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Prospective Study Testing a Simplified Paclitaxel Premedication Regimen in Patients with Early Breast Cancer

BACKGROUND: In early trials, hypersensitivity reactions (HSRs) to paclitaxel were common, thus prompting the administration of antihistamines and corticosteroids before every paclitaxel dose. We tested the safety of omitting corticosteroids after cycle 2 during the paclitaxel portion of the dose‐den...

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Autores principales: Barroso‐Sousa, Romualdo, Vaz‐Luis, Ines, Di Meglio, Antonio, Hu, Jiani, Li, Tianyu, Rees, Rebecca, Sinclair, Natalie, Milisits, Lindsey, Leone, Jose Pablo, Constantine, Michael, Faggen, Meredith, Briccetti, Frederick, Block, Caroline, Partridge, Ann, Burstein, Harold, Waks, Adrienne G., Tayob, Nabihah, Trippa, Lorenzo, Tolaney, Sara M., Hassett, Michael J., Winer, Eric P., Lin, Nancy U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571744/
https://www.ncbi.nlm.nih.gov/pubmed/34472667
http://dx.doi.org/10.1002/onco.13960
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author Barroso‐Sousa, Romualdo
Vaz‐Luis, Ines
Di Meglio, Antonio
Hu, Jiani
Li, Tianyu
Rees, Rebecca
Sinclair, Natalie
Milisits, Lindsey
Leone, Jose Pablo
Constantine, Michael
Faggen, Meredith
Briccetti, Frederick
Block, Caroline
Partridge, Ann
Burstein, Harold
Waks, Adrienne G.
Tayob, Nabihah
Trippa, Lorenzo
Tolaney, Sara M.
Hassett, Michael J.
Winer, Eric P.
Lin, Nancy U.
author_facet Barroso‐Sousa, Romualdo
Vaz‐Luis, Ines
Di Meglio, Antonio
Hu, Jiani
Li, Tianyu
Rees, Rebecca
Sinclair, Natalie
Milisits, Lindsey
Leone, Jose Pablo
Constantine, Michael
Faggen, Meredith
Briccetti, Frederick
Block, Caroline
Partridge, Ann
Burstein, Harold
Waks, Adrienne G.
Tayob, Nabihah
Trippa, Lorenzo
Tolaney, Sara M.
Hassett, Michael J.
Winer, Eric P.
Lin, Nancy U.
author_sort Barroso‐Sousa, Romualdo
collection PubMed
description BACKGROUND: In early trials, hypersensitivity reactions (HSRs) to paclitaxel were common, thus prompting the administration of antihistamines and corticosteroids before every paclitaxel dose. We tested the safety of omitting corticosteroids after cycle 2 during the paclitaxel portion of the dose‐dense (DD) doxorubicin‐cyclophosphamide (AC)–paclitaxel regimen. PATIENTS, MATERIALS, AND METHODS: In this prospective, single‐arm study, patients who completed four cycles of DD‐AC for stage I–III breast cancer received paclitaxel 175 mg/m(2) every 2 weeks for four cycles. Patients received a standard premedication protocol containing dexamethasone, diphenhydramine, and a histamine H2 blocker prior to the first two paclitaxel cycles. Dexamethasone was omitted in cycles three and four if there were no HSRs in previous cycles. We estimated the rate of grade 3–4 HSRs. RESULTS: Among 127 patients enrolled, 125 received more than one dose of protocol therapy and are included in the analysis. Fourteen (11.2%; 90% confidence interval, 6.9%–20.0%) patients had any‐grade HSRs, for a total of 22 (4.5%; 3.1%–6.4%) HSRs over 486 paclitaxel cycles. Any‐grade HSRs occurred in 1.6% (0.3%–5.0%), 6.5% (3.3%–11.3%), 7.4% (3.9%–12.5%), and 2.6% (0.7%–6.6%) of patients after paclitaxel cycles 1, 2, 3, and 4, respectively. Dexamethasone use was decreased by 92.8% in cycles 3 and 4. Only one patient experienced grade 3 HSR in cycles 3 or 4, for a rate of grade 3/4 HSR 0.4% (0.02%–2.0%) (1/237 paclitaxel infusions). That patient had grade 2 HSR during cycle 2, and the subsequent grade 3 event occurred despite usual dexamethasone premedication. A sensitivity analysis restricted to patients not known to have received dexamethasone in cycles 3 and 4 found that any‐grade HSRs occurred in 2.7% (3/111; 0.7%–6.8%) and 0.9% (1/109; 0.05%–4.3%) of patients in cycle 3 and 4, respectively. CONCLUSION: Corticosteroid premedication can be safely omitted in cycles 3 and 4 of dose‐dense paclitaxel if HSRs are not observed during cycles 1 and 2. IMPLICATIONS FOR PRACTICE: Because of the potential for hypersensitivity reactions (HSRs) to paclitaxel, corticosteroids are routinely prescribed prior to each dose, on an indefinite basis. This prospective study, including 125 patients treated with 486 paclitaxel cycles, demonstrates that corticosteroids can be safely omitted in future cycles if HSRs did not occur during cycles 1 and 2 of paclitaxel and that this strategy reduces the use of corticosteroids in cycles 3 and 4 by 92.8% relative to current standard of care.
