Less Toxic Chemotherapy in Locally Advanced Breast Cancer.
Adult
Aged
Antineoplastic Agents
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Bevacizumab
/ administration & dosage
Breast Neoplasms
/ drug therapy
Combined Modality Therapy
/ adverse effects
Cyclophosphamide
/ administration & dosage
Doxorubicin
/ administration & dosage
Female
Humans
Middle Aged
Paclitaxel
/ administration & dosage
Pilot Projects
Journal
Southern medical journal
ISSN: 1541-8243
Titre abrégé: South Med J
Pays: United States
ID NLM: 0404522
Informations de publication
Date de publication:
11 2020
11 2020
Historique:
entrez:
3
11
2020
pubmed:
4
11
2020
medline:
11
2
2021
Statut:
ppublish
Résumé
Preoperative chemotherapy produces tumor shrinkage in most patients with locally advanced breast cancer, including some pathological complete responses (pCRs). We attempted this using a much less toxic sequential regimen, given with concurrent bevacizumab. Patients with locally advanced breast cancer received 3 intravenous doses each of preoperative sequential liposome encapsulated doxorubicin 25 mg/m Between March 2008 and December 2009, 32 patients received treatment. There was no cardiotoxicity, and other toxicity was mild (no grade 4 or 5 toxicity). No long-term toxicity, including cardiotoxicity, has been observed. Every patient had ≥30% reduction in tumor size; 9 of 31 patients who completed chemotherapy had pCR at operation. Seven years later, 22 of 32 patients remain free of recurrence and 27 of 32 are alive. The preoperative chemotherapy used appears to be comparably effective, but much less toxic than that used in most conventional regimens and should be studied further. Concurrent treatment with bevacizumab (reported separately) did not provide any additional benefit.
Identifiants
pubmed: 33140109
doi: 10.14423/SMJ.0000000000001169
pii: SMJ50854
pmc: PMC8787856
mid: NIHMS1764927
doi:
Substances chimiques
Antineoplastic Agents
0
Bevacizumab
2S9ZZM9Q9V
Doxorubicin
80168379AG
Cyclophosphamide
8N3DW7272P
Paclitaxel
P88XT4IS4D
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
559-563Subventions
Organisme : NCI NIH HHS
ID : P30 CA013148
Pays : United States
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