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Study: Breast cancer implant study suggests links with illness but has serious flaws

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Why is this study important? In-depth
Study findings Conclusions
Questions to ask your provider References     
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This study is about:

The long-term safety of patients with breast implants.

This report was sensationalized in the media and covered in a recent headline hype blog.  

THIS INFORMATION HAS BEEN UPDATED: In October 2021, the issued guidance for people with breast implants Read our latest review on this topic.  

Why is this study important?

Following U.S. approval of silicone breast implants in 2006, the agency ordered manufacturers to conduct post-approval studies involving nearly 100,000 patients. The shared the results from these studies in 2011 and also posted on the post-approval study websites for manufacturers Allergan in 2015 and Mentor in 2018.

In a recent article published in the Annals of Surgery, Coroneos and colleagues report on the long-term outcomes of the 100,000 patients who were enrolled in the FDA-mandated post-approval studies. The authors emphasize that their results implicate silicone implants in an increased risk for certain conditions.

This study has significant problems, including the methods used, potential bias, and inconsistencies in reporting of results. These flaws prohibit any meaningful conclusions that might be drawn from this report’s results regarding silicone implants and health outcomes.

Unfortunately, the conclusions of this study are likely to cause unnecessary alarm to women have or are considering breast implants.

Study findings: 

Because this is study was poorly conducted, the following results are untrustworthy.

Compared to the general population, patients with silicone implants had an incidence of specific conditions that was statistically more than double for the following conditions. Oddly, patients with Mentor implants only reported these conditions; none of the physicians of the patients with Allergan reported these conditions:

  • Rheumatoid arthritis
  • Sjorgen syndrome
  • Scleroderma
  • Melanoma

Compared to the general population, patients with silicone implants also had incidence rates that were statistically significant but less than double for the following conditions:

  • Overall cancer diagnosis (patients with either Mentor and Allergan implants).
  • Neurological disorders (patients with either Mentor and Allegan implants).
  • Multiple sclerosis (only in patients with Mentor implants).
  • Myositis (only in patients with Mentor implants).

A variety of patient-reported health conditions, including chronic fatigue, memory problems, rheumatoid arthritis, fibromyalgia, and many others have been referred to as “breast implant illness.” Based on the results of hundreds of studies in different countries, the advises that while implants have inherent problems, no research has ever associated them with the conditions described. The lack of evidence to support or refute a link to rheumatological or connective tissue disorders does not suggest that certain patients who are suffering may not benefit from removal of their implants.

While anecdotal and case reports claim that there is a link between silicone implants and fibromyalgia, this study found that women with silicone implants had lower rates of fibromyalgia, regardless of the manufacturer.  They also had lower rates of lung cancer.

Importantly, due to the many limitations of this study, there is not enough evidence to show an association between breast implants and immune or connective tissue diseases.

The many limitations of this study data include:

  • The number of study participants and design were inadequate for testing for rare events.
  • Only a subset of the data was evaluated.
  • Different collection methods were used for different test groups.
  • A poorly matched control group was used.
  • Poor follow-up rates of participants increased the likelihood of biased responses.
  • The potential for statistical error exists.
  • The study results are illogical.
  • There were unreported conflicts of interest

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What does this mean for me?

While many patients with breast implants are satisfied with their results, breast implants are associated with known risks, including capsular contracture (hardening of the breast area around the implant), reoperation, removal, and rupture. Saline and silicone implants are also associated with extremely rare occurrences of breast implant-associated anaplastic large cell (BIA-ALCL), a type of non-Hodgkin’s .  See our XRAYS reviews here and here.

Although newer generations of breast implants are believed to be greatly improved over earlier models, they are not lifetime devices and they are not without problems. They may last 10 to 20 years, or need to be replaced within a year of placement. Although some women do not experience any problems with their implants, the overall incidence of problems, including those that require reoperation and/or replacement is high. The longer a patient has implants the more likely she is to experience rupture, wrinkling, rippling, asymmetry, breast pain and numerous other issues that require medical intervention to resolve.

The held a public meeting of the General and Plastic Surgery Devices Panel at the ’s headquarters in Silver Spring, Maryland March 25-26, 2019. FORCE attended and made public comments at the meeting. The and the Plastic Surgery Foundation have developed the Patient Registry and Outcomes For breast Implants and anaplastic large cell (ALCL) etiology and Epidemiology (PROFILE) to collect real world data on patients who have a confirmed diagnosis of BIA-ALCL.  The is also creating the National Breast Implant Registry to collect real world data on the safety and performance of breast implants. 

