Patients treated with immune checkpoint inhibitors have better quality of life: Study
TAMPA, Fla. - Immune checkpoint inhibitors that activate the immune system to target cancer cells have greatly impacted the lives of cancer patients by improving survival and providing an alternative to chemotherapy. However, it is unclear how immune checkpoint inhibitors affect patients' quality of life, symptoms and physical functioning. In a new article published in the Journal of the National Cancer Institute, Moffitt Cancer Center researchers report that patients treated with immune checkpoint inhibitors have a higher self-reported quality of life than patients treated with other types of therapy.
Immune checkpoint inhibitors are approved to treat a variety of solid tumor types and lymphomas. The therapy works by blocking the activity of the proteins PD-1, PD-L1 or CTLA-4, resulting in stimulation of the immune system and promotion of anti-tumor activity. Current immune checkpoint inhibitors include the drugs atezolizumab, avelumab, durvalumab, ipilimumab, nivolumab and pembrolizumab.
There is limited information about how treatment with immune checkpoint inhibitors impacts a patient's life, and how that compares to standard treatment options. In general, it is hoped that cancer treatments will ultimately improve the overall quality of life as the tumor recedes, and patients enter remission. However, all cancer therapies, including immune checkpoint inhibitors, are associated with side effects that could affect a patient's daily life, such as their ability to work. Chemotherapy tends to be associated with more severe adverse events than targeted therapies such as immune checkpoint inhibitors because of the nondiscriminatory impact of chemotherapy on both cancer cells as well as normal cells. Ultimately, the anti-tumor activity of various treatment regimens combined with their associated side effects can result in both positive and negative effects on patients' quality of life.
https://academic.oup.com/jnci/advance-article-abstract/doi/10.1093/jnci/djab171/6368683?redirectedFrom=fulltext
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