Articles Posted in Mesothelioma Attorney

The U.S. Food and Drug Administration (FDA) recently granted final approval of a new brand of a chemotherapy drug already in use by oncologists to treat malignant pleural mesothelioma and advanced stage non small cell lung cancer. Starting in February 2020, doctors will be allowed to prescribe Pemfexy, a type of chemotherapy drug called pemetrexed, and provide an alternative treatment to the name brand drug Alimta.

The new chemotherapy works as an injection, which is combined with cisplatin for patients with malignant pleural mesothelioma whose disease is unresectable or who are otherwise ineligible for curative surgery in combination with cisplatin. This new type of pemetrexed injection was already tentatively approved for use by the FDA in 2017 after the agency determined that the drug met all required quality, safety, and efficacy standards.

However, patients in the United States were not eligible to receive the treatment because the company that holds the patent for the standard pemetrexed treatment held patent protections on the product. Now, with a settlement agreement between the two sides, Eagle pharmaceuticals will be able to bring limited supplies of Pemfexy beginning in February 2020 and uncapped entry in April 2020.

Virginia Governor Ralph Northam recently signed into law legislation passed by the state legislature which extends the deadlines for which asbestos cancer victims have to file lawsuits against companies they believe are responsible for their diagnosis. House Bill 781 passed unanimously through the House and Senate and will circumvent a decision from the Virginia Supreme Court that ruled the statute of limitations begins on the first diagnosis of any condition related to asbestos exposure.

That ruling from the Virginia Supreme Court came in 2013 from the state’s Third Circuit Court of Appeals. In that case, Kiser v. A.W. Chesterton, the Court was asked to determine whether the statute of limitations in an asbestos cancer lawsuit begins at the time of a mesothelioma diagnosis or, as in this case, when a doctor makes a separate diagnosis of a non-mesothelioma cancer diagnosis. Virginia, like other states, has various laws on statutes of limitations as they apply to injury claims and the time periods in which they can be filed.

In Kiser, the plaintiff sued numerous asbestos manufacturers and distributors in 1988 for damages related to the nonmalignant pleural thickening of his lungs, as well as asbestosis. 20 years later, the plaintiff was diagnosed with mesothelioma, a rare and deadly form of lung cancer directly linked to asbestos exposure. Sadly, the plaintiff passed away from his mesothelioma cancer just three months after receiving his diagnosis, and his family filed a wrongful death lawsuit on his behalf in 2010 against another group of defendants not named in the 1988 lawsuit.

Pharmaceutical and cosmetics giant Johnson & Johnson recently agreed to a settlement in a talcum powder asbestos cancer lawsuit brought by a woman who claims her rare form of cancer was caused by decades of using the company’s cosmetics products. While the terms of the settlement were not immediately clear, the resolution is nonetheless significant because Johnson & Johnson has settled very few lawsuits brought by plaintiffs alleging similar claims against the company.

According to the talcum powder asbestos cancer lawsuit, filed in a Manhattan New York Supreme Court, the 62-year-old plaintiff developed mesothelioma from decades of using Johnson & Johnson’s iconic Baby Powder product. The plaintiff claimed she developed mesothelioma from carcinogenic asbestos fibers contained within the talcum powder and that Johnson & Johnson knew for years about the risk of contamination in its talc-based products but provided no warning to consumers.

The settlement was reached in the judge’s chambers just before attorneys for both sides were to commence with their opening statements in the trial. Thus far, Johnson & Johnson has chosen to litigate and defend to trial most of the talcum powder cancer lawsuits brought against it in state courts across the country and has chosen to resolve very few before or during trial. Many of those trials have resulted in significant verdicts on behalf of the plaintiffs who claimed they developed various forms of cancer, including mesothelioma, from years of using talc-based products, like Baby Powder and Shower to Shower, contaminated with asbestos fibers.

The family of a former Penn State University professor recently filed an asbestos cancer lawsuit against the school alleging that the victim passed away from mesothelioma cancer that he developed after years of working in dangerous conditions at the educational institution. The lawsuit seeks to recover compensation for the victim’s pain and suffering and hold the university responsible for knowingly placing the victim at undue risk in unsafe work environments.

