Stomato-pharyngology
Online ISSN : 1884-4316
Print ISSN : 0917-5105
ISSN-L : 0917-5105
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Practice of superselective intraarterial high-dose cisplatin chemoradiotherapy in the oral cavity
Tomoyuki YoshidaHiroyuki ItoKazuhiro NakamuraAkira ShimizuKiyoaki TsukaharaTaro InagakiDaisuke TakataIsaku OkamotoTakahito Kondo
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2011 Volume 24 Issue 1 Pages 81-86

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Abstract
Objectives: Superselective intraarterial infusion enables high-dose chemotherapeutic agents to be administered via tumor feeding vessels to neutralize and limit the adverse cisplatin effects acceptable. Between 1998 and 2008, we evaluated the efficacy of first-line therapy and adverse events in 30 subjects with oral squamous cell cancer undergoing simultaneous superselective intra arterial high-dose chemotherapy and radiotherapy.
Methods: The 30 subjects—23 men and 7 women aged 40 to 72—consisted of 3 T2, 12 T3, and 15 T4. Four patients had N0, 8 N1, 7 N2b, 8 N2c, and 3 N3 disease. Two were in CS II, 6 III, 17 IVa, and 5 IVb (III>93%, IV: 73%). Superselective intra arterial chemotherapy delivered through the femoral artery used the Seldinger technique. A single cisplatin dose of 100-550 mg/m2 (mean 440 mg/m2). Five minutes after intra arterial infusion, sodium thiosulphate (9g/m2) was administered via a peripheral cutaneous vein in the contralateral forearm. Concurrent radiotherapy started on Day 2 at 2 Gy per session for a total of 60 Gy. Two to 3 weeks later, 15 under went the second course of superselective intra arterial chemotherapy after tumor feeding vessels were visualized angiographically.
Results: Four (13.3%) subjects with Grade 3 or greater myelosuppression required G-CSF. Grade 3 or greater mucositis was observed in 57% and Grade 4 mucositis occurred in 5 (16.7%). All adverse effects were reversible and no serious adverse events were prolonged. Among those responding to first-line therapy, 24 of the 30 (80%) achieved CR and 6 (20%) PR, but no SD or NC. Overall response was 100%. Histopathologically, 2 of 9 undergoing postchemoradiotherapy had no tumors. Clinical and pathological CR was 86.7%.
Conclusion: Adverse events associated with this therapy associated events were considered relatively mild and within allowable limits.
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© 2011 Japan Society of Stomato-pharyngology
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