• James Cleary, Henry Ddungu, Sandra R Distelhorst, Carla Ripamonti, Gary M Rodin, Mohammad A Bushnaq, Joe N Clegg-Lamptey, Stephen R Connor, Msemo B Diwani, Alexandru Eniu, Joe B Harford, Suresh Kumar, M R Rajagopal, Beti Thompson, Julie R Gralow, and Benjamin O Anderson.
• University of Wisconsin Comprehensive Cancer Center, Madison, WI, USA.
• Breast. 2013 Oct 1;22(5):616-27.

AbstractMany women diagnosed with breast cancer in low- and middle-income countries (LMICs) present with advanced-stage disease. While cure is not a realistic outcome, site-specific interventions, supportive care, and palliative care can achieve meaningful outcomes and improve quality of life. As part of the 5th Breast Health Global Initiative (BHGI) Global Summit, an expert international panel identified thirteen key resource recommendations for supportive and palliative care for metastatic breast cancer. The recommendations are presented in three resource-stratified tables: health system resource allocations, resource allocations for organ-based metastatic breast cancer, and resource allocations for palliative care. These tables illustrate how health systems can provide supportive and palliative care services for patients at a basic level of available resources, and incrementally add services as more resources become available. The health systems table includes health professional education, patient and family education, palliative care models, and diagnostic testing. The metastatic disease management table provides recommendations for supportive care for bone, brain, liver, lung, and skin metastases as well as bowel obstruction. The third table includes the palliative care recommendations: pain management, and psychosocial and spiritual aspects of care. The panel considered pain management a priority at a basic level of resource allocation and emphasized the need for morphine to be easily available in LMICs. Regular pain assessments and the proper use of pharmacologic and non-pharmacologic interventions are recommended. Basic-level resources for psychosocial and spiritual aspects of care include health professional and patient and family education, as well as patient support, including community-based peer support.Copyright © 2013 The Authors. Published by Elsevier Ltd.. All rights reserved.

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