Answer / Rajat Prakash Singh

Emerging therapies like gene editing (CRISPR) and targeted immunotherapies are revolutionizing hematology practice. Gene editing holds promise for treating genetic disorders like sickle cell disease and beta-thalassemia by correcting the mutated genes responsible for these conditions. Targeted immunotherapies, on the other hand, can help in managing cancerous blood cells, such as chronic myeloid leukemia (CML). These advancements could lead to improved patient outcomes, reduced side effects, and personalized medicine. However, they also present challenges related to cost, accessibility, and ethical considerations.

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