Literature DB >> 25825476

Dual Blockade with AFatinib and Trastuzumab as NEoadjuvant Treatment for Patients with Locally Advanced or Operable Breast Cancer Receiving Taxane-Anthracycline Containing Chemotherapy-DAFNE (GBG-70).

Claus Hanusch1, Andreas Schneeweiss2, Sibylle Loibl3, Michael Untch4, Stefan Paepke5, Sherko Kümmel6, Christian Jackisch7, Jens Huober8, Jörn Hilfrich9, Bernd Gerber10, Holger Eidtmann11, Carsten Denkert12, Serban Costa13, Jens Uwe Blohmer14, Knut Engels15, Nicole Burchardi16, Gunter von Minckwitz17.   

Abstract

PURPOSE: Dual anti-HER2 blockade with trastuzumab/pertuzumab or trastuzumab/lapatinib in combination with anthracycline/taxane-based chemotherapy can reach pathologic complete response (pCR) rates of up to 60% in HER2-positive breast cancer. The DAFNE (Dual blockade with AFatinib and trastuzumab as NEoadjuvant treatment) phase II study (NCT015591477) investigated a dual blockade with the irreversible pan-HER inhibitor afatinib and trastuzumab in this setting. EXPERIMENTAL
DESIGN: Participants with untreated, centrally HER2-positive breast cancer were treated for 6 weeks with afatinib (20 mg/d) and trastuzumab [(8) 6 mg/kg/3 weeks] alone; followed by 12-week treatment with paclitaxel (80 mg/m(2)/1 week), trastuzumab, and afatinib; followed by 12 weeks with epirubicin (90 mg/m(2)/3 weeks), cyclophosphamide (600 mg/m(2)/3 weeks), and trastuzumab before surgery. Primary objective was pCR rate, defined as ypT0/is ypN0. We expected a pCR rate of 70%; 65 patients were needed to exclude a rate of ≤55%.
RESULTS: pCR rate was 49.2% [90% confidence interval (CI), 38.5-60.1] in 65 treated patients. Patients with hormone receptor-negative (N = 19) or hormone receptor-positive (N = 46) tumors showed pCR rates of 63.2% and 43.5%, respectively (P = 0.153). Patients with (N = 9) or without (N = 56) lymphocyte predominant breast cancer (LPBC) showed pCR rates of 100% and 41.1%, respectively (P < 0.001). PCR rate was not different in patients with or without PIK3CA tumor mutations (P = 0.363). Clinical responses were seen in 96.3% of 54 evaluable patients, and breast conserving surgery was possible in 59.4% of 62 assessable patients. Most frequent nonhematologic grade 3-4 toxicities were diarrhea (7.7%), increased creatinine (4.6%), and infection (4.6%). One patient developed symptomatic congestive heart failure.
CONCLUSIONS: Neoadjuvant treatment with afatinib, trastuzumab, and chemotherapy showed acceptable tolerability, and a pCR rate comparable with that of other anti-HER2 doublets but below challenging expectations. ©2015 American Association for Cancer Research.

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Year:  2015        PMID: 25825476     DOI: 10.1158/1078-0432.CCR-14-2774

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  12 in total

Review 1.  Neoadjuvant Therapy for Breast Cancer: Established Concepts and Emerging Strategies.

Authors:  Tessa G Steenbruggen; Mette S van Ramshorst; Marleen Kok; Sabine C Linn; Carolien H Smorenburg; Gabe S Sonke
Journal:  Drugs       Date:  2017-08       Impact factor: 9.546

Review 2.  Mutation distributions and clinical correlations of PIK3CA gene mutations in breast cancer.

Authors:  Ebubekir Dirican; Mustafa Akkiprik; Ayşe Özer
Journal:  Tumour Biol       Date:  2016-02-26

3.  PIK3CA mutations are associated with reduced pathological complete response rates in primary HER2-positive breast cancer: pooled analysis of 967 patients from five prospective trials investigating lapatinib and trastuzumab.

Authors:  S Loibl; I Majewski; V Guarneri; V Nekljudova; E Holmes; E Bria; C Denkert; C Schem; C Sotiriou; S Loi; M Untch; P Conte; R Bernards; M Piccart; G von Minckwitz; J Baselga
Journal:  Ann Oncol       Date:  2016-05-13       Impact factor: 32.976

Review 4.  Tyrosine kinase inhibitors in breast cancer (Review).

Authors:  George Iancu; Dragos Serban; Cristinel Dumitru Badiu; Ciprian Tanasescu; Mihai Silviu Tudosie; Corneliu Tudor; Daniel Ovidiu Costea; Anca Zgura; Raluca Iancu; Danut Vasile
Journal:  Exp Ther Med       Date:  2021-12-03       Impact factor: 2.447

5.  Phase I trial of afatinib and 3-weekly trastuzumab with optimal anti-diarrheal management in patients with HER2-positive metastatic cancer.

Authors:  Nicolas Martin; Nicolas Isambert; Carlos Gomez-Roca; Rainer-Georg Goeldner; Sylvie Zanetta; Behbood Sadrolhefazi; Hélène de Mont-Serrat; Mario Campone; Jean-Pierre Delord
Journal:  Cancer Chemother Pharmacol       Date:  2018-10-22       Impact factor: 3.333

Review 6.  Afatinib: first global approval.

Authors:  Rosselle T Dungo; Gillian M Keating
Journal:  Drugs       Date:  2013-09       Impact factor: 9.546

Review 7.  Early HER2-Positive Breast Cancer: Current Treatment and Novel Approaches.

Authors:  Marija Ban; Branka Petrić Miše; Eduard Vrdoljak
Journal:  Breast Care (Basel)       Date:  2020-10-28       Impact factor: 2.860

Review 8.  PIK3CA mutations and their response to neoadjuvant treatment in early breast cancer: A systematic review and meta-analysis.

Authors:  Hongwei Fan; Chao Li; Qian Xiang; Ling Xu; Zhuo Zhang; Qianxin Liu; Tonttong Zhang; Ying Zhou; Xia Zhao; Yimin Cui
Journal:  Thorac Cancer       Date:  2018-03-25       Impact factor: 3.500

9.  Preferential Response of Basal-Like Head and Neck Squamous Cell Carcinoma Cell Lines to EGFR-Targeted Therapy Depending on EREG-Driven Oncogenic Addiction.

Authors:  Sylvie Job; Aurélien de Reyniès; Betty Heller; Amélie Weiss; Eric Guérin; Christine Macabre; Sonia Ledrappier; Cyril Bour; Christine Wasylyk; Nelly Etienne-Selloum; Laurent Brino; Christian Gaiddon; Bohdan Wasylyk; Alain C Jung
Journal:  Cancers (Basel)       Date:  2019-06-08       Impact factor: 6.639

10.  Network-based approach to identify biomarkers predicting response and prognosis for HER2-negative breast cancer treatment with taxane-anthracycline neoadjuvant chemotherapy.

Authors:  Cui Jiang; Shuo Wu; Lei Jiang; Zhichao Gao; Xiaorui Li; Yangyang Duan; Na Li; Tao Sun
Journal:  PeerJ       Date:  2019-09-03       Impact factor: 2.984

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