Practice of superselective intraarterial high-dose cisplatin chemoradiotherapy in the oral cavity
Creators
- 1. Tokyo Medical Univ., Hachioji Medical Center, Hachioji, Tokyo (Japan)
- 2. Tokyo Medical Univ., Medical School, Tokyo (Japan)
Description
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. 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 (9 g/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. Four (13.3%) subjects with Grade 3 or greater myelosuppression required granulocyte-colony stimulating factor (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 complete response (CR) and 6 (20%) partial response (PR), but no stable disease (SD) or no change (NC). Overall response was 100%. Histopathologically, 2 of 9 undergoing postchemoradiotherapy had no tumors. Clinical and pathological CR was 86.7%. Adverse events associated with this therapy associated events were considered relatively mild and within allowable limits. (author)
Additional details
Publishing Information
- Journal Title
- Koku Intoka
- Journal Volume
- 24
- Journal Issue
- 1
- Journal Page Range
- p. 81-86
- ISSN
- 0917-5105
INIS
- Country of Publication
- Japan
- Country of Input or Organization
- Japan
- INIS RN
- 42098614
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CARCINOMAS; CHEMOTHERAPY; COMBINED THERAPY; FRACTIONATED IRRADIATION; ORAL CAVITY; PATIENTS; RADIATION DOSES; RADIOTHERAPY; SURVIVAL CURVES
- Descriptors DEC
- DIGESTIVE SYSTEM; DISEASES; DOSES; IRRADIATION; MEDICINE; NEOPLASMS; NUCLEAR MEDICINE; RADIOLOGY; THERAPY