Skip to main content
Log in

Trastuzumab Emtansine: First Global Approval

  • R&D Insight Report
  • Published:
Drugs Aims and scope Submit manuscript

Abstract

Genentech and ImmunoGen are collaborating on the development of trastuzumab emtansine, a HER2 antibody-drug conjugate that comprises Genentech’s trastuzumab antibody linked to ImmunoGen’s anti-mitotic agent, mertansine (a maytansine derivative; also known as DM1). The conjugate combines two strategies: the anti-HER2 activity of trastuzumab, and the targeted intracellular delivery of mertansine, a tubulin polymerisation inhibitor which interferes with mitosis and promotes apoptosis. The linker in trastuzumab emtansine is a non-reducible thioether linker, N-succinimidyl-4-(N-maleimidomethyl) cyclohexane-1-carboxylate (SMCC, designated MCC after conjugation). Trastuzumab emtansine (Kadcyla™) has been launched in the USA as second-line monotherapy for HER2-positive metastatic breast cancer, and has been filed for approval in the EU and Japan in this indication. Trastuzumab emtansine is in phase III development as first-line combination therapy or monotherapy for metastatic HER2-positive breast cancer, and as third-line monotherapy for metastatic HER2-positive breast cancer. Phase II development is underway for early-stage breast cancer and phase II/III development is underway in patients with HER2-positive gastric cancer. This article summarizes the milestones in the development of trastuzumab emtansine leading to this first approval for the treatment of patients with HER2-positive, metastatic breast cancer who previously received trastuzumab and a taxane, separately or in combination.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. World Health Organization. Breast cancer: prevention and control. 2012. http://www.who.int/cancer/detection/breastcancer/en/index1.html. Accessed 11 Mar 2013.

  2. Dawood S, Broglio K, Buzdar AU, et al. Prognosis of women with metastatic breast cancer by HER2 status and trastuzumab treatment: an institutional-based review. J Clin Oncol. 2010;28(1):92–8.

    Article  PubMed  CAS  Google Scholar 

  3. Hurvitz SA, Kakkar R. The potential for trastuzumab emtansine in human epidermal growth factor receptor 2 positive metastatic breast cancer: latest evidence and ongoing studies. Ther Adv Med Oncol. 2012;4(5):235–45.

    Article  PubMed  Google Scholar 

  4. US FDA. FDA approves new treatment for late-stage breast cancer [media release]. 22 Feb 2013. http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm340704.htm.

  5. Genentech Inc. Kadcyla™ (ado-trastuzumab emtansine): US prescribing information. 2013. http://www.gene.com/download/pdf/kadcyla_prescribing.pdf. Accessed 12 Mar 2013.

  6. ImmunoGen Inc. ImmunoGen Inc. announces FDA approval of Kadcyla (ado-trastuzumab emtansine; also known as T-DM1) [media release]. 22 Feb 2013. http://www.immunogen.com

  7. Genentech. FDA grants Genentech’s trastuzumab emtansine (T-DM1) priority review for HER2- positive metastatic breast cancer [media release]. 6 Nov 2012. http://www.gene.com.

  8. ImmunoGen Inc. ImmunoGen Inc. announces trastuzumab emtansine (T-DM1) significantly improved survival in the EMILIA phase III trial [media release]. 27 Aug 2012. http://www.immunogen.com.

  9. Roche. FDA approves Roche’s Kadcyla (trastuzumab emtansine), the first antibody-drug conjugate for treating HER2-positive metastatic breast cancer [media release]. 22 Feb 2013. http://www.roche.com.

  10. ImmunoGen Inc. ImmunoGen Inc. reports second quarter fiscal year 2013 financial results and provides quarterly update [media release]. 25 Jan 2013. http://www.immunogen.com.

  11. Chugai Pharmaceutical Co. Ltd. New drug application filed for antibody-drug conjugate trastuzumab emtansine for the treatment of HER2-positive metastatic or recurrent breast cancer [media release]. 29 Jan 2013. http://www.chugai-pharm.co.jp.

  12. Hoffmann-La Roche. A study of trastuzumab emtansine (T-DM1) plus pertuzumab/pertuzumab placebo versus trastuzumab (herceptin) plus a taxane in patients with metastatic breast cancer (MARIANNE) [ClinicalTrials.gov identifier NCT01120184]. US National Institutes of Health, ClinicalTrials.gov. 2013. http://clinicaltrials.gov/show/NCT01120184. Accessed 12 Mar 2013.

