Journal of Clinical Oncology, Vol 12, 1592-1599, Copyright © 1994 by American Society of Clinical Oncology
Tumor response, toxicity, and survival after neoadjuvant organ- preserving chemotherapy for advanced laryngeal carcinoma. The Department of Veterans Affairs Cooperative Laryngeal Cancer Study Group
MB Spaulding, SG Fischer and GT Wolf
Department of Medicine, State University of New York at Buffalo.
PURPOSE: In 1984, the Department of Veterans Affairs Cooperative Studies
Program began a trial in which patients with resectable squamous cell
carcinoma of the larynx were randomized to receive standard surgery
followed by radiation therapy or to receive neoadjuvant therapy with
cisplatin and fluorouracil (5-FU) followed by radiation therapy for those
achieving a greater than 50% tumor response to chemotherapy. This analysis
reviews the tumor responses, toxicity, compliance, and long-term survival
for those patients randomized to the chemotherapy arm. PATIENTS AND
METHODS: One hundred sixty-six patients were randomized to the chemotherapy
arm. Standard tumor response data, chemotherapy toxicity, and survival have
been examined using standard statistical methods. RESULTS: The high
response rates and acceptable toxicity to cisplatin and 5-FU of previously
untreated patients were confirmed. Long-term disease-free survival was more
likely to occur in patients who achieved a complete response to
chemotherapy, particularly in those who had a confirmed histologic response
to chemotherapy. Pretreatment histologic growth patterns were highly
predictive of responses to chemotherapy. CONCLUSION: Neoadjuvant
chemotherapy was well tolerated and did not negatively affect the
definitive treatment that followed. The survival of nonresponding patients
who underwent prompt salvage surgery was also not impaired. The role of
organ preservation should be explored in other head and neck sites.

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