Literature DB >> 11180520

Phase II study of combined 5-fluorouracil/ Ginkgo biloba extract (GBE 761 ONC) therapy in 5-fluorouracil pretreated patients with advanced colorectal cancer.

B Hauns1, B Häring, S Köhler, K Mross, C Unger.   

Abstract

The aim of the study was to evaluate the efficacy, tolerability and quality of life in 5-fluorouracil (5-FU) pretreated colorectal cancer patients after combined 5-FU and Ginkgo biloba extract GBE 761 ONC (i.e. the Ginkgo biloba special extract EGb 761(R)) therapy. Following conventional 5-FU therapy, 44 patients (32 evaluable for response) with advanced progressive colorectal cancer were treated every 3 weeks with courses of 350 mg GBE 761 ONC as a 30 min i.v. infusion on days 1-6 followed by 500 mg/m(2)/d 5-FU as a 30 min i.v. infusion on days 2-6. The response to therapy was evaluated after the second and fourth course of treatment. The data of 32 patients could be evaluated for efficacy. We observed a progression of disease in 22 patients, no change in 8 patients and a partial response in 2 patients (overall response = 6.3%). Seventeen of 22 patients with observed progressive disease showed further progression after two cycles, two after three cycles and three after four cycles. The median survival time was 9.5 months (7.7-11.5 months). GBE 761 ONC was well tolerated. Adverse events that occurred during the study were mainly myelosuppression and gastrointestinal symptoms and were judged to be 5-FU related or consistent with liver toxicity and thus tumour related. Our results suggest a good benefit-risk ratio of the combined 5-FU and GBE 761 ONC therapy as second line treatment in metastatic colorectal cancer. The survival time was similar to that known from second line treatment according to the Ardalan scheme. Since an improvement was observed in some patients despite the failure of the conventional 5-FU pretreatment, it would be interesting to evaluate whether the application of 5-FU plus GBE 761 ONC as a first line treatment is of benefit. Copyright 2001 John Wiley & Sons, Ltd.

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Year:  2001        PMID: 11180520     DOI: 10.1002/1099-1573(200102)15:1<34::aid-ptr755>3.0.co;2-2

Source DB:  PubMed          Journal:  Phytother Res        ISSN: 0951-418X            Impact factor:   5.878


  4 in total

1.  The effect of EGB on proliferation of gastric carcinoma SGC7901 cells.

Authors:  Y Qian; L Xia; W Shi; J J Sun; Y Q Sun
Journal:  Clin Transl Oncol       Date:  2015-10-21       Impact factor: 3.405

2.  Natural Compounds as Occult Ototoxins? Ginkgo biloba Flavonoids Moderately Damage Lateral Line Hair Cells.

Authors:  Sarah Neveux; Nicole K Smith; Anna Roche; Bruce E Blough; Wimal Pathmasiri; Allison B Coffin
Journal:  J Assoc Res Otolaryngol       Date:  2016-11-28

3.  Ginkgo biloba extract 761 enhances 5-fluorouracil chemosensitivity in colorectal cancer cells through regulation of high mobility group-box 3 expression.

Authors:  Xi Chen; Lingbing Zeng
Journal:  Am J Transl Res       Date:  2018-06-15       Impact factor: 4.060

4.  Ginkgo biloba induces different gene expression signatures and oncogenic pathways in malignant and non-malignant cells of the liver.

Authors:  Carolin Czauderna; Mayrel Palestino-Dominguez; Darko Castven; Diana Becker; Luis Zanon-Rodriguez; Jovana Hajduk; Friederike L Mahn; Monika Herr; Dennis Strand; Susanne Strand; Stefanie Heilmann-Heimbach; Luis E Gomez-Quiroz; Marcus A Wörns; Peter R Galle; Jens U Marquardt
Journal:  PLoS One       Date:  2018-12-21       Impact factor: 3.240

  4 in total

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