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 Table of Contents  
SELECTED SUMMARY
Year : 2020  |  Volume : 33  |  Issue : 3  |  Page : 158-159

Adjuvant trastuzumab emtansine in human epidermal growth factor receptor 2-positive breast cancer: Take-home points from the KATHERINE trial


Department of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India

Date of Web Publication17-Apr-2021

Correspondence Address:
Atul Batra
Department of Medical Oncology, All India Institute of Medical Sciences, New Delhi
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0970-258X.314006


How to cite this article:
Vanidassane I, Naik RD, Sharma V, Khurana S, Batra A. Adjuvant trastuzumab emtansine in human epidermal growth factor receptor 2-positive breast cancer: Take-home points from the KATHERINE trial. Natl Med J India 2020;33:158-9

How to cite this URL:
Vanidassane I, Naik RD, Sharma V, Khurana S, Batra A. Adjuvant trastuzumab emtansine in human epidermal growth factor receptor 2-positive breast cancer: Take-home points from the KATHERINE trial. Natl Med J India [serial online] 2020 [cited 2021 Oct 20];33:158-9. Available from: http://www.nmji.in/text.asp?2020/33/3/158/314006

Von Minckwitz G, Huang CS, Mano MS, Loibl S, Mamounas EP, Untch M, Wolmark N, Rastogi P, Schneeweiss A, Redondo A, Fischer HH, Jacot W, Conlin AK, Arce-Salinas C, Wapnir IL, Jackisch C, DiGiovanna MP, Fasching PA, Crown JP, Wülfing P, Shao Z, Rota Caremoli E, Wu H, Lam LH, Tesarowski D, Smitt M, Douthwaite H, Singel SM, Geyer CE Jr for the KATHERINE Investigators. (German Breast Group, Neu-Isenburg, the Center for Hematology and Oncology Bethanien, Frankfurt, the AGO-B and HELIOS Klinikum Berlin-Buch, Berlin, the National Center for Tumor Diseases, Heidelberg University Hospital and German Cancer Research Center, Heidelberg, Evangelische Kliniken Gelsenkirchen, Gelsenkirchen, the Arbeitsgemeinschaft Gynäkologische Onkologie–Breast and Sana Klinikum Offenbach, Offenbach, the Department of Gynecology and Obstetrics, University Hospital Erlangen, Comprehensive Cancer Center Erlangen–EMN, Friedrich–Alexander University Erlangen–Nuremberg, Erlangen, and Mammazentrum Hamburg am Krankenhaus Jerusalem, Hamburg––all in Germany; the National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan; Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil; the National Surgical Adjuvant Breast and Bowel Project (NSABP) Foundation and Orlando Health University of Florida Health Cancer Center, Orlando, USA; the NSABP Foundation and Allegheny Health Network Cancer Institute and the NSABP Foundation and University of Pittsburgh Cancer Institute, School of Medicine, Pittsburgh, USA; Hospital Universitario La Paz–Instituto de Investigación Hospital Universitario La Paz, Madrid, Spain; Institut Régional du Cancer de Montpellier, Université de Montpellier, INSERM Unité 1194, Montpellier, France; the NSABP Foundation and Providence Portland Medical Center, Portland, Oregon, USA; the National Cancer Institute, Mexico City, Mexico; the NSABP Foundation and Stanford University School of Medicine, Stanford, and Genentech, South San Francisco—both in California, USA; Yale University School of Medicine, Yale Cancer Center, and Smilow Cancer Hospital, New Haven, Connecticut, USA; the Ireland Cooperative Oncology Research Group, Dublin, Ireland; Fudan University Shanghai Cancer Center and Roche (China) Holding, Shanghai, China; the Cancer Center Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy; F. Hoffmann–La Roche, Welwyn Garden City, UK; and the NSABP Foundation and Virginia Commonwealth University Massey Cancer Center, Richmond, Virginia, USA.) Trastuzumab emtansine for residual invasive HER 2-positive breast cancer.


