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. 2009 Jun 15:1:17.
doi: 10.1186/1758-3284-1-17.

Radical radiotherapy with concurrent weekly cisplatin in loco-regionally advanced squamous cell carcinoma of the head and neck: a single-institution experience

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Radical radiotherapy with concurrent weekly cisplatin in loco-regionally advanced squamous cell carcinoma of the head and neck: a single-institution experience

Tejpal Gupta et al. Head Neck Oncol. .

Abstract

Background: The dominant pattern of failure for squamous cell carcinoma of head and neck remains loco-regional, although distant metastases are now being increasingly documented. Radical radiotherapy with concurrent chemotherapy is contemporary standard of care in the non-surgical management of these loco-regionally advanced cancers, based on large randomized controlled trials utilizing high-dose cisplatin (80-100 mg/m2) cycled every three-weekly during definitive radiotherapy. Although efficacious, this is associated with high acute morbidity necessitating intensive supportive care with attendant resource implications. The aim of this retrospective study was to assess the efficacy and acute toxicity of an alternative schedule i.e. concurrent weekly cisplatin-based radical radiotherapy and it's potential to be an optimal regimen in advanced head and neck cancers.

Methods: Outcome data of patients with Stage III & IV head and neck squamous cell carcinoma, excluding nasopharynx, planned for radical radiotherapy (66-70 Gy) with concurrent weekly cisplatin (30 mg/m2) treated in a single unit between 1996-2004 was extracted.

Results: The dataset consisted of 264 patients with a median age of 54 years. The median radiotherapy dose was 70 Gy (range 7.2-72 Gy) and median number of chemotherapy cycles was 6 (range 1-7). Two-thirds (65%) of patients received > or = 85% of planned cisplatin dose. With a mean follow-up of 19 months, the 5-year local control; loco-regional control; and disease free survival was 57%; 46%; and 43% respectively. Acute grade 3 or worse mucositis and dermatitis was seen in 77 (29%) and 92 (35%) patients respectively, essentially in patients receiving doses > or = 66 Gy and 6 or more cycles of chemotherapy. Other toxicities (hematologic, nausea and vomiting) were mild and self-limiting. Overall, the acute toxicity of this concurrent weekly chemo-radiation regimen though mildly increased did not mandate intensive supportive care. Stage grouping, primary site, and intensity of treatment were significant predictors of loco-regional control and disease free survival.

Conclusion: Radical radiotherapy with concurrent weekly cisplatin has moderate efficacy and acceptable acute toxicity with potential to be an optimal regimen in loco-regionally advanced squamous cell carcinoma of the head and neck, particularly in limited-resource settings. Stage grouping, primary site, and treatment intensity are important determinants of outcome.

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Figures

Figure 1
Figure 1
Stage grouping as prognostic factor for local control (a), loco-regional control (b), and disease-free survival (c) in SCCHN treated with concurrent chemo-radiotherapy.
Figure 2
Figure 2
Impact of intensity of chemotherapy on local control (a), loco-regional control (b), and disease-free survival (c) in weekly cisplatin-based concurrent chemo-radiotherapy for SCCHN.
Figure 3
Figure 3
Correlation of primary site with local control (a), loco-regional control (b), and disease-free survival (c) in loco-regionally advanced SCCHN treated with concurrent chemo-radiotherapy.

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References

    1. GLOBOCAN 2002 . Version 20 IARC Cancer Base No5. Lyon: IARC Press; 2004. Cancer incidence, mortality, and prevalence worldwide.
    1. Forastiere A, Koch W, Trotti A, Sidransky D. Medical progress- Head and Neck cancer. N Engl J Med. 2001;345:1890–1900. doi: 10.1056/NEJMra001375. - DOI - PubMed
    1. Chin D, Boyle GM, Porceddu S, Theile DR, Parsons PG, Coman WB. Head and neck cancer- past, present, and future. Expert Rev Anticancer Ther. 2006;6:1111–1118. doi: 10.1586/14737140.6.7.1111. - DOI - PubMed
    1. Garavello W, Ciardo A, Spreafico R, Gaini RM. Risk factors for distant metastases in head and neck squamous cell carcinoma. Arch Otolaryngol Head Neck Surg. 2006;132:762–766. doi: 10.1001/archotol.132.7.762. - DOI - PubMed
    1. Pignon JP, Bourhis J, Domenge C, Designe L. Chemotherapy added to locoregional treatment for head and neck squamous-cell carcinoma: three meta-analyses of updated individual data. Lancet. 2000;355:949–955. - PubMed