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Update on Emerging Therapies for Advanced Colorectal Cancer.
Alese, Olatunji B; Wu, Christina; Chapin, William J; Ulanja, Mark B; Zheng-Lin, Binbin; Amankwah, Millicent; Eads, Jennifer.
Afiliação
  • Alese OB; Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA.
  • Wu C; Mayo Clinic, Phoenix, AZ.
  • Chapin WJ; Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
  • Ulanja MB; Christus Ochsner St Patrick Hospital, Lake Charles, LA.
  • Zheng-Lin B; Mayo Clinic, Phoenix, AZ.
  • Amankwah M; Louisiana State University Health Shreveport, Shreveport, LA.
  • Eads J; Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
Am Soc Clin Oncol Educ Book ; 43: e389574, 2023 May.
Article em En | MEDLINE | ID: mdl-37155942
Colorectal cancer (CRC) is the third most common malignancy worldwide. It is projected to increase by 3.2 million new cases and account for 1.6 million deaths by 2040. Mortality is largely due to limited treatment options for patients who present with advanced disease. Thus, the development of effective and tolerable therapies is crucial. Chemotherapy has been the backbone of systemic treatment of advanced CRC, but utility has been limited because of invariable resistance to therapy, narrow mechanisms of action, and unfavorable toxicity profile. Tumors that are mismatch repair-deficient have demonstrated remarkable response to immune checkpoint inhibitor therapy. However, most CRC tumors are mismatch repair-proficient and represent an unmet medical need. Although ERBB2 amplification occurs only in a few cases, it is associated with left-sided tumors and a higher incidence of brain metastasis. Numerous combinations of HER2 inhibitors have demonstrated efficacy, and antibody-drug conjugates against HER2 represent innovative strategies in this area. The KRAS protein has been classically considered undruggable. Fortunately, new agents targeting KRAS G12C mutation represent a paradigm shift in the management of affected patients and could lead the advancement in drug development for the more common KRAS mutations. Furthermore, aberrant DNA damage response is present in 15%-20% of CRCs, and emerging innovative combinations with poly (ADP-ribose) polymerase (PARP) inhibitors could improve the current therapeutic landscape. Multiple novel biomarker-driven approaches in the management of patients with advanced CRC tumors are reviewed in this article.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Neoplasias Colorretais Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Neoplasias Colorretais Idioma: En Ano de publicação: 2023 Tipo de documento: Article