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SOX as Salvage Treatment in Nasopharyngeal Carcinoma

This study has been terminated.
(poor accrual of eligible patients)
Information provided by (Responsible Party):
Ye Guo, Fudan University Identifier:
First received: July 26, 2011
Last updated: August 19, 2014
Last verified: August 2014
The aim of the study is to evaluate the efficacy and safety of SOX regimen (S-1 plus oxaliplatin) as salvage treatment in patients with relapsed or metastatic nasopharyngeal carcinoma.

Condition Intervention Phase
Nasopharyngeal Carcinoma Drug: S-1 plus oxaliplatin Phase 2

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase II Study of SOX in Patients With Platinum-resistant Nasopharyngeal Carcinoma

Resource links provided by NLM:

Further study details as provided by Ye Guo, Fudan University:

Primary Outcome Measures:
  • Median progression-free survival [ Time Frame: 1 year ]

Secondary Outcome Measures:
  • Overall response rate [ Time Frame: 6 weeks ]
  • Median overall survival [ Time Frame: 1.5 year ]

Enrollment: 16
Study Start Date: July 2011
Estimated Study Completion Date: December 2015
Estimated Primary Completion Date: December 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: S-1 plus oxaliplatin
S-1 60 mg BID at day 1-14 Oxaliplatin 100 mg/m2 at day 1 Frequence of cycles: every 3 weeks for 6 cycles
Drug: S-1 plus oxaliplatin
S-1 60 mg BID at day 1-14 Oxaliplatin 100 mg/m2 at day 1 Frequence of cycles: every 3 weeks
Other Names:
  • S-1
  • Oxaliplatin

Detailed Description:
The treatment option in patients with platinum-resistant relapsed or metastatic nasopharyngeal carcinoma is limited. Previous studies showed that both S-1 and oxaliplatin were effective in head and neck cancer. Moreover, SOX (S-1 plus oxaliplatin) was proved to be tolerable in advanced stage gastric cancer. Therefore, we aim to evaluate this regimen in salvage setting of nasopharyngeal carcinoma.

Ages Eligible for Study:   18 Years to 75 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Age range: 18-75 years old
  • Histological confirmed incurable relapsed or metastatic nasopharyngeal carcinoma
  • Prior exposure of at least one line of platinum-containing regimen
  • ECOG performance status 0-1
  • Life expectancy of more than 3 months
  • Bone marrow function: ANC≧1.5×109/L, PLT≧100×109/L, Hb≧80g/L
  • Liver function: total bilirubin, ALT and AST <1.5×UNL
  • Renal function: Cr<1.5×UNL, CCR≧50ml/min
  • Without > 1 grade of neuropathy

Exclusion Criteria:

  • With curable treatment option
  • With CNS involvement
  • Prior platinum exposure only in neo-adjuvant/adjuvant setting or concurrently used with radiotherapy
  • Treated with > 2 lines of palliative chemotherapy
  • With prior exposure of S-1 or oxaliplatin
  • History of other malignancies except cured basal cell carcinoma of skin and carcinoma in-situ of uterine cervix
  • Significant active infection
  • Pregnant or lactating women
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Please refer to this study by its identifier: NCT01403259

Fudan University Shanghai Cancer Center
Shanghai, China
Sponsors and Collaborators
Fudan University
Principal Investigator: Ye Guo, MD Fudan University
  More Information

Responsible Party: Ye Guo, Dr., Fudan University Identifier: NCT01403259     History of Changes
Other Study ID Numbers: HNTG 11-02
Study First Received: July 26, 2011
Last Updated: August 19, 2014

Keywords provided by Ye Guo, Fudan University:
Nasopharyngeal carcinoma

Additional relevant MeSH terms:
Nasopharyngeal Neoplasms
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Pharyngeal Neoplasms
Otorhinolaryngologic Neoplasms
Head and Neck Neoplasms
Neoplasms by Site
Nasopharyngeal Diseases
Pharyngeal Diseases
Stomatognathic Diseases
Otorhinolaryngologic Diseases
Antineoplastic Agents processed this record on September 21, 2017