Prospective Long-Term Follow-Up of Pulmonary Diffusion Capacity Reduction Caused by Dose-Dense Chemotherapy in Patients with Breast Cancer.


Journal

Journal of oncology
ISSN: 1687-8450
Titre abrégé: J Oncol
Pays: Egypt
ID NLM: 101496537

Informations de publication

Date de publication:
2019
Historique:
received: 25 12 2018
revised: 05 08 2019
accepted: 04 09 2019
entrez: 28 11 2019
pubmed: 28 11 2019
medline: 28 11 2019
Statut: epublish

Résumé

Our previous study of pulmonary function in 34 patients with early breast cancer without preexisting lung disease showed that anthracycline- and taxane-based adjuvant dose-dense chemotherapy (DDC) caused a significant 16.4% mean reduction in carbon monoxide diffusing capacity (DLCO). The present study reports the pulmonary and oncological outcomes of these patients on long-term follow-up. The primary endpoint was DLCO measured by the pulmonary function test (PFT) performed at a median of 27 months after DDC (range, 8-97) in 25 patients without disease recurrence. DLCO values were recorded as a percentage of predicted values according to age, height, and hemoglobin level and analyzed relative to baseline pre-DDC DLCO values. The secondary endpoints were symptoms, additional therapies, and cancer outcomes during a median of 11 years' follow-up (range, 4.4-11.4). A longitudinal general linear model showed significant effects of time on DLCO and its trend ( The significant reduction in DLCO seen after DDC in patients with potentially curable breast cancer is evident years afterwards, especially in older patients. While most patients partly recover, some will have a lasting symptomatic DLCO impairment.

Sections du résumé

BACKGROUND BACKGROUND
Our previous study of pulmonary function in 34 patients with early breast cancer without preexisting lung disease showed that anthracycline- and taxane-based adjuvant dose-dense chemotherapy (DDC) caused a significant 16.4% mean reduction in carbon monoxide diffusing capacity (DLCO). The present study reports the pulmonary and oncological outcomes of these patients on long-term follow-up.
PATIENTS AND METHODS METHODS
The primary endpoint was DLCO measured by the pulmonary function test (PFT) performed at a median of 27 months after DDC (range, 8-97) in 25 patients without disease recurrence. DLCO values were recorded as a percentage of predicted values according to age, height, and hemoglobin level and analyzed relative to baseline pre-DDC DLCO values. The secondary endpoints were symptoms, additional therapies, and cancer outcomes during a median of 11 years' follow-up (range, 4.4-11.4).
RESULTS RESULTS
A longitudinal general linear model showed significant effects of time on DLCO and its trend (
CONCLUSIONS CONCLUSIONS
The significant reduction in DLCO seen after DDC in patients with potentially curable breast cancer is evident years afterwards, especially in older patients. While most patients partly recover, some will have a lasting symptomatic DLCO impairment.

Identifiants

pubmed: 31772578
doi: 10.1155/2019/2584859
pmc: PMC6854974
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2584859

Informations de copyright

Copyright © 2019 Yosef Landman et al.

Déclaration de conflit d'intérêts

The authors have declared no conflicts of interest.

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Auteurs

Yosef Landman (Y)

Institute of Oncology, Davidoff Cancer Center, Rabin Medical Center, Petach Tikva, Israel.

Salomon Marcello Stemmer (SM)

Institute of Oncology, Davidoff Cancer Center, Rabin Medical Center, Petach Tikva, Israel.
Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Aaron Sulkes (A)

Institute of Oncology, Davidoff Cancer Center, Rabin Medical Center, Petach Tikva, Israel.
Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Victoria Neiman (V)

Institute of Oncology, Davidoff Cancer Center, Rabin Medical Center, Petach Tikva, Israel.

Tal Granot (T)

Institute of Oncology, Davidoff Cancer Center, Rabin Medical Center, Petach Tikva, Israel.

Daniel Hendler (D)

Institute of Oncology, Davidoff Cancer Center, Rabin Medical Center, Petach Tikva, Israel.

Mordechai Reuven Kramer (MR)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Institute of Pulmonology, Rabin Medical Center, Petach Tikva, Israel.

Karen Gelmon (K)

Department of Medical Oncology, British Columbia Cancer Agency, Vancouver, Canada.

Rinat Yerushalmi (R)

Institute of Oncology, Davidoff Cancer Center, Rabin Medical Center, Petach Tikva, Israel.
Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Classifications MeSH