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. 2020 Dec 29;22(1):240. doi: 10.3390/ijms22010240

Table 1.

Variation of anti-cancer drugs in HNSCC.

Category Sub-Category Drug Name Mechanism Main Site of Drug Metabolism Main AEs The Others of AEs Clinical Research Effectiveness
Cytotoxic anti-cancer agents Platinum-based Cisplatin DNA crosslink Kidney Bone-marrow suppression, kidney dysfunction Allergy, peripheral nerve disorder, nausea Ref. [5] RR: 88.5%
Carboplatin Cell-cycle non-specific
Taxane-based Docetaxel Depolymerization inhibitor Liver Bone-marrow suppression, hair loss, nausea Allergy, edema, peripheral nerve disorder Ref. [6,7,8] RR: 33–53%
Paclitaxel Stop at M phase
Pyrimidine-based 5-fluorouracil (5-FU) DNA synthesis inhibitor Liver Bone-marrow suppression, mucositis, nausea Allergy, Myocardial ischemia, Diarrhea Ref. [5] RR: 88.5% (Platinum-combination therapy)
Tegafur, Gimeracil, and Oteracil potassium (S-1) S phase specific
Molecular-targeted agents Antibody-drug Cetuximab EGFR inhibitor - Rash, skin dryness, paronychia Infusion reaction, hypomagnesemia, interstitial pneumonia LA-HNSCC: Ref. [1] OS: 49 months
R/M-HNSCC: Ref. [2] OS: 10.1 months
Immune checkpoint inhbitor Anti PD-1 antibody Nivolumab PD-1 receptor inhibitior - Diarrhea, Dysthyroidism, Rash Colitis, diabetes mellitus, interstitial pneumonia Platinum-resistance: Ref. [3] OS: 7.7 months
Pembrolizumab Ref. [4] OS: 14.7/14.9 months (Pem-combination/monotherapy)

EGFR: epidermal growth factor receptor, PD-1: programmed cell death-1, AEs: adverse events, Pem: pembrolizumab, OS: median over all survival, RR: response rate, LA-HNSCC: locally advanced head and neck squamous cell carcinoma, R/M-HNSCC: recurrent/metastatic head and neck squamous cell carcinoma.