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Randomized Phase III Study of High-Dose Fluorouracil Given As a Weekly 24-Hour Infusion With or Without Leucovorin Versus Bolus Fluorouracil Plus Leucovorin in Advanced Colorectal Cancer: European Organization of Research and Treatment of Cancer Gastrointestinal Group Study 40952
Abstract
Purpose: This trial was conducted to determine whether high-dose fluorouracil (FU) given as a weekly 24-hour infusion is more active than bolus FU + leucovorin (LV), and whether high-dose infusional FU can be modulated by LV. Patients and Methods: A total of 497 patients with previously untreated metastatic colorectal cancer were randomly assigned to receive bolus FU 425 mg/m 2 intravenously + LV 20 mg/m 2 on days 1 to 5 and repeated on day 28 (FU + LV), or FU 2,600 mg/m 2 as a 24-hour infusion alone (FU 24h) or in combination with 500 mg/m 2 LV (FU 24h + LV)—all given weekly ×6 followed by a 2-week rest period. Survival was the major study end point. Results: With a median follow-up of more than 3 years, survival did not differ among the treatment groups (median FU + LV, 11.1 months [95% CI, 10.2 to 15.0 months]; FU 24h, 13.0 months [95% CI, 10.4 to 15.4 months]; FU 24h + LV, 13.7 months [95% CI, 12.0 to 16.4 months]; P = .724). Progression-free survival (PFS) was significantly longer for FU 24h + LV (median FU + LV, 4.0 months [95% CI, 3.4 to 4.9]; FU 24h, 4.1 months [95% CI, 3.4 to 5.0]; FU 24h + LV 5.6 months [95% CI, 4.4 to 6.7]; P = .029). The response rates in the subgroup of patients with measurable disease were 12%, 10%, and 17% for FU + LV, FU 24h, and FU 24h + LV, respectively (not significant). Occurrence of grade 3 and 4 diarrhea was higher in the FU 24h + LV arm (22%) compared with the FU 24h (6%) or FU + LV (9%) arms; however, stomatitis (11% in FU + LV v 3% in FU 24h v 5% in FU 24h + LV arms) and hematologic toxicity were higher in the bolus FU + LV arm. Global quality of life did not differ within the three arms. Conclusion: Neither FU 24h + LV nor FU 24h prolong survival, relative to bolus FU + LV. Leucovorin increases PFS if added to FU 24h, but increases toxicity.
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Cited by
Köhne, C.-H., van Cutsem, E., Wils, J., Bokemeyer, C., El-Serafi, M., Lutz, M. P., Lorenz, M., Reichardt, P., Rückle-Lanz, H., Frickhofen, N., et al. (2005) · Journal of Clinical Oncology · doi:10.1200/jco.2005.05.546 · Cited by 331
Self-citationTherapy for Metastatic Colorectal Cancer
Goldberg, R. M. (2006) · The Oncologist · doi:10.1634/theoncologist.11-9-981 · Cited by 78
Metadata
- Authors
- Köhne, C.-H., Wils, J., Lorenz, M., Schöffski, P., Voigtmann, R., Bokemeyer, C., Lutz, M., Kleeberg, U., Ridwelski, K., Souchon, R., El-Serafi, M., Weiss, U., Burkhard, O., Rückle, H., Lichinitser, M., Langenbuch, T., Scheithauer, W., Baron, B., Couvreur, M. L., & Schmoll, H. J.
- Venue
- Journal of Clinical Oncology
- Published
- 2003-10-15
- Volume
- 21
- Issue
- 20
- Pages
- 3721-3728
- ISSN
- 0732-183X (ISSN-L)
- 1527-7755
- OpenAlex
- W2115366398
- Cited by
- 160
- References
- 0
- FWCI
- 9.55
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Randomized Phase III Study of High-Dose Fluorouracil Given As a Weekly 24-Hour Infusion With or Without Leucovorin Versus Bolus Fluorouracil Plus Leucovorin in Advanced Colorectal Cancer: European Organization of Research and Treatment of Cancer Gastrointestinal Group Study 40952. https://app.cochat.ai/papers/10.1200/jco.2003.11.122
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- Köhne, C.-H., Wils, J., Lorenz, M., Schöffski, P., Voigtmann, R., Bokemeyer, C., Lutz, M., Kleeberg, U., Ridwelski, K., Souchon, R., El-Serafi, M., Weiss, U., Burkhard, O., Rückle, H., Lichinitser, M., Langenbuch, T., Scheithauer, W., Baron, B., Couvreur, M. L., & Schmoll, H. J. (2003). Randomized Phase III Study of High-Dose Fluorouracil Given As a Weekly 24-Hour Infusion With or Without Leucovorin Versus Bolus Fluorouracil Plus Leucovorin in Advanced Colorectal Cancer: European Organization of Research and Treatment of Cancer Gastrointestinal Group Study 40952. Journal of Clinical Oncology. https://doi.org/10.1200/jco.2003.11.122
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