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1. Biologie
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Winslow
and his colleagues plan to use their approach to investigate not just
the genetic mutations involved in the development of pancreatic cancer,
but also those responsible for its progression and metastasis.
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5. Traitements
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The
study, published in The Lancet today, is relevant to postmenopausal
women with ER-positive breast cancer, which accounts for over 80% of
cases which occur after the menopause.
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Many
womb cancers contain faults in the genes that encode components of
their DNA repair toolkits, and since the end of 2014, Dr Kristeleit and
her team have been making preparations for a clinical trial to test a
new PARP inhibitor in women with the disease.
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"Before
doctors give this drug to all post-menopausal women at high risk of
breast cancer, more thorough clinical trials are needed".
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In
IMAGE 1, patients with advanced pancreatic cancer and WHO performance
score 0-2 (n = 110) were assigned randomly to receive IMM-101
intradermally plus gemcitabine (n = 75) or gemcitabine alone (n = 35)
for a 12-cycle maximum. The efficacy endpoint of primary interest was
overall survival (OS).
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Trials
showed that the drugs stopped breast tumour cells from spreading to the
bones, the most common site for secondary cancers, and reduced the risk
of dying from the disease by 18% in the first ten years after
diagnosis.
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5.2 Pharma
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Filing Based on Data From Phase 3 Head-To-Head ENDEAVOR Study.
Relapsed Multiple Myeloma Patients Treated With Kyprolis in Study Lived Twice as Long Without Disease Worsening.
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Variations
include Opdivo in previously treated non-squamous, non-small cell lung
cancer (NSCLC) and Opdivo in combination with Yervoy (ipilimumab) in
advanced melanoma.
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5.2.1 Pharma - Partenariats
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Moses
attributed Merck's interest in its technology to its ability to link
two or three nanobodies together to target multiple immune checkpoints
simultaneously.
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5.3 Traitements - FDA, EMA,...
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Company
to Proceed Expeditiously With Marketing Authorization Application in
Europe and Will Evaluate Regulatory and Clinical Strategies to Gain
Marketing Approval in the U.S.
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The
FDA wanted the additional evidence before Sunesis files its marketing
application for the drug, the company said in a statement on Thursday.
The European Medicines Agency (EMA) however, gave the company the nod to
submit a marketing application for vosaroxin, Sunesis said.
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5.4 Traitements - Economie
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"A
lot of my patients cry — they're frustrated," says Dr. Ayalew Tefferi, a
hematologist at the Mayo Clinic. "Many of them spend their life savings
on cancer drugs and end up being bankrupt."
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Here’s
the best idea they propose: An independent, government-chartered group
that evaluated the value of drugs (option 1) would give insurance
companies a powerful new negotiating tool. Like the U.S. Preventative
Services Task Force, which evaluates screening, it would provide a basis
for public discussion about these drugs, even if it had not power of
its own.
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6. Lutte contre les cancers
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All
the available research points in the opposite direction. Studies have
found that providing genetic risk information will not, long-term, help
people quit smoking or lose weight. It will not encourage them to get
cancer screening. And, more damning, it will not help individuals at
risk for diabetes adopt a healthy lifestyle, even when that
personalized, genetically informed advice is provided by experts.
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Some
oncologists said that while the study tackled a difficult question
carefully, patients and doctors should avoid generalizing based on its
results.
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6.6 Publications
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This
is a really strong recommendation. It not only indicates the
usefulness of unique identifiers in information systems (such as in
recommendation number 11, which advocates the increased use of ISNIs as
organizational identifiers), it specifically suggests that ORCID iDs
should be mandated in the national Research Excellence Framework (the
REF).
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6.7.3 DMP
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Today’s
EHRs impede workflow, are a roadblock to easy information transfer, and
can cause significant downtime because of the need for specialized
technical assistance. The EHR has unintentionally become more important
than the patient.
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6.9 Controverses
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Failure to publish the results of all clinical trials is skewing medical science.
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