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Indian Journal of Medical and Paediatric Oncology
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DRUG REVIEW
Year : 2020  |  Volume : 41  |  Issue : 1  |  Page : 54-56  

Trastuzumab: A milestone in human epidermal growth factor receptor 2-positive breast cancer


Department of Medical Oncology, Cancer Institute (WIA), Chennai, Tamil Nadu, India

Date of Submission16-Dec-2019
Date of Acceptance06-Feb-2020
Date of Web Publication24-Apr-2020

Correspondence Address:
Dr. Manikandan Dhanushkodi
Department of Medical Oncology, Cancer Institute (WIA), 38, Sardar Patel Road, Chennai . 600 036, Tamil Nadu
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijmpo.ijmpo_252_19

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  Abstract 


Human epidermal growth factor receptor 2 (HER2) overexpression is seen in 25% of breast cancers. Patients with HER2-positive breast cancer have aggressive disease and inferior survival. HER2 overexpression is assessed by immunohistochemistry or fluorescent in situ hybridization-based methods. Trastuzumab has shown to improve survival in HER2-positive breast cancer. It is recommended in patients with >T1c for 1-year duration in adjuvant setting, preferably given concurrently with taxane.

Keywords: Breast cancer, human epidermal growth factor receptor 2-positive disease, trastuzumab


How to cite this article:
Dhanushkodi M. Trastuzumab: A milestone in human epidermal growth factor receptor 2-positive breast cancer. Indian J Med Paediatr Oncol 2020;41:54-6

How to cite this URL:
Dhanushkodi M. Trastuzumab: A milestone in human epidermal growth factor receptor 2-positive breast cancer. Indian J Med Paediatr Oncol [serial online] 2020 [cited 2020 May 28];41:54-6. Available from: http://www.ijmpo.org/text.asp?2020/41/1/54/283105




  Introduction Top


Human epidermal growth factor receptor 2 (HER2) overexpression is seen in 25% of breast cancers.[1] Patients with HER2-positive breast cancer have aggressive disease, higher chance of metastasis, and inferior survival.[2] HER2 overexpression is assessed by immunohistochemistry (IHC) or fluorescent in situ hybridization (FISH)-based methods. Trastuzumab has shown to improve survival in HER2-positive breast cancer.


  Mechanism of Action Top


Trastuzumab is an IgG1 kappa recombinant DNA-derived humanized monoclonal antibody that selectively binds with high affinity to the extracellular domain of (HER2) protein and prevents the activation of intracellular tyrosine kinase. Other mechanisms include prevention of HER2 receptor dimerization, increased endocytic destruction of receptor, and antibody-dependent cell-mediated cytotoxicity.[3] There are a few differences in the mechanism of action between trastuzumab and newer anti-HER2 therapy. Pertuzumab binds to subdomain 2 of HER2 receptors and blocks its ligand-dependent heterodimerization with HER1, HER3, and HER4. Lapatinib binds to the intracellular domain of epidermal growth factor receptor and HER2 and prevents the downstream signaling.


  Discovery Top


In 1979, Robert Weinberg identified that HER2 gene was involved in multiple cancer pathways. Many years later, Dennis Slamon (UCLA) collaborated with Axel Ullrich (Genentech) and showed that HER2 positivity was associated with poor prognosis and trastuzumab improved survival.[4]


  Approval Top


In 1998, trastuzumab was Food and Drug Administration (FDA) approved for the treatment of HER2-positive metastatic breast cancer. In 2006, trastuzumab was FDA approved for the treatment of HER2-positive breast cancer as an adjuvant therapy. In 2010, trastuzumab was FDA approved for the treatment of HER2-positive metastatic gastric cancer.


  Human Epidermal Growth Factor Receptor 2 Positivity (Asco/cap Guideline) Top


Breast cancer and gastroesophageal cancer – HER2 is positive when IHC for HER2 neu is 2+ and FISH for HER2 neu is positive or IHC 3+.


  Indication Top


The National Comprehensive Cancer Network and the European Society of Medical Oncology guidelines recommend trastuzumab for patients with ≥T1c HER2-positive breast cancer in adjuvant setting. Patients with pT1b can be considered for trastuzumab if the tumor is hormone negative or Grade 3. Trastuzumab is preferably given concurrently with a taxane. The key trials on trastuzumab in HER2-positive breast cancer are mentioned in [Table 1].
Table 1: Clinical trials with trastuzumab

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  Other Indication Top


Trastuzumab-based chemotherapy is recommended in advanced HER2-positive gastric or gastroesophageal junction adenocarcinoma. Addition of trastuzumab to chemotherapy in advanced gastric/gastroesophageal junction adenocarcinoma improves overall survival (OS) by 2 months.[10]


  Strength Top


Trastuzumab is available as 440 and 150 mg vial. The reconstituted vial can be used until 28 days when stored at 2°C–8°C.


