Effectiveness of incorporating cetuximab into docetaxel/cisplatin/fluorouracil induction chemotherapy and chemoradiotherapy for inoperable squamous cell carcinoma of the oral cavity: A phase II study
Background Inoperable oral cavity squamous cell carcinoma (SCC) is a highly invasive disease associated with the extensive destruction of locoregional tissues and a dismal prognosis. Management strategies for these patients are limited. Methods This study was a single arm, prospective, open‐label ph...
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Published in | Head & neck Vol. 39; no. 7; pp. 1333 - 1342 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.07.2017
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Subjects | |
Online Access | Get full text |
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Summary: | Background
Inoperable oral cavity squamous cell carcinoma (SCC) is a highly invasive disease associated with the extensive destruction of locoregional tissues and a dismal prognosis. Management strategies for these patients are limited.
Methods
This study was a single arm, prospective, open‐label phase II trial. A regimen consisting of cetuximab‐docetaxel, cisplatin, and fluorouracil (C‐TPF) followed by bio‐chemoradiotherapy (bio‐CRT) with cisplatin and cetuximab was administered to patients who responded to induction chemotherapy. The objective response rate to C‐TPF was the primary endpoint.
Results
Forty‐three patients were enrolled in this study. The objective response rate of C‐TPF was 88.4%; 88.9% (32/36) of the responders completed the full bio‐CRT course, and the objective response rate of bio‐CRT was 64.7%. The most common grade 3/4 adverse events for induction chemotherapy were leucopenia (32.6%) and febrile neutropenia (14.0%). The 1‐year progression‐free survival (PFS) and overall survival (OS) rates were 43% and 68%, respectively.
Conclusion
C‐TPF is an effective and tolerable induction chemotherapy regimen for inoperable oral cavity SCC. |
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Bibliography: | Funding information These authors contributed equally to this study. This study was supported in part by Merck Serono (Darmstadt, Germany), the Taiwan Clinical Oncology Research Foundation, the Taipei Veterans General Hospital (V104‐E8‐001, V104‐C‐040 to M.‐H.Y.), and a grant from the Ministry of Health and Welfare, Center of Excellence for Cancer Research (MOHW104‐TDU‐B‐211‐124‐001 to M.‐H.Y.). This work was presented as an e‐poster #e17016 at the American Society of Clinical Oncology (ASCO) 2015, 51st Annual Meeting, Chicago, Illinois, May 29 to June 2, 2015. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 1043-3074 1097-0347 |
DOI: | 10.1002/hed.24766 |