• `Research autopsy' enable scientists stu

    From ScienceDaily@1:317/3 to All on Tue Sep 28 21:30:44 2021
    `Research autopsy' enable scientists study why certain cancer therapies
    stop working
    Patients agree in life to donate biological samples in death for cancer research

    Date:
    September 28, 2021
    Source:
    Ohio State University Wexner Medical Center
    Summary:
    A new research study turns cancer scientists into molecular
    detectives, searching for clues for why certain cancers are able
    to spread and evolve by studying tissues collected within hours
    of death.



    FULL STORY ==========================================================================
    A new research study at The Ohio State University Comprehensive Cancer
    Center - - Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC -- James) turns cancer scientists into molecular
    detectives, searching for clues for why certain cancers are able to
    spread and evolve by studying tissues collected within hours of death.


    ==========================================================================
    Led by Dr. Sameek Roychowdhury, this unique clinical research study --
    known as the Rapid Cancer Research Autopsy Trial -- allows scientists to
    gather biological samples after a patient's death to conduct research
    otherwise not possible, with the goal of better understanding how the
    cancer cells overcame different treatments.

    "As patients undergo cancer treatment and, in some instances, succumb to
    their disease, there's limited opportunity to understand their cancer and
    what made it so lethal and what took their lives," said Roychowdhury,a
    medical oncologist and researcher with the OSUCCC -- James Translational Therapeutics Program.

    "The rapid autopsy program allows us to sample every site of cancer
    in the body. This can help us understand how the cancer cells overcame different treatments and then go back to the drawing board to develop
    better therapies targeted to different genes and types of cancer."
    For this Pelotonia-funded study, patients consent during life to donate biological samples upon death for the purposes of cancer research. When
    the patient passes, researchers rapidly mobilize to perform an autopsy
    before tissues degrade. Samples are preserved to "freeze/pause" the
    tissue characteristics at that moment so that they can go back to the
    lab and identify potential genetic mutations or cellular characteristics
    that could explain why therapy stopped working, in hopes of guiding
    future therapies.

    Study Findings Impacting Cancer Care Since the trial's launch in
    2016, the OSUCCC -- James rapid research autopsy team has performed 55 autopsies. Data gathered from these autopsies has already led to novel
    findings about drug resistance mechanisms for a recently approved, novel targeted therapy called infigratinib (pronounced "IN fig RA ti nib,"
    marketed as Truseltiq, pronounced "troo-SEL-tik"). This drug targets
    FGFR2 gene mutations known as fusions in cholangiocarcinoma and other
    cancer types.

    The team recently published findings in the medical journal Lancet: Gastroenterology & Hepatology from a single-arm, multicenter, phase 2
    study of the drug infigratinib in previously treated patients with locally advanced or metastatic cholangiocarcinoma, a rare and difficult-to-treat
    form that occurs in the bile duct. Results showed meaningful impact
    on tumor response and led to the FDA-approval of this therapy for cholangiocarcinoma and these specific FGFR2 fusions in May 2021. Going
    beyond cholangiocarcinoma, OSUCCC -- James investigators are enrolling
    patients to a phase 2 study of infigratinib for patients with other
    cancer types that harbor FGFR gene mutations. This study was designed and developed by the OSUCCC -- James team as an investigator- initiated trial
    in partnership with the drug development industry. Roychowdhury notes this study could provide evidence that more patients with FGFR gene mutations
    could benefit from new therapy approaches that directly target FGFR.

    "This represents a strong potential new therapy option for diseases that
    have limited treatment options," Roychowdhury said. "We are so humbled
    by our patients' selflessness by participating in research that will help others. It is a legacy of hope and exciting to see both precision cancer medicine and the research autopsy trial translating into discoveries at
    the patient's bedside." Roychowdhury says his team is continually humbled
    by patients' eagerness to help advance research in any way possible, even
    if those discoveries will not come in time to eradicate their own disease.

    "Everyone on our team sees it as a privilege and duty to care for them
    in that research study and to use that autopsy to help others as that
    patient would have wanted," he said. "We're understanding how to better
    take care of patients with cancer, find better ways to develop therapies
    and to understand biology.

    But even more rewarding is the fact that almost
    every single family member has said to me how grateful
    they are that their loved one could be part of the study." ========================================================================== Story Source: Materials provided by Ohio_State_University_Wexner_Medical_Center. Note: Content may be edited
    for style and length.


    ========================================================================== Journal Reference:
    1. Milind Javle, Sameek Roychowdhury, Robin Kate Kelley, Saeed Sadeghi,
    Teresa Macarulla, Karl Heinz Weiss, Dirk-Thomas Waldschmidt, Lipika
    Goyal, Ivan Borbath, Anthony El-Khoueiry, Mitesh J Borad, Wei Peng
    Yong, Philip A Philip, Michael Bitzer, Surbpong Tanasanvimon,
    Ai Li, Amit Pande, Harris S Soifer, Stacie Peacock Shepherd,
    Susan Moran, Andrew X Zhu, Tanios S Bekaii-Saab, Ghassan K
    Abou-Alfa. Infigratinib (BGJ398) in previously treated patients
    with advanced or metastatic cholangiocarcinoma with FGFR2 fusions
    or rearrangements: mature results from a multicentre, open-label,
    single-arm, phase 2 study. The Lancet Gastroenterology & Hepatology,
    2021; 6 (10): 803 DOI: 10.1016/S2468-1253 (21)00196-5 ==========================================================================

    Link to news story: https://www.sciencedaily.com/releases/2021/09/210928121338.htm

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