  Summary Top


Patients with human epidermal growth factor receptor 2-(HER 2)positive early breast cancer have an aggressive clinical course than those with hormone-positive cancer. Patients harbouring HER 2 neu gene amplification tend to have increased risk of recurrence or death with residual invasive carcinoma after neoadjuvant chemotherapy and/ or targeted therapy. Trastuzumab emtansine (T-DM1) is an antibody drug conjugate of trastuzumab and emtansine, a microtubule inhibitor. The drug, apart from inhibiting the HER 2 pathway, also releases emtansine to HER 2 overexpressing cell, overcoming trastuzumab resistance and tumour killing. The KATHERINE trial was a multicentric, open-label, randomized study. A total of 1486 patients with HER 2-positive early breast cancer, who had residual invasive disease post-neoadjuvant therapy, were included in the study. Post-surgery, eligible patients were randomly assigned to either the T-DM1 group (14 cycles every q3weeks) or the trastuzumab group. The primary outcome of the study was invasive disease-free survival (IDFS) and the secondary outcome was safety. Planned interim analysis showed fewer invasive disease or death in the T-DM1 group than in the trastuzumab group (12.2% v. 22.2%). Three-year IDFS was statistically significantly higher in the T-DM1 group than in the trastuzumab group (hazard ratio 0.50; 95% CI 0.39–0.64, p≤0.001). The safety profile with T-DM1 was consistent with previous reports; however, there was an increased incidence of thrombocytopenia, liver dysfunction and neuropathy with T-DM1 than with trastuzumab. The trial concluded that among patients with HER 2-positive early breast cancer who had residual invasive disease after completion of neoadjuvant therapy, the risk of recurrence of invasive breast cancer or death was 50% lower with adjuvant T-DM1 than with trastuzumab alone.


  Comment Top


Breast cancer is the most common cancer worldwide and the leading cause of cancer-related mortality in women. With the invention of targeted therapy, the treatment paradigm of breast cancer has shifted from a nihilistic to an optimistic approach. HER 2 gene amplification is seen in 15%–20% of primary invasive breast cancer and is associated with poor survival.[1] Targeted agents such as trastuzumab, pertuzumab, T-DM1 and lapatinib block the activation of the HER 2 pathway, increasing pathological complete remission (pCR) rates when administered in the neoadjuvant setting. Despite the significant benefit, 50% of patients progress within 1 year of trastuzumab-based therapy due to acquired resistance.[2] T-DM1 overcomes trastuzumab resistance by virtue of its different mechanism of inhibition of HER 2 overexpression and also causing cell death by emtansine.[3] The correlation residual invasive carcinoma post-neoadjuvant therapy was best established in triple-negative breast cancer followed by HER-2-positive tumours. To overcome the adverse effect of residual disease, the KATHERINE trial intended to intensify/modify adjuvant therapy. This study has shown that there was 50% reduction in invasive disease recurrence when treated with T-DM1 in the adjuvant setting.

This well-designed study had pCR as a new surrogate marker to predict outcomes in breast cancer, which has advantages over using the new treatment to the entire HER-2-positive breast cancer scenario. Inclusion of all HER-2-positive early breast cancer means long duration of follow-up and thus delaying approval of a potentially beneficial drug.[4] Second, choosing a high-risk subset not achieving pCR is a logical and financially efficient way to prove the beneficial effect of T-DM1. The trial also emphasizes the importance of neoadjuvant-targeted therapy in HER-2-positive early breast cancer.