  Dose and Administration Top


The 3 weekly dose is 8 mg/kg loading intravenous over 90 min followed by maintenance 6 mg/kg over 30 min. The weekly dose is 4 mg/kg loading intravenous over 90 min followed by 2 mg/kg maintenance over 30 min. Subcutaneous trastuzumab has also shown to be noninferior to intravenous trastuzumab.[11] The recommended dose is 600 mg trastuzumab with 10,000 units hyaluronidase Q 3 weekly subcutaneous over 2–5 min. Intrathecal trastuzumab 20–50 mg can be used in HER2-positive leptomeningeal disease.[12]


  Regimens in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Top


  • <3 cm, node negative: weekly paclitaxel for 12 cycles along with trastuzumab (1 year)[13]
  • Node positive and higher stage: TCH (docetaxel, carboplatin, and trastuzumab) or AC (adriamycin and cyclophosphamide) followed paclitaxel with trastuzumab[7]
  • Advanced/metastatic: THP (docetaxel, trastuzumab, and pertuzumab).[14]



  Duration Top


Trastuzumab is continued lifelong for patients with metastatic disease and 1 year for patients with non-metastatic disease. Persephone trial in early-stage breast cancer from the UK has shown 6 months of trastuzumab to be non-inferior to 1-year duration.[15] Short-course trastuzumab (weekly for 9 weeks) has shown to improve survival as compared to no trastuzumab.[16],[17]


  Toxicity Top


Cardiotoxicity

Clinical trials have shown that the incidence of clinically significant cardiotoxicity with chemotherapy and trastuzumab was about 2%.[7] The risk factors for trastuzumab-induced cardiotoxicity are prior anthracycline usage, coronary artery disease, baseline systolic dysfunction (left ventricular ejection fraction <50%), diabetes, hypertension, dyslipidemia, and atrial fibrillation. Cardiotoxicity is lesser in patients who received short duration trastuzumab (6 months: 4%) as compared to long duration (1 year: 6%).[15]

Monitoring

No blood investigations are necessary before administration of trastuzumab. Echocardiogram has to be done before starting trastuzumab, every 3 monthly while on trastuzumab, and 6 monthly for 2 years after completion of trastuzumab. Patients who have received prior anthracycline need to be monitored for 5 years after completion of trastuzumab. Trastuzumab should be temporarily withheld if LVEF drop is >10% and permanently withheld if patients develop symptomatic heart failure or after 2 withholds.

Biosimilar

Biosimilars are game-changers in oncology and have made cancer care affordable and cost-effective. In 2017, the FDA approved the first biosimilar trastuzumab (Mylan) based on the Heritage trial.[18] This was a phase 3 randomized controlled trial with 500 patients with HER2-positive metastatic breast cancer, where trastuzumab biosimilar showed equivalent response rate (69% for biosimilar and 64% for innovator) at 24 weeks. The OS was also similar in both groups.[19]

Newer anti-HER2 therapy

FDA approved other anti-HER2 therapy includes lapatinib, trastuzumab emtansine, pertuzumab, neratinib, and trastuzumab deruxtecan.[20] Tucatinib[21] is a newer anti-HER2 therapy that has shown promise in heavily pretreated advanced breast cancer.


  Conclusion Top


Trastuzumab has significantly improved survival in early, locally advanced, and metastatic HER2-positive breast cancer. It can cause cardiotoxicity and needs periodic monitoring with echocardiogram.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Mitri Z, Constantine T, O'Regan R. The HER2 receptor in breast cancer: Pathophysiology, clinical use, and new advances in therapy. Chemother Res Pract 2012;2012:743193.  Back to cited text no. 1
    
2.
Slamon DJ, Clark GM, Wong SG, Levin WJ, Ullrich A, McGuire WL. Human breast cancer: Correlation of relapse and survival with amplification of the HER-2/neu oncogene. Science 1987;235:177-82.  Back to cited text no. 2
    
3.
Hudis CA. Trastuzumab – Mechanism of action and use in clinical practice. N Engl J Med 2007;357:39-51.  Back to cited text no. 3
    
4.
Delaney P. HER-2: The making of herceptin, a revolutionary treatment for breast cancer. J Natl Cancer Inst 1999;91:1329-30.  Back to cited text no. 4
    
5.
Perez EA, Romond EH, Suman VJ, Jeong JH, Sledge G, Geyer CE Jr, et al. Trastuzumab plus adjuvant chemotherapy for human epidermal growth factor receptor 2-positive breast cancer: planned joint analysis of overall survival from NSABP B-31 and NCCTG N9831. J Clin Oncol 2014;32:3744-52.  Back to cited text no. 5
    
6.
Cameron D, Piccart-Gebhart MJ, Gelber RD, Procter M, Goldhirsch A, de Azambuja E, et al. 11 years' follow-up of trastuzumab after adjuvant chemotherapy in HER2-positive early breast cancer: Final analysis of the HERceptin Adjuvant (HERA) trial. Lancet 2017;389:1195-205.  Back to cited text no. 6
    