Posted 2/21/19


Coroneos CJ, Selber JC, Offodile AC, et al. “US Breast Implant Postapproval Studies Long-term Outcomes in 99,993 Patients.Annals of Surgery; 2019. 269(1):30–36.

Ashar BS. “Assessing the Risks of Breast Implants and 's Vision for the National Breast Implant Registry.Annals of Surgery. 2019; 269(1): 37–38.

Colwell AS, Mehrara B. “US Breast Implant Postapproval Studies—Long-term Outcomes in 99,993 Patients.” Annals of Surgery. January 2019; 269(1): 39–40.

Balk EM, Earley A, Avendano EA, et al. “Long-term health outcomes in women with silicone gel breast implants:  a systematic review.Annals of Internal Medicine. 2016; 164: 164-175.



Note: FORCE receives funding from industry sponsors, including companies that manufacture implants. All XRAYS articles are reviewed by members of our Scientific Advisory Board prior to publication to assure scientific integrity.

This article is relevant for:

Women with or considering breast implant reconstruction

This article is also relevant for:

people with breast cancer

people with ER/PR + cancer

people with Her2-positive cancer

people with a genetic mutation linked to cancer risk


people with triple negative breast cancer

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Study background:

In the early 1990s, numerous anecdotal and case reports of silicone breast implants causing connective tissue disorders, cancer and autoimmune diseases resulted in a voluntary moratorium of their use. Subsequently, a new generation of silicone implants were approved in 2006.

As a condition of that approval, the ordered breast implant manufacturers Allergan and Mentor to follow implant patients for 10 years to identify common complications and rare events. The shared results of these studies, which involved nearly 100,000 patients in a report published in 2011.

In addition to the ’s 2011 report, an extensive literature review in 2016 by Balk and colleagues of more than 5,000 citations concluded that case reports and anecdotes did not conclusively associate breast implants with any health outcomes, including connective tissue disease, cancer, neurological disorders or reproductive problems.

Researchers of this study wanted to know:

The long-term safety and efficacy of breast implants.

Study design:

The subset of data used for this study include information from the following patients from the original post-approval studies:

  • Silicone implants: 41,342 patients from Allergan; 41,975 patients from Mentor
  • Saline implants: 15,646 patients with Allergan; 1,030 patients from Mentor

Allergan patients with Natrelle® silicone gel or saline implants were recruited from February 2007 to March 2010 from 873 sites.  Mentor patients with saline or MemoryGel® silicone implants were recruited from February 2007 to July 2009 from 2,342 sites. Collected clinical outcome data included deaths, rare adverse events (e.g., connective tissue disease) and local complications. For each manufacturer, participants were assessed at 3 to 4 postoperative visits at predefined intervals, and by annual remote (mail, telephone, internet) patient questionnaires. 

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Study findings:

The conclusions of this study cannot be deemed as scientific or reliable, based on the way data was collected, the analysis method, and the overall bias involved.

Compared to the general population, patients with silicone implants had a statistically significant, more than double incidence of the following conditions:

  • Rheumatoid arthritis (observed only in Mentor implants)
    • 0.05% per person per year in the general population
    • 0.3% per person per year in women with implants (nearly 6-fold more)
  • Sjorgen syndrome (observed only in Mentor implants)
    • 0.007% per person per year in the general population
    • 0.057% per person per year in women with implants (nearly 8-fold more)
  • Scleroderma (observed only in Mentor implants)
    • 0.006% per person per year in the general population
    • 0.04% per person per year in women with implants (7-fold more)
  • Melanoma (observed only in Mentor implants)
    • 0.021% per person per year in the general population
    • 0.08% per person per year in women with implants (nearly 4-fold more)

For patients with silicone implants, incidence rates were statistically significant, but less than double that of the general population for the following:

  • Overall cancer diagnosis (in patients with either Mentor or Allergan implants):
    • 0.41% per person per year in the general population
    • 0.16% per person per year in women with Allergan implants (less than the general population)
    • 0.64% per person per year in women with Mentor implants (1.5-fold more often)
  • Neurological disorder (in patients with either Mentor or Allegan implants)
    • 0.23% per person per year in the general population
    • 0.036% per person per year in women with o with Allergan implants (less than the general population)
    • 0.36% per person per year in women with Mentor implants (1.5-fold more often)
  • Multiple sclerosis (observed only in Mentor implants)
    • 0.25% per person per year in the general population
    • 0.4% per person per year in women with Mentor implants (1.7 fold more often)
  • Myositis (observed only in Mentor implants)
    • 0.008% per person per year in the general population
    • 0.15% per person per year in women with Mentor implants (1.8-fold more often)
  • Regardless of the manufacturer, women with silicone implants had lower rates of fibromyalgia. Patients with Mentor implants had lower rates of lung cancer.

