Abstract
OBJECTIVE: To analyze the relationship of health insurance status and delivery systems to breast cancer outcomes — stage at diagnosis, treatment selected, survival — focusing on comparisons among women aged 65 or more having Medicare alone, Medicare/Medicaid, or Medicare with group model HMO, non-group model HMO, or private fee-for-service (FFS) supplement.
DESIGN: Retrospectively defined cohort from Sacramento, Calif, regional cancer registry.
SETTING: Thirteen-county region in northern California with mature managed care market.
PATIENTS: Female invasive breast cancer patients aged 65 or more (N=1,146), diagnosed 1987–1993.
MEASUREMENTS AND MAIN RESULTS: Health insurance was determined from hospital records. Outcomes were analyzed with multivariate regression models, controlling for age, ethnicity, time, and SES measures. Stage I diagnosis was more likely among group model HMO patients than among private FFS insured (odds ratio [OR], 1.42; 95% confidence interval [CI], 0.84 to 2.40). Stage I tumors were significantly less likely for Medicaid patients (OR, 0.50; 95% CI, 0.31 to 0.82). Use of breast-conserving surgery plus radiation (BCS+) varied significantly by hospital type (including HMO-owned and various-sized community hospitals) and time. Survival of patients with private FFS, group-, and non-group model HMO insurance was not significantly different, but was for those with Medicaid or Medicare alone.
CONCLUSIONS: This study sheds new light on the relationship of insurance to stage and survival among older breast cancer patients, highlighting the importance of distinguishing types of HMOs and types of FFS plans. These outcomes do not differ significantly between women with Medicare who are in HMOs and those with private FFS supplemental insurance. However, patients with Medicare/Medicaid or Medicare alone are at risk for poorer outcomes.
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References
Hoechst Marion Roussel. HMO-PPO/Medicare-Medicaid Digest. Managed Care Digest Series 1997. Kansas City, Mo: Hoechst Marion Roussel; 1997.
Hoechst Marion Roussel. HMO-PPO/Medicare-Medicaid Digest. Managed Care Digest Series 1998. Kansas City, Mo: Hoechst Marion Roussel; 1998.
Ries LAG, Kosary CL, Hankey BF, Miller BA, Edwards BK, eds. SEER Cancer Statistics Review, 1973–1995. Bethesda, Md: National Cancer Institute; 1998.
Ries LAG, Kosary CL, Hankey BF, Harras A, Miller BA, Edwards BK, eds. SEER Cancer Statistics Review, 1973–1993: Tables and Graphs. Bethesda, Md: National Cancer Institute; 1996.
Morris CR, Cohen R, Perkins CI, Allen M, Kwong SL, Schlag R, Wright WE. Cancer in California: 1988–1996. Sacramento, Calif: California Department of Health Services, Cancer Surveillance Section; March 1999.
Breen N, Kessler L. Changes in the use of screening mammography: evidence from the 1987 and 1990 National Health Interview Surveys. Am J Public Health. 1994;84:62–7.
Morris CR, Wright WE, eds. Breast Cancer in California. Sacramento, Calif: California Department of Health Services, Cancer Surveillance Section; March 1996.
Centers for Disease Control. Self-reported use of mammography among women aged ≥40 years — United States, 1989 and 1995. MMWR. 1997;46:937–41.
Veronesi U, Saccozzi R, DelVecchio M, et al. Comparing radical mastectomy with quadrantectomy, axillary dissection, and radio-therapy in patients with small cancer of the breast. N Engl J Med. 1981;305:6–11.
Sarrazin D, Le M, Rouesse J, et al. Conservative treatment versus mastectomy in breast cancer tumors with macroscopic diameter of 20 millimeters or less. Cancer. 1984;53:1209–13.
Fisher B, Bauer M, Margolese R, et al. Five-year results of a randomized clinical trial comparing total mastectomy and segmental mastectomy with or without radiation. N Engl J Med. 1985;312:665–73.
NIH Consensus Conference. Treatment of early-stage breast cancer. JAMA. 1991;265:391–5.
Lazovich D, White E, Thomas DB, Moe RE. Underutilization of breast-conserving surgery and radiation therapy among women with stage I or II breast cancer. JAMA. 1991;266:3433–8.
