Literature DB >> 26827687

Prognostic risk factors for treatment decision in pT1a,b N0M0 HER2-positive breast cancers.

Antonino Musolino1, Daniela Boggiani2, Angelica Sikokis2, Anita Rimanti2, Benedetta Pellegrino2, Rosa Vattiato3, Paolo Sgargi2, Fabio Falcini3, Caterina Caminiti4, Maria Michiara2, Francesco Leonardi2.   

Abstract

Although outcomes for women with breast cancers may vary by biologic subtype, patients with T1a,b N0M0 tumors have an excellent prognosis across all subgroups. HER2 overexpression occurs in 15-20% of primary breast tumors, and is associated with diminished disease-free and overall survival. The anti-HER2 monoclonal antibody trastuzumab in combination with chemotherapy is an effective treatment for all stages of HER2 positive breast cancer (bc). However, the absolute benefit decreases as the risk of recurrence lessens and no available randomized adjuvant trial has evaluated the role of trastuzumab in women with pT1a,b N0M0, HER2-positive breast tumors. These findings may explain the debate about the appropriate indication for adjuvant chemotherapy plus trastuzumab in this setting of patients. The aim of this review was to describe known and novel prognostic risk factors to be used for tailored treatment decision in pT1a,b N0M0 HER2-positive tumors. Whether patients with small HER2-positive bc may be suitable for (chemo)therapy reduction strategies, the current available data cannot exclude the need for a more aggressive treatment in a small subset of these subjects. Novel clinical prognostic factors such as interval cancer (IC) detection may help to address this clinically important controversy. A multicenter population-based cancer registry study is currently evaluating whether IC detection may identify patients with pT1a N0M0 HER2-positive tumors in whom the rate of recurrence justifies consideration for use of conventional, trastuzumab-based chemotherapy regimens.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Breast cancer; HER2-positive; Interval cancer risk; Prognostic factors; pT1a,b

Mesh:

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Year:  2015        PMID: 26827687     DOI: 10.1016/j.ctrv.2015.11.010

Source DB:  PubMed          Journal:  Cancer Treat Rev        ISSN: 0305-7372            Impact factor:   12.111


  3 in total

1.  Immunoglobulin G fragment C receptor polymorphisms and efficacy of preoperative chemotherapy plus trastuzumab and lapatinib in HER2-positive breast cancer.

Authors:  A Musolino; N Naldi; M V Dieci; D Zanoni; A Rimanti; D Boggiani; P Sgargi; D G Generali; F Piacentini; M Ambroggi; K Cagossi; L Gianni; S Sarti; G Bisagni; A Ardizzoni; P F Conte; V Guarneri
Journal:  Pharmacogenomics J       Date:  2016-07-05       Impact factor: 3.550

2.  Would 1.0 cm be a more suitable cutoff to subdivide pT1 tumors in hormone receptor-negative and HER2-positive breast cancer?

Authors:  Changjun Wang; Yidong Zhou; Hanjiang Zhu; Wei Huang; Ziyuan Chen; Feng Mao; Yan Lin; Xiaohui Zhang; Songjie Shen; Ying Zhong; Yan Li; Qiang Sun
Journal:  Cancer Med       Date:  2018-10-01       Impact factor: 4.452

3.  Clinico-Immunological Profile of a 67-Year-Old Woman Affected by HER2-Positive Breast Cancer and Autoimmune Dermatomyositis.

Authors:  Benedetta Pellegrino; Giulia Mazzaschi; Denise Madeddu; Cristina Mori; Costanza Anna Maria Lagrasta; Gabriele Missale; Federico Quaini; Antonino Musolino
Journal:  Front Oncol       Date:  2020-02-25       Impact factor: 6.244

  3 in total

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