» Articles » PMID: 19803732

Aerosol Gemcitabine: Preclinical Safety and in Vivo Antitumor Activity in Osteosarcoma-bearing Dogs

Overview
Date 2009 Oct 7
PMID 19803732
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Osteosarcoma is the most common skeletal malignancy in the dog and in young humans. Although chemotherapy improves survival time, death continues to be attributed to metastases. Aerosol delivery can provide a strategy with which to improve the lung drug delivery while reducing systemic toxicity. The purpose of this study is to assess the safety of a regional aerosol approach to chemotherapy delivery in osteosarcoma-bearing dogs, and second, to evaluate the effect of gemcitabine on Fas expression in the pulmonary metastasis.

Methods: We examined the systemic and local effects of aerosol gemcitabine on lung and pulmonary metastasis in this relevant large-animal tumor model using serial laboratory and arterial blood gas analysis and histopathology and immunohistochemistry, respectively.

Results And Conclusions: Six hundred seventy-two 1-h doses of aerosol gemcitabine were delivered. The treatment was well tolerated by these subjects with osteosarcoma (n = 20). Aerosol-treated subjects had metastatic foci that demonstrated extensive, predominately central, intratumoral necrosis. Fas expression was decreased in pulmonary metastases compared to the primary tumor (p = 0.008). After aerosol gemcitabine Fas expression in the metastatic foci was increased compared to lung metastases before treatment (p = 0.0075), and even was higher than the primary tumor (p = 0.025). Increased apoptosis (TUNEL) staining was also detected in aerosol gemcitabine treated metastasis compared to untreated controls (p = 0.028). The results from this pivotal translational study support the concept that aerosol gemcitabine may be useful against pulmonary metastases of osteosarcoma. Additional studies that evaluate the aerosol route of administration of gemcitabine in humans should be safe and are warranted.

Citing Articles

Improving Osteosarcoma Treatment: Comparative Oncology in Action.

Tarone L, Mareschi K, Tirtei E, Giacobino D, Camerino M, Buracco P Life (Basel). 2022; 12(12).

PMID: 36556464 PMC: 9783386. DOI: 10.3390/life12122099.


Osteosarcoma and Metastasis.

Sheng G, Gao Y, Yang Y, Wu H Front Oncol. 2021; 11:780264.

PMID: 34956899 PMC: 8702962. DOI: 10.3389/fonc.2021.780264.


Adoptive Natural Killer Cell Immunotherapy for Canine Osteosarcoma.

Kisseberth W, Lee D Front Vet Sci. 2021; 8:672361.

PMID: 34164452 PMC: 8215197. DOI: 10.3389/fvets.2021.672361.


The Histone Deacetylase Inhibitor Entinostat/Syndax 275 in Osteosarcoma.

Kiany S, Harrison D, Gordon N Adv Exp Med Biol. 2020; 1257:75-83.

PMID: 32483732 DOI: 10.1007/978-3-030-43032-0_7.


Understanding and Modeling Metastasis Biology to Improve Therapeutic Strategies for Combating Osteosarcoma Progression.

Fan T, Roberts R, Lizardo M Front Oncol. 2020; 10:13.

PMID: 32082995 PMC: 7006476. DOI: 10.3389/fonc.2020.00013.


References
1.
Gandhi V, Plunkett W, Du M, Ayres M, Estey E . Prolonged infusion of gemcitabine: clinical and pharmacodynamic studies during a phase I trial in relapsed acute myelogenous leukemia. J Clin Oncol. 2002; 20(3):665-73. DOI: 10.1200/JCO.2002.20.3.665. View

2.
Berg J, Weinstein M, Springfield D, Rand W . Results of surgery and doxorubicin chemotherapy in dogs with osteosarcoma. J Am Vet Med Assoc. 1995; 206(10):1555-60. View

3.
Rodriguez Jr C, Stellrecht C, Gandhi V . Mechanisms for T-cell selective cytotoxicity of arabinosylguanine. Blood. 2003; 102(5):1842-8. DOI: 10.1182/blood-2003-01-0317. View

4.
Jones P, de Lorimier L, Kitchell B, Losonsky J . Gemcitabine as a radiosensitizer for nonresectable feline oral squamous cell carcinoma. J Am Anim Hosp Assoc. 2003; 39(5):463-7. DOI: 10.5326/0390463. View

5.
Hawkins D, Arndt C . Pattern of disease recurrence and prognostic factors in patients with osteosarcoma treated with contemporary chemotherapy. Cancer. 2003; 98(11):2447-56. DOI: 10.1002/cncr.11799. View