The benefit of T-DM1 comes along with increased toxicity and cost of therapy. The T-DM1 group had significantly more side-effects than the trastuzumab group. Even the cost of T-DM1 was higher. Although T-DM1 demonstrated clinical benefits, the absolute benefit in terms of cost-effectiveness was not ascertained. About 20% of patients in the trastuzumab group did not complete 14 cycles. Twenty-three patients randomized to the trastuzumab group did not receive planned therapy, while only 4 patients did not receive therapy in the T-DM1 group. This may have a bearing on observed outcomes. Whether the addition of T-DM1 changes the disease biology or natural course may be answered once survival data are available. The choice of a HER-2-targeted agent for relapse in T-DM1 and trastuzumab-exposed patients should be addressed in future trials.

Indian scenario

Many patients in the Indian subcontinent present in an advanced stage with large tumour bulk. Therefore, the probability of residual disease in Indian patients is high. The KATHERINE trial results could be the answer for many patients in India. However, the use of HER-2-targeted therapy is limited due to financial constraints for many patients.[5] The expected cost of treating breast cancer with adjuvant T-DM1 could be ₹3 600 000–₹5 000 000. The majority of patients in India are not covered by insurance nor can they afford the drug, ultimately abandoning the expensive option irrespective of the benefit. Initially, the cost may be prohibitive for upfront use of T-DM1 in India. Hence, it is important to ascertain the cost–benefit analysis of this treatment to counsel our patients. Second, centralized HER 2 testing was limited only to the pre-treatment biopsy samples in this study. Guarneri et al. reported loss of HER 2 expression in 15% of patients receiving neoadjuvant chemotherapy with anti-HER 2 agents.[6] The possibility of loss of HER-2 expression after neoadjuvant treatment and its influence on further decision-making and outcomes is important, especially in resource-limited settings. The side-effect profile of the Indian population should also be reviewed. Initiating trials involving adjuvant T-DM1 therapy in India and enrolling our patients is one way to address the above two concerns.

In a nutshell, the KATHERINE trial addresses the unmet need of a poor risk subset of HER-2-positive early breast cancers. It showed clinically meaningful decrease in IDFS with adjuvant T-DM1. The study has brought a new drug in the forefront using a relatively new predictive biomarker, i.e. pCR, in the management of HER-2-positive early breast cancer, setting a new standard of care in this population.

Conflicts of interest. None declared

 
  References Top

1.
King CR, Kraus MH, Aaronson SA. Amplification of a novel v-erbB-related gene in a human mammary carcinoma. Science 1985;229:974–6.  Back to cited text no. 1
    
2.
Marty M, Cognetti F, Maraninchi D, Snyder R, Mauriac L, Tubiana-Hulin M, et al. Randomized phase II trial of the efficacy and safety of trastuzumab combined with docetaxel in patients with human epidermal growth factor receptor 2-positive metastatic breast cancer administered as first-line treatment: The M77001 study group. J Clin Oncol 2005;23:4265–74.  Back to cited text no. 2
    
3.
Giordano SH, Temin S, Kirshner JJ, Chandarlapaty S, Crews JR, Davidson NE, et al. Systemic therapy for patients with advanced human epidermal growth factor receptor 2-positive breast cancer: American Society of Clinical Oncology Clinical Practice Guideline. J Clin Oncol 2014;32:2078–99.  Back to cited text no. 3
    
4.
Prowell TM, Beaver JA, Pazdur R. Residual disease after neoadjuvant therapy—Developing drugs for high-risk early breast cancer. N Engl J Med 2019;380: 612–15.  Back to cited text no. 4
    
5.
Adusumilli P, Konatam ML, Gundeti S, Bala S, Maddali LS. Treatment challenges and survival analysis of human epidermal growth factor receptor 2-positive breast cancer in the real world. Indian J Med Paediatr Oncol 2017;38:22–7.  Back to cited text no. 5
    
6.
Guarneri V, Dieci MV, Barbieri E, Piacentini F, Omarini C, Ficarra G, et al. Loss of HER 2 positivity and prognosis after neoadjuvant therapy in HER2-positive breast cancer patients. Ann Oncol 2013;24:2990–4.  Back to cited text no. 6
    




 

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