A fresh glimmer of hope has emerged for
pancreatic cancer patients. A first-of-its-kind telehealth-based cancer
clinical trial offers patients targeted therapy from the comfort of
their homes. Dubbed "smart drugs," these precision therapies singularly
pinpoint the genetic anomalies responsible for driving the proliferation
of cancer cells.
The primary objective of this trial was to investigate fibroblast growth
factor receptors (FGFR), identified in around one percent of patients
with pancreatic cancer. Through the implementation of telehealth
techniques in this study, patients throughout the United States can gain
access to oral targeted drug therapies conveniently, eliminating the
need for extensive travel.
Dr. Sameek Roychowdhury, a medical
oncologist at The Ohio State University Cancer Center, stresses that
bringing clinical trial treatments to patients and collaborating with
local oncologists nationwide significantly enhances patient access to
these therapies. This approach also improves the potential for impactful
discoveries through the enrollment of larger groups of patients,
according to a press statement.
Pancreatic cancer, though rare, is a highly
aggressive disease that impacts approximately 64,000 people every year.
Detection often takes place during the advanced stages, which
complicates the treatment process. Surgical procedures show promise in
the early stages, yet early identification remains a challenge, which
limits the availability of recommended treatment selections. This study
aims to enhance the availability of clinical trials for targeted drug
therapies, thus addressing a pivotal void in pancreatic cancer
treatment.
In cancer patients, numerous gene mutations
could be present, but identifying the ones influencing cancer behavior
and utilizing innovative treatments to address these mutations forms the
foundation of 'smart drug’ – or precision cancer medicine – research,
says Roychowdhury. Clinical trials for precision oncology are hindered
by the rarity of certain gene mutations, which deters pharmaceutical
companies from undertaking such trials due to a lack of interest and
feasibility.
This trial draws inspiration from FGFR
research supported by Gateway for Cancer Research, a nonprofit
organization dedicated to funding early-phase clinical trials for
various types of cancer. Gateway is a proponent of decentralized
oncology research and seeks to raise awareness about telemedicine-based
trials, ensuring that patients comprehend their options no matter how
close they are to a research site.
With ten years of expertise in FGFR intelligent medications, Dr.
Roychowdhury spearheads this groundbreaking therapy. Along with the
clinical trial, his team has established a patient registry to advance
research into rare forms of pancreatic cancer.
Patient enrollment for the trial is set to begin in the second half of
2023. To find out more about taking part in the research or becoming a
member of the registry, reach out to Sameek.Roychowdhury@osumc.edu.
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Labels: fibroblast growth receptors, genetic anomalies, Pancreatic Cancer
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