Publications by authors named "Heamanthaa Padmanabhan"

Cascade testing for families with BRCA pathogenic variants is important to identify relatives who are carriers. These relatives can benefit from appropriate risk management and preventative strategies arising from an inherited increased risk of breast, ovarian, prostate, melanoma, and pancreatic cancers. Cascade testing has the potential to enable cost-effective cancer control even in low- and middle-income settings, but few studies have hitherto evaluated the psychosocial impact of cascade testing in an Asian population, where the cultural and religious beliefs around inheritance and destiny have previously been shown to influence perception and attitudes toward screening.

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Article Synopsis
  • The rise of PARPi therapies has shifted genetic testing for breast and ovarian cancers from risk management to treatment decisions, but a shortage of genetic counselors remains a challenge.
  • Despite high interest (77%) among oncologists and surgeons in providing genetic counseling, 85% prefer referring patients to specialized services, pointing to concerns about costs and availability of genetic support.
  • The study highlights a need for training non-genetics healthcare professionals in genetic counseling, particularly in low-to-middle income countries, emphasizing a focus on risk management over direct access to new therapies.
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Article Synopsis
  • An increasing number of cancer patients are opting for genetic testing due to lower costs and new therapies, even without a strong family history or high risk of carrying mutations.
  • Studies on the psychosocial outcomes for breast cancer patients, especially those of Asian descent, remain limited, despite a significant number of low-risk carriers identified in research.
  • Results showed that with proper counseling, low-risk carriers had improved risk perception and a greater intention to adopt proactive health measures, demonstrating psychological resilience even in the absence of a family history of cancer.
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Background: Identifying patients with mutations is clinically important to inform on the potential response to treatment and for risk management of patients and their relatives. However, traditional referral routes may not meet clinical needs, and therefore, mainstreaming cancer genetics has been shown to be effective in some high-income and high health-literacy settings. To date, no study has reported on the feasibility of mainstreaming in low-income and middle-income settings, where the service considerations and health literacy could detrimentally affect the feasibility of mainstreaming.

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