Gemcitabine-Induced Pulmonary Toxicity: A Case Report of Pulmonary Veno-Occlusive Disease

Introduction Gemcitabine is a chemotherapeutic agent frequently used by for the treatment of several malignancies both in the adjuvant and metastatic setting. Although myelosuppression is the most adverse event of this therapy, gemcitabine might induce severe pulmonary toxicities. We describe a case...

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Main Authors: Célia Turco, Marine Jary, Stefano Kim, Mélanie Moltenis, Bruno Degano, Philippe Manzoni, Thierry Nguyen, Bruno Genet, Marie-Blanche Valnet Rabier, Bruno Heyd, Christophe Borg
Format: Article
Language:English
Published: SAGE Publishing 2015-01-01
Series:Clinical Medicine Insights: Oncology
Online Access:https://doi.org/10.4137/CMO.S26537
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spelling doaj-8bdcf98a41c943b5bc1bd5beefb4db9a2020-11-25T02:48:08ZengSAGE PublishingClinical Medicine Insights: Oncology1179-55492015-01-01910.4137/CMO.S26537Gemcitabine-Induced Pulmonary Toxicity: A Case Report of Pulmonary Veno-Occlusive DiseaseCélia Turco0Marine Jary1Stefano Kim2Mélanie Moltenis3Bruno Degano4Philippe Manzoni5Thierry Nguyen6Bruno Genet7Marie-Blanche Valnet Rabier8Bruno Heyd9Christophe Borg10INSERM, Unit 1098, University of Franche-Comté, Besançon, France.INSERM, Unit 1098, University of Franche-Comté, Besançon, France.Department of Medical Oncology, University Hospital of Besançon, Besançon, France.Regional center of Pharmacovigilance, University Hospital of Besançon, Besançon, France.Functional Explorations, University Hospital of Besançon, Besançon, France.Radiology and Interventional Pain Management Unit, University Hospital of Besançon, Besançon, France.Department of Medical Oncology, University Hospital of Besançon, Besançon, France.Department of Cardiology, University Hospital of Besançon, Besançon, France.Regional center of Pharmacovigilance, University Hospital of Besançon, Besançon, France.Department of Digestive Surgery and Liver Transplantation, University Hospital of Besançon, Besançon, France.INSERM, Unit 1098, University of Franche-Comté, Besançon, France.Introduction Gemcitabine is a chemotherapeutic agent frequently used by for the treatment of several malignancies both in the adjuvant and metastatic setting. Although myelosuppression is the most adverse event of this therapy, gemcitabine might induce severe pulmonary toxicities. We describe a case of pulmonary veno-occlusive disease (PVOD) related to gemcitabine. Case Presentation The patient was an 83-year-old man with a metastatic pancreatic cancer who was treated by gemcitabine as first-line therapy. He was in good health and received no other chemotherapy. A dose of 1000 mg/m 2 of gemcitabine was administered over a 30-minute intravenous infusion on days 1, 8, and 15 of a 28-day cycle. After a period of 6 months, a complete response was observed. Nevertheless, the patient developed a severe dyspnea, with arterial hypoxemia and very low lung diffusion for carbon monoxide. A CT scan showed diffuse ground glass opacities with septal lines, bilateral pleural effusion, and lymph node enlargement. On echocardiography, there was a suspicion of pulmonary hypertension with elevated systolic pulmonary artery pressure and normal left ventricular pressures. Right heart catheterization confirmed pulmonary hypertension and normal pulmonary artery occlusion pressure. Diagnosis of PVOD was made, and a gemcitabine-induced toxicity was suspected. A symptomatic treatment was started. At last follow-up, patient was in functional class I with near-normal of CT scan, arterial blood gases, and echocardiography. A gemcitabine-induced PVOD is the more likely diagnosis.https://doi.org/10.4137/CMO.S26537
collection DOAJ
language English
format Article
sources DOAJ
author Célia Turco
Marine Jary
Stefano Kim
Mélanie Moltenis
Bruno Degano
Philippe Manzoni
Thierry Nguyen
Bruno Genet
Marie-Blanche Valnet Rabier
Bruno Heyd
Christophe Borg
spellingShingle Célia Turco
Marine Jary
Stefano Kim
Mélanie Moltenis
Bruno Degano
Philippe Manzoni
Thierry Nguyen
Bruno Genet
Marie-Blanche Valnet Rabier
Bruno Heyd
Christophe Borg
Gemcitabine-Induced Pulmonary Toxicity: A Case Report of Pulmonary Veno-Occlusive Disease
Clinical Medicine Insights: Oncology
author_facet Célia Turco
Marine Jary
Stefano Kim
Mélanie Moltenis
Bruno Degano
Philippe Manzoni
Thierry Nguyen
Bruno Genet
Marie-Blanche Valnet Rabier
Bruno Heyd
Christophe Borg
author_sort Célia Turco
title Gemcitabine-Induced Pulmonary Toxicity: A Case Report of Pulmonary Veno-Occlusive Disease
title_short Gemcitabine-Induced Pulmonary Toxicity: A Case Report of Pulmonary Veno-Occlusive Disease
title_full Gemcitabine-Induced Pulmonary Toxicity: A Case Report of Pulmonary Veno-Occlusive Disease
title_fullStr Gemcitabine-Induced Pulmonary Toxicity: A Case Report of Pulmonary Veno-Occlusive Disease
title_full_unstemmed Gemcitabine-Induced Pulmonary Toxicity: A Case Report of Pulmonary Veno-Occlusive Disease
title_sort gemcitabine-induced pulmonary toxicity: a case report of pulmonary veno-occlusive disease
publisher SAGE Publishing
series Clinical Medicine Insights: Oncology
issn 1179-5549
publishDate 2015-01-01
description Introduction Gemcitabine is a chemotherapeutic agent frequently used by for the treatment of several malignancies both in the adjuvant and metastatic setting. Although myelosuppression is the most adverse event of this therapy, gemcitabine might induce severe pulmonary toxicities. We describe a case of pulmonary veno-occlusive disease (PVOD) related to gemcitabine. Case Presentation The patient was an 83-year-old man with a metastatic pancreatic cancer who was treated by gemcitabine as first-line therapy. He was in good health and received no other chemotherapy. A dose of 1000 mg/m 2 of gemcitabine was administered over a 30-minute intravenous infusion on days 1, 8, and 15 of a 28-day cycle. After a period of 6 months, a complete response was observed. Nevertheless, the patient developed a severe dyspnea, with arterial hypoxemia and very low lung diffusion for carbon monoxide. A CT scan showed diffuse ground glass opacities with septal lines, bilateral pleural effusion, and lymph node enlargement. On echocardiography, there was a suspicion of pulmonary hypertension with elevated systolic pulmonary artery pressure and normal left ventricular pressures. Right heart catheterization confirmed pulmonary hypertension and normal pulmonary artery occlusion pressure. Diagnosis of PVOD was made, and a gemcitabine-induced toxicity was suspected. A symptomatic treatment was started. At last follow-up, patient was in functional class I with near-normal of CT scan, arterial blood gases, and echocardiography. A gemcitabine-induced PVOD is the more likely diagnosis.
url https://doi.org/10.4137/CMO.S26537
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