Hanna Timothy P, King Will D, Thibodeau Stephane, Jalink Matthew, Paulin Gregory A, Harvey-Jones Elizabeth, O'Sullivan Dylan E, Booth Christopher M, Sullivan Richard, Aggarwal Ajay
Division of Cancer Care and Epidemiology, Cancer Research Institute at Queen's University, 10 Stuart Street, 2nd Level, Kingston, ON K7L3N6, Canada.
Department of Oncology, Queen's University, Kingston, ON, Canada.
BMJ. 2020 Nov 4;371:m4087. doi: 10.1136/bmj.m4087.
To quantify the association of cancer treatment delay and mortality for each four week increase in delay to inform cancer treatment pathways.
Systematic review and meta-analysis.
Published studies in Medline from 1 January 2000 to 10 April 2020.
Curative, neoadjuvant, and adjuvant indications for surgery, systemic treatment, or radiotherapy for cancers of the bladder, breast, colon, rectum, lung, cervix, and head and neck were included. The main outcome measure was the hazard ratio for overall survival for each four week delay for each indication. Delay was measured from diagnosis to first treatment, or from the completion of one treatment to the start of the next. The primary analysis only included high validity studies controlling for major prognostic factors. Hazard ratios were assumed to be log linear in relation to overall survival and were converted to an effect for each four week delay. Pooled effects were estimated using DerSimonian and Laird random effect models.
The review included 34 studies for 17 indications (n=1 272 681 patients). No high validity data were found for five of the radiotherapy indications or for cervical cancer surgery. The association between delay and increased mortality was significant (P<0.05) for 13 of 17 indications. Surgery findings were consistent, with a mortality risk for each four week delay of 1.06-1.08 (eg, colectomy 1.06, 95% confidence interval 1.01 to 1.12; breast surgery 1.08, 1.03 to 1.13). Estimates for systemic treatment varied (hazard ratio range 1.01-1.28). Radiotherapy estimates were for radical radiotherapy for head and neck cancer (hazard ratio 1.09, 95% confidence interval 1.05 to 1.14), adjuvant radiotherapy after breast conserving surgery (0.98, 0.88 to 1.09), and cervix cancer adjuvant radiotherapy (1.23, 1.00 to 1.50). A sensitivity analysis of studies that had been excluded because of lack of information on comorbidities or functional status did not change the findings.
Cancer treatment delay is a problem in health systems worldwide. The impact of delay on mortality can now be quantified for prioritisation and modelling. Even a four week delay of cancer treatment is associated with increased mortality across surgical, systemic treatment, and radiotherapy indications for seven cancers. Policies focused on minimising system level delays to cancer treatment initiation could improve population level survival outcomes.
量化癌症治疗延迟每增加四周与死亡率之间的关联,以为癌症治疗途径提供参考。
系统评价和荟萃分析。
2000年1月1日至2020年4月10日发表在Medline上的研究。
纳入膀胱癌、乳腺癌、结肠癌、直肠癌、肺癌、宫颈癌以及头颈癌手术、全身治疗或放疗的治愈性、新辅助和辅助治疗指征。主要结局指标是每种指征每延迟四周的总生存风险比。延迟时间从诊断到首次治疗,或从一种治疗完成到下一种治疗开始计算。初步分析仅纳入了控制主要预后因素的高有效性研究。假定风险比与总生存呈对数线性关系,并转换为每延迟四周的效应值。采用DerSimonian和Laird随机效应模型估计合并效应。
该评价纳入了针对17种指征的34项研究(n=1272681例患者)。在5种放疗指征或宫颈癌手术方面未发现高有效性数据。17种指征中有13种的延迟与死亡率增加之间的关联具有统计学意义(P<0.05)。手术方面的结果一致,每延迟四周的死亡风险为1.06-1.08(例如,结肠切除术1.06,95%置信区间1.01至1.12;乳腺癌手术1.08,1.03至1.13)。全身治疗的估计值有所不同(风险比范围为1.01-1.28)。放疗方面的估计值为头颈癌根治性放疗(风险比1.09,95%置信区间1.05至1.14)、保乳手术后辅助放疗(0.98,0.88至1.09)以及宫颈癌辅助放疗(1.23,1.00至1.50)。对因缺乏合并症或功能状态信息而被排除的研究进行的敏感性分析未改变研究结果。
癌症治疗延迟是全球卫生系统中存在的一个问题。现在可以量化延迟对死亡率的影响,以便进行优先级排序和建模。即使癌症治疗延迟四周,在七种癌症的手术、全身治疗和放疗指征方面也与死亡率增加相关。专注于尽量减少癌症治疗开始时系统层面延迟的政策可能会改善人群层面的生存结局。