SEOM guidelines for the treatment of malignant pleural mesothelioma

Pilar Lianes1, Jordi Remon, Isabel Bover

  • 1Servicio de Oncología Médica, Hospital de Mataró, Mataró, Barcelona, Spain. plianes@csdm.cat

Insights

Malignant pleural mesothelioma (MPM), primarily caused by asbestos exposure, is a rare cancer with increasing incidence. Multimodal treatment strategies are evolving, with neoadjuvant chemotherapy showing promise.

Area of Science:

  • Oncology
  • Thoracic Surgery
  • Medical Oncology

Background:

  • Malignant pleural mesothelioma (MPM) is a rare cancer strongly linked to asbestos exposure, accounting for approximately 80% of cases.
  • The incidence of MPM is rising and is projected to peak within the next decade.
  • MPM presents in three main histological types: epithelial, sarcomatous, and mixed.

Framework:

  • No universally accepted standard treatment approach exists for MPM.
  • Multimodal therapy, including surgery (extra-pleural pneumonectomy or pleurectomy/decortication), chemotherapy, and radiotherapy, is often employed.
  • Treatment decisions are complex and require a multidisciplinary team approach, with surgery reserved for carefully selected patients.

Implementation:

  • Neoadjuvant chemotherapy is favored over adjuvant chemotherapy due to better patient compliance and reduced surgical morbidity.
  • Radiotherapy can be utilized for prophylaxis against recurrence, to enhance locoregional control, and for symptom palliation.
  • For unresectable disease, chemotherapy regimens including platinum and pemetrexed or raltitrexed are the primary treatment option.

Implications:

  • The optimal sequence and combination of treatments within multimodal therapy for MPM remain under investigation.
  • There is currently no widely approved salvage therapy for patients who do not respond to initial treatments.
  • Further research is needed to establish standardized treatment protocols and improve outcomes for MPM patients.