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Outcome of eribulin as a late treatment line for Thai metastatic breast cancer patients

BACKGROUND: We report the safety and efficacy of eribulin as a late treatment line in Thai metastatic breast cancer (MBC) patients. PATIENTS AND METHODS: A total of 30 MBC patients treated with eribulin between January 2014 and January 2017 were retrospectively analyzed. The patients were scheduled...

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Autores principales: Ditsatham, Chagkrit, Chitapanarux, Imjai, Somwangprasert, Areewan, Watcharachan, Kirati, Wongmaneerung, Panchaporn, Charoentum, Chaiyut, Chewaskulyong, Busyamas, Chakrabandhu, Somvilai, Onchan, Wimrak, Teeyasuntranonn, Anongnart, Sripan, Patumrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074808/
https://www.ncbi.nlm.nih.gov/pubmed/30104885
http://dx.doi.org/10.2147/OTT.S166399
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author Ditsatham, Chagkrit
Chitapanarux, Imjai
Somwangprasert, Areewan
Watcharachan, Kirati
Wongmaneerung, Panchaporn
Charoentum, Chaiyut
Chewaskulyong, Busyamas
Chakrabandhu, Somvilai
Onchan, Wimrak
Teeyasuntranonn, Anongnart
Sripan, Patumrat
author_facet Ditsatham, Chagkrit
Chitapanarux, Imjai
Somwangprasert, Areewan
Watcharachan, Kirati
Wongmaneerung, Panchaporn
Charoentum, Chaiyut
Chewaskulyong, Busyamas
Chakrabandhu, Somvilai
Onchan, Wimrak
Teeyasuntranonn, Anongnart
Sripan, Patumrat
author_sort Ditsatham, Chagkrit
collection PubMed
description BACKGROUND: We report the safety and efficacy of eribulin as a late treatment line in Thai metastatic breast cancer (MBC) patients. PATIENTS AND METHODS: A total of 30 MBC patients treated with eribulin between January 2014 and January 2017 were retrospectively analyzed. The patients were scheduled to receive 1.4 mg/m(2) of eribulin on day 1, day 8 and subsequently every 21 days. All patients had previously received at least three chemotherapy regimens including anthracycline and taxane. Response rate and progression-free survival (PFS) were analyzed. RESULTS: The median age was 56 years (range, 40–74 years), with a median follow-up time of 5.7 months (range, 0.2–25 months). The overall response rate was 30% (nine patients): four patients had triple-negative breast cancer, three patients had luminal B breast cancer and two patients had luminal A breast cancer. The median PFS was 2.9 months (range, 0.2–14 months). The median number of previous chemotherapy regimens was 4 (range, 3–9). Univariate analysis showed that the number of regimens (four or fewer) prior to eribulin was statistically associated with superior PFS (P = 0.009). Multivariate analysis also showed similar statistical association between number of prior regimens (four or fewer) and better PFS adjusted by age group (≥50 years; hazard ratio = 1.29; 95% CI: 1.0–1.65; P = 0.046). There were no toxic deaths or grade 4 toxicities. Nine (30%) patients had grade 3 anemia toxicities, and the other common toxicities were leukopenia and neutropenia. Four (13%) patients required dose reduction and 16 (53%) patients required dose delay because of toxicities. CONCLUSION: Eribulin is an effective drug for heavily pretreated MBC patients with tolerable toxicities. The benefit was superior in patients who received fewer than four previous chemotherapy regimens.
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spelling pubmed-60748082018-08-13 Outcome of eribulin as a late treatment line for Thai metastatic breast cancer patients Ditsatham, Chagkrit Chitapanarux, Imjai Somwangprasert, Areewan Watcharachan, Kirati Wongmaneerung, Panchaporn Charoentum, Chaiyut Chewaskulyong, Busyamas Chakrabandhu, Somvilai Onchan, Wimrak Teeyasuntranonn, Anongnart Sripan, Patumrat Onco Targets Ther Original Research BACKGROUND: We report the safety and efficacy of eribulin as a late treatment line in Thai metastatic breast cancer (MBC) patients. PATIENTS AND METHODS: A total of 30 MBC patients treated with eribulin between January 2014 and January 2017 were retrospectively analyzed. The patients were scheduled to receive 1.4 mg/m(2) of eribulin on day 1, day 8 and subsequently every 21 days. All patients had previously received at least three chemotherapy regimens including anthracycline and taxane. Response rate and progression-free survival (PFS) were analyzed. RESULTS: The median age was 56 years (range, 40–74 years), with a median follow-up time of 5.7 months (range, 0.2–25 months). The overall response rate was 30% (nine patients): four patients had triple-negative breast cancer, three patients had luminal B breast cancer and two patients had luminal A breast cancer. The median PFS was 2.9 months (range, 0.2–14 months). The median number of previous chemotherapy regimens was 4 (range, 3–9). Univariate analysis showed that the number of regimens (four or fewer) prior to eribulin was statistically associated with superior PFS (P = 0.009). Multivariate analysis also showed similar statistical association between number of prior regimens (four or fewer) and better PFS adjusted by age group (≥50 years; hazard ratio = 1.29; 95% CI: 1.0–1.65; P = 0.046). There were no toxic deaths or grade 4 toxicities. Nine (30%) patients had grade 3 anemia toxicities, and the other common toxicities were leukopenia and neutropenia. Four (13%) patients required dose reduction and 16 (53%) patients required dose delay because of toxicities. CONCLUSION: Eribulin is an effective drug for heavily pretreated MBC patients with tolerable toxicities. The benefit was superior in patients who received fewer than four previous chemotherapy regimens. Dove Medical Press 2018-07-31 /pmc/articles/PMC6074808/ /pubmed/30104885 http://dx.doi.org/10.2147/OTT.S166399 Text en © 2018 Ditsatham et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Ditsatham, Chagkrit
Chitapanarux, Imjai
Somwangprasert, Areewan
Watcharachan, Kirati
Wongmaneerung, Panchaporn
Charoentum, Chaiyut
Chewaskulyong, Busyamas
Chakrabandhu, Somvilai
Onchan, Wimrak
Teeyasuntranonn, Anongnart
Sripan, Patumrat
Outcome of eribulin as a late treatment line for Thai metastatic breast cancer patients
title Outcome of eribulin as a late treatment line for Thai metastatic breast cancer patients
title_full Outcome of eribulin as a late treatment line for Thai metastatic breast cancer patients
title_fullStr Outcome of eribulin as a late treatment line for Thai metastatic breast cancer patients
title_full_unstemmed Outcome of eribulin as a late treatment line for Thai metastatic breast cancer patients
title_short Outcome of eribulin as a late treatment line for Thai metastatic breast cancer patients
title_sort outcome of eribulin as a late treatment line for thai metastatic breast cancer patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074808/
https://www.ncbi.nlm.nih.gov/pubmed/30104885
http://dx.doi.org/10.2147/OTT.S166399
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