Roche Information Solutions, Roche Diagnostics, Grenzacherstrasse 124, Building 71, CH-4070, Basel, Switzerland.
Roche Information Solutions, Roche Diagnostics, Santa Clara, CA, USA.
J Cancer Res Clin Oncol. 2023 Jul;149(7):3691-3700. doi: 10.1007/s00432-022-04179-8. Epub 2022 Aug 17.
This study assessed the impact of adherence to guidelines-recommended diagnostic testing on treatment selection and overall survival (OS) in patients with diffuse large B-cell lymphoma (DLBCL) initiated on rituximab-based first line of treatment (1-LOT).
This retrospective cohort study used a nationwide electronic health record-derived de-identified database, including diagnostic testing information on immunohistochemistry (IHC), fluorescence in situ hybridization (FISH) and karyotype analysis that were abstracted from pathology reports or clinical visit notes, where available. The study included patients above 18 years old who were diagnosed with DLBCL between January 2011 and December 2019 and initiated on rituximab-based 1-LOT. Patients were classified into 'non-adherence,' 'partial-adherence' and 'complete-adherence' groups according to the evidence/documentation of a confirmed known result for IHC and molecular profiling tests (FISH and karyotyping) on a selection of the markers prior to the initiation of 1-LOT. Logistic regression was used to evaluate associations of adherence to diagnostic testing with 1-LOT between R-CHOP and other rituximab-based regimens. Median OS after the start of rituximab-based 1-LOT was calculated using the Kaplan-Meier method. Multivariable-adjusted Cox proportional hazards regression was used to assess the risk of all-cause death after initiation of 1-LOT by the degrees of adherence to guidelines-recommended diagnostic testing.
In total, 3730 patients with DLBCL who initiated on rituximab-based 1-LOT were included. No association was found between adherence to guidelines-recommended diagnostic testing and treatment selection of 1-LOT for R-CHOP versus other rituximab-based regimens. Patients with a higher degree of adherence to guidelines-recommended diagnostic testing survived longer (median OS at 5.1, 6.9 and 7.1 years for 'non-adherence,' 'partial-adherence' and 'complete-adherence' groups, respectively [log-rank p < 0.001]) and had a decreased mortality risk (multivariable-adjusted hazard ratio with 95% confidence intervals at 0.83 [0.70-0.99] for 'partial-adherence' and 0.77 [0.64-0.91] for 'complete-adherence' groups, respectively).
Patients' adherence to guidelines-recommended diagnostic testing were associated with better survival benefit, reinforcing the need for adoption of diagnostic testing guidelines in routine clinical care.
本研究评估了在接受利妥昔单抗为基础的一线治疗(1-LOT)的弥漫性大 B 细胞淋巴瘤(DLBCL)患者中,遵循指南推荐的诊断检测对治疗选择和总生存(OS)的影响。
本回顾性队列研究使用了一个全国性的电子病历衍生的去识别数据库,其中包括从病理报告或临床就诊记录中提取的免疫组化(IHC)、荧光原位杂交(FISH)和核型分析的诊断检测信息。该研究纳入了 2011 年 1 月至 2019 年 12 月期间被诊断为 DLBCL 且接受利妥昔单抗为基础的 1-LOT 的年龄在 18 岁以上的患者。根据在 1-LOT 开始前对一系列标志物进行的 IHC 和分子分析测试(FISH 和核型分析)的确认已知结果的证据/记录,患者被分为“不遵守”、“部分遵守”和“完全遵守”组。采用逻辑回归评估诊断检测遵守情况与 R-CHOP 与其他利妥昔单抗为基础方案之间的 1-LOT 选择之间的关联。使用 Kaplan-Meier 法计算利妥昔单抗为基础的 1-LOT 开始后的中位 OS。采用多变量调整 Cox 比例风险回归评估遵循指南推荐的诊断检测程度与 1-LOT 开始后全因死亡的风险。
共有 3730 名接受利妥昔单抗为基础的 1-LOT 的 DLBCL 患者被纳入研究。未发现遵循指南推荐的诊断检测与 R-CHOP 与其他利妥昔单抗为基础方案之间的 1-LOT 治疗选择之间存在关联。更高程度遵循指南推荐的诊断检测的患者存活时间更长(“不遵守”、“部分遵守”和“完全遵守”组的中位 OS 分别为 5.1、6.9 和 7.1 年[log-rank p<0.001]),且死亡率降低(多变量调整后的风险比,95%置信区间分别为 0.83[0.70-0.99]和 0.77[0.64-0.91])。
患者对指南推荐的诊断检测的遵守与生存获益相关,这加强了在常规临床护理中采用诊断检测指南的必要性。