Gemcitabine and docetaxel combination chemotherapy is the standard of care for patients with unresectable recurrent or metastatic leiomyosarcoma of the uterus. Although they are generally well-tolerated agents, they can also cause severe and life-threatening pulmonary toxicities. Here, we describe a case of grade 4 pneumonitis due to gemcitabine and docetaxel in a 74-year-old woman with recurrent, metastatic uterine leiomyosarcoma. Despite early recognition of chemotherapy-induced lung injury and early administration of corticosteroid, she developed noncardiogenic pulmonary edema, diffuse alveolar hemorrhage, and acute respiratory distress syndrome. She required multiple intubations and a tracheostomy. Physicians should not only be aware of...
Docetaxel is a semisynthetic cytostatic drug that belongs to the family of taxoids. Docetaxel inhibi...
Interstitial lung disease associated with docetaxel in a patient treated for breast cancer — a case ...
The aim of this phase I/II dose escalating study was to establish the maximum tolerated dose (MTD) o...
Pneumonitis is a rare but serious complication of docetaxel treatment. We report a 63-year-old woman...
Development of pulmonary infiltrates with respiratory symptoms in patients with advanced cancer pres...
Gemcitabine is a chemotherapy agent that may cause unpredictable side effects. In this report, we de...
Gemcitabine is a nucleoside analog that has been increasingly used in the chemotherapy of solide tum...
Background: Pulmonary toxicity is a well-known complication observed with several anticancer drugs. ...
Gemcitabine was introduced into clinical practice in 1989. This purine analogue anti-metabolite has ...
Incidence of diffuse alveolar damage is rarely seen after administration of docetaxel used alone or ...
Gemcitabine is a chemotherapeutic agent used for the treatment of a number of malignancies. Although...
Abstract Taxane‐induced pneumotoxicity is rare. However, 1–5% of patients taking docetaxel may devel...
Introduction Gemcitabine is a chemotherapeutic agent frequently used by for the treatment of several...
Docetaxel has proven effective in many solid tumors, including breast cancer. Hypersensitivity react...
Several chemotherapeutic agents are known to develop pulmonary toxicities in cancer patients, althou...
Docetaxel is a semisynthetic cytostatic drug that belongs to the family of taxoids. Docetaxel inhibi...
Interstitial lung disease associated with docetaxel in a patient treated for breast cancer — a case ...
The aim of this phase I/II dose escalating study was to establish the maximum tolerated dose (MTD) o...
Pneumonitis is a rare but serious complication of docetaxel treatment. We report a 63-year-old woman...
Development of pulmonary infiltrates with respiratory symptoms in patients with advanced cancer pres...
Gemcitabine is a chemotherapy agent that may cause unpredictable side effects. In this report, we de...
Gemcitabine is a nucleoside analog that has been increasingly used in the chemotherapy of solide tum...
Background: Pulmonary toxicity is a well-known complication observed with several anticancer drugs. ...
Gemcitabine was introduced into clinical practice in 1989. This purine analogue anti-metabolite has ...
Incidence of diffuse alveolar damage is rarely seen after administration of docetaxel used alone or ...
Gemcitabine is a chemotherapeutic agent used for the treatment of a number of malignancies. Although...
Abstract Taxane‐induced pneumotoxicity is rare. However, 1–5% of patients taking docetaxel may devel...
Introduction Gemcitabine is a chemotherapeutic agent frequently used by for the treatment of several...
Docetaxel has proven effective in many solid tumors, including breast cancer. Hypersensitivity react...
Several chemotherapeutic agents are known to develop pulmonary toxicities in cancer patients, althou...
Docetaxel is a semisynthetic cytostatic drug that belongs to the family of taxoids. Docetaxel inhibi...
Interstitial lung disease associated with docetaxel in a patient treated for breast cancer — a case ...
The aim of this phase I/II dose escalating study was to establish the maximum tolerated dose (MTD) o...