Molecular Tumor Board Improves Outcomes for Hispanic Patients With Advanced Solid Tumors

Author:

Sotelo-Rodríguez Carolina12ORCID,Vallejo-Ardila Dora12ORCID,Ruiz-Patiño Alejandro12ORCID,Chamorro Diego F.12,Rodríguez July12,Moreno-Pérez Darwin A.12,Carranza Hernán12ORCID,Otero Jorge12,Vargas Carlos12,Archila Pilar12,Rojas Leonardo3ORCID,Zuluaga Jairo3,Rubio Cladelis1ORCID,Ordóñez-Reyes Camila12ORCID,Garcia-Robledo Juan Esteban4ORCID,Mejía Sergio5ORCID,Jaller Elvira12ORCID,Arrieta Oscar6ORCID,Cardona Andrés F.37

Affiliation:

1. Foundation for Clinical and Applied Cancer Research—FICMAC, Bogotá, Colombia

2. Molecular Oncology and Biology Systems Research Group (Fox-G), Universidad El Bosque, Bogotá, Colombia

3. Thoracic Oncology Unit, Luis Carlos Sarmiento Angulo Cancer Treatment and Research Center (CTIC), Bogotá, Colombia

4. Hematology/Oncology Division, Mayo Clinic, Scottsdale, AZ

5. Thoracic Oncology Unit, Clínica Las Américas, Medellín, Colombia

6. Thoracic Oncology Unit, National Cancer Institute (INCan), México City, México

7. Direction of Research, Science and Education, Luis Carlos Sarmiento Angulo Cancer Treatment and Research Center (CTIC), Bogotá, Colombia

Abstract

PURPOSE Multidisciplinary molecular tumor boards (MTBs) decode complex genomic data into clinical recommendations. Although MTBs are well-established in the oncology practice in developed countries, this strategy needs to be better explored in developing countries. Herein, we describe the possible benefits and limitations of the first MTB established in Colombia. METHODS Demographic, clinical, and genomic information was collected between August 2020 and November 2021. By mid-2020, an MTB strategy was created to discuss clinical cases with one or more genomic alterations identified by next-generation sequencing using an open-access virtual platform. We characterized the patient population as benefiting from the recommended treatment option. We assessed the benefits and access to available targeted therapies that have the potential to change clinical management by making recommendations to treating oncologists on the basis of genomic profiling. However, we did not assess the treatment oncologists' compliance with MTB recommendations because they were not intended to replace clinical judgment/standard of care. RESULTS A total of 146 patients were included in the discussions of the MTB. The median age was 59 years, and 59.6% were women. Genomic results prompting a change in therapeutic decisions were obtained in 53.1% of patients (95% CI, 44.9 to 61.3). The most prevalent malignancy was non–small-cell lung cancer (51%). Other malignancies represented 60%, 50%, and 30% of patients with soft-tissue sarcomas, brain tumors, and breast cancer, respectively. CONCLUSION Using an open-access virtual platform, MTBs were feasible in low- and middle-income countries on the basis of the capability to provide the benefits and access to available targeted therapies that are not standard of care. Furthermore, MTB recommendations were made available to the treating oncologist in different locations across Colombia, providing the option to modify clinical management in most of these patients.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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