Trastuzumab Deruxtecan Effectively Treats HER2-Expressing Cancers Regardless of Tumor Location

For immediate release
June 5, 2023

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Rachel Cagan Facci
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ASCO Perspective

“This study provides data for an unmet need for patients who have exhausted standard therapeutic options with tumors that overexpress HER2 for which no drug is yet approved. While additional follow-up is needed, there is robust activity across multiple HER2 expressing tumors with over 50% response rate in those with the highest levels of HER2 expression coupled with an encouraging safety profile. Trastuzumab deruxtecan could provide a new treatment option for these patients,” said Bradley Alexander McGregor, MD, ASCO Expert.

ALEXANDRIA, Va. — Trastuzumab deruxtecan (Enhertu®) is an effective treatment option for people with difficult-to-treat HER2-expressing solid tumors, according to the findings of an international study. The research will be presented at the 2023 American Society of Clinical Oncology (ASCO) Annual Meeting.

Study at a Glance

Focus

Effectiveness of trastuzumab deruxtecan on biliary tract, bladder, cervical, endometrial, ovarian, pancreatic, and other solid tumors

Population

267 patients with HER2-expressing (immunohistochemistry [IHC] 3+ or IHC 2+ by local or central testing) locally advanced or metastatic cancer – biliary tract, bladder, cervical, endometrial, ovarian, pancreatic, or other tumors – that has gotten worse after at least one systemic treatment or that has no treatment options

Findings

  • At median follow-up of 9.7 months, trastuzumab deruxtecan resulted in an objective response rate (ORR) of 37.1% in the overall study population.
  • Median duration of response (mDOR) was 11.8 months. 
  • In patients with higher levels of IHC expression (IHC 3+), ORR was 61.3% and mDOR was 22.1 months compared to 27.2% ORR and 9.8 months mDOR for patients with IHC 2+ expression.

Significance

Trastuzumab deruxtecan may be a potential new treatment option for patients with HER2-expressing solid tumors.

Key Findings

In the phase II open-label DESTINY-PanTumor02 study, patients with HER2-expressing (immunohistochemistry [IHC] 3+ or IHC 2+) locally advanced or metastatic disease that had worsened after at least one systemic treatment or that had no treatment options were treated with at least one dose of trastuzumab deruxtecan. At the median follow-up of 9.7 months, the treatment resulted in an ORR of 37.1% (ORR is a measure of the number of partial and complete responses to a treatment). The amount of time that tumors continued to respond to treatment—measured by the mDOR—was 11.8 months. In patients with higher levels of HER2 expression (i.e., IHC 3+), trastuzumab deruxtecan was even more effective, resulting in an ORR of 61.3% and an mDOR of 22.1 months. Across different disease sites, trastuzumab deruxtecan resulted in the following ORRs:

  • Endometrial cancer: 57.5% for all patients, 84.6% for IHC 3+, and 47.1% for IHC 2+
  • Cervical cancer: 50% for all patients, 75% for IHC 3+, 40% for IHC 2+
  • Ovarian cancer: 45% for all patients, 63.6% for IHC 3+, 36.8% for IHC 2+
  • Urothelial cancer: 39% for all patients, 56.3% for IHC 3+, 35% for IHC 2+
  • Biliary tract cancer: 22% for all patients, 56.3% for IHC 3+, 0% for IHC 2+
  • Pancreatic cancer: 4% for all patients, 0% for IHC 3+, 5.3% for IHC 2+

The study participants were mostly able to tolerate treatment with trastuzumab deruxtecan, however, 11.6% of participants stopped treatment due to adverse events. The most common treatment-related side effects were nausea, fatigue, and low levels of blood cells (cytopenia).

