A phase II study of Epirubicin in oxaliplatin-resistant patients with metastatic colorectal cancer and TOP2A gene amplification. Issue 1 (December 2016)
- Record Type:
- Journal Article
- Title:
- A phase II study of Epirubicin in oxaliplatin-resistant patients with metastatic colorectal cancer and TOP2A gene amplification. Issue 1 (December 2016)
- Main Title:
- A phase II study of Epirubicin in oxaliplatin-resistant patients with metastatic colorectal cancer and TOP2A gene amplification
- Authors:
- Tarpgaard, Line
Qvortrup, Camilla
Nygård, Sune
Nielsen, Signe
Andersen, Diana
Jensen, Niels
Stenvang, Jan
Detlefsen, Sönke
Brünner, Nils
Pfeiffer, Per - Abstract:
- Abstract ᅟ The overall purpose of this study is to provide proof of concept for introducing the anthracycline epirubicin as an effective, biomarker-guided treatment for metastatic colorectal cancer (mCRC) patients who are refractory to treatment with oxaliplatin-based chemotherapy and haveTOP2A gene amplification in their tumor cells. Background Epirubicin is an anthracycline that targets DNA topoisomerase 2-α enzyme encoded by theTOP2A gene. It is used for treatment of several malignancies, but currently not in CRC.TOP2A gene amplifications predict improved efficacy of epirubicin in patients with breast cancer and thus could be an alternative option for patients with CRC and amplifiedTOP2A gene. We have previously analysed the frequency ofTOP2A gene aberrations in CRC and found that 46.6 % of these tumors hadTOP2A copy gain and 2.0 % had loss ofTOP2A when compared to adjacent normal tissue. TheTOP2A gene is located on chromosome 17 and when theTOP2A /CEN-17 ratio was applied to identify tumors with gene loss or amplifications, 10.5 % had a ratio ≥ 1.5 consistent with gene amplification and 2.6 % had a ratio ≤ 0.8 suggesting gene deletions. Based on these observations and the knowledge gained from treatment of breast cancer patients, we have initiated a prospective clinical, phase II protocol using epirubicin (90 mg/m2 iv q 3 weeks) in mCRC patients, who are refractory to treatment with oxaliplatin. Methods/Design The study is an open label, single arm, phase II study,Abstract ᅟ The overall purpose of this study is to provide proof of concept for introducing the anthracycline epirubicin as an effective, biomarker-guided treatment for metastatic colorectal cancer (mCRC) patients who are refractory to treatment with oxaliplatin-based chemotherapy and haveTOP2A gene amplification in their tumor cells. Background Epirubicin is an anthracycline that targets DNA topoisomerase 2-α enzyme encoded by theTOP2A gene. It is used for treatment of several malignancies, but currently not in CRC.TOP2A gene amplifications predict improved efficacy of epirubicin in patients with breast cancer and thus could be an alternative option for patients with CRC and amplifiedTOP2A gene. We have previously analysed the frequency ofTOP2A gene aberrations in CRC and found that 46.6 % of these tumors hadTOP2A copy gain and 2.0 % had loss ofTOP2A when compared to adjacent normal tissue. TheTOP2A gene is located on chromosome 17 and when theTOP2A /CEN-17 ratio was applied to identify tumors with gene loss or amplifications, 10.5 % had a ratio ≥ 1.5 consistent with gene amplification and 2.6 % had a ratio ≤ 0.8 suggesting gene deletions. Based on these observations and the knowledge gained from treatment of breast cancer patients, we have initiated a prospective clinical, phase II protocol using epirubicin (90 mg/m2 iv q 3 weeks) in mCRC patients, who are refractory to treatment with oxaliplatin. Methods/Design The study is an open label, single arm, phase II study, investigating the efficacy of epirubicin in patients with oxaliplatin refractory mCRC and with a cancer cellTOP2A /CEN-17 ratio ≥ 1.5.TOP2A gene amplification measured by fluorescence in situ hybridization. A total of 25 evaluable patients (15 + 10 in two steps) will be included (Simon's two-stage minimax design). Every nine weeks, response is measured by computed tomography imaging and evaluated according to RECIST 1.1. The primary end-point of the study is progression-free survival. Trial registration Eudract no.2013-001648-79 . … (more)
- Is Part Of:
- BMC cancer. Volume 16:Issue 1(2016)
- Journal:
- BMC cancer
- Issue:
- Volume 16:Issue 1(2016)
- Issue Display:
- Volume 16, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 16
- Issue:
- 1
- Issue Sort Value:
- 2016-0016-0001-0000
- Page Start:
- 1
- Page End:
- 5
- Publication Date:
- 2016-12
- Subjects:
- Cancer -- Periodicals
616.994005 - Journal URLs:
- http://www.biomedcentral.com/bmccancer/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=16 ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s12885-016-2124-5 ↗
- Languages:
- English
- ISSNs:
- 1471-2407
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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