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Australian scientists developed a targeted immunotherapy for myelofibrosis, a rare blood cancer, based on specific gene mutations.
Australian researchers have developed a new targeted therapy for myelofibrosis, a rare blood cancer causing fatigue and spleen enlargement.
Published in Blood, the study identifies two distinct targets for immunotherapy based on Type 1 and Type 2 calreticulin mutations, enabling the immune system to precisely attack abnormal cells while sparing healthy tissue.
This precision approach, led by Daniel Thomas and Angel Lopez at SAHMRI, marks a world-first distinction in treatment strategies and represents a shift from symptom management to disease-targeted therapy.
While human trials are still pending, the findings offer hope for more effective, long-lasting treatments.
Científicos australianos desarrollaron una inmunoterapia dirigida para la mielofibrosis, un cáncer de sangre raro, basada en mutaciones genéticas específicas.