Tegafur is a prodrug of 5-fluorouracil (5-FU) with a similar spectrum of antitumor activity. It is used in the treatment of advanced gastroin-testinal neoplasms. Over 5-FU, tegafur has the advantage of oral administration and less hematologic toxicity. Gastrointestinal toxicity is its main dose-limiting factor. The cutaneous adverse effects of tegafur include mucositis, photosensitivity, diffuse or nail-restricted hyper-pigmentation, palmoplantar erythrodysesthesia syndrome, palmoplantar keratoderma, sclero-dactyly and Raynaud phenomenon. We report here the case of a patient who developed acral hyperpigmentation during treatment wit
Progress in the understanding of many tumors has enabled the development of new therapies, such as t...
A 60-year-old female patient with gastric cancer and lymph node and liver metastases was treat-ed wi...
Purpose: Vemurafenib is a potent inhibitor of V600 mutant BRAF with significant impact on progressio...
Tegafur is a prodrug of 5-fluorouracil (5-FU) with a similar spectrum of antitumor activity. It is u...
5-fluorouracil, a fluoropyrimidine antineoplastic drug, is used to topically treat actinic keratoses...
TS-1 is an oral fluoropyrimidine anticancer drug that contains tegafur, gimeracil, and oteracil. A 7...
Targeted anticancer therapies, unlike the traditional cytotoxic chemotherapies which lead to systemi...
Skin toxicity is a frequent complication of anti-epidermal growth factor receptor therapy, which can...
Regorafenib is an oral multikinase inhibitor targeting several tyrosine kinase receptors including B...
Introduction. Vemurafenib is a selective inhibitor of serine-threonine kinase BRAF used in the tr...
There is a variety of adverse effects and toxicities of newer and older chemotherapeutic agents whic...
Introduction: Anti-EGFR targeted anti-cancer treatment is associated with various skin adverse event...
A wide spectrum of skin toxicities has been described in patients receiving epidermal growth factor ...
The use of targeted therapies, when added to conventional chemotherapy, has significantly improved c...
The last few years, new therapies targeting the epidermal growth factor receptor (EGFR) have shown t...
Progress in the understanding of many tumors has enabled the development of new therapies, such as t...
A 60-year-old female patient with gastric cancer and lymph node and liver metastases was treat-ed wi...
Purpose: Vemurafenib is a potent inhibitor of V600 mutant BRAF with significant impact on progressio...
Tegafur is a prodrug of 5-fluorouracil (5-FU) with a similar spectrum of antitumor activity. It is u...
5-fluorouracil, a fluoropyrimidine antineoplastic drug, is used to topically treat actinic keratoses...
TS-1 is an oral fluoropyrimidine anticancer drug that contains tegafur, gimeracil, and oteracil. A 7...
Targeted anticancer therapies, unlike the traditional cytotoxic chemotherapies which lead to systemi...
Skin toxicity is a frequent complication of anti-epidermal growth factor receptor therapy, which can...
Regorafenib is an oral multikinase inhibitor targeting several tyrosine kinase receptors including B...
Introduction. Vemurafenib is a selective inhibitor of serine-threonine kinase BRAF used in the tr...
There is a variety of adverse effects and toxicities of newer and older chemotherapeutic agents whic...
Introduction: Anti-EGFR targeted anti-cancer treatment is associated with various skin adverse event...
A wide spectrum of skin toxicities has been described in patients receiving epidermal growth factor ...
The use of targeted therapies, when added to conventional chemotherapy, has significantly improved c...
The last few years, new therapies targeting the epidermal growth factor receptor (EGFR) have shown t...
Progress in the understanding of many tumors has enabled the development of new therapies, such as t...
A 60-year-old female patient with gastric cancer and lymph node and liver metastases was treat-ed wi...
Purpose: Vemurafenib is a potent inhibitor of V600 mutant BRAF with significant impact on progressio...