Literature DB >> 29244528

Phase III, Randomized Study of Dual Human Epidermal Growth Factor Receptor 2 (HER2) Blockade With Lapatinib Plus Trastuzumab in Combination With an Aromatase Inhibitor in Postmenopausal Women With HER2-Positive, Hormone Receptor-Positive Metastatic Breast Cancer: ALTERNATIVE.

Stephen R D Johnston1, Roberto Hegg1, Seock-Ah Im1, In Hae Park1, Olga Burdaeva1, Galina Kurteva1, Michael F Press1, Sergei Tjulandin1, Hiroji Iwata1, Sergio D Simon1, Sarah Kenny1, Severine Sarp1, Miguel A Izquierdo1, Lisa S Williams1, William J Gradishar1.   

Abstract

Purpose Human epidermal growth factor receptor 2 (HER2) targeting plus endocrine therapy (ET) improved clinical benefit in HER2-positive, hormone receptor (HR)-positive metastatic breast cancer (MBC) versus ET alone. Dual HER2 blockade enhances clinical benefit versus single HER2 blockade. The ALTERNATIVE study evaluated the efficacy and safety of dual HER2 blockade plus aromatase inhibitor (AI) in postmenopausal women with HER2-positive/HR-positive MBC who received prior ET and prior neo(adjuvant)/first-line trastuzumab (TRAS) plus chemotherapy. Methods Patients were randomly assigned (1:1:1) to receive lapatinib (LAP) + TRAS + AI, TRAS + AI, or LAP + AI. Patients for whom chemotherapy was intended were excluded. The primary end point was progression-free survival (PFS; investigator assessed) with LAP + TRAS + AI versus TRAS + AI. Secondary end points were PFS (comparison of other arms), overall survival, overall response rate, clinical benefit rate, and safety. Results Three hundred fifty-five patients were included in this analysis: LAP + TRAS + AI (n = 120), TRAS + AI (n = 117), and LAP + AI (n = 118). Baseline characteristics were balanced. The study met its primary end point; superior PFS was observed with LAP + TRAS + AI versus TRAS + AI (median PFS, 11 v 5.7 months; hazard ratio, 0.62; 95% CI, 0.45 to 0.88; P = .0064). Consistent PFS benefit was observed in predefined subgroups. Overall response rate, clinical benefit rate, and overall survival also favored LAP + TRAS + AI. The median PFS with LAP + AI versus TRAS + AI was 8.3 versus 5.7 months (hazard ratio, 0.71; 95% CI, 0.51 to 0.98; P = .0361). Common adverse events (AEs; ≥ 15%) with LAP + TRAS + AI, TRAS + AI, and LAP + AI were diarrhea (69%, 9%, and 51%, respectively), rash (36%, 2%, and 28%, respectively), nausea (22%, 9%, and 22%, respectively), and paronychia (30%, 0%, and 15%, respectively), mostly grade 1 or 2. Serious AEs were reported similarly across the three groups, and AEs leading to discontinuation were lower with LAP + TRAS + AI. Conclusion Dual HER2 blockade with LAP + TRAS + AI showed superior PFS benefit versus TRAS + AI in patients with HER2-positive/HR-positive MBC. This combination offers an effective and safe chemotherapy-sparing alternative treatment regimen for this patient population.

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Year:  2017        PMID: 29244528     DOI: 10.1200/JCO.2017.74.7824

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  35 in total

Review 1.  The trastuzumab era: current and upcoming targeted HER2+ breast cancer therapies.

Authors:  Jordyn Kreutzfeldt; Brett Rozeboom; Nandini Dey; Pradip De
Journal:  Am J Cancer Res       Date:  2020-04-01       Impact factor: 6.166

Review 2.  The changing treatment of metastatic her2-positive breast cancer.

