1999
DOI: 10.1016/s0959-8049(99)81010-7
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Weekly gemcitabine (GEM) and 5-fluorouracil (5-FU) in pancreatic carcinoma. Phase I–II study

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Cited by 2 publications
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“…In this small series, no WHO Grade 3 or 4 toxicities were observed. Moreover, the interim median overall survival was 13 months, compared with only 7 months and 4.4 months, respectively, in the trials by Cascinu et al31 and Berlin et al32 The ongoing trial of Tarantini et al,35 using escalating doses of both gemcitabine and 5‐FU, achieved a PR in four patients and a high rate of CBR, but was associated with high levels of toxicity (Table 1).…”
Section: Gemcitabine With Bolus 5‐fumentioning
confidence: 95%
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“…In this small series, no WHO Grade 3 or 4 toxicities were observed. Moreover, the interim median overall survival was 13 months, compared with only 7 months and 4.4 months, respectively, in the trials by Cascinu et al31 and Berlin et al32 The ongoing trial of Tarantini et al,35 using escalating doses of both gemcitabine and 5‐FU, achieved a PR in four patients and a high rate of CBR, but was associated with high levels of toxicity (Table 1).…”
Section: Gemcitabine With Bolus 5‐fumentioning
confidence: 95%
“…To date, there is a wealth of published reports of Phase I‐II trials of gemcitabine in combination with 5‐FU with or without FA for the treatment of patients with advanced pancreatic cancer (Tables 1 and 2). Although the dose and schedule of administration of gemcitabine has been similar in nearly all the trials, the administration of 5‐FU varies from protracted continuous infusion to 24‐hour continuous infusion to weekly bolus infusion at differing dose levels with16–24 or without FA 25–35. In five fully completed trials,16, 17, 25, 31, 32 four different treatment schedules for 5‐FU were used.…”
Section: Gemcitabine In Combination With 5‐fumentioning
confidence: 99%
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