环境下的预期结果相当。这项研究证明了sqR-CHOP的可行性、安全性和有效性,增加了乌干达的研究基础设施,并将改善其他资源有限地区的护理。
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来源期刊
JCO Global Oncology
JCO Global Oncology Medicine-Oncology
CiteScore
6.70
自引率
6.70%
发文量
310
审稿时长
7 weeks
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