Farrow DC, Hunt WC, Samet JM. Geographic variation in the treatment of localized breast cancer. N Engl J Med. 1992;326:1097–101.
Hunter CP, Redmond CK, Chen VW, et al. Breast cancer: factors associated with stage at diagnosis in black and white women. J Natl Cancer Inst. 1993;85:1129–37.
Eley JW, Hill HA, Chen VW, Austin DF, et al. Racial differences in survival from breast cancer. Results of the National Cancer Institute Black/White Cancer Survival Study. JAMA. 1994;272:947–54.
Lee-Feldstein A, Anton-Culver H, Feldstein PJ. Treatment differences and other prognostic factors related to breast cancer survival. Delivery systems and medical outcomes. JAMA. 1994;271:1163–8.
Riley GF, Potosky AL, Lubitz JD, Brown ML. Stage of cancer at diagnosis for Medicare HMO and fee-for-service enrollees. Am J Public Health. 1994;84:1598–604.
Foster RS, Farwell ME, Costanza MC. Breast-conserving surgery for breast cancer: patterns of care in a geographic region and estimation of potential applicability. Ann Surg Oncol. 1995;2:275–80.
Johantgen ME, Coffey RM, Harris DR, Levy H, Clinton JJ. Treating early-stage breast cancer: hospital characteristics associated with breast-conserving surgery. Am J Public Health. 1995;85:1432–4.
Ballard-Barbash R, Potosky AL, Harlan LC, Nayfield SG, Kessler LG. Factors associated with surgical and radiation therapy for early stage breast cancer in older women. J Natl Cancer Inst. 1996;88:716–26.
Potosky AL, Merrill RM, Riley GF, Taplin SH, Barlow W, Fireman VH, Ballard-Barbash R. Breast cancer survival and treatment in health maintenance organization and fee-for-service settings. J Natl Cancer Inst. 1997;89:1683–91.
Riley GF, Potosky AL, Klabunde CN, Warren JL, Ballard-Barbash R. Stage at diagnosis and treatment patterns among older women with breast cancer: an HMO and fee-for-service comparison. JAMA. 1999;281:720–4.
Osteen RT, Winchester DP, Hussey DH, et al. Insurance coverage of patients with breast cancer in the 1991 Commission on Cancer Patient Care evaluation study. Ann Surg Oncol. 1994;1:462–7.
Gabel R. Ten ways HMOs have changed during the 1990s. Health Aff. 1997;16:134–45.
Nattinger AB, Gottlieb MS, Veum J, Yahnke D, Goodwin JS. Geographic variation in the use of breast-conserving treatment for breast cancer. N Engl J Med. 1992;326:1102–7.
Nattinger AB, Gottlieb MS, Hoffman RG, Walker AP, Goodwin JS. Minimal increase in use of breast-conserving surgery from 1986 to 1990. Med Care. 1996;34:479–89.
Young WW, Marks SM, Kohler SA, Hsu AY. Dissemination of clinical results. Mastectomy versus lumpectomy and radiation therapy. Med Care. 1996;34:1003–17.
Kotwall CA, Covington DL, Rutledge R, Churchill MP, Meyer AA. Patient, hospital, and surgeon factors associated with breast conservation surgery. A statewide analysis in North Carolina. Ann Surg. 1996;224:419–29.
Perkins CI, Morris CR, Wright WE. Cancer Incidence and Mortality in California by Race/Ethnicity, 1988–1993. Sacramento, Calif: California Department of Health Services, Cancer Surveillance Section; March 1996.
Percy C, Van Holten V, Muir C, eds. International Classification of Diseases for Oncology. 2nd ed. Geneva, Switzerland: World Health Organization; 1990.
American Joint Committee on Cancer. Manual for Staging of Cancer. 4th ed. Philadelphia, Pa: JB Lippincott, 1992.
Seiffert J, ed. SEER Program Comparative Staging Guide for Cancer, Version 1.1. Bethesda, Md: National Institutes of Health; 1993. NIH publication 93-3640.
Hayward RA, Shapiro MF, Freeman HE, Corey CR. Who gets screened for cervical and breast cancer? Results from a new national survey. Arch Intern Med. 1988;148:1177–81.
