Immunotherapies against HER2-Positive Breast Cancer

Santiago Duro-Sánchez1,2,3,4, Macarena Román Alonso1,2,3,4, Joaquín Arribas1,2,3,4,5,6

  • 1Preclinical & Translational Research Program, Vall d'Hebron Institute of Oncology (VHIO), 08035 Barcelona, Spain.

Cancers
|February 25, 2023
PubMed

Insights

Immunotherapy shows promise for HER2-positive breast cancer, offering new strategies beyond standard treatments. These approaches aim to boost the immune system to fight cancer, potentially preventing relapse and metastasis.

Area of Science:

  • Oncology
  • Immunology

Background:

  • Breast cancer is a leading cause of cancer deaths in women globally.
  • HER2-positive breast cancer, characterized by HER2 receptor overexpression, affects 15-20% of patients.
  • Current treatments face challenges with patient response, leading to relapse, metastasis, and poor prognosis.

Purpose of the Study:

  • To review various immunotherapeutic strategies for HER2-positive breast cancer.
  • To evaluate the potential of immunotherapy in preventing tumor progression and treating resistant tumors.
  • To highlight the benefits and drawbacks of different immunotherapeutic approaches.

Main Methods:

  • Review of existing literature on immunotherapeutic strategies.
  • Examination of cancer vaccines, immune checkpoint blockade, and adoptive cell therapy.
  • Analysis of clinical utility and potential applications in HER2-positive breast cancer.

Main Results:

  • Immunotherapy aims to enhance antitumor immune response to prevent relapse and metastasis.
  • Various immunotherapeutic strategies are under investigation for HER2-positive breast cancer.
  • These approaches may complement standard-of-care therapies for resistant tumors.

Conclusions:

  • Immunotherapy holds significant promise for treating HER2-positive breast cancer.
  • It offers potential for complete tumor cell eradication and disease progression prevention.
  • Further research is needed to confirm the utility of immunotherapies in this patient population.

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