Authors:  Maria Mitsogianni; Ioannis P Trontzas; Georgia Gomatou; Stephanie Ioannou; Nikolaos K Syrigos; Elias A Kotteas
Journal:  Oncol Lett       Date:  2021-02-12       Impact factor: 2.967

Review 3.  Mechanism, safety and efficacy of three tyrosine kinase inhibitors lapatinib, neratinib and pyrotinib in HER2-positive breast cancer.

Authors:  Jun-Cheng Xuhong; Xiao-Wei Qi; Yi Zhang; Jun Jiang
Journal:  Am J Cancer Res       Date:  2019-10-01       Impact factor: 6.166

4.  Stereotactic radiosurgery with concurrent HER2-directed therapy is associated with improved objective response for breast cancer brain metastasis.

Authors:  Joseph M Kim; Jacob A Miller; Rupesh Kotecha; Samuel T Chao; Manmeet S Ahluwalia; David M Peereboom; Alireza M Mohammadi; Gene H Barnett; Erin S Murphy; Michael A Vogelbaum; Lilyana Angelov; Jame Abraham; Halle Moore; G Thomas Budd; John H Suh
Journal:  Neuro Oncol       Date:  2019-05-06       Impact factor: 12.300

Review 5.  The role of HER2 alterations in clinicopathological and molecular characteristics of breast cancer and HER2-targeted therapies: a comprehensive review.

Authors:  Shafighe Asgari-Karchekani; Armin Aryannejad; Seied Asadollah Mousavi; Shirin Shahsavarhaghighi; Seyed Mohammad Tavangar
Journal:  Med Oncol       Date:  2022-09-29       Impact factor: 3.738

6.  Phenethyl isothiocyanate hampers growth and progression of HER2-positive breast and ovarian carcinoma by targeting their stem cell compartment.

Authors:  Ada Koschorke; Simona Faraci; Debora Giani; Claudia Chiodoni; Egidio Iorio; Rossella Canese; Mario P Colombo; Alessia Lamolinara; Manuela Iezzi; Michael Ladomery; Claudio Vernieri; Filippo de Braud; Massimo Di Nicola; Elda Tagliabue; Lorenzo Castagnoli; Serenella M Pupa
Journal:  Cell Oncol (Dordr)       Date:  2019-08-02       Impact factor: 6.730

Review 7.  Towards personalized treatment for early stage HER2-positive breast cancer.

Authors:  Kristina Goutsouliak; Jamunarani Veeraraghavan; Vidyalakshmi Sethunath; Carmine De Angelis; C Kent Osborne; Mothaffar F Rimawi; Rachel Schiff
Journal:  Nat Rev Clin Oncol       Date:  2019-12-13       Impact factor: 66.675

Review 8.  Cardiotoxicity in HER2-positive breast cancer patients.

Authors:  Diana Gonciar; Lucian Mocan; Alexandru Zlibut; Teodora Mocan; Lucia Agoston-Coldea
Journal:  Heart Fail Rev       Date:  2021-01-06       Impact factor: 4.214

9.  Triple Targeting of Breast Tumors Driven by Hormonal Receptors and HER2.

Authors:  Elena Shagisultanova; Lyndsey S Crump; Michelle Borakove; Jessica K Hall; Aryana R Rasti; Benjamin A Harrison; Peter Kabos; Traci R Lyons; Virginia F Borges
Journal:  Mol Cancer Ther       Date:  2021-11-02       Impact factor: 6.261

10.  Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases.

Authors:  Emad A Rakha; Islam M Miligy; Cecily M Quinn; Elena Provenzano; Abeer M Shaaban; Caterina Marchiò; Michael S Toss; Grace Gallagy; Ciara Murray; Janice Walshe; Ayaka Katayama; Karim Eldib; Nahla Badr; Bruce Tanchel; Rebecca Millican-Slater; Colin Purdie; Dave Purnell; Sarah E Pinder; Ian O Ellis; Andrew H S Lee
Journal:  Br J Cancer       Date:  2021-03-24       Impact factor: 7.640

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