According to the mesothelioma cancer lawsuit, filed in a Pennsylvania state court in Pittsburgh in 2016, the victim developed mesothelioma as a result of working in buildings which the university knew were constructed with asbestos in floor and ceiling tiles and insulation. The lawsuit alleges that the victim was diagnosed with mesothelioma cancer in 2014 and passed away just four months later, 12 years after retiring from teaching as a wood sciences professor.

The asbestos cancer lawsuit against Penn State cites a study conducted by the university in the 1970s which showed that almost one hundred buildings on its campus were built with asbestos materials. However, despite this knowledge, the school eventually ceased asbestos abatement in 1989 after administrators cited budgetary concerns, noting that “In all future projects, our goal should be to minimize the removal of asbestos to only what is absolutely required. Obviously, this will help us a lot in the area of project budgets.”

An Illinois state appeals court recently upheld a substantial $4.6 million verdict in a mesothelioma cancer lawsuit brought by a union pipefitter who worked with products manufactured by John Crane, Inc. during the 1950s. In its ruling, the First District Appellate Court determined the trial court was right to allow the plaintiff’s attorneys to present expert testimony showing the victim’s asbestos cancer diagnosis was a result of exposure to asbestos fibers while working with John Crane products.

In his lawsuit, the plaintiff testified that he suffered from significant asbestos exposure from valves and gaskets, including those manufactured by the defendant. At trial, the plaintiff’s expert witness testified that the products manufactured by John Crane were a substantial contributing factor to the victim’s mesothelioma cancer diagnosis. Defense attorneys harped on testimony by this expert for the plaintiffs in which he explained the nuances in the relationship between asbestos exposure and developing mesothelioma cancer.

Additionally, the defendant took issue with the jury instructions given to the panel to help them reach a decision during their deliberations. These jury instructions are a standard part of our judicial system and both inform the jury of the legal standards for reaching a verdict and how they must apportion responsibility in civil cases. John Crane’s attorneys had asked the judge to give the jurors specialized jury instructions pattered for the particular case, though the trial judge determined that the Illinois state pattern instructions were sufficient.

A recent Duke University study published in The American Journal of Surgical Pathology examined hundreds of women diagnosed with diffuse mesothelioma, looking to an analyzing trends among the group which could eventually shed light on new treatment and detection methods. One of the key findings in the mesothelioma cancer study found that women with objective markers were diagnosed with pleural mesothelioma and that their average age of diagnosis was older compared to those diagnosed with another common type of the cancer, peritoneal mesothelioma.

The mesothelioma cancer study, which was a continuation study of an ongoing study by Duke University, examined 354 female mesothelioma patients of which the overwhelmingly majority were known to have been exposed to asbestos. The authors state that this exposure came from household contact, primarily from a family member who would have been exposed to asbestos fibers in an industrial setting. Of those studied, 275 patients had a pleural mesothelioma diagnosis which corresponds to linings of tissue surrounding the lungs and 79 cases were those of peritoneal mesothelioma which affects tissue linings around the abdominal cavity.

The researchers found that survival rates were longer for those with epithelial subtypes of peritoneal mesothelioma, though their average age of diagnosis was younger at 52 years of age compared to 62 years of age for those diagnosed with pleural mesothelioma. Further, researchers found that tremolite asbestos was a common form of the mineral which the patients were exposed to, followed by amphibole asbestos – considered one of the most deadly forms of the mineral. Some of these types of asbestos are found in cosmetics products such as talcum powder.

After nearly a two-week-long asbestos cancer trial, pharmaceutical and cosmetics giant Johnson & Johnson agreed to a rare settlement with the plaintiff who alleges she developed a rare and deadly form of lung cancer as a result of using one of the company’s most popular and iconic talc-based products. As part of the settlement, the New Jersey-based company reportedly agreed to pay the plaintiff $2 million and resolve the case without admitting any wrongdoing in the matter.

The settlement is a rare move by Johnson & Johnson, which faces an estimated nearly 17,000 other cases alleging plaintiffs developed serious forms of cancer, including mesothelioma, from using asbestos-contaminated talcum powder products produced and marketed by the company. To date, jurors in state courts in California, Missouri, and New Jersey have handed down verdicts in favor of plaintiffs totaling over $5 billion in total compensation, including punitive damages for what the juries deemed especially reckless conduct on Johnson & Johnson’s part.