“HER2 is present in many cancer types, such as breast, gastric, lung, gynecologic, and urothelial cancers, and patients with HER2-expressing, hard-to-treat cancers need new treatment options,” said Funda Meric-Bernstam, MD, chair of the Department of Investigational Cancer Therapeutics at the University of Texas MD Anderson Cancer Center and lead author of the study. “These results advance our clinical understanding of HER2 expression, reaffirm HER2 as an actionable biomarker across a broad range of tumor types, and show that trastuzumab deruxtecan could potentially provide a new treatment option for patients with advanced disease across these tumors, especially in patients with HER2 IHC 3+ or 2+ expression.”

About the Study

Patients with HER2-expressing biliary tract, bladder, cervical, endometrial, ovarian, pancreatic, or other tumors (excluding breast, gastric, colorectal and non-small cell lung cancers) were enrolled in the study. There were 267 patients, including 75 patients with IHC 3+ expression and 125 with IHC 2+ expression. IHC is the amount of HER2 receptor protein present in cells. 

Although HER2 is expressed across a variety of tumor types, there are currently no approved HER2-targeted therapies for many types of cancer, especially those that are hard to treat. Trastuzumab deruxtecan is an antibody drug conjugate targeting HER2 that is currently approved by the U.S. Food and Drug Administration for HER2-expressing breast cancer, HER2+ gastric cancer, and lung cancers with HER2-mutations. This study is the first global study of tumor-agnostic applications for trastuzumab deruxtecan across a broad range of HER2-expressing solid tumors.

Next Steps

The researchers are currently collecting additional survival outcomes in the DESTINY-PanTumor02 study.

This study was sponsored and designed by Astra Zeneca in collaboration with Daiichi Sankyo.

View the full embargoed abstract: 

LBA3000: Efficacy and safety of trastuzumab deruxtecan (T-DXd) in patients (pts) with HER2-expressing solid tumors: DESTINY-PanTumor02 (DP-02) interim results.  

Authors: Funda Meric-Bernstam, Vicky Makker, Ana Oaknin, Do-Youn Oh, Susana N. Banerjee, Antonio Gonzalez Martin, Kyung Hae Jung, Iwona A. Lugowska, Luis Manso, Aránzazu Manzano, Bohuslav Melichar, Salvatore Siena, Daniil Stroyakovskiy, Chiedozie Anoka, Yan Ma, Soham D. Puvvada, JUNG-YUN LEE; University of Texas MD Anderson Cancer Center, Houston, TX; Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY; Gynaecologic Cancer Programme, Vall d'Hebron Institute of Oncology (VHIO), Hospital Universitari Vall d’Hebron, Vall d’Hebron Barcelona Hospital Campus, Barcelona, Spain; Seoul National University College of Medicine, Seoul, Korea, Republic of (South); The Royal Marsden NHS Foundation Trust and Institute of Cancer Research, London, United Kingdom; Cancer Center Clínica Universidad de Navarra, Madrid, Spain; Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea, Republic of (South); Maria Sklodowska-Curie National Research Institute and Oncology Centre (MSCI), Warsaw, Poland; Hospital Universitario 12 de Octubre, Madrid, Spain; Hospital Clínico San Carlos and IdISSC, Madrid, Spain; University Hospital, Palacký University, Olomouc, Czech Republic; Università degli Studi di Milano (La Statale) and Niguarda Cancer Center, Grande Ospedale Metropolitano Niguarda, Milan, Italy; Moscow City Oncology Hospital No.62, Moscow, Russian Federation; Late-Stage Development, Oncology R&D, AstraZeneca, Gaithersburg, MD; Late-stage Development, Oncology R&D, AstraZeneca, Cambridge, United Kingdom; Yonsei University College of Medicine, Seoul, South Korea  

