Literature DB >> 17962613

Recent advances with topotecan in the treatment of lung cancer.

Mary O'Brien1, John Eckardt, Rodryg Ramlau.   

Abstract

Topotecan is a semisynthetic derivative of camptothecin that specifically targets topoisomerase I. It has well-established antineoplastic properties and has been successfully combined with other antineoplastic agents with activity dependent on DNA disruption, such as cisplatin and etoposide. Topotecan is indicated for the treatment of small cell lung cancer (SCLC) sensitive disease after failure of first-line chemotherapy and metastatic ovarian carcinoma after failure of initial or subsequent chemotherapy. Since the approval of topotecan for the second-line treatment of SCLC, studies have been conducted in the first-line setting. Recent studies demonstrate the utility of i.v. topotecan in combination with cisplatin for untreated SCLC. Further, an oral formulation of topotecan is currently under investigation and may provide added convenience for patients. Oral topotecan has been studied in the first- and second-line settings for both SCLC and non-small cell lung cancer (NSCLC). Three recent phase III trials have demonstrated the activity of oral topotecan. In the first study of chemotherapy-naïve patients with extensive-disease SCLC, oral topotecan plus cisplatin provided efficacy and safety similar to those of etoposide plus cisplatin. In a second study of patients with relapsed SCLC, treatment with oral topotecan showed a statistically significant and clinically meaningful longer overall survival time and improvement in dyspnea and quality of life compared with best supportive care alone in all prognostic groups. Finally, in previously treated patients with NSCLC, single-agent oral topotecan was shown to be noninferior in 1-year survival rate relative to the current standard of i.v. docetaxel. In future studies, oral topotecan will represent a good candidate for combination therapy with other i.v. or oral chemotherapy agents, monoclonal antibodies, and small molecule tyrosine kinase inhibitors.

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Year:  2007        PMID: 17962613     DOI: 10.1634/theoncologist.12-10-1194

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  11 in total

1.  Current Treatment Options in Gastroenteropancreatic Neuroendocrine Carcinoma.

Authors:  Katharine E H Thomas; Brianne A Voros; J Philip Boudreaux; Ramcharan Thiagarajan; Eugene A Woltering; Robert A Ramirez
Journal:  Oncologist       Date:  2019-01-11

2.  Capsaicin synergizes with camptothecin to induce increased apoptosis in human small cell lung cancers via the calpain pathway.

Authors:  Jamie R Friedman; Haley E Perry; Kathleen C Brown; Ying Gao; Ju Lin; Cathyrn D Stevenson; John D Hurley; Nicholas A Nolan; Austin T Akers; Yi Charlie Chen; Krista L Denning; Linda G Brown; Piyali Dasgupta
Journal:  Biochem Pharmacol       Date:  2017-01-16       Impact factor: 5.858

3.  Pelitinib (EKB-569) targets the up-regulation of ABCB1 and ABCG2 induced by hyperthermia to eradicate lung cancer.

Authors:  Kenneth K W To; Daniel C Poon; Yuming Wei; Fang Wang; Ge Lin; Liwu Fu
Journal:  Br J Pharmacol       Date:  2015-06-26       Impact factor: 8.739

4.  Extrapulmonary small cell carcinoma: involvement of the brain without evidence of extracranial malignancy by serial PET/CT scans.

Authors:  Christopher N Hueser; Nghi C Nguyen; Medhat Osman; Necat Havlioglu; Anjali J Patel
Journal:  World J Surg Oncol       Date:  2008-09-25       Impact factor: 2.754

5.  Selective cytotoxicity and combined effects of camptothecin or paclitaxel with sodium-R-alpha lipoate on A549 human non-small cell lung cancer cells.

Authors:  Sherif Ibrahim; Dayuan Gao; Patrick J Sinko
Journal:  Nutr Cancer       Date:  2013-09-24       Impact factor: 2.900

6.  The prognostic significance of the circulating neuroendocrine markers chromogranin A, pro-gastrin-releasing peptide, and neuron-specific enolase in patients with small-cell lung cancer.

Authors:  Marina Petrović; Zoran Bukumirić; Vladimir Zdravković; Slobodanka Mitrović; Henry Dushan Atkinson; Vladimir Jurišić
Journal:  Med Oncol       Date:  2013-12-30       Impact factor: 3.064

7.  SULF2 methylation is prognostic for lung cancer survival and increases sensitivity to topoisomerase-I inhibitors via induction of ISG15.

Authors:  M Tessema; C M Yingling; C L Thomas; D M Klinge; A M Bernauer; Y Liu; S Dacic; J M Siegfried; S E Dahlberg; J H Schiller; S A Belinsky
Journal:  Oncogene       Date:  2011-12-12       Impact factor: 9.867

8.  Significance of c-MET overexpression in cytotoxic anticancer drug-resistant small-cell lung cancer cells.

Authors:  Hiroaki Ozasa; Tetsuya Oguri; Ken Maeno; Osamu Takakuwa; Eiji Kunii; Yoshitaka Yagi; Takehiro Uemura; Daishi Kasai; Mikinori Miyazaki; Akio Niimi
Journal:  Cancer Sci       Date:  2014-07-25       Impact factor: 6.716

9.  Topoisomerase I inhibitors, shikonin and topotecan, inhibit growth and induce apoptosis of glioma cells and glioma stem cells.

Authors:  Feng-Lei Zhang; Ping Wang; Yun-Hui Liu; Li-Bo Liu; Xiao-Bai Liu; Zhen Li; Yi-Xue Xue
Journal:  PLoS One       Date:  2013-11-26       Impact factor: 3.240

10.  Inhalation delivery of topotecan is superior to intravenous exposure for suppressing lung cancer in a preclinical model.

Authors:  Philip J Kuehl; Marcie J Grimes; Devon Dubose; Michael Burke; David A Revelli; Andrew P Gigliotti; Steven A Belinsky; Mathewos Tessema
Journal:  Drug Deliv       Date:  2018-11       Impact factor: 6.419

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