Publications by authors named "Malvika Vyas"

Background: The academia-industry interface is important, and, despite challenges that inevitably occur, bears the potential for positive synergies to emerge. Perceived barriers to wider collaboration in academia-industry oncology research in Europe need to be addressed, current academic cooperative group and industry models for collaboration need to be discussed, and a common terminology to facilitate understanding of both sectors' concerns needs to be established with an eye towards improving academia-industry partnerships on clinical trials for the benefit of patients with cancer.

Methodology: CAREFOR (Clinical Academic Cancer Research Forum), a multi-stakeholder platform formed to improve the direction for academic clinical trials in the field of oncology in Europe, formed the CAREFOR-Industry Working Group comprised of experienced professionals from European academic cooperative groups joined by industry representatives selected based on their activities in the area of medical oncology.

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Article Synopsis
  • The article summarizes the ESMO Asia 2018 Congress session focused on the availability and effectiveness of cancer medicines in Asia, particularly for breast, colorectal, and lung cancers, which contribute to a significant number of cancer deaths in the region.
  • It highlights the negative impact of limited access to medications on patient outcomes and discusses disparities in medicine accessibility based on income levels among Asian countries, citing data from the ESMO International Consortium Study.
  • The session emphasizes various global policy initiatives supported by ESMO to enhance cancer care and proposes potential strategies to address barriers to accessing anticancer treatments in low- and middle-income countries.
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Article Synopsis
  • The ESMO conducted a survey to evaluate the knowledge and comfort level of oncologists regarding the use of biosimilars, highlighting gaps in understanding related to their development and safety.
  • Nearly half of the prescribers reported using biosimilars, with most rating their knowledge as average to high, yet concerns about potential risks like immunogenicity were prevalent.
  • The results indicate a strong demand for further education on biosimilars, with preferences for both online and face-to-face learning options, particularly emphasizing the need for global consistency in definitions and guidelines.
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With the imminent arrival of oncology biosimilars in the therapeutic paradigm, stakeholders including a clinician, specialist nurse, patient advocate, regulator and economist provide their perspective on optimising the uptake of these new agents in the treatment of cancer. A number of key messages emerge, based on the discussion that took place during a session of the European Society for Medical Oncology's Annual Congress, ESMO Madrid 2017. First, for successful integration of biosimilars into the global healthcare paradigm, informing and educating the full scope of stakeholders, including clinicians, nurses, pharmacists and patients, is primordial.

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The cancer burden is rising globally, exerting significant strain on populations and health systems at all income levels. In May 2017, world governments made a commitment to further invest in cancer control as a public health priority, passing the World Health Assembly Resolution 70.12 on cancer prevention and control within an integrated approach.

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Biosimilars present a necessary and timely opportunity for physicians, patients and healthcare systems. If suitably developed clinically, manufactured to the correct standards and used appropriately, they can positively impact on the financial sustainability of healthcare systems. A critical consideration regarding the introduction of biosimilars into the clinic centres on the required information concerning all the respective procedures.

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