Memahami hubungan antara MRD dan terapi CAR T-Cell
What is MRD in cancer treatment? Measurable Residual Disease, or MRD, is the name for the very few cancer cells that stay in the body after or during treatment. Flow cytometry, polymerase chain reaction (PCR), or next-generati..
Terapi sel induk mesenkim pada gangguan neurologis
Neurological diseases are big problems around the world because they cause a lot of death and disability. Traditional treatments haven't always worked, which has led to a change toward new methods like cell-based therapies. Beca..
Penunjukan obat yatim piatu diberikan oleh FDA kepada CART T-Cell Therapy A2B530 untuk pengobatan kanker kolorektal
In March 2024, a news release said that A2B530 (A2 Biotherapeutics), a CAR T-cell therapy, had been given Orphan Drug Designation to treat colorectal cancer that expresses carcinoembryonic antigen (CEA) and has lost HLA-A*02 expr..
Amtagvi Iovance disetujui oleh USFDA sebagai terapi sel T pertama untuk tumor padat
Iovance Biotherapeutics' first-of-its-kind immunotherapy was approved by the FDA. This means that T-cell therapy, which has changed the way some types of blood cancer are treated, can now be used directly on solid tumors.The drug..
Amivantamab-vmjw disetujui oleh USFDA untuk indikasi kanker paru-paru non-sel kecil yang bermutasi penyisipan EGFR exon 20
The Food and Drug Administration approved amivantamab-vmjw (Rybrevant, Janssen Biotech, Inc.) in combination with carboplatin and pemetrexed on March 1, 2024. Patients with epidermal growth factor receptor (EGFR) exon 20 insertio..
Osimertinib dengan kemoterapi disetujui oleh USFDA untuk kanker paru-paru non-sel kecil yang bermutasi EGFR
The Food and Drug Administration approved osimertinib (Tagrisso, AstraZeneca Pharmaceuticals LP) in combination with platinum-based chemotherapy for patients with locally advanced or metastatic non-small cell lung cancer (la/mNSC..
Lifileucel disetujui oleh USFDA untuk melanoma yang tidak dapat dioperasi atau metastasis
The Food and Drug Administration granted accelerated approval to lifileucel (Amtagvi, Iovance Biotherapeutics, Inc.) on February 16, 2024. This approval is for adult patients with unresectable or metastatic melanoma who have been..
Tepotinib disetujui oleh USFDA untuk kanker paru-paru non-sel kecil yang bermetastasis
The Food and Drug Administration officially approved tepotinib (Tepmetko, EMD Serono, Inc.) on February 15, 2024, for adult patients with metastatic non-small cell lung cancer (NSCLC) that had mesenchymal-epithelial transition (M..
Liposom Irinotecan disetujui oleh USFDA untuk pengobatan lini pertama adenokarsinoma pankreas metastatik
The Food and Drug Administration approved irinotecan liposome (Onivyde, Ipsen Biopharmaceuticals, Inc.) with oxaliplatin, fluorouracil, and leucovorin on February 13, 2024, for treating metastatic pancreatic adenocarcinoma as the..
Erdafitinib disetujui oleh USFDA untuk karsinoma urothelial stadium lanjut atau metastasis lokal
Erdafitinib (Balversa, Janssen Biotech) was approved by the Food and Drug Administration on January 19, 2024, for adult patients with FGFR3 genetic changes who have locally advanced or metastatic urothelial carcinoma (mUC). Patie..