Post-Neoadjuvant Treatment Strategies in Breast Cancer.

breast cancer individualized treatment post-neoadjuvant

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
28 Feb 2022
Historique:
received: 10 01 2022
revised: 17 02 2022
accepted: 20 02 2022
entrez: 10 3 2022
pubmed: 11 3 2022
medline: 11 3 2022
Statut: epublish

Résumé

Neoadjuvant chemotherapy enables close monitoring of tumor response in patients with breast cancer. Being able to assess tumor response during treatment provides an opportunity to evaluate new therapeutic strategies. Thus, for triple-negative breast tumors, it was demonstrated that additional immunotherapy could improve prognosis compared with chemotherapy alone. Furthermore, adjuvant therapy can be escalated or de-escalated correspondingly. The CREATE-X trial randomly assigned HER2-negative patients with residual tumor after neoadjuvant therapy to either observation or capecitabine. In HER2-negative patients with positive BRCA testing, the OlympiA study randomly assigned patients to either observation or olaparib. HER2-positive patients without pathologic remission were randomly assigned to trastuzumab or trastuzumab-emtansine within the KATHERINE study. These studies were all able to show an improvement in oncologic outcome associated with the escalation of therapy in patients presenting with residual tumor after neoadjuvant treatment. On the other hand, this individualization of therapy may also offer the possibility to de-escalate treatment, and thereby reduce morbidity. Among WSG-ADAPT HER2+/HR-, HER2-positive patients achieved comparable results without chemotherapy after complete remission following neoadjuvant treatment. In summary, the concept of post-neoadjuvant therapy constitutes a great opportunity for individualized cancer treatment, potentially improving outcome. In this review, the most important trials of post-neoadjuvant therapy are compiled and discussed.

Identifiants

pubmed: 35267554
pii: cancers14051246
doi: 10.3390/cancers14051246
pmc: PMC8909560
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Christiane Matuschek (C)

Department of Radiation Oncology, University Hospital Dusseldorf, Medical Faculty, Heinrich-Heine-University Dusseldorf, Moorenstr. 5, 40225 Dusseldorf, Germany.

Danny Jazmati (D)

Department of Radiation Oncology, University Hospital Dusseldorf, Medical Faculty, Heinrich-Heine-University Dusseldorf, Moorenstr. 5, 40225 Dusseldorf, Germany.

Edwin Bölke (E)

Department of Radiation Oncology, University Hospital Dusseldorf, Medical Faculty, Heinrich-Heine-University Dusseldorf, Moorenstr. 5, 40225 Dusseldorf, Germany.

Bálint Tamaskovics (B)

Department of Radiation Oncology, University Hospital Dusseldorf, Medical Faculty, Heinrich-Heine-University Dusseldorf, Moorenstr. 5, 40225 Dusseldorf, Germany.

Stefanie Corradini (S)

Department of Radiation Oncology, LMU University of Munich, 81388 Munich, Germany.

Wilfried Budach (W)

Department of Radiation Oncology, University Hospital Dusseldorf, Medical Faculty, Heinrich-Heine-University Dusseldorf, Moorenstr. 5, 40225 Dusseldorf, Germany.

David Krug (D)

Department of Radiation Oncology, University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.

Svjetlana Mohrmann (S)

Department of Gynecology & Obstetrics, Heinrich-Heine University, 40225 Dusseldorf, Germany.

Eugen Ruckhäberle (E)

Department of Gynecology & Obstetrics, Heinrich-Heine University, 40225 Dusseldorf, Germany.

Tanja Fehm (T)

Department of Gynecology & Obstetrics, Heinrich-Heine University, 40225 Dusseldorf, Germany.

Carolin Nestle Krämling (C)

Department of Senology: EVK Dusseldorf, 40217 Dusseldorf, Germany.

Markus Dommach (M)

Department of Internal Medicine, Sana Krankenhaus, 40625 Dusseldorf, Germany.

Jan Haussmann (J)

Department of Radiation Oncology, University Hospital Dusseldorf, Medical Faculty, Heinrich-Heine-University Dusseldorf, Moorenstr. 5, 40225 Dusseldorf, Germany.

Classifications MeSH