Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (16)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Hughes, M. J.
Right arrow Articles by Kaye, S. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hughes, M. J.
Right arrow Articles by Kaye, S. B.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Annals of Oncology 7:208-210, 1996
© 1996 European Society for Medical Oncology


other

A pilot study of combination therapy with interferon-{alpha}-2a and 5-fluorouracil in metastatic carcinoid and malignant endocrine pancreatic tumours

M. J. Hughes1, D. J. Kerr2, J. Cassidy3, M. Soukop4, K. McGregor1, N. Blackburn5, H. Yosef1 and S. B. Kaye1

1Medical Oncology Unit, Beatson Oncology Centre Glasgow
2Department of Clinical Oncology, Queen Elizabeth Medical Centre Birmingham
3Department of Medical Oncology, Aberdeen Royal Infirmary Aberdeen
4Medical Oncology Unit, Glasgow Royal Infirmary Glasgow
5Department of Clinical Research, Roche Products Ltd. Welwyn Garden City, UK

M. J. Hughes, M.D. Medical Oncology Unit Beatson Oncology Centre Glasgow G11 6NT, U.K.

Background: In view of the encouraging single agent response rates to interferon and 5-fluorouracil (5-FU) in malignant carcinoid and endocrine pancreatic tumours and the theoretical benefits of combination therapy with 5-FU and interferon in other tumours a study was designed to look at the feasibility of this combination, given for 12 months, in these tumours.

Patients and methods: Patients were treated with 5-FU 750 mg/m2 by intravenous bolus every week and 3 Mega Units of recombinant interferon-{alpha}-2a subcutaneously 3 times per week increasing, as tolerated, to 6 then 9 MU. Fifteen patients were entered into the study.

Results: One patient died suddenly of an unrelated illness and is not assessed. None of the remaining 14 patients had radiological evidence of response to treatment, although 6 had stable disease lasting for 7 to 64 weeks (median 40 weeks). Two patients did have biochemical evidence of a response, i.e., a 50% reduction in baseline urinary 5HIAA for 26 and 52 weeks. Treatment toxicity was significant. Six patients stopped treatment prematurely because of either nausea and/or diarrhoea. Overall treatment duration ranged from 4 to 64 weeks (median 7.5 weeks).

Conclusion: Overall we found the treatment to be disappointing in terms of tolerance and response rate and do not recommend its use in malignant carcinoid or endocrine pancreatic tumours.

{alpha}-interferon, carcinoid, 5-fluorouracil, islet cell, neuroendocrine tumours


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Endocr. Rev.Home page
G. A. Kaltsas, G. M. Besser, and A. B. Grossman
The Diagnosis and Medical Management of Advanced Neuroendocrine Tumors
Endocr. Rev., June 1, 2004; 25(3): 458 - 511.
[Abstract] [Full Text] [PDF]


Home page
JCOHome page
Y. Z. Patt, M. M. Hassan, R. D. Lozano, T. D. Brown, J. N. Vauthey, S. A. Curley, and L. M. Ellis
Phase II Trial of Systemic Continuous Fluorouracil and Subcutaneous Recombinant Interferon Alfa-2b for Treatment of Hepatocellular Carcinoma
J. Clin. Oncol., February 1, 2003; 21(3): 421 - 427.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.