Crizotinib for ROS1-rearranged lung cancer and pulmonary tumor thrombotic microangiopathy under venoarterial extracorporeal membrane oxygenation.
Daisetsu AoyamaShigefumi FukuiHaruhiko HirataKeiko Ohta-OgoHideo MatamaEmi TateishiTatsuya NishiiYasuhide AsaumiMamoru ToyofukuTatsuyoshi IkeueTakeshi OgoHatsue Ishibashi-UedaSatoshi YasudaPublished in: Pulmonary circulation (2022)
Pulmonary tumor thrombotic microangiopathy (PTTM) is a rapidly progressive subtype of pulmonary hypertension (PH) associated with impaired right ventricular adaptation and very poor prognosis in cancer, and its rapid progression makes antemortem diagnosis and treatment extremely difficult. We describe the case of a 35-year-old woman who developed severe PH with subsequent circulatory collapse. The patient was clinically diagnosed with PTTM induced by lung adenocarcinoma harboring the c-ros oncogene 1 (ROS1) rearrangement within 1-2 weeks, while hemodynamics were stabilized by rescue venoarterial extracorporeal membrane oxygenation support. Crizotinib, an oral tyrosine kinase inhibitor targeting anaplastic lymphoma kinase, MET, and ROS1 kinase domains dramatically resolved PH, resulting in more than 3 years of survival. Targeted gene-tailored therapy with mechanical support can improve survival in PTTM.
Keyphrases
- extracorporeal membrane oxygenation
- pulmonary hypertension
- poor prognosis
- acute respiratory distress syndrome
- cell death
- dna damage
- reactive oxygen species
- respiratory failure
- long non coding rna
- tyrosine kinase
- pulmonary artery
- advanced non small cell lung cancer
- multiple sclerosis
- cancer therapy
- pulmonary arterial hypertension
- mechanical ventilation
- protein kinase
- genome wide
- papillary thyroid
- squamous cell carcinoma
- diffuse large b cell lymphoma
- free survival
- young adults
- early onset
- oxidative stress
- epidermal growth factor receptor
- gene expression
- intensive care unit
- cell therapy
- stem cells
- squamous cell
- smoking cessation
- dna methylation
- mesenchymal stem cells
- genome wide identification
- drug induced
- bone marrow