Background: T-DXd is an antibody drug conjugate targeting HER2 and is approved in HER2-expressing breast (BC) and gastric (GC) cancers. HER2 expression is prevalent in other solid tumors. The efficacy of current treatments (Tx) in these populations, including studies with HER2-directed Tx, is modest, revealing a significant unmet medical need. Clinically meaningful activity of T-DXd was seen in HER2-expressing tumors in a phase 1 study (NCT02564900).  Methods: DP-02 (NCT04482309) is an open-label phase 2 study of T-DXd 5.4 mg/kg q3w in pts with HER2-expressing (immunohistochemistry [IHC] 3+ or IHC 2+ by local or central testing) locally advanced or metastatic disease that progressed after ≥1 systemic Tx or that has no Tx options. Cohorts with biliary tract (BTC), bladder (URO), cervical (CC), endometrial (EC), ovarian (OC), pancreatic (PC), or other tumors (excluding BC, GC, colorectal cancer, and non-small cell lung cancer) were enrolled. Efficacy and safety were analyzed in all pts who received ≥1 dose of T-DXd. The primary endpoint was investigator-assessed confirmed objective response rate (ORR). Secondary endpoints included duration of response (DOR), disease control rate, progression-free and overall survival, and safety.  Results: At data cutoff (16 Nov 2022; median follow-up, 9.7 mo), 267 pts had been treated (median, 2 prior lines of Tx [range, 0-13]); 75 pts were IHC 3+ and 125 were IHC 2+ by central testing. In all 267 pts, the ORR was 37.1% and median DOR (mDOR) was 11.8 mo; in pts with IHC 3+ expression, the ORR was 61.3% and mDOR was 22.1 mo. ORR per cohort is shown in all pts and those with centrally confirmed HER2 IHC 3+ or IHC 2+ expression. Grade (G) ≥3 adverse events (AEs) occurred in 58.4% of pts; 11.6% discontinued Tx due to AEs. Adjudicated drug-related interstitial lung disease/pneumonitis occurred in 18 pts (6.7% [G1, n=6; G2, n=11; G5, n=1]).  Conclusions: This is the first tumor-agnostic global study of T-DXd in a broad range of HER2-expressing solid tumors. T-DXd showed encouraging ORR, particularly in pts with IHC 3+ expression, durable clinical benefit, and a manageable safety profile in this heavily pretreated population. These interim results show T-DXd to be a potential new Tx option for pts with HER2-expressing solid tumors.  

 
 
 
 
 
 
 

  

 
 
 
 

EC  

 
 
 
 

CC  

 
 
 
 

OC  

 
 
 
 

URO  

 
 
 
 

Othera  

 
 
 
 

BTC  

 
 
 
 

PC  

 
 
 
 

Total  

 
 
 
 

All pts  

 
 

  

 
 

  

 
 

  

 
 

  

 
 

  

 
 

  

 
 

  

 
 

  

 
 
 
 

n  

 
 

40  

 
 

40  

 
 

40  

 
 

41  

 
 

40  

 
 

41  

 
 

25  

 
 

267  

 
 
 
 

ORR, %b  

 
 

57.5  

 
 

50.0  

 
 

45.0  

 
 

39.0  

 
 

30.0  

 
 

22.0  

 
 

4.0  

 
 

37.1  

 
 
 
 

Central IHC 3+c  

 
 

  

 
 
 
 

n  

 
 

13  

 
 

8  

 
 

11  

 
 

16  

 
 

9  

 
 

16  

 
 

2  

 
 

75  

 
 
 
 

ORR, %b  

 
 

84.6  

 
 

75.0  

 
 

63.6  

 
 

56.3  

 
 

44.4  

 
 

56.3  

 
 

0  

 
 

61.3  

 
 
 
 

Central IHC 2+c  

 
 

  

 
 
 
 

n  

 
 

17  

 
 

20  

 
 

19  

 
 

20  

 
 

16  

 
 

14  

 
 

19  

 
 

125  

 
 
 
 

ORR, %b  

 
 

47.1  

 
 

40.0  

 
 

36.8  

 
 

35.0  

 
 

18.8  

 
 

0  

 
 

5.3  

 
 

27.2  

a Responses in extramammary Paget disease, head and neck cancer, oropharyngeal neoplasm, and salivary gland cancer.  

b By investigator assessment per RECIST 1.1.  

c Central assessment of HER2 expression was done retrospectively for pts enrolled based on local testing; 67 pts were not centrally confirmed as IHC 3+ or IHC 2+.  

View disclosures for:

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