4.4 Review

New Treatment Strategies for the Inflammatory Breast Cancer

Journal

CURRENT TREATMENT OPTIONS IN ONCOLOGY
Volume 22, Issue 6, Pages -

Publisher

SPRINGER
DOI: 10.1007/s11864-021-00843-2

Keywords

Inflammatory breast cancer (IBC); Tumor emboli; Molecular pathways; Targeted treatment; Immunotherapy; Microscopic disease

Categories

Funding

  1. Associazione per lo Sviluppo della Scienza Oncologica (ASSO), Siena, Italy

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Inflammatory breast cancer remains the most aggressive type of breast cancer, and despite significant progress in refining diagnostic criteria and treatment strategies, outcomes for patients with this subtype are still unsatisfactory. Global efforts are now focused on identifying novel strategies to improve treatment response and prolong survival for metastatic patients.
Opinion statement Inflammatory breast cancer (IBC) remains the most aggressive type of breast cancer. During the past decade, enormous progress has been made to refine diagnostic criteria and establish multimodality treatment strategies as keys for the improvement of survival outcomes. Multiple genomic studies enabled a better understanding of underlying tumor biology, which is responsible for the complex and aggressive nature of IBC. Despite these important achievements, outcomes for this subgroup of patients remain unsatisfactory compared to locally advanced non-IBC counterparts. Global efforts are now focused on identifying novel strategies that will improve treatment response, prolong survival for metastatic patients, achieve superior local control, and possibly increase the cure rate for locally advanced disease. Genomic technologies constitute the most important tool that will support future clinical progress. Gene-expressing profiling of the tumor tissue and liquid biopsy are important parts of the everyday clinical practice aiming to guide treatment decisions by providing information on tumor molecular drivers or primary and acquired resistance to treatment. The International IBC expert panel and IBC International Consortium made a tremendous effort to define IBC as a distinct entity of BC, and they will continue to lead and support the research for this rare and very aggressive disease. Finally, a uniform platform is now required to develop and lead large, multi-arm, proof-of-concept clinical trials that perform rapid, focused, and cost-effective evaluations of potential novel therapeutics in IBC.

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