𩺠å
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ð äžé éé»
- 22E: synthetic lethality (PARP), targeted protein degradation (PROTAC), mRNA cancer vaccines
- Taiwan: å¥ä¿ CDK4/6, BCL-2, BRAF/MEK, PD-1/PD-L1 inhibitors
ð Pearls (10)
- Synthetic lethality: PARP + BRCA = HR-deficient lethal
- PROTAC (proteolysis-targeting chimera) emerging for âundruggableâ targets
- Tumor-agnostic therapies: pembrolizumab MSI-H, larotrectinib NTRK fusion, dabrafenib BRAF V600E
- mRNA cancer vaccines (BioNTech, Moderna trials)
- CAR-T for hematologic malignancies
- BiTE (bispecific T cell engager): blinatumomab, mosunetuzumab
- Antibody-drug conjugate (ADC): T-DXd, sacituzumab, polatuzumab
- Tumor mutational burden (TMB) predicts immunotherapy response
- Microsatellite instability (MSI-H) universal CRC screening
- Liquid biopsy ctDNA for monitoring + early detection
ð Taiwan
- å¥ä¿ CDK4/6 (palbociclib, ribociclib, abemaciclib) for breast
- å¥ä¿ BRAF/MEK for melanoma + NSCLC
- å¥ä¿ PD-1/PD-L1 å€ cancer
- å¥ä¿ CGP NGS panel æ¢ä»¶
- å¥ä¿ CAR-T éå¶
ð å
§å°éé»
- Cell cycle + CDK4/6
- Apoptosis + BCL-2
- Major signaling (MAPK, PI3K, JAK)
- Targeted therapies
- Immunotherapy era
- Tumor agnostic (22E)
â ïž AI èçš¿ã