Dr. Michael Misialek’s first outreach letter to Cigna Insurance
Dear Mr. Cordani,
I am a pathologist in Boston who has seen the power of 3-D mammography (DBT). Simply put, women’s lives have been saved by it. Practicing at Newton-Wellesley Hospital in Newton, MA, where we were the FIRST hospital in the country to routinely PROVIDE ALL patients with screening DBT, I have diagnosed twice as many early invasive cancers than conventional digital mammography. As such, women are treated sooner, at lesser cost, and have a greater potential for long term survival.
Please reconsider your decision to deny DBT coverage in 2016.
Michael J. Misialek, MD
Associate Chair of Pathology
Response to Dr. Misialek from Cigna Insurance
Dear Mr. Misialek,
Thank you for your inquiry to Cigna. We appreciate you contacting us regarding 3D Mammograms. Cigna will continue to review the research on this technology and will also follow the USPSTF’s guidelines if it should recommend coverage for breast cancer screening. Cigna’s coverage policies are based on an extensive examination of peer-reviewed medical and scientific studies, journal articles and other evidence, as well as guidelines from professional medical societies. Coverage policies are reviewed regularly and are changed based on new evidence.
Again, thank for your inquiry to Cigna. Please let us know if you have additional questions..
Dr. Michael Misialek’s Second Outreach to Cigna Insurance
I would appreciate your forwarding this comprehensive review of the literature to the executive management team.
Digital breast tomosynthesis (DBT, 3D mammography) finds more cancers earlier and as a result helps save lives. Medicare generally covers DBT, however private payers have been reluctant to provide coverage. DBT should be covered as an effective screening strategy for breast cancer. The rationale behind this request is that coverage is already provided for full-field digital mammography (FFDM), based on its ability to improve interpretive performance compared with standard film-screen mammography. The evidence described and cited below documents that DBT shows an even greater improvement in cancer detection than that found for FFDM, with the additional benefit of reducing the frequency of false-positive examinations.
Conventional mammography (either film-screen or FFDM) produces planar images, in which overlapping tissue can result both in unnecessary recalls from screening mammograms (false positive studies) and in missed cancers (false negative studies). Approximately 10%-20% of the cases in which a woman must be recalled from screening mammography are due to superimposed normal tissue simulating a lesion. This additional imaging causes patient anxiety, inconvenience, and increased cost. In addition, overlying tissue can obscure cancers, with as many as 20%-30% of cancers being missed by conventional planar mammography,.
The latest advancement in mammography – digital breast tomosynthesis (DBT) – helps address the problem of overlapping tissues in planar FFDM and reduces interpretation inaccuracy. DBT is a mammography-based system that acquires low-dose images of the breast at multiple angles during a short scan time. The individual images are then reconstructed into a series of thin, high-resolution slices. This provides a clearer depiction of the internal architecture of the breast, making underlying breast cancers more easily perceptible and facilitating confirmation that superimposed normal glandular tissue does not represent an abnormality. Conventional, planar mammographic images are still necessary to demonstrate the anatomic distribution of findings and to characterize calcifications. Furthermore, DBT cannot produce magnification images, still useful for some mammographically-detected lesions in determining which do and do not require biopsy.
DBT was approved by the U.S. Food & Drug Administration (FDA) on February 11, 2011 for the same indications as planar FFDM. This includes breast cancer screening, diagnosis, and intervention. On August 26, 2014, a second vendor received FDA approval for DBT. Other vendors are expected to apply for approval. Since receiving FDA approval, there have been numerous published studies demonstrating the clinical benefits of DBT. These studies consistently report substantial decreases in the recall rate from screening (reduced false positives) and substantial increases in the cancer detection rate (increased true positives).
The first prospective screening trial to compare DBT to planar FFDM was published by Skaane et al. Researchers compared FFDM+DBT to FFDM alone, in 12,631 screening examinations. Skaane’s study demonstrated increased sensitivity in the detection of breast cancer without compromising specificity or increasing the rate of false positive results. In an interim analysis, they found that the addition of DBT resulted in a:
The Screening with Tomosynthesis or Routine Mammography (STORM) trial was a prospective comparative study of 7292 women from two institutions. The cancer detection rate was 51% higher for FFDM+DBT than FFDM alone, while FFDM+DBT was also associated with a 17% statistically significant reduction in false positive recalls.
Haas et al., in a study of 6100 women receiving FFDM+DBT, reported a 30% statistically significant reduction in recall rate with DBT screening. Rose et al., in a study of 9499 women receiving FFDM+DBT, reported a 53% increase in the detection of invasive cancers and a statistically significant increase in the positive predictive value for screening recalls (PPV1) with FFDM+DBT compared to FFDM alone.
The largest study to date, by Friedewald et al, was published in 2014 in the Journal of the American Medical Association. This multi-center trial compared 281,187 conventional mammograms to 173,663 DBT exams. The study reported the following findings:
Given the above information, CMS decided to add additional reimbursement for Medicare patients receiving DBT, beginning in January of 2015.
In conclusion, the following facts are known:
Therefore, I urge all insurance companies to provide coverage of digital breast tomosynthesis as a medically necessary screening and diagnostic mammography service.
Michael J. Misialek, MD
Associate Chair of Pathology
 Pisano, ED et al. Diagnostic Performance of Digital versus Film Mammography for Breast-Cancer Screening. N Engl J Med 2005 353: 1773-1783.
 Rosenberg RD, Yankaskas BC, Abraham LA, Sickles EA, Lehman CD, Geller BM, Carney PA, Kerlikowske K, Buist DS, Weaver DL, Barlow WE, Ballard-Barbash R. Performance benchmarks for screening mammography. Radiology. 2006 Oct;241(1):55-66. Erratum in: Radiology. 2014 May;271(2):620.
 Schell MJ et al. Evidence-based target recall rates for screening mammography. Radiology, June 2007; 243: 681-689.
 Holland R, Mravunac M, Hendriks JH, Bekker BV. So-called interval cancers of the breast: pathologic and radiologic analysis of sixty-four cases. Cancer 1982;49(12):2527-2533.
 Skaane P, Bandos AI, Gullien R, et al. Comparison of Digital Mammography Alone and Digital Mammography Plus Tomosynthesis in a Population-based Screening Program. Radiology 2013, Apr; 267(1): 47-56.
 Ciatto S, Houssami N, Bernardi D, Caumo F, Pellegrini M, Brunelli S, Tuttobene P, Bricolo P, Fantò C, Valentini M, Montemezzi S, Macaskill P. Integration of 3D digital mammography with tomosynthesis for population breast-cancer screening (STORM): a prospective comparison study. Lancet Oncol. 2013 Jun;14(7):583-9.
 Haas BM, Kaira V, Geisel J, Raghy M, Durand M, Philpotts LE. Comparison of tomosynthesis plus digital mammography and digital mammography alone for breast cancer screening. Radiology 2013; 269:694–700
 Rose SL, Tidwell AL, Bujnoch LJ, Kushwaha AC, Nordmann AS, Sexton R. Implementation of breast tomosynthesis in a routine screening practice: an observational study. AJR 2013; 200:1401–1408
 Friedewald S M, Rafferty E A, Rose S L, Durand M A, Plecha D M, Greenberg J S, Hayes M K, Copit D S, Carlson K L, Cink T M, Barke L D, Greer L N, Miller D P, Conant E F Breast Cancer Screening Using Tomosynthesis in Combination with Digital Mammography, JAMA. 2014;311(24):2499-2507