Role of Detection Method in Predicting Breast Cancer Survival: Analysis of Randomized Screening Trials (original) (raw)

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Affiliations of authors: Department of Biostatistics and Applied Mathematics, M. D. Anderson Cancer Center, University of Texas, Houston, TX (YS, YY, MFM, DAB); Department of Biostatistics, University of Washington, Seattle, WA (LYTI); Department of Public Health Sciences, University of Toronto, Canada (ABM)

Correspondence to: Donald A. Berry, PhD, Department of Biostatistics and Applied Mathematics, Unit 447, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030 (e-mail: dberry@mdanderson.org ).

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Affiliations of authors: Department of Biostatistics and Applied Mathematics, M. D. Anderson Cancer Center, University of Texas, Houston, TX (YS, YY, MFM, DAB); Department of Biostatistics, University of Washington, Seattle, WA (LYTI); Department of Public Health Sciences, University of Toronto, Canada (ABM)

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Affiliations of authors: Department of Biostatistics and Applied Mathematics, M. D. Anderson Cancer Center, University of Texas, Houston, TX (YS, YY, MFM, DAB); Department of Biostatistics, University of Washington, Seattle, WA (LYTI); Department of Public Health Sciences, University of Toronto, Canada (ABM)

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Affiliations of authors: Department of Biostatistics and Applied Mathematics, M. D. Anderson Cancer Center, University of Texas, Houston, TX (YS, YY, MFM, DAB); Department of Biostatistics, University of Washington, Seattle, WA (LYTI); Department of Public Health Sciences, University of Toronto, Canada (ABM)

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Affiliations of authors: Department of Biostatistics and Applied Mathematics, M. D. Anderson Cancer Center, University of Texas, Houston, TX (YS, YY, MFM, DAB); Department of Biostatistics, University of Washington, Seattle, WA (LYTI); Department of Public Health Sciences, University of Toronto, Canada (ABM)

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Affiliations of authors: Department of Biostatistics and Applied Mathematics, M. D. Anderson Cancer Center, University of Texas, Houston, TX (YS, YY, MFM, DAB); Department of Biostatistics, University of Washington, Seattle, WA (LYTI); Department of Public Health Sciences, University of Toronto, Canada (ABM)

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Received:

24 January 2005

Revision received:

02 June 2005

Published:

17 August 2005

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Yu Shen, Ying Yang, Lurdes Y. T. Inoue, Mark F. Munsell, Anthony B. Miller, Donald A. Berry, Role of Detection Method in Predicting Breast Cancer Survival: Analysis of Randomized Screening Trials, JNCI: Journal of the National Cancer Institute, Volume 97, Issue 16, 17 August 2005, Pages 1195–1203, https://doi.org/10.1093/jnci/dji239
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Abstract

Background: Screening mammography detects breast cancers earlier than those detected symptomatically, and so mammographically detected breast cancers tend to have better prognoses. The so-called stage shift that results from screen detection is subject to lead-time and length biases, and so earlier detection may not translate into longer survival. We used data from three large breast cancer screening trials—Health Insurance Plan (HIP) of New York and two Canadian National Breast Cancer Screening Studies (CNBSS)—to investigate survival benefits of breast cancer screening beyond stage shift. We also address whether method of detection is an independent prognostic factor in breast cancer. Methods: The HIP trial randomly assigned approximately 62 000 women to screening and control groups. The two CNBSS trial cohorts CNBSS-1 and CNBSS-2 included a total of 44 970 women in the screening group and 44 961 in the control group. After adjusting for stage and other tumor characteristics in a Cox proportional hazards model, survival distributions were compared by method of breast cancer detection with both univariate and multivariable analyses. All P values are two-sided. Results: Breast cancers detected by screening mammography had a shift in stage distribution to earlier stages (for HIP, P <.001; for CNBSS-1, P = .03; and for CNBSS-2, P <.001). After adjusting for tumor size, lymph node status, and disease stage in a Cox proportional hazards model, method of detection was a statistically significant independent predictor of disease-specific survival. Patients with interval cancers had a 53% (95% confidence interval [CI] = 17% to 100%) greater hazard of death from breast cancer than patients with screen-detected cancers, and patients with cancer in the control groups had a 36% (95% CI = 10% to 68%) greater hazard of death than patients with screen-detected cancer. Conclusion: There was an apparent survival benefit beyond stage shift for patients with screen-detected breast cancers compared with patients with breast cancers detected otherwise. Method of detection appears to be an important prognostic factor, even after adjusting for known tumor characteristics. This finding suggests that clinical trialists should routinely collect information about method of detection.

© The Author 2005. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oupjournals.org.

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