SWOG clinical trial number
S0007
Evaluation of 3 Hour Infusion of Paclitaxel Plus Cisplatin and 5-Fluorouracil in Patients with Advanced or Recurrent Squamous Cell Carcinoma of the Head and Neck (SCCHN)
Closed
Phase
Accrual
100%
Published
Research committees
Head and Neck Cancer
Treatment
Cisplatin
5-Fluorouracil
Paclitaxel
Eligibility Criteria Expand/Collapse
Pts. must have histologically proven SCCHN that is met. at dx or persisted, met. or recurred following definitive surgery and/or RT (* 28 days prior to reg.). Pts. whose only measurable dz is within a prior RT port must have clearly prog. dz prior to reg. Newly diag., non-met. dz are not eligible. Pts. must have measurable or non-measurable dz; pts. must not have received prior chemo for recurrent or newly diagnosed met dz. Pts. w/ neuropathy - sensory * Grade 2 are not eligible.
Publication Information Expand/Collapse
2016
PMid: PMID27325863 | PMC number: PMC5012713
2006
A phase II evaluation of a 3-hour infusion of paclitaxel, cisplatin, and 5-fluorouracil in patients with advanced or recurrent squamous cell carcinoma of the head and neck: Southwest Oncology Group Study 0007
2004
A phase II evaluation of a 3-hour infusion of paclitaxel (P), cisplatin (CDDP) & 5-fluorouracil (5FU) in patients with advanced or recurrent squamous cell carcinoma of the head and neck (SCCHN). A Southwest Oncology Group (SWOG) study