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There are important and significant problems with this study.

The data used was inadequate for testing rare events.

The authors of this study performed their analysis on data that was known to be problematic. Although their original post-approval studies enrolled a sufficient number of patients (99,993), other experts warned that using physician-reported or patient-reported data was inadequate, especially for studying rare events, and should not be used to make statistically significant conclusions. The study follow-up was also poorly conducted.

Only a subset of the data was evaluated.

Ethical, accurate study procedure calls for objective analysis of all data in a study. Yet, the authors of this study “cherry-picked” only certain data to include and subsets of the results data to calculate rates of adverse effects. This “picking and choosing” of data skews observations and results. It is unacceptable scientific process without the standard stringent internal validation.

A poorly matched control group was used.

The number of adverse events in this study’s subset of patients was compared to controls.  The authors chose the general population rates reported in the literature as controls, rather than control participants who participated in this study. From a scientific perspective, this is highly irregular, since the study test group and the control group from the general population may differ in ways (e.g., environmental exposure to chemicals or differences in ethnicity) that are not related to the presence or absence of breast implants. A more reliable control would be a comparison of rates in the same study of harmful events between women with silicone implants and women with saline implants. In fact, the authors had this data, but they did not use it.

Different data collection methods were used for different test groups.

This study violated another basic rule of scientific methodology: that the method of data collection should be the same among groups that are compared. This study’s comparison of Allergan and Mentor data was highly inappropriate, since they were collected by different methods. Study authors used rates of adverse events that were calculated from physician-reported data in the Allergen study of 25,219 patients. In contrast, rates of adverse events were calculated from patient-reported data (without physician confirmation) for the Mentor study of 8,437 patients. Using patient-reported data for connective tissue diseases or other conditions without clinical confirmation is unreliable. These diseases can vary considerably in presentation and may require physician expertise or laboratory tests to confirm a diagnosis.

Poor follow-up rates increase the likelihood of biased responses.

Rates of patient follow-up were poor. The 2-year follow-up data included 60.5% of Allergan patients, but just 24% of Mentor patients. Even fewer (20%) of women participated in the 7-year follow-up. Poor follow-up rates like these can introduce substantial bias. One reason is that patients without symptoms or concerns are less likely to follow-up, while patients with symptoms or concerns may be more likely to keep their follow-up visits and/or respond to questionnaires. Despite this obvious shortcoming, which was worse with the Mentor study, the authors heavily base their conclusions on that data.

The potential for statistical error exists.

Because large data sets inherently have variations, a subset of data can almost always be randomly found to fit a given pre-formed hypothesis. Objective studies do the opposite: they collect and analyze reliable data and come to objective conclusions.

In one of the two accompanying editorials, Amy S. Colwell, MD, and Babak Mehrara, MD, state that:

“This [type of statistical error] may arise from deliberate academic dishonesty or as an honest mistake. Type I [statistical] errors have a pernicious effect because they cause patient/physician anxiety and lead to medical errors and flawed conclusions.”

Nor did the current analysis evaluate other patient data such as geography, lifestyle, UV light exposure, smoking, alcohol use, cancer history, weight, depression, medications or reproductive history that might impact this study’s outcomes. Failing to control for the potential of statistical and other confounding factors means the statistical conclusions of the current study are untrustworthy.

Results of the study are illogical.

For unknown reasons, the current study emphasizes the patient-reported data from 8,437 Mentor patients, while virtually ignoring the physician-reported data from the larger group of 25,219 Allergan patients:

  • While the authors emphasize the increased risk of rheumatoid arthritis in patients with Mentor implants, they ignore data that suggests a protective effect in patients with Allergan implants.
  • The authors also emphasize an increased rate of scleroderma and Sjogren’s syndrome in patients with Mentor implants, again ignoring their data showing no reported cases of scleroderma or Sjogren’s syndrome in patients who have Allergan implants.
  • The authors emphasize the statistically increased risk of neurological disorders for patients with silicone breast implants.  However, they fail to highlight that while Mentor implants are associated with a statistically significant increased risk, Allegan implants are associated with a statistically significant decreased risk. This suggests that Allergan implants, but not Mentor implants are protective for neurological disorders.
  • Mentor implants were associated with increased melanoma risk while no cases of melanoma were reported in patients with Allergan implants.

