Although the initial choice to evaluate a 3-hour infusion of paclitaxel (Taxol; Bristol-Myers Squibb Company, Princeton, NJ) was arbitrary, the attenuated schedule has since proven safe and active against several neoplasms. Shorter infusions are easier to administer, particularly in combination chemotherapy and combined-modality therapy, prompting our investigations of 1-hour paclitaxel infusions in more than 500 patients and approximately 2,000 treatment courses. The toxicity, activity, and pharmacology of 1- and 3-hour infusions of paclitaxel appear to be similar. Results of phase II trials document that 1-hour paclitaxel infusions can be administered safely, and notable activity has been seen against several neoplasms, including cancers of the lung, breast, and urothelium, as well as advanced squamous carcinomas and tumors of unknown origin. This report also describes some limited pharmacologic data of 1-hour paclitaxel compared with longer infusions.
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Hosp Pharm
September 2024
Medical Oncology, IRCCS Sacro Cuore Don Calabria Hospital, Negrar di Valpolicella, Verona, Italy.
Eur J Cancer
May 2024
Cancer Therapeutics Program, UPMC Hillman Cancer Center, Pittsburgh, PA, USA; Department of Pharmaceutical Sciences, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA, USA; Division of Hematology-Oncology, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. Electronic address:
Paclitaxel, one of the most frequently used anticancer drugs, is dosed by body surface area, which leads to substantial inter-individual variability in systemic drug exposure. We evaluated clinical evidence regarding the scientific rationale and clinical benefit of individualized paclitaxel dosing based on measured systemic concentrations, known as therapeutic drug monitoring (TDM). In retrospective studies, higher systemic exposure is associated with greater toxicity and efficacy of paclitaxel treatment across several disease types and dosing regimens.
View Article and Find Full Text PDFFront Cardiovasc Med
September 2023
Department of Engineering, Wake Forest University, Winston-Salem, NC, United States.
Prev Chronic Dis
August 2023
Division of General Pediatrics, Stanford University School of Medicine, Palo Alto, California.
Cancer Manag Res
September 2022
Department of Medical Oncology 4, National Cancer Hospital of Vietnam, Hanoi, Vietnam.
Objective: To evaluate the outcome and safety of the paclitaxel, carboplatin, and capecitabine (TCX) regimen in patients with advanced gastric cancer.
Methods: Advanced gastric cancer patients received the TCX regimen for up to six cycles, which were 3 weeks apart. Paclitaxel (175 mg/m2) was given over a 3-hour infusion, followed by carboplatin in a 1-hour infusion on day 1.
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