  13. Ellis PA, Barrios CH, Im Y, et al. MARIANNE: A phase III, randomized study of trastuzumab-DM1 (T-DM1) with or without pertuzumab (P) compared with trastuzumab (H) plus taxane for first- line treatment of HER2-positive, progressive, or recurrent locally advanced or metastatic breast cancer (MBC) [abstract no. TPS102]. J Clin Oncol. 2011;29(15 Suppl).

  14. Hoffmann-La Roche. A study of trastuzumab emtansine in comparison with treatment of physician’s choice in patients with HER2-positive breast cancer who have received at least two prior regimens of HER2-directed therapy (TH3RESA) [ClinicalTrials.gov identifier NCT01419197]. US National Institutes of Health, ClinicalTrials.gov. 2013. http://clinicaltrials.gov/ct2/show/NCT01419197?term=NCT01419197&rank=1. Accessed 12 Mar 2013.

  15. Krop IE, LoRusso P, Miller KD, et al. A phase II study of trastuzumab emtansine in patients with human epidermal growth factor receptor 2-positive metastatic breast cancer who were previously treated with trastuzumab, lapatinib, an anthracycline, a taxane, and capecitabine. J Clin Oncol. 2012;30(26):3234–41.

    Article  PubMed  CAS  Google Scholar 

  16. Hoffmann-La Roche. A study of trastuzumab emtansine (T-DM1) sequentially with anthracycline-based chemotherapy, as adjuvant or neoadjuvant therapy for patients with early stage HER2-positive breast cancer [ClinicalTrials.gov identifier NCT01196052]. US National Institutes of Health, ClinicalTrials.gov. 2013. http://www.clinicaltrials.gov/ct2/show/record/NCT01196052?term=NCT01196052&rank=1. Accessed 13 Mar 2013.

  17. ImmunoGen Inc. ImmunoGen Inc. announces development of trastuzumab emtansine for early stage HER2-positive breast cancer [media release]. 3 Jun 2012. http://www.immunogen.com.

  18. Hoffmann-La Roche. A study of trastuzumab emtansine versus taxane in patients with advanced gastric cancer [ClinicalTrials.gov identifier NCT01641939]. US National Institutes of Health, ClinicalTrials.gov. 2013. http://clinicaltrials.gov/ct2/show/NCT01641939?term=NCT01641939&rank=1. Accessed 13 Mar 2013.

  19. ImmunoGen Inc. ImmunoGen Inc. announces Genentech’s fifth TAP technology license [media release]. 9 Dec 2008. http://www.immunogen.com.

  20. ImmunoGen Inc. ImmunoGen Inc. to develop commercial-scale manufacturing process for trastuzumab-DM1 for Genentech; companies also amend 2000 agreement for TAP compounds targeting HER2, potentially providing increased royalties and milestones to ImmunoGen [media release]. 4 May 2006. http://www.businesswire.com.

  21. ImmunoGen Inc. ImmunoGen Inc. announces Genentech's renewal of technology access agreement [media release]. 3 May 2005. http://www.immunogen.com.

  22. Roche. Roche Completes Acquisition of Genentech [media release]. 26 Mar 2009. http://www.roche.com.

  23. ImmunoGen Inc. ImmunoGen Inc. reports second quarter fiscal year 2008 financial results [media release]. 1 Feb 2008. http://www.immunogen.com.

  24. Junttila TT, Li G, Parsons K, et al. Trastuzumab-DM1 (T-DM1) retains all the mechanisms of action of trastuzumab and efficiently inhibits growth of lapatinib insensitive breast cancer. Breast Cancer Res Treat. 2011;128(2):347–56.

    Article  PubMed  CAS  Google Scholar 

  25. Junttila T, Fields C, Li G, et al. Trastuzumab-mertansine retains all the mechanisms of action of trastuzumab and is extremely effective in combination with docetaxel [abstract no. 515]. 20th-EORTC-NCI-AACR symposium on molecular targets and cancer therapeutics, Geneva, 21–24 Oct 2008.

  26. Lewis Phillips GD, Li G, Dugger DL, et al. Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate. Cancer Res. 2008;68(22):9280–90.

    Google Scholar 

  27. Li G, Fields CT, Parsons KL. Trastuzumab-DM1: mechanisms of action and mechanisms of resistance [abstract no. 223]. 22nd EORTC-NCI-AACR symposium on molecular targets and cancer therapeutics, 16–19 Nov 2010.

  28. Honig A, Diessner J, Dietl J, et al. T-DM1 and pertuzumab as new tools for HER2 specific antibody-therapy against breast cancer stem cells in HER2-positive mammary carcinoma [abstract no. P1-04-05 plus poster]. Cancer Res. 2011;71(24 Suppl 3).

