Cancer Surveillance Branch, International Agency for Research on Cancer, Lyon, France.
Department of Health Sciences, University of Leicester, Leicester, UK.
Int J Cancer. 2021 Sep 1;149(5):1013-1020. doi: 10.1002/ijc.33620. Epub 2021 May 20.
Survival from lung cancer remains low, yet is the most common cancer diagnosed worldwide. With survival contrasting between the main histological groupings, small-cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), it is important to assess the extent that geographical differences could be from varying proportions of cancers with unspecified histology across countries. Lung cancer cases diagnosed 2010-2014, followed until 31 December 2015 were provided by cancer registries from seven countries for the ICBP SURVMARK-2 project. Multiple imputation was used to reassign cases with unspecified histology into SCLC, NSCLC and other. One-year and three-year age-standardised net survival were estimated by histology, sex, age group and country. In all, 404 617 lung cancer cases were included, of which 47 533 (11.7%) and 262 040 (64.8%) were SCLC and NSCLC. The proportion of unspecified cases varied, from 11.2% (Denmark) to 29.0% (The United Kingdom). After imputation with unspecified histology, survival variations remained: 1-year SCLC survival ranged from 28.0% (New Zealand) to 35.6% (Australia) NSCLC survival from 39.4% (The United Kingdom) to 49.5% (Australia). The largest survival change after imputation was for 1-year NSCLC (4.9 percentage point decrease). Similar variations were observed for 3-year survival. The oldest age group had lowest survival and largest decline after imputation. International variations in SCLC and NSCLC survival are only partially attributable to differences in the distribution of unspecified histology. While it is important that registries and clinicians aim to improve completeness in classifying cancers, it is likely that other factors play a larger role, including underlying risk factors, stage, comorbidity and care management which warrants investigation.
肺癌的生存率仍然很低,但却是全球最常见的癌症诊断。由于小细胞肺癌(SCLC)和非小细胞肺癌(NSCLC)这两个主要组织学分组之间的生存率存在差异,因此评估各国之间由于癌症组织学未明确的比例不同而导致的差异程度非常重要。ICBP SURVMARK-2 项目的癌症登记处提供了 2010-2014 年诊断的肺癌病例,并随访至 2015 年 12 月 31 日。使用多次插补将组织学未明确的病例重新分配到 SCLC、NSCLC 和其他类型。根据组织学、性别、年龄组和国家,估计了 1 年和 3 年的年龄标准化净生存率。共纳入 404617 例肺癌病例,其中 SCLC 和 NSCLC 分别为 47533(11.7%)和 262040(64.8%)。未明确病例的比例各不相同,从 11.2%(丹麦)到 29.0%(英国)。在对未明确组织学的病例进行插补后,生存差异仍然存在:1 年 SCLC 生存率范围为 28.0%(新西兰)至 35.6%(澳大利亚),NSCLC 生存率范围为 39.4%(英国)至 49.5%(澳大利亚)。插补后 NSCLC 1 年生存率变化最大(下降 4.9 个百分点)。3 年生存率也观察到类似的变化。最年长的年龄组在插补后生存率最低,降幅最大。SCLC 和 NSCLC 生存率的国际差异部分归因于未明确组织学的分布差异。虽然登记处和临床医生应该努力提高癌症分类的完整性,但其他因素可能发挥更大的作用,包括潜在的危险因素、分期、合并症和护理管理,这值得进一步研究。