Department of Medicine, University of Toronto, Toronto, ON.
Br J Haematol. 2015 Feb;168(4):492-500. doi: 10.1111/bjh.13150. Epub 2014 Oct 17.
There is a paucity of data on the impact of diagnostic and treatment delays on outcomes in haematological malignancies, particularly in patients with diffuse large B-cell lymphoma (DLBCL). Our database of patients treated for DLBCL between 2002 and 2010 was interrogated. Univariate and multivariate analyses were performed to determine the relationship between sociodemographic or disease-specific variables and delays. Cox Regression analysis was used to discern the impact of delays on survival. Patients (n = 278) waited a median of 4 weeks before seeking medical attention. It took a median of 8 weeks for a non-haematology physician to diagnose DLBCL and refer to a haematologist. A median of 3 weeks elapsed between specialist consultation and chemotherapy initiation. In multivariate logistic regression analysis, bone marrow involvement [odds ratio (OR) = 0·41, P = 0·018], Charlson comorbidity index (OR = 1·42, P = 0·017) and urgent inpatient chemotherapy (OR = 0·40, P = 0·012) were associated with diagnostic delays >6 weeks. Lack of pathological diagnosis at the time of haematology referral was the only factor that independently predicted for treatment delays >4 weeks (OR = 8·25, P < 0·01). Diagnostic or treatment delays did not impact survival or progression-free survival. In conclusion, selected disease and patient-related factors are associated with delays in management of DLBCL, but do not impact outcomes.
关于诊断和治疗延迟对血液恶性肿瘤(尤其是弥漫性大 B 细胞淋巴瘤)患者结局的影响,数据很少。我们对 2002 年至 2010 年间接受弥漫性大 B 细胞淋巴瘤治疗的患者数据库进行了查询。采用单变量和多变量分析来确定社会人口统计学或疾病特异性变量与延迟之间的关系。采用 Cox 回归分析来辨别延迟对生存的影响。患者(n=278)在寻求医疗帮助之前平均等待 4 周。非血液科医生诊断弥漫性大 B 细胞淋巴瘤并转介给血液科医生平均需要 8 周。从专家会诊到开始化疗平均需要 3 周。在多变量逻辑回归分析中,骨髓受累(OR=0·41,P=0·018)、Charlson 合并症指数(OR=1·42,P=0·017)和紧急住院化疗(OR=0·40,P=0·012)与诊断延迟>6 周相关。血液科转介时缺乏病理诊断是唯一独立预测治疗延迟>4 周的因素(OR=8·25,P<0·01)。诊断或治疗延迟均未影响生存或无进展生存期。总之,一些疾病和患者相关因素与弥漫性大 B 细胞淋巴瘤的治疗延迟相关,但不影响结局。