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Relative dose intensity delivered to patients with early breast cancer: Canadian experience

Adjuvant chemotherapy for early breast cancer improves disease-free and overall survival in pre- and postmenopausal women. The importance of maintaining relative dose intensity (rdi) is well-known; however, little information is available from routine clinical practice regarding how well dose intens...

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Autores principales: Raza, S., Welch, S., Younus, J.
Formato: Texto
Lenguaje:English
Publicado: Multimed Inc. 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2794674/
https://www.ncbi.nlm.nih.gov/pubmed/20016741
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author Raza, S.
Welch, S.
Younus, J.
author_facet Raza, S.
Welch, S.
Younus, J.
author_sort Raza, S.
collection PubMed
description Adjuvant chemotherapy for early breast cancer improves disease-free and overall survival in pre- and postmenopausal women. The importance of maintaining relative dose intensity (rdi) is well-known; however, little information is available from routine clinical practice regarding how well dose intensity is maintained with modern chemotherapy regimens. In a retrospective review of patients undergoing chemotherapy for early breast cancer at a single institution in Canada from January 2006 to November 2007, a total of 263 patients received one of the following regimens: ac-t [doxorubicin (Adriamycin: Pharmacia, Kalamazoo, MI, U.S.A.)–cyclophosphamide, paclitaxel (Taxol: Bristol–Myers Squibb, Princeton, NJ, U.S.A.)]; fec-100 (5-fluorouracil–epirubicin–cyclophosphamide); fec-d (5-fluorouracil–epirubicin–cyclophosphamide, docetaxel). Overall, only 14.4% of patients had a rdi less than 85%. Dose delay or reduction (or both) occurred in 46%, 37%, and 20% of patients receiving fec-100, ac-t, and fec-d respectively. Optimal rdi was delivered to 96%, 95%, and 70.7% of patients for ac-t, fec-d and fec-100 regimens respectively. Patients over 65 years of age accounted for 14% of the total cohort and were more likely to receive a suboptimal rdi than were patients younger than 65 years of age (35% vs. 6.6%). Optimal chemotherapy rdi (>85%) for early breast cancer can be achieved at an academic cancer centre. This goal is less often accomplished in elderly patients, and thus a proactive approach is required for managing toxicity in that population.
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spelling pubmed-27946742009-12-16 Relative dose intensity delivered to patients with early breast cancer: Canadian experience Raza, S. Welch, S. Younus, J. Curr Oncol Medical Oncology Adjuvant chemotherapy for early breast cancer improves disease-free and overall survival in pre- and postmenopausal women. The importance of maintaining relative dose intensity (rdi) is well-known; however, little information is available from routine clinical practice regarding how well dose intensity is maintained with modern chemotherapy regimens. In a retrospective review of patients undergoing chemotherapy for early breast cancer at a single institution in Canada from January 2006 to November 2007, a total of 263 patients received one of the following regimens: ac-t [doxorubicin (Adriamycin: Pharmacia, Kalamazoo, MI, U.S.A.)–cyclophosphamide, paclitaxel (Taxol: Bristol–Myers Squibb, Princeton, NJ, U.S.A.)]; fec-100 (5-fluorouracil–epirubicin–cyclophosphamide); fec-d (5-fluorouracil–epirubicin–cyclophosphamide, docetaxel). Overall, only 14.4% of patients had a rdi less than 85%. Dose delay or reduction (or both) occurred in 46%, 37%, and 20% of patients receiving fec-100, ac-t, and fec-d respectively. Optimal rdi was delivered to 96%, 95%, and 70.7% of patients for ac-t, fec-d and fec-100 regimens respectively. Patients over 65 years of age accounted for 14% of the total cohort and were more likely to receive a suboptimal rdi than were patients younger than 65 years of age (35% vs. 6.6%). Optimal chemotherapy rdi (>85%) for early breast cancer can be achieved at an academic cancer centre. This goal is less often accomplished in elderly patients, and thus a proactive approach is required for managing toxicity in that population. Multimed Inc. 2009-12 /pmc/articles/PMC2794674/ /pubmed/20016741 Text en 2009 Multimed Inc. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Medical Oncology
Raza, S.
Welch, S.
Younus, J.
Relative dose intensity delivered to patients with early breast cancer: Canadian experience
title Relative dose intensity delivered to patients with early breast cancer: Canadian experience
title_full Relative dose intensity delivered to patients with early breast cancer: Canadian experience
title_fullStr Relative dose intensity delivered to patients with early breast cancer: Canadian experience
title_full_unstemmed Relative dose intensity delivered to patients with early breast cancer: Canadian experience
title_short Relative dose intensity delivered to patients with early breast cancer: Canadian experience
title_sort relative dose intensity delivered to patients with early breast cancer: canadian experience
topic Medical Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2794674/
https://www.ncbi.nlm.nih.gov/pubmed/20016741
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