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Adjuvant trastuzumab and vinorelbine for early-stage HER2+ breast cancer

BACKGROUND: The single-arm phase II APT trial established trastuzumab and paclitaxel (TH) as the standard adjuvant regimen for small human epidermal growth factor receptor 2 (HER2+) tumors. However, paclitaxel causes alopecia and has high rates of neuropathy and hypersensitivity reactions. In patien...

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Autores principales: McLaughlin, Shannon, Nakajima, Erika, Bar, Yael, Hutchinson, Jennifer A., Shin, Jennifer, Moy, Beverly, Isakoff, Steven J., Bardia, Aditya, Kuter, Irene, Spring, Laura M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837262/
https://www.ncbi.nlm.nih.gov/pubmed/36643653
http://dx.doi.org/10.1177/17588359221146133
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author McLaughlin, Shannon
Nakajima, Erika
Bar, Yael
Hutchinson, Jennifer A.
Shin, Jennifer
Moy, Beverly
Isakoff, Steven J.
Bardia, Aditya
Kuter, Irene
Spring, Laura M.
author_facet McLaughlin, Shannon
Nakajima, Erika
Bar, Yael
Hutchinson, Jennifer A.
Shin, Jennifer
Moy, Beverly
Isakoff, Steven J.
Bardia, Aditya
Kuter, Irene
Spring, Laura M.
author_sort McLaughlin, Shannon
collection PubMed
description BACKGROUND: The single-arm phase II APT trial established trastuzumab and paclitaxel (TH) as the standard adjuvant regimen for small human epidermal growth factor receptor 2 (HER2+) tumors. However, paclitaxel causes alopecia and has high rates of neuropathy and hypersensitivity reactions. In patients with metastatic HER2+ breast cancer (BC), the combination of trastuzumab and vinorelbine (TV) is effective and well tolerated. There is a need for alternative non-anthracycline/taxane-based regimens for patients with HER2+ early-stage BC, especially for those with contraindications or who wish to avoid side effects of taxane-based regimens. Here we describe our institutional experience with adjuvant TV for patients with early-stage HER2+ BC. METHODS: Clinicopathological characteristics, treatment details, and outcomes of patients with localized HER2+ BC treated with adjuvant TV from 2007 to 2021 at a large academic medical institution were collected. Study endpoints included invasive disease-free survival (IDFS), overall survival (OS), and safety/tolerability. IDFS and OS were measured from start date of TV treatment to date of event/last follow-up and date of death/last follow-up, respectively. RESULTS: A total of 30 patients were treated with TV. All patients received trastuzumab at standard dosing and vinorelbine at a starting dose of 25 mg/m(2) either on days 1/8 or on days 1/8/21 (weekly) of a 21-day cycle with four planned cycles. Median age at diagnosis was 59 years (range: 36–81). 90.3% of patients had anatomic pathologic stage IA BC and 9.7% stage IIA BC. Of the 30 patients, 24 of them opted to pursue TV due to concerns related to alopecia, neuropathy, and other toxicities, and 6 switched from treatment with TH to TV due to toxicities. Eight patients experienced neutropenia with no cases of febrile neutropenia. No patients experienced alopecia or long-term neuropathy. With a median follow-up of 68 months (5.7 years), the 5-year IDFS rate was 90.9%, with one local and one distant recurrence. The 5-year OS was 100%. CONCLUSIONS: Trastuzumab in combination with vinorelbine in the adjuvant, early-stage setting for low-risk HER2+ BC demonstrated clinical efficacy and appeared to be well tolerated. TV warrants further evaluation as an alternative regimen to TH for patients with early-stage HER2+ BC.
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spelling pubmed-98372622023-01-14 Adjuvant trastuzumab and vinorelbine for early-stage HER2+ breast cancer McLaughlin, Shannon Nakajima, Erika Bar, Yael Hutchinson, Jennifer A. Shin, Jennifer Moy, Beverly Isakoff, Steven J. Bardia, Aditya Kuter, Irene Spring, Laura M. Ther Adv Med Oncol Original Research BACKGROUND: The single-arm phase II APT trial established trastuzumab and paclitaxel (TH) as the standard adjuvant regimen for small human epidermal growth factor receptor 2 (HER2+) tumors. However, paclitaxel causes alopecia and has high rates of neuropathy and hypersensitivity reactions. In patients with metastatic HER2+ breast cancer (BC), the combination of trastuzumab and vinorelbine (TV) is effective and well tolerated. There is a need for alternative non-anthracycline/taxane-based regimens for patients with HER2+ early-stage BC, especially for those with contraindications or who wish to avoid side effects of taxane-based regimens. Here we describe our institutional experience with adjuvant TV for patients with early-stage HER2+ BC. METHODS: Clinicopathological characteristics, treatment details, and outcomes of patients with localized HER2+ BC treated with adjuvant TV from 2007 to 2021 at a large academic medical institution were collected. Study endpoints included invasive disease-free survival (IDFS), overall survival (OS), and safety/tolerability. IDFS and OS were measured from start date of TV treatment to date of event/last follow-up and date of death/last follow-up, respectively. RESULTS: A total of 30 patients were treated with TV. All patients received trastuzumab at standard dosing and vinorelbine at a starting dose of 25 mg/m(2) either on days 1/8 or on days 1/8/21 (weekly) of a 21-day cycle with four planned cycles. Median age at diagnosis was 59 years (range: 36–81). 90.3% of patients had anatomic pathologic stage IA BC and 9.7% stage IIA BC. Of the 30 patients, 24 of them opted to pursue TV due to concerns related to alopecia, neuropathy, and other toxicities, and 6 switched from treatment with TH to TV due to toxicities. Eight patients experienced neutropenia with no cases of febrile neutropenia. No patients experienced alopecia or long-term neuropathy. With a median follow-up of 68 months (5.7 years), the 5-year IDFS rate was 90.9%, with one local and one distant recurrence. The 5-year OS was 100%. CONCLUSIONS: Trastuzumab in combination with vinorelbine in the adjuvant, early-stage setting for low-risk HER2+ BC demonstrated clinical efficacy and appeared to be well tolerated. TV warrants further evaluation as an alternative regimen to TH for patients with early-stage HER2+ BC. SAGE Publications 2023-01-10 /pmc/articles/PMC9837262/ /pubmed/36643653 http://dx.doi.org/10.1177/17588359221146133 Text en © The Author(s), 2023. https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
McLaughlin, Shannon
Nakajima, Erika
Bar, Yael
Hutchinson, Jennifer A.
Shin, Jennifer
Moy, Beverly
Isakoff, Steven J.
Bardia, Aditya
Kuter, Irene
Spring, Laura M.
Adjuvant trastuzumab and vinorelbine for early-stage HER2+ breast cancer
title Adjuvant trastuzumab and vinorelbine for early-stage HER2+ breast cancer
title_full Adjuvant trastuzumab and vinorelbine for early-stage HER2+ breast cancer
title_fullStr Adjuvant trastuzumab and vinorelbine for early-stage HER2+ breast cancer
title_full_unstemmed Adjuvant trastuzumab and vinorelbine for early-stage HER2+ breast cancer
title_short Adjuvant trastuzumab and vinorelbine for early-stage HER2+ breast cancer
title_sort adjuvant trastuzumab and vinorelbine for early-stage her2+ breast cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837262/
https://www.ncbi.nlm.nih.gov/pubmed/36643653
http://dx.doi.org/10.1177/17588359221146133
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