Johnson & Johnson was not the only defendant in the case to reach a settlement. The 61-year old plaintiff also named London-based Rio Tinto Minerals as a defendant, which reportedly mined the talc that was used in the Johnson & Johnson Baby Powder the plaintiff allegedly developed mesothelioma from. As a result of settlements with all parties involved, the Oakland County jury was dismissed and will no longer need to deliver a verdict in the case.

The Food and Drug Administration (FDA) recently announced that it will host a public forum discussing the methods used to test for asbestos fibers in talc-based products, as well as the terminology and criteria that can be used to measure the carcinogen in consumer products. During that forum, the FDA will discuss preliminary recommendations from the Interagency Working Group on Asbestos in Consumer Products (IWGAC)—an interagency working group formed in 2018 to support the development of standardized testing methods for asbestos and other harmful particles.

The purpose of the IWGAC is to address the terminology and definitions of asbestos, recommend improvements for measuring asbestos in talc-based products, and recommend testing standards to test these products. The FDA forum comes two-years after the agency first began investigating reports of asbestos in talcum powder products, during which time it tested 50 such products and confirmed the presence of asbestos in some. One of those examinations in October 2019 revealed the presence of asbestos fibers in a lot of Johnson & Johnson’s Baby Powder, which caused the company to voluntarily recall 33,000 bottles of the iconic product.

Specifically, the IWGAC recommends adopting the term elongate mineral particles (EMP) to be “any mineral particle with a minimum aspect ratio of 3:1,” as to resolve ambiguity and disagreement of asbestos vs non-asbestos identification. Testing laboratories report all EMP having a length of over 500 nm and that testing methods specify reportable EMP identified as certain types of asbestos.

Johnson & Johnson CEO Alex Gorsky recently appeared in a New Brunswick, New Jersey courtroom to testify in a talcum powder asbestos cancer lawsuit brought by four plaintiffs who claim they developed a serious form of cancer from years of using one of the company’s most iconic products. The talcum powder lawsuit alleges that the plaintiffs developed mesothelioma as a result of asbestos exposure from using Johnson & Johnson products like Baby Powder and Shower to Shower while the pharmaceutical and cosmetics giant knew about the risk posed to consumers but chose not to provide any safety warnings on the products.

During his testimony, Gorsky indicated that he relied on company experts when he announced on national television that Johnson & Johnson’s Baby Powder does not contain asbestos and was safe for consumers to use. Despite Gorsky claiming that he did not have firsthand knowledge of the science behind Baby Powder risks, revelations have surfaced in recent months that the company knew for decades about possible risks and that the company still chose to market its products to vulnerable and marginalized communities.

Furthermore, Johnson & Johnson was forced to issue a recall of 33,000 bottles of Baby Powder after independent testing conducted on behalf of the Food and Drug Administration (FDA) discovered the presence of asbestos fibers in the product lot. Those tests have since spurred Congressional oversight committees to call for standardized testing methods and terminology to dispel ambiguity about how results are interpreted and ensure the public at large is protected from products containing deadly asbestos.

A recent study conducted by an international team of pathologists has reportedly identified a new protein which is often found in the tumor cells of patients diagnosed with pleural mesothelioma, a rare and deadly form of lung cancer which commonly affects the thin lining of tissue surrounding the lungs. With the discovery, researchers hope that doctors can make a more accurate prognosis for their patients and craft more effective and targeted treatment options to help these individuals live longer, more comfortable lives.

Published in The Journal of Pathology, the study found that the presence of protein CD70 correlates with a worse prognosis in patients with malignant pleural mesothelioma through immune evasion and enhanced invasiveness. The study was led by researchers at Aichi Medical University School of Medicine in Nagakute, Japan, with contributions from doctors based in the U.S., Poland, and Germany.

In the paper, the authors determined that about 20% of the mesothelioma tumor cells examined showed high levels of the CD70 protein, which resulted in a median survival of only six and a half months compared to a survival rate of a year and a half for patients without the over expression of the protein. Researchers believe these findings may explain the significant differences in survival periods between patients with the disease. The same protein has been studied in other serious forms of cancer, including certain types of kidney cancers and brain cancers.

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