Binita S. Ashar, MD, Divisional Director and author of the other editorial that accompanied this study, states:

“Unfortunately, as the authors acknowledge, they failed to account for methodological differences between studies, inconsistencies in the data, differential loss to follow-up, confounding and other potential sources of bias.”

Conflicts of interest are not reported

Importantly, the authors report no financial conflicts of interest. Annals of Surgery conforms to the disclosure policy published by the International Committee of Medical Journal Editors, instructing authors to “report all sources of revenue paid (or promised to be paid) directly to you or your institution on your behalf over the 36 months prior to submission of the work.” According to the Propublica online database Dollars for Docs, Mark W. Clemens, MD and senior author of the study received $64,013 from Allergan in 2016 for promoting its Natrelle and Seri products. In 2015, he received $134,782 from Allergan. Awareness of possible bias is essential for proper evaluation of study conclusions.

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Social media often amplifies fears about breast implants.  As a result, increasing numbers of women see plastic surgeons for evaluation of systemic symptoms of “breast implant illness” that they attribute to their breast implants. However, breast implant illness is not a medical diagnosis. Currently, no simple test confirms the relationship between implants and a patient’s symptoms. Despite the claims of the authors of this scientifically flawed study, no sufficient scientific evidence supports a link between breast implants and autoimmune-related disorders or other diseases. Breast implants (primarily implants with textured surfaces) are linked by evidence to BIA-ALCL, although this is extremely rare. Other known, non-disease risks associated with breast implants include capsular contracture, reoperation, removal, and implant rupture. These remain the most common problems that occur with breast implants.

Posted 2/21/19

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Expert Guidelines
Expert Guidelines

The issued guidelines for the use of breast implants: 

  • Breast implant manufacturers are required to include a label warning and a patient decision checklist with all implants. The checklist should include the following:
    • the current incidence rates of breast implant-associated anaplastic large cell (BIA-ALCL) and breast implant illness (BII).
    • specific information regarding ongoing patient registries.
  • The has provided breast implant manufacturers with specific language for an informational card that should be given to all patients following placement of breast implants. The card should include:
    • the serial number, lot number, device style, device size and the unique device identifier (UDI) of the implant.
    • weblinks to the most up-to-date access to the patient device checklist, boxed warning and labeling of the specific implant.
  • In collaboration with the and breast implant manufacturers, the American Society of Plastic Surgeons and the Plastic Surgery Foundation launched the National Breast Implant Registry (NBIR) in September 2018. This database collects information from plastic surgeons on breast implant procedures to help improve the quality of care for all patients.

Updated: 12/15/2021

Questions To Ask Your Doctor
Questions To Ask Your Doctor

  • How often should I see a board-certified plastic surgeon, even if I have no concerns about my breast implants?
  • How often should I have an to evaluate the integrity of my silicone breast implants?
  • How can I obtain a copy of the manufacturer’s safety information for the implants I have or I am considering?
  • Regarding the breast implants I have or I am considering, how long can I expect to have them before they need to be replaced?

Open Clinical Trials
Open Clinical Trials

The following studies are related to mastectomy and breast reconstruction.

Updated: 11/20/2023

Find Experts
Find Experts

The following resources can help you find a plastic surgeon who specializes in breast reconstruction:

Finding a plastic surgeon

Other ways to find experts

  • Register for the FORCE Message Boards and post on the Find a Specialist board to connect with other people who share your situation.
  • The website for The Complete Guide to Breast Reconstruction  provides information on Choosing the Right Surgeon.

Updated: 11/20/2023

Who covered this study?


Long-term safety of silicone breast implants still unclear This article rates 5.0 out of 5 stars

Medical Express

Silicone breast implants linked to increased risk of some rare harms This article rates 2.0 out of 5 stars

Medical News Today

The long-term outcomes of breast implants studied This article rates 2.0 out of 5 stars

Science Daily

Silicone breast implants linked to increased risk of some rare harms This article rates 2.0 out of 5 stars

Medical Express

Long-term outcomes of breast implants explored This article rates 1.5 out of 5 stars

How we rated the media

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