7.
Slamon D, Eiermann W, Robert N, Pienkowski T, Martin M, Press M, et al. Adjuvant trastuzumab in HER2-positive breast cancer. N Engl J Med 2011;365:1273-83.  Back to cited text no. 7
    
8.
Slamon DJ, Leyland-Jones B, Shak S, Fuchs H, Paton V, Bajamonde A, et al. Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. N Engl J Med 2001;344:783-92.  Back to cited text no. 8
    
9.
Joensuu H, Kellokumpu-Lehtinen PL, Bono P, Alanko T, Kataja V, Asola R, et al. Adjuvant docetaxel or vinorelbine with or without trastuzumab for breast cancer. N Engl J Med 2006;354:809-20.  Back to cited text no. 9
    
10.
Bang YJ, Van Cutsem E, Feyereislova A, Chung HC, Shen L, Sawaki A, et al. Trastuzumab in combination with chemotherapy versus chemotherapy alone for treatment of HER2-positive advanced gastric or gastro-oesophageal junction cancer (ToGA): A phase 3, open-label, randomised controlled trial. Lancet 2010;376:687-97.  Back to cited text no. 10
    
11.
Jackisch C, Hegg R, Stroyakovskiy D, Ahn JS, Melichar B, Chen SC, et al. HannaH phase III randomised study: Association of total pathological complete response with event-free survival in HER2-positive early breast cancer treated with neoadjuvant-adjuvant trastuzumab after 2 years of treatment-free follow-up. Eur J Cancer 2016;62:62-75.  Back to cited text no. 11
    
12.
Figura NB, Long W, Yu M, Robinson TJ, Mokhtari S, Etame AB, et al. Intrathecal trastuzumab in the management of HER2+ breast leptomeningeal disease: A single institution experience. Breast Cancer Res Treat 2018;169:391-6.  Back to cited text no. 12
    
13.
Tolaney SM, Barry WT, Dang CT, Yardley DA, Moy B, Marcom PK, et al. Adjuvant paclitaxel and trastuzumab for node-negative, HER2-positive breast cancer. N Engl J Med 2015;372:134-41.  Back to cited text no. 13
    
14.
Swain SM, Baselga J, Kim SB, Ro J, Semiglazov V, Campone M, et al. Pertuzumab, trastuzumab, and docetaxel in HER2-positive metastatic breast cancer. N Engl J Med 2015;372:724-34.  Back to cited text no. 14
    
15.
Earl HM, Hiller L, Vallier AL, Loi S, McAdam K, Hughes-Davies L, et al. 6 versus 12 months of adjuvant trastuzumab for HER2-positive early breast cancer (PERSEPHONE): 4-year disease-free survival results of a randomised phase 3 non-inferiority trial. Lancet 2019;393:2599-612.  Back to cited text no. 15
    
16.
Joensuu H, Bono P, Kataja V, Alanko T, Kokko R, Asola R, et al. Fluorouracil, epirubicin, and cyclophosphamide with either docetaxel or vinorelbine, with or without trastuzumab, as adjuvant treatments of breast cancer: Final results of the FinHer Trial. J Clin Oncol 2009;27:5685-92.  Back to cited text no. 16
    
17.
Sethjiwala T, Dhanushkodi M, Radhakrishnan V, Kalaiarasi JP, Mehra N, Joshi A, et al. Adjuvant short-course trastuzumab in breast cancer. Indian J Gynecol 2019;17:68.  Back to cited text no. 17
    
18.
Rugo HS, Barve A, Waller CF, Hernandez-Bronchud M, Herson J, Yuan J, et al. Effect of a proposed trastuzumab biosimilar compared with trastuzumab on overall response rate in patients with ERBB2 (HER2)-positive metastatic breast cancer: A randomized clinical trial. JAMA 2017;317:37-47.  Back to cited text no. 18
    
19.
Waller CF, Manikhas V, Pennella EJ, Bondarenko V, Mukhametshina G, Tiambeng ML, et al. Biosimilar trastuzumab-dkst monotherapy versus trastuzumab monotherapy after combination therapy: Final overall survival (OS) from the phase III HERITAGE Trial. J Clin Oncol 2019;37:1021.  Back to cited text no. 19
    
20.
Modi S, Saura C, Yamashita T, Park YH, Kim S, Tamura K, et al. Trastuzumab deruxtecan in previously treated HER2-positive breast cancer. N Engl J Med 2019;382:610-21.  Back to cited text no. 20
    
21.
Murthy RK, Loi S, Okines A, Paplomata E, Hamilton E, Hurvitz SA, et al. Tucatinib, trastuzumab, and capecitabine for HER2-positive metastatic breast cancer. N Engl J Med 2019;382:597-609.  Back to cited text no. 21
    



 
 
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  In this article
   Abstract
  Introduction
  Mechanism of Action
  Discovery
  Approval
   Human Epidermal ...
  Indication
  Other Indication
  Strength
   Dose and Adminis...
   Regimens in Huma...
  Duration
  Toxicity
  Conclusion
   References
   Article Tables

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