Krieger N. Social class and the black/white crossover in the age-specific incidence of breast cancer: a study linking census-derived data to population-based registry records. Am J Epidemiol. 1990;131:804–14.
Lerman C, Rimer B, Trock B, Balshem A, Engstrom PF. Factors associated with repeat adherence to breast cancer screening. Prev Med. 1990;19:279–90.
Mandelblatt J, Andrews H, Kerner J, Zauber A, Burnett W. Determinants of late stage diagnosis of breast and cervical cancer: the impact of age, race, social class, and hospital type. Am J Public Health. 1991;81:646–9.
Wells BL, Horm JW. Stage at diagnosis in breast cancer: race and socioeconomic factors. Am J Public Health. 1992;82:1383–5.
Katz SJ, Hofer TP. Socioeconomic disparities in preventive care persist despite universal coverage. Breast and cervical cancer screening in Ontario and the United States. JAMA. 1994;272:530–4.
Breen N, Figueroa JB. Stage of breast and cervical cancer diagnosis in disadvantaged neighborhoods: a prevention policy perspective. Am J Prev Med. 1996;12:319–36.
Michalski TA, Nattinger AB. The influence of black race and socioeconomic status on the use of breast-conserving surgery for Medicare beneficiaries. Cancer. 1997;79:314–9.
Krieger N, Williams DR, Moss NE. Measuring social class in US public health research: concepts, methodologies, and guidelines. Annu Rev Public Health. 1997;18:341–78.
State of California, Department of Health Services, Medi-Cal Policy Division. Hospital Peer Grouping. Sacramento, Calif: State of California, Department of Health Services; 1991.
American Hospital Association. 1990 American Hospital Association Guide to the Health Care Field. Chicago, Ill: American Hospital Association; 1991.
SAS Institute Inc. SAS/STAT User’s Guide. Version 6. Cary, NC: SAS Institute; 1990.
SAS Institute Inc. SAS/STAT Software: Changes and Enhancements through Release 6.11. Cary, NC: SAS Institute; 1996.
Hosmer DW, Lemeshow S. Applied Logistic Regression. New York, NY: Wiley; 1989.
Stokes ME, Davis CS, Koch GG. Categorical Data Analysis Using the SAS System. Cary, NC: SAS Institute; 1995.
Cox DR. Regression models and life tables. J R Stat Soc B. 1972;34:187–220.
Allison PD. Survival Analysis Using the SAS System: A Practical Guide. Cary, NC: SAS Institute; 1995.
Kaplan EL, Meier PL. Nonparametric estimation from imcomplete observations. J Am Stat Assoc. 1958;53:457–81.
Mantel N, Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst. 1959;22:719–48.
Makuc DM, Freid VVM, Parsons PE. Health insurance and cancer screening among women. Advance Data from Vital and Health Statistics; no. 254. Hyattsville, Md: National Center for Health Statistics; 1994.
Blustein J. Medicare coverage, supplemental insurance, and the use of mammography by older women. N Engl J Med. 1995;332:1138–42.
Potosky AL, Breen N, Braubard BI, Pearsons PE. The association between health care coverage and the use of cancer screening tests. Med Care. 1998;36:257–70.
Lee-Feldstein A, Feldstein PJ, Buchmueller T, Katterhagen G. The relationship of HMOs, health insurance, and delivery systems to breast cancer outcomes. Med Care. 2000;38:705–18.
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Cancer incidence data have been provided by the California Department of Health Services and its agent, the Public Health Institute, as part of its statewide cancer reporting program, mandated by Health and Safety Code Section 103875 and 103885. The ideas and opinions expressed herein are those of the authors, and no endorsement of the State of California, Department of Health Services or the Public Health Institute, is intended or should be inferred.
This research was supported by grant number CA-71236 from the National Cancer Institute. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the National Cancer Institute.
Dr. Katterhagen was formerly Medical Director, Cancer Program and Breast Center, Mills-Peninsula Hospital, Burlingame, Calif.
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Lee-Feldstein, A., Feldstein, P.J., Buchmueller, T. et al. Breast cancer outcomes among older women. J GEN INTERN MED 16, 189–199 (2001). https://doi.org/10.1111/j.1525-1497.2001.91112.x
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DOI: https://doi.org/10.1111/j.1525-1497.2001.91112.x