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Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
Published on: September 20, 2016
Primary tumors of the lung other than lung cancer
1UCLA School of Medicine, Department of Medicine 90024-1699.
Abstract:
Neoplasms of the lung other than lung cancer are rare and have varying biologic behavior. Diffuse malignant mesothelioma remains a difficult clinical problem, with efforts directed at combined modality therapy. A nude mouse xenograft model may hold promise in the identification of active chemotherapy agents. Continuing evidence suggests that typical and atypical pulmonary carcinoids represent a spectrum of neuroendocrine disease, with small cell lung cancer representing the most virulent subtype. Therapy for advanced invasive thymoma includes neoadjuvant chemotherapy, surgery, and postoperative radiation. Nonseminomatous germ cell neoplasms of the mediastinum respond much less favorably to cisplatin-based chemotherapy than do similar tumors arising elsewhere, and new advances in treatment are needed. Rare mesenchymal tumors usually respond favorably to surgical excision.
Insights
This study reviews rare lung neoplasms, including mesothelioma and carcinoids, and their varied treatments. Research into chemotherapy agents and mediastinal germ cell tumors is ongoing.
Area of Science:
- Thoracic oncology
- Rare pulmonary neoplasms
- Neoadjuvant chemotherapy
Background:
- Neoplasms of the lung other than primary lung cancer are uncommon and exhibit diverse biological behaviors.
- Diffuse malignant mesothelioma presents a significant clinical challenge, necessitating combined modality therapeutic approaches.
- Pulmonary carcinoids are increasingly recognized as part of a neuroendocrine disease spectrum, with small cell lung cancer as the most aggressive form.
Purpose of the Study:
- To provide an overview of the diagnosis and management of various rare thoracic neoplasms.
- To highlight the challenges and current therapeutic strategies for conditions like malignant mesothelioma and mediastinal germ cell tumors.
- To identify areas for future research, particularly in chemotherapy agent development and treatment of resistant neoplasms.
Main Methods:
- Review of current literature on rare lung and mediastinal neoplasms.
- Discussion of therapeutic modalities including chemotherapy, surgery, and radiation.
- Exploration of preclinical models, such as nude mouse xenografts, for chemotherapy screening.
Main Results:
- Malignant mesothelioma requires combined modality therapy.
- Pulmonary carcinoids and small cell lung cancer represent a spectrum of neuroendocrine tumors.
- Advanced invasive thymoma treatment involves neoadjuvant chemotherapy, surgery, and radiation.
- Nonseminomatous germ cell neoplasms of the mediastinum show limited response to cisplatin-based chemotherapy.
- Rare mesenchymal tumors generally respond well to surgical excision.
Conclusions:
- Effective management of rare thoracic neoplasms requires tailored, often multimodal, therapeutic strategies.
- Further research is crucial for improving outcomes in challenging conditions like malignant mesothelioma and mediastinal germ cell tumors.
- Preclinical models offer a promising avenue for identifying novel chemotherapy agents for thoracic malignancies.
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