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spelling pubmed-85717442021-11-10 Prospective Study Testing a Simplified Paclitaxel Premedication Regimen in Patients with Early Breast Cancer Barroso‐Sousa, Romualdo Vaz‐Luis, Ines Di Meglio, Antonio Hu, Jiani Li, Tianyu Rees, Rebecca Sinclair, Natalie Milisits, Lindsey Leone, Jose Pablo Constantine, Michael Faggen, Meredith Briccetti, Frederick Block, Caroline Partridge, Ann Burstein, Harold Waks, Adrienne G. Tayob, Nabihah Trippa, Lorenzo Tolaney, Sara M. Hassett, Michael J. Winer, Eric P. Lin, Nancy U. Oncologist Breast Cancer BACKGROUND: In early trials, hypersensitivity reactions (HSRs) to paclitaxel were common, thus prompting the administration of antihistamines and corticosteroids before every paclitaxel dose. We tested the safety of omitting corticosteroids after cycle 2 during the paclitaxel portion of the dose‐dense (DD) doxorubicin‐cyclophosphamide (AC)–paclitaxel regimen. PATIENTS, MATERIALS, AND METHODS: In this prospective, single‐arm study, patients who completed four cycles of DD‐AC for stage I–III breast cancer received paclitaxel 175 mg/m(2) every 2 weeks for four cycles. Patients received a standard premedication protocol containing dexamethasone, diphenhydramine, and a histamine H2 blocker prior to the first two paclitaxel cycles. Dexamethasone was omitted in cycles three and four if there were no HSRs in previous cycles. We estimated the rate of grade 3–4 HSRs. RESULTS: Among 127 patients enrolled, 125 received more than one dose of protocol therapy and are included in the analysis. Fourteen (11.2%; 90% confidence interval, 6.9%–20.0%) patients had any‐grade HSRs, for a total of 22 (4.5%; 3.1%–6.4%) HSRs over 486 paclitaxel cycles. Any‐grade HSRs occurred in 1.6% (0.3%–5.0%), 6.5% (3.3%–11.3%), 7.4% (3.9%–12.5%), and 2.6% (0.7%–6.6%) of patients after paclitaxel cycles 1, 2, 3, and 4, respectively. Dexamethasone use was decreased by 92.8% in cycles 3 and 4. Only one patient experienced grade 3 HSR in cycles 3 or 4, for a rate of grade 3/4 HSR 0.4% (0.02%–2.0%) (1/237 paclitaxel infusions). That patient had grade 2 HSR during cycle 2, and the subsequent grade 3 event occurred despite usual dexamethasone premedication. A sensitivity analysis restricted to patients not known to have received dexamethasone in cycles 3 and 4 found that any‐grade HSRs occurred in 2.7% (3/111; 0.7%–6.8%) and 0.9% (1/109; 0.05%–4.3%) of patients in cycle 3 and 4, respectively. CONCLUSION: Corticosteroid premedication can be safely omitted in cycles 3 and 4 of dose‐dense paclitaxel if HSRs are not observed during cycles 1 and 2. IMPLICATIONS FOR PRACTICE: Because of the potential for hypersensitivity reactions (HSRs) to paclitaxel, corticosteroids are routinely prescribed prior to each dose, on an indefinite basis. This prospective study, including 125 patients treated with 486 paclitaxel cycles, demonstrates that corticosteroids can be safely omitted in future cycles if HSRs did not occur during cycles 1 and 2 of paclitaxel and that this strategy reduces the use of corticosteroids in cycles 3 and 4 by 92.8% relative to current standard of care. John Wiley & Sons, Inc. 2021-09-24 2021-11 /pmc/articles/PMC8571744/ /pubmed/34472667 http://dx.doi.org/10.1002/onco.13960 Text en © 2021 The Authors. The Oncologist published by Wiley Periodicals LLC on behalf of AlphaMed Press. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Breast Cancer
Barroso‐Sousa, Romualdo
Vaz‐Luis, Ines
Di Meglio, Antonio
Hu, Jiani
Li, Tianyu
Rees, Rebecca
Sinclair, Natalie
Milisits, Lindsey
Leone, Jose Pablo
Constantine, Michael
Faggen, Meredith
Briccetti, Frederick
Block, Caroline
Partridge, Ann
Burstein, Harold
Waks, Adrienne G.
Tayob, Nabihah
Trippa, Lorenzo
Tolaney, Sara M.
Hassett, Michael J.
Winer, Eric P.
Lin, Nancy U.
Prospective Study Testing a Simplified Paclitaxel Premedication Regimen in Patients with Early Breast Cancer
title Prospective Study Testing a Simplified Paclitaxel Premedication Regimen in Patients with Early Breast Cancer
title_full Prospective Study Testing a Simplified Paclitaxel Premedication Regimen in Patients with Early Breast Cancer
title_fullStr Prospective Study Testing a Simplified Paclitaxel Premedication Regimen in Patients with Early Breast Cancer
title_full_unstemmed Prospective Study Testing a Simplified Paclitaxel Premedication Regimen in Patients with Early Breast Cancer
title_short Prospective Study Testing a Simplified Paclitaxel Premedication Regimen in Patients with Early Breast Cancer
title_sort prospective study testing a simplified paclitaxel premedication regimen in patients with early breast cancer
topic Breast Cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571744/
https://www.ncbi.nlm.nih.gov/pubmed/34472667
http://dx.doi.org/10.1002/onco.13960
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