'Decadose' Effects of Cisplatin on Squamous Cell Carcinoma of the Upper Aerodigestive Tract. II. Clinical Studies
Autor: | Stephen B. Howell, William Hryniuk, K. Thomas Robbins, Anna Maria Storniolo |
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Rok vydání: | 1996 |
Předmět: |
Adult
Male Drug medicine.medical_specialty Pathology media_common.quotation_subject medicine.medical_treatment Urology Antineoplastic Agents medicine Humans Infusions Intra-Arterial Aged media_common Cisplatin Chemotherapy Cell growth business.industry Head and neck cancer Middle Aged medicine.disease Clinical trial Upper aerodigestive tract Otorhinolaryngology Epidermoid carcinoma Drug Resistance Neoplasm Head and Neck Neoplasms Carcinoma Squamous Cell Female Neoplasm Recurrence Local business medicine.drug |
Zdroj: | The Laryngoscope. 106:37-42 |
ISSN: | 1531-4995 0023-852X |
DOI: | 10.1097/00005537-199601000-00008 |
Popis: | There is evidence that solid tumors rapidly acquire cellular resistance to cisplatin. This resistance is usually mild to moderate and could be circumvented with higher concentrations of drug exposure if ancillary methods were available to avoid systemic cytotoxicity. The purpose of this study was to determine whether a tenfold increase in dose (decadose) would overcome cisplatin resistance. In a clinical trial, response effects of cisplatin at dose intensities ranging from 32.5 to 200 mg/m2 per week, which were delivered by highly selective intra-arterial infusions with a simultaneously administered intravenous neutralizing agent, were measured in 31 patients with squamous cell carcinoma (SCC) of the upper aerodigestive tract (UADT). The overall response rate (complete response [CR] and partial response [PR]) to cisplatin therapy at dose intensity intervals of 0 to 74, 75 to 149, and 150 to 200 mg/m2 per week were 45.5%, 72.7%, and 100%, respectively. The average received dose intensities for nonresponders and responders (CR and PR) were 57.8 and 120.7 mg/m2 per week, respectively (P = .031). The results indicate that resistance to standard doses of cisplatin by SCC of the UADT, both previously untreated and recurrent, can be substantially overcome with “decadose” cisplatin therapy. Progress toward improving survival of patients with head and neck cancer, and possibly other site-specific malignancies, may be achieved by incorporating decadose cisplatin therapy into a multimodality treatment plan. |
Databáze: | OpenAIRE |
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