Chinese breast cancer patients with CYP2D6*10 mutant genotypes have a better prognosis with toremifene than with tamoxifen. Issue 2 (30th June 2021)
- Record Type:
- Journal Article
- Title:
- Chinese breast cancer patients with CYP2D6*10 mutant genotypes have a better prognosis with toremifene than with tamoxifen. Issue 2 (30th June 2021)
- Main Title:
- Chinese breast cancer patients with CYP2D6*10 mutant genotypes have a better prognosis with toremifene than with tamoxifen
- Authors:
- Wang, Hongyue
Ma, Xinchi
Zhang, Bin
Zhang, Yaotian
Han, Ning
Wei, Linlin
Sun, Chaonan
Sun, Shichen
Zeng, Xue
Guo, Hong
Li, Yubing
Zhang, Yanyu
Zhao, Jiaming
Qin, Zilan
Liu, Zhuang
Zhang, Na - Abstract:
- Abstract: Purpose: To evaluate the prognosis of estrogen receptor‐positive breast cancer patients with CYP2D6*10 mutant genotypes under tamoxifen or toremifen therapy. Methods: Estrogen receptor‐positive breast cancer patients were selected and CYP2D6*10 genotypes (C/C, C/T, and T/T) were determined by Sanger sequencing. Patients were divided into tamoxifen, toremifene, or tamoxifen + toremifene groups according to prior therapy. The correlation between CYP2D6*10 genotype and disease‐free survival was analyzed. Results: In total, 293 estrogen receptor‐positive breast cancer patients treated with tamoxifen or toremifene between 2008 and 2017 were studied. Median follow‐up was 39 months (10–141). Of these, 107 (36.52%), 112 (38.23%), and 74 (25.26%) patients had C/C, C/T, and T/T genotypes, respectively. Genotype was significantly associated with disease‐free survival in tamoxifen patients. Patients with C/T and T/T genotypes showed worse disease‐free survival than patients with a C/C genotype. Genotype and disease‐free survival in toremifene and tamoxifen+toremifene patients were not correlated. Of patients with a C/T genotype, toremifene or tamoxifen+toremifene groups showed better disease‐free survival than tamoxifen patients. Although disease‐free survival of patients with a T/T genotype in the three groups was not statistically different, tamoxifen patients showed worse disease‐free survival. There was no correlation between different treatments and disease‐free survivalAbstract: Purpose: To evaluate the prognosis of estrogen receptor‐positive breast cancer patients with CYP2D6*10 mutant genotypes under tamoxifen or toremifen therapy. Methods: Estrogen receptor‐positive breast cancer patients were selected and CYP2D6*10 genotypes (C/C, C/T, and T/T) were determined by Sanger sequencing. Patients were divided into tamoxifen, toremifene, or tamoxifen + toremifene groups according to prior therapy. The correlation between CYP2D6*10 genotype and disease‐free survival was analyzed. Results: In total, 293 estrogen receptor‐positive breast cancer patients treated with tamoxifen or toremifene between 2008 and 2017 were studied. Median follow‐up was 39 months (10–141). Of these, 107 (36.52%), 112 (38.23%), and 74 (25.26%) patients had C/C, C/T, and T/T genotypes, respectively. Genotype was significantly associated with disease‐free survival in tamoxifen patients. Patients with C/T and T/T genotypes showed worse disease‐free survival than patients with a C/C genotype. Genotype and disease‐free survival in toremifene and tamoxifen+toremifene patients were not correlated. Of patients with a C/T genotype, toremifene or tamoxifen+toremifene groups showed better disease‐free survival than tamoxifen patients. Although disease‐free survival of patients with a T/T genotype in the three groups was not statistically different, tamoxifen patients showed worse disease‐free survival. There was no correlation between different treatments and disease‐free survival in patients with a C/C genotype. Cox proportional hazard analysis revealed toremifene patients had a better prognosis than tamoxifen patients; toremifene was an independent protective factoremifene for disease‐free survival. Conclusions: Tamoxifen was less effective in patients with CYP2D6*10 C/T and T/T genotypes. Estrogen receptor‐positive breast cancer patients with a CYP2D6*10 mutation genotype have a better prognosis with toremifen than tamoxifen. Abstract : DFS of patients with different genotypes in the TAM, TOR and TAM+TOR group. TAM tamoxifen, TOR toremifene, DFS disease‐free survival, C/C wild‐type CYP2D6 *10, C/T heterozygous CYP2D6 *10, T/T mutant CYP2D6 *10 … (more)
- Is Part Of:
- Asia-Pacific journal of clinical oncology. Volume 18:Issue 2(2022)
- Journal:
- Asia-Pacific journal of clinical oncology
- Issue:
- Volume 18:Issue 2(2022)
- Issue Display:
- Volume 18, Issue 2 (2022)
- Year:
- 2022
- Volume:
- 18
- Issue:
- 2
- Issue Sort Value:
- 2022-0018-0002-0000
- Page Start:
- e148
- Page End:
- e153
- Publication Date:
- 2021-06-30
- Subjects:
- breast cancer -- CYP2D6*10 -- tamoxifen -- toremifene
Oncology -- Pacific Area -- Periodicals
Cancer -- Treatment -- Pacific Area -- Periodicals
Cancer -- Pacific Area -- Periodicals
Cancer -- Treatment -- Periodicals
616.9940095 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1743-7563/issues ↗
http://www.blackwell-synergy.com/openurl?genre=journal&eissn=1743-7563 ↗
http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/ajco ↗ - DOI:
- 10.1111/ajco.13571 ↗
- Languages:
- English
- ISSNs:
- 1743-7555
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1742.260681
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21277.xml