  29. Schwall RH, Dugger D, Erickson SL, et al. Potent preclinical efficacy of herceptin-DM1 against HER2-over-expressing breast tumors in vivo [abstract no. 652]. AACR-NCI-EORTC international conference on molecular targets and cancer therapeutics, Maimi (FL); 29 Oct–2 Nov 2001.

  30. Barok M, Tanner M, Koninki K, et al. Trastuzumab-DM1 is highly effective in preclinical models of HER2-positive gastric cancer. Cancer Lett. 2011;306(2):171–9.

    Article  PubMed  CAS  Google Scholar 

  31. Fields C, Li G, Prior WW, et al. Enhanced in vitro and in vivo activity of trastuzumab-DM1 antibody-drug conjugate combined with GDC-0941, a small molecule inhibitor of Pl3 kinase [abstract no. 3239]. 100th annual meeting of the American Association for Cancer Research, Denver (CO), 18–22 Apr 2009.

  32. Gupta M, Wang B, Carrothers T, et al. Exposure-response analysis in patients with HER2-positive (HER2+) metastatic breast cancer (MBC) to assess the effect of T-DM1 on QTc prolongation [abstract no. PII-64]. Clin Pharmacol Ther. 2011;89 Suppl 1:S58.

    Google Scholar 

  33. Girish S, Gupta M, Wang B, et al. Clinical pharmacology of trastuzumab emtansine (T-DM1): an antibody-drug conjugate in development for the treatment of HER2-positive cancer. Cancer Chemother Pharmacol. 2012;69(5):1229–40.

    Article  PubMed  CAS  Google Scholar 

  34. Gupta M, Lorusso PM, Wang B, et al. Clinical implications of pathophysiological and demographic covariates on the population pharmacokinetics of trastuzumab emtansine, a HER2-targeted antibody-drug conjugate, in patients with HER2-positive metastatic breast cancer. J Clin Pharmacol. 2012;52(5):691–703.

    Article  PubMed  CAS  Google Scholar 

  35. Krop IE, Beeram M, Modi S, et al. Phase I study of trastuzumab-DM1, an HER2 antibody-drug conjugate, given every 3 weeks to patients with HER2-positive metastatic breast cancer. J Clin Oncol. 2010;28(16):2698–704.

    Article  PubMed  CAS  Google Scholar 

  36. Lu D, Burris HA 3rd, Wang B, et al. Drug interaction potential of trastuzumab emtansine (T-DM1) combined with pertuzumab in patients with HER2-positive metastatic breast cancer. Curr Drug Metab. 2012;13(7):911–22.

    Article  PubMed  CAS  Google Scholar 

  37. Verma S, Miles D, Gianni L, et al. Trastuzumab emtansine for HER2-positive advanced breast cancer. N Engl J Med. 2012;367(19):1783–91.

    Article  PubMed  CAS  Google Scholar 

  38. Hurvitz SA, Dirix L, Kocsis J, et al. Phase II randomized study of trastuzumab emtansine versus trastuzumab plus docetaxel in patients with human epidermal growth factor receptor 2-postive metastatic breast cancer. J Clin Oncol. 2013;31(9):1157-63.

    Google Scholar 

  39. Burris HA 3rd, Rugo HS, Vukelja SJ, et al. Phase II study of the antibody drug conjugate trastuzumab-DM1 for the treatment of human epidermal growth factor receptor 2 (HER2)-positive breast cancer after prior HER2-directed therapy. J Clin Oncol. 2011;29(4):398–405.

    Article  PubMed  CAS  Google Scholar 

  40. Dieras V, Harbeck N, Albain K, et al. A phase Ib/II trial of trastuzumab-DM1 (T-DM1) with pertuzumab for patients with HER2-positive, locally advanced or metastatic breast cancer: interim efficacy and safety results [abstract no. P3-14-01 plus poster]. 33rd annual San Antonio breast cancer symposium, San Antonio (TX), 8–12 Dec 2010.

  41. Beeram M, Krop IE, Burris HA, et al. A phase 1 study of weekly dosing of trastuzumab emtansine (T-DM1) in patients with advanced human epidermal growth factor 2-positive breast cancer. Cancer. 2012;118(23):5733–40.

    Article  PubMed  CAS  Google Scholar 

  42. Aogi K, Ando M, Iwata H, et al. Phase I study of single agent trastuzumab emtansine in Japanese patients with human epidermal growth factor receptor2 (HER2)-positive metastatic breast cancer (JO22591) [abstract no. P1-12-19]. Cancer Res. 2011;71(24 Suppl 3).

  43. Mahapatra K, Darbonne W, Bumbaca D, et al. T-DM1-induced thrombocytopenia results from impaired platelet production in a HER2-independent manner [abstract no. A135]. 23rd AACR-NCI-EORTC international conference on molecular targets and cancer therapeutics, San Fransisco (CA), 12–16 Nov 2011.

