All-cause mortality in randomized trials of cancer screening
- PMID: 11830606
- DOI: 10.1093/jnci/94.3.167
All-cause mortality in randomized trials of cancer screening
Abstract
Background: The most widely accepted end point in randomized cancer screening trials is disease-specific mortality. The validity of this end point, however, rests on the assumption that cause of death can be determined accurately. An alternative end point is all-cause mortality, which depends only on the accurate ascertainment of deaths and when they occur. We compared disease-specific and all-cause mortality in published randomized cancer-screening trials to indirectly assess the validity of the disease-specific mortality end point.
Methods: We examined all 12 published randomized trials of cancer screening for which both end points were available (seven of mammography, three of fecal occult blood detection, and two of chest x-ray screening for lung cancer). For each randomized trial, we subtracted disease-specific mortality observed in the screened group from that observed in the control group and all-cause mortality in the screened group from that in the control group. We then compared the differences in these two mortality measures.
Results: In five of the 12 trials, differences in the two mortality rates went in opposite directions, suggesting opposite effects of screening. In four of these five trials, disease-specific mortality was lower in the screened group than in the control group, whereas all-cause mortality was the same or higher. In two of the remaining seven trials, the mortality rate differences were in the same direction but their magnitudes were inconsistent; i.e., the difference in all-cause mortality exceeded the disease-specific mortality in the control group. Thus, results of seven of the 12 trials were inconsistent in their direction or magnitude.
Conclusion: Major inconsistencies were identified in disease-specific and all-cause mortality end points in randomized cancer screening trials. Because all-cause mortality is not affected by bias in classifying the cause of death, it should be examined when interpreting the results of randomized cancer-screening trials.
Comment in
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Interleukin-8 in neonatal sepsis.Acta Paediatr. 2001 Sep;90(9):961-2. doi: 10.1080/080352501316977995. Acta Paediatr. 2001. PMID: 11683205 Review. No abstract available.
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Screening trials are even more difficult than we thought they were.J Natl Cancer Inst. 2002 Feb 6;94(3):156-7. doi: 10.1093/jnci/94.3.156. J Natl Cancer Inst. 2002. PMID: 11830599 No abstract available.
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Do disease-specific mortality effects correlate with all-cause mortality effects in cancer screening trials?J Fam Pract. 2002 May;51(5):480. J Fam Pract. 2002. PMID: 12019063 No abstract available.
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Re: All-cause mortality in randomized trials of cancer screening.J Natl Cancer Inst. 2002 Jun 5;94(11):861; author reply 865-6. doi: 10.1093/jnci/94.11.861. J Natl Cancer Inst. 2002. PMID: 12048277 No abstract available.
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Re: All-cause mortality in randomized trials of cancer screening.J Natl Cancer Inst. 2002 Jun 5;94(11):862; author reply 865-6. doi: 10.1093/jnci/94.11.862. J Natl Cancer Inst. 2002. PMID: 12048278 No abstract available.
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Re: All-cause mortality in randomized trials of cancer screening.J Natl Cancer Inst. 2002 Jun 5;94(11):863-4; author reply 865-6. doi: 10.1093/jnci/94.11.863-a. J Natl Cancer Inst. 2002. PMID: 12048279 No abstract available.
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Re: All-cause mortality in randomized trials of cancer screening.J Natl Cancer Inst. 2002 Jun 5;94(11):863; author reply 865-6. doi: 10.1093/jnci/94.11.863. J Natl Cancer Inst. 2002. PMID: 12048280 No abstract available.
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Re: All-cause mortality in randomized trials of cancer screening.J Natl Cancer Inst. 2002 Jun 5;94(11):864-5; author reply 865-6. doi: 10.1093/jnci/94.11.864. J Natl Cancer Inst. 2002. PMID: 12048281 No abstract available.
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