Radiotherapy & Oncology
Volume 89, Issue 1 , Pages 44-50, October 2008

A phase II trial of low-dose gemcitabine and radiation alternated to cisplatin and 5-fluorouracil: An active and manageable regimen for stage IV squamous cell carcinoma of the head and neck

  • Marco Benasso

      Affiliations

    • Department of Medical Oncology A, National Institute for Cancer Research, Genoa, Italy
    • Corresponding Author InformationCorresponding author. Marco Benasso, S.C. Oncologia Medica A, National Institute for Cancer Research, Largo Rosanna Benzi, 10, 16132 Genova, Italy.
  • ,
  • Viviana Vigo

      Affiliations

    • Department of Medical Oncology A, National Institute for Cancer Research, Genoa, Italy
  • ,
  • Almalina Bacigalupo

      Affiliations

    • Department of Radiation Oncology, National Institute for Cancer Research, Genoa, Italy
  • ,
  • Anna Ponzanelli

      Affiliations

    • Department of Medical Oncology A, National Institute for Cancer Research, Genoa, Italy
  • ,
  • Michela Marcenaro

      Affiliations

    • Department of Radiation Oncology, National Institute for Cancer Research, Genoa, Italy
  • ,
  • Renzo Corvò

      Affiliations

    • Department of Otholaryngology, National Institute for Cancer Research, Genoa, Italy
  • ,
  • Giovanni Margarino

      Affiliations

    • Department of Otholaryngology, National Institute for Cancer Research, Genoa, Italy

Received 14 December 2007; received in revised form 13 March 2008; accepted 1 April 2008. published online 23 April 2008.

Abstract 

Background

The addition of gemcitabine may be a reasonable way to enhance the activity of the alternating cisplatin/5-fluorouracil and radiation regimen considered the referring approach for patients with advanced squamous cell carcinoma (SCC) of the head and neck at the National Institute for Cancer Research of Genoa.

Methods

Three courses of cisplatin, 20mg/m2/day and 5-fluorouracil, 200mg/m2/day, days 1–5 (weeks 1, 4, and 7) alternated to 3 courses of radiotherapy at standard fractionation (weeks 2–3, 5–6, 8–9) up to 60Gy, and gemcitabine, 50mg/m2 on monday of each week of radiation, were administered to 47 patients with stage IV (42 patients) or relapsed after surgery (5 patients), SCC of the oral cavity, pharynx or larynx.

Results

Eighty-five percent of the patients completed the planned treatment. Main grade 3–4 acute toxicities were: mucositis (40%), neutropenia (26%) and thrombocytopenia (30%). Twenty-seven patients reached a complete response (57%). Seven partial responders were rendered disease-free by surgery (final complete response rate: 72%). At a median follow-up of 37 months, 3-year overall survival, progression-free survival and loco-regional control are 50%, 43% and 54%, respectively.

Conclusions

The addition of gemcitabine at low dose to our referring alternating regimen is feasible and very active. It may improve the long-term outcomes despite an acceptable increase of acute mucoseal toxicity.

Keywords: Head and neck, Chemo-radiotherapy, Gemcitabine

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0167-8140(08)00196-5

doi:10.1016/j.radonc.2008.04.002

Radiotherapy & Oncology
Volume 89, Issue 1 , Pages 44-50, October 2008