Literature DB >> 7619747

Etoposide: twenty years later.

J D Hainsworth1, F A Greco.   

Abstract

Since the beginning of its clinical development 20 years ago, etoposide has become an important and widely used agent in clinical oncology. Its integral role in the treatment of germ cell tumors and small-cell lung cancer seems unlikely to diminish in the future, and its use in non-Hodgkin's lymphoma and in various high dose regimens will probably continue to increase. Active investigation continues regarding the optimal dose and schedule of etoposide, and it is likely that these investigations will result in further improvement of its clinical activity in patients with sensitive tumor types. Continued clinical investigation may result in the identification of active etoposide containing combination regimens for ovarian cancer, breast cancer, and some of the childhood malignancies. Exciting possibilities for the future include exploration of etoposide in combination with the topoisomerase I inhibitors, as well as the development of drugs to reverse drug resistance. During the next 10 years, the applications and importance of this unique drug will continue to increase.

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Year:  1995        PMID: 7619747     DOI: 10.1093/oxfordjournals.annonc.a059180

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  22 in total

1.  Artemisia absinthium (AA): a novel potential complementary and alternative medicine for breast cancer.

Authors:  Gowhar Shafi; Tarique N Hasan; Naveed Ahmed Syed; Amal A Al-Hazzani; Ali A Alshatwi; A Jyothi; Anjana Munshi
Journal:  Mol Biol Rep       Date:  2012-02-05       Impact factor: 2.316

2.  E2F-1 cooperates with topoisomerase II inhibition and DNA damage to selectively augment p53-independent apoptosis.

Authors:  J Nip; D K Strom; B E Fee; G Zambetti; J L Cleveland; S W Hiebert
Journal:  Mol Cell Biol       Date:  1997-03       Impact factor: 4.272

3.  Oral etoposide in patients with hematological malignancies: a clinical and pharmacokinetic study.

Authors:  E Osby; E Liliemark; M Björkholm; J Liliemark
Journal:  Med Oncol       Date:  2001       Impact factor: 3.064

4.  Clinical and pharmacokinetic phase I trial of oral dimethylaminoetoposide (NK611) administered for 21 days every 35 days.

Authors:  I Rassmann; H Schrödel; T Schilling; M Zucchetti; A Kaeser-Fröhlich; J Rastetter; A R Hanauske
Journal:  Invest New Drugs       Date:  1996       Impact factor: 3.850

5.  Etoposide with or without mannitol for the treatment of recurrent or primarily unresponsive brain tumors: a Children's Cancer Group Study, CCG-9881.

Authors:  N L Kobrinsky; R J Packer; J M Boyett; P Stanley; T Shiminski-Maher; J C Allen; J H Garvin; D J Stewart; J L Finlay
Journal:  J Neurooncol       Date:  1999       Impact factor: 4.130

6.  Enhanced expression of DNA topoisomerase II genes in human medulloblastoma and its possible association with etoposide sensitivity.

Authors:  Toshio Uesaka; Tadahisa Shono; Daisuke Kuga; Satoshi O Suzuki; Hiroaki Niiro; Kyoko Miyamoto; Kenichi Matsumoto; Masahiro Mizoguchi; Masaru Ohta; Toru Iwaki; Tomio Sasaki
Journal:  J Neurooncol       Date:  2007-03-15       Impact factor: 4.130

Review 7.  Camptothecin and podophyllotoxin derivatives: inhibitors of topoisomerase I and II - mechanisms of action, pharmacokinetics and toxicity profile.

Authors:  Jörg T Hartmann; Hans-Peter Lipp
Journal:  Drug Saf       Date:  2006       Impact factor: 5.606

8.  DNA-AP sites generation by etoposide in whole blood cells.

Authors:  Emilio Rojas; Patricia Mussali; Efrain Tovar; Mahara Valverde
Journal:  BMC Cancer       Date:  2009-11-16       Impact factor: 4.430

9.  Phase II study of combination chemotherapy with etoposide and ifosfamide in patients with heavily pretreated recurrent or persistent epithelial ovarian cancer.

Authors:  Heeseok Kang; Tae-Joong Kim; Chel Hun Choi; Jeong-Won Lee; Je-Ho Lee; Duk-Soo Bae; Byoung-Gie Kim
Journal:  J Korean Med Sci       Date:  2009-09-24       Impact factor: 2.153

10.  ABL-N-induced apoptosis in human breast cancer cells is partially mediated by c-Jun NH2-terminal kinase activation.

Authors:  Bin Liu; Mei Han; Rong-Hua Sun; Jun-Jie Wang; Yan-Ping Zhang; Di-Qun Zhang; Jin-Kun Wen
Journal:  Breast Cancer Res       Date:  2010-01-25       Impact factor: 6.466

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