Literature DB >> 8826868

A phase II randomised trial of 5-fluorouracil with or without interferon alpha-2a in advanced colorectal cancer.

A Piga1, S Cascinu, L Latini, M Marcellini, M Bavosi, L Acito, R Bascioni, L Giustini, G Francini, A Pancotti, G Rossi, M Del Papa, F Carle, R Cellerino.   

Abstract

With the association of 5-fluorouracil (5-FU) and alpha-interferon (IFN), objective responses as high as 26 63% have been reported in untreated patients with advanced colorectal cancer. However, grade 3-4 toxicity has also been reported. We have conducted a prospective phase II randomised study comparing 5-FU to 5-FU + IFN, to investigate whether the addition of IFN to a weekly 5-FU regimen devoid of significant toxicity used at our institutions could improve the effectiveness of 5-FU while maintaining acceptable toxicity. Patients with histologically proven advanced colorectal carcinoma were randomised to receive 5-FU 500 mg m-2 intravenous (i.v.) bolus on days 1-5 followed by 5-FU 500 mg m-2 i.v. bolus weekly from day 15, with or without IFN alpha-2a intramuscularly (i.m.) 1.5 mU daily on days 6-12 and 3 mU i.m. daily thereafter. The treatment was administered on an outpatient basis. Response was evaluated every 3 months, and treatment continued until progression or after two consecutive judgements of stable disease. Response rate was the main end point of the study. Of 141 patients eligible, 72 were randomised to 5-FU alone (arm A) and 69 to 5-FU + IFN (arm B). Responses were 9/72 (12.5%) in arm A and 6/69 (8.7%) in arm B; complete responses were three in arm A and two in arm B. Progression-free survival (median 4 months) and survival (median 12 months) were identical in the two arms. Toxicity was almost absent in arm A and moderate in arm B, represented mainly by haematological toxicity (usually leucopenia). In conclusion, overall survival was good in both arms of treatment and toxicity was moderate. While the response rate with 5-FU alone was in accord with the literature data, response to 5-FU + IFN was lower than expected. At least at this dosage and schedule, the association of 5-FU and IFN is no better than 5-FU alone and is of no clinical interest.

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Year:  1996        PMID: 8826868      PMCID: PMC2074731          DOI: 10.1038/bjc.1996.467

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  16 in total

1.  Interferon effects upon fluorouracil metabolism by HL-60 cells.

Authors:  L Elias; J M Sandoval
Journal:  Biochem Biophys Res Commun       Date:  1989-09-15       Impact factor: 3.575

2.  Chemotherapy for colorectal carcinoma: one small step forward, one step backward.

Authors:  N Kemeny
Journal:  J Clin Oncol       Date:  1995-06       Impact factor: 44.544

3.  Interferon alpha-2a and 5-fluorouracil for advanced colorectal carcinoma. Assessment of activity and toxicity.

Authors:  N Kemeny; A Younes; K Seiter; D Kelsen; P Sammarco; L Adams; S Derby; P Murray; C Houston
Journal:  Cancer       Date:  1990-12-15       Impact factor: 6.860

4.  Fluorouracil and recombinant alfa-2a-interferon: an active regimen against advanced colorectal carcinoma.

Authors:  S Wadler; E L Schwartz; M Goldman; A Lyver; M Rader; M Zimmerman; L Itri; V Weinberg; P H Wiernik
Journal:  J Clin Oncol       Date:  1989-12       Impact factor: 44.544

5.  Interaction of gamma interferon and 5-fluorouracil in the H630 human colon carcinoma cell line.

Authors:  E Chu; S Zinn; D Boarman; C J Allegra
Journal:  Cancer Res       Date:  1990-09-15       Impact factor: 12.701

6.  Reporting results of cancer treatment.

Authors:  A B Miller; B Hoogstraten; M Staquet; A Winkler
Journal:  Cancer       Date:  1981-01-01       Impact factor: 6.860

7.  Phase II evaluation of recombinant alpha-2a-interferon and continuous infusion fluorouracil in previously untreated metastatic colorectal adenocarcinoma.

Authors:  R Pazdur; J A Ajani; Y Z Patt; J Gomez; B Bready; B Levin
Journal:  Cancer       Date:  1993-02-15       Impact factor: 6.860

8.  A prospective randomized comparison of continuous infusion fluorouracil with a conventional bolus schedule in metastatic colorectal carcinoma: a Mid-Atlantic Oncology Program Study.

Authors:  J J Lokich; J D Ahlgren; J J Gullo; J A Philips; J G Fryer
Journal:  J Clin Oncol       Date:  1989-04       Impact factor: 44.544

Review 9.  Clinical relevance of biochemical modulation of 5-fluorouracil.

Authors:  G J Peters; C J van Groeningen
Journal:  Ann Oncol       Date:  1991-07       Impact factor: 32.976

10.  Phase II trial of fluorouracil and recombinant interferon alfa-2a in patients with advanced colorectal carcinoma: an Eastern Cooperative Oncology Group study.

Authors:  S Wadler; B Lembersky; M Atkins; J Kirkwood; N Petrelli
Journal:  J Clin Oncol       Date:  1991-10       Impact factor: 44.544

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  2 in total

1.  Retrospective evaluation of 5-fluorouracil-interferon-a aTreatment of advanced colorectal cancer patients.

Authors:  C András; Z Csiki; I Gál; I Takács; L Antal; G Szegedi
Journal:  Pathol Oncol Res       Date:  2000       Impact factor: 3.201

2.  Alpha-interferon does not increase the efficacy of 5-fluorouracil in advanced colorectal cancer.

Authors:  P Thirion; P Piedbois; M Buyse; P J O'Dwyer; D Cunningham; A Man; F A Greco; G Colucci; C H Köhne; F Di Constanzo; A Piga; S Palmeri; P Dufour; A Cassano; G Pajkos; R A Pensel; N F Aykan; J Marsh; M T Seymour
Journal:  Br J Cancer       Date:  2001-03-02       Impact factor: 7.640

  2 in total

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