  44. Agilent Technologies. FDA approves two Dako assays as companion diagnostics for genentech’s new breast cancer medicine Kadcyla [media release]. 5 Mar 2013. http://www.agilent.com.

  45. Hoffmann-La Roche. A study of trastuzumab emtansine in patients with HER2 positive breast cancer who have received prior anti-HER2 and chemotherapy-based treatment [ClinicalTrials.gov identifier NCT01702571]. US National Institutes of Health, ClinicalTrials.gov. 2013. http://clinicaltrials.gov/ct2/show/NCT01702571?term=NCT01702571&rank=1. Accessed 12 Mar 2013.

  46. ImmunoGen Inc. ImmunoGen Inc. reports second quarter fiscal year 2012 financial results and provides quarterly update [media release]. 27 Jan 2012. http://www.immunogen.com.

  47. Genentech. A study of trastuzumab-MCC-DM1 in patients with HER2-positive locally advanced or metastatic breast cancer [ClinicalTrials.gov identifier NCT01120561]. US National Institutes of Health, ClinicalTrials.gov. 2013. http://www.clinicaltrials.gov/show/NCT01120561. Accessed 13 Mar 2013.

  48. Roche. Roche submits application to FDA for trastuzumab-DM1 in previously treated advanced HER2-positive breast cancer [media release]. 7 Jul 2010. http://www.roche.com.

  49. Genentech. An extension study of trastusumab emtansine in patients previously treated with trastusumab emtansine [ClinicalTrials.gov identifier NCT00781612]. US National Institutes of Health, ClinicalTrials.gov. 2012. http://clinicaltrials.gov/show/NCT00781612. Accessed 13 Mar 2013.

  50. Genentech. A study of trastuzumab emtansine, paclitaxel, and pertuzumab in patients with HER2-positive, locally advanced or metastatic breast cancer [ClinicalTrials.gov identifier NCT00951665]. US National Institutes of Health, ClinicalTrials.gov. 2012. http://clinicaltrials.gov/show/NCT00951665. Accessed 13 Mar 2013.

  51. Krop IE, Modi S, Elias A, et al. A dose-escalation study of trastuzumab-DM1(T-DM1), paclitaxel (T), and pertuzumab (P) in patients with HER2-positive, locally advanced or metastatic breast cancer (MBC) previously treated with a trastuzumab-containing regimen [abstract no. P3-14-10]. Cancer Res. 2010;70(24 Suppl 2).

  52. Hoffmann-La Roche. A study of trastuzumab emtansine (T-DM1) in combination with docetaxel, and potentially pertuzumab, in patients with advanced breast cancer [ClinicalTrials.gov identifier NCT00934856]. US National Institutes of Health, ClinicalTrials.gov. 2013. http://clinicaltrials.gov/show/NCT00934856. Accessed 13 Mar 2013.

  53. Genentech. Trastuzumab and trastuzumab-MCC-DM1 administered intravenously and GDC-0941 administered orally to patients with HER2-positive metastatic breast cancer who have progressed on previous trastuzumab-based therapy [ClinicalTrials.gov identifier NCT00928330]. US National Institutes of Health, ClinicalTrials.gov. 2012. http://clinicaltrials.gov/ct2/show/NCT00928330?term=NCT00928330&rank=1. Accessed 13 Mar 2013.

  54. Krop IE, Wolff AC, Winer EP, et al. A phase Ib study evaluating safety, tolerability, pharmacokinetics (PK), and activity of the phosphoinositide-3 kinase (PI3 K) inhibitor GDC-0941 in combination with trastuzumab-MCC-DM1 (T-DM1) in patients with advanced HER2-positive breast cancer [abstract no. P6-15-02]. Cancer Res. 2010;70(24 Suppl 2).

  55. Hoffmann-La Roche. A combination study of trastuzumab emtansine and capecitabine in patients with breast cancer or gastric cancer [ClinicalTrials.gov identifier NCT01702558]. US National Institutes of Health, ClinicalTrials.gov. 2013. http://clinicaltrials.gov/show/NCT01702558. Accessed 13 Mar 2013.

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Anita Ballantyne.

Additional information

This profile has been extracted and modified from the Adis R&D Insight drug pipeline database. Adis R&D Insight tracks drug development worldwide through the entire development process, from discovery, through pre-clinical and clinical studies to market launch.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ballantyne, A., Dhillon, S. Trastuzumab Emtansine: First Global Approval. Drugs 73, 755–765 (2013). https://doi.org/10.1007/s40265-013-0050-2

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40265-013-0050-2

Keywords

Navigation