Management of adverse events in patients with HER2+ metastatic breast cancer treated with tucatinib, trastuzumab, and capecitabine (HER2CLIMB).

Authors

null

Alicia Frances Clare Okines

The Royal Marsden NHS Foundation Trust, London, United Kingdom

Alicia Frances Clare Okines , Elisavet Paplomata , Tanya A. Wahl , Gail Lynn Shaw Wright , Stephanie Sutherland , Erik Jakobsen , Frances Valdes , Arlene Chan , Amy Sanders Clark , Alison Katherine Conlin , Maryam B. Lustberg , Jennifer M. Specht , Timothy J. Pluard , Xiaofu Zhu , Ian E. Krop , Karen A. Gelmon , Dennis J. Slamon , Jorge Ramos , Grace An , Erika Paige Hamilton

Organizations

The Royal Marsden NHS Foundation Trust, London, United Kingdom, Winship Cancer Institute of Emory University School of Medicine, Atlanta, GA, Swedish Cancer Institute, Issaquah, WA, Florida Cancer Specialists and Research Institute, New Port Richey, FL, Mount Vernon Hospital, Northwood, United Kingdom, Vejle Hospital, Vejle, Denmark, University of Miami, Miami, FL, Breast Cancer Research Centre-Western Australia and Curtin University, Perth, Australia, University of Pennsylvania Abramson Cancer Center, Philadelphia, PA, Providence Cancer Center Oncology and Hematology Care Clinic, Portland, OR, The Ohio State University Comprehensive Cancer Center, Columbus, OH, University of Washington, Seattle, WA, St Luke's Cancer Institute, Kansas City, MO, Cross Cancer Institute, Edmonton, AB, Canada, Dana-Farber Cancer Institute, Boston, MA, Department of Medical Oncology, BC Cancer, Vancouver, BC, Canada, University of California, Los Angeles, CA, Seattle Genetics, Inc., Bothell, WA, Sarah Cannon Research Institute and Tennessee Oncology, Nashville, TN

Research Funding

Pharmaceutical/Biotech Company
Seattle Genetics, Inc.

Background: Tucatinib (TUC) is an investigational TKI, highly selective for HER2 without significant inhibition of EGFR. HER2CLIMB is a randomized trial of TUC vs placebo in combination with trastuzumab and capecitabine in patients (pts) with HER2+ breast cancer (NCT02614794, Murthy NEJM 2019). The most common G ≥3 adverse events (AEs) with higher incidence on the TUC arm (diarrhea, palmar-plantar erythrodysesthesia syndrome [PPE], and elevated liver enzymes) are described herein. Methods: Given that pts on the TUC arm had a longer duration of tx than those on the control arm, time-at-risk exposure-adjusted incidence rates of diarrhea, AST, ALT, and PPE were calculated as the number of pts with an event divided by the total exposure time-at-risk of an initial occurrence of the event among pts in the tx group. Time-to-event analyses were conducted for AST/ALT/bilirubin (in aggregate), diarrhea, and PPE. Results: Diarrhea and elevated AST/ALT/bilirubin on both the TUC and control arms were primarily G1/2 and manageable with dose modifications, and in some cases of diarrhea, with antidiarrheal tx. Median time to diarrhea onset was shorter on the TUC arm compared to control. For AST/ALT/bilirubin and PPE, median time to first onset was Cycles 1 and 2. On the TUC arm, antidiarrheals were used in 49.7% of cycles in which diarrhea was reported (39.8% on the control arm), and when used, the median duration of use on each arm was 3 days per cycle. Prophylactic antidiarrheals were not required per protocol. When adjusted for exposure (time-at-risk exposure-adjusted incidence rate per 100 person-years), the difference in G ≥3 events between tx arms becomes similar for diarrhea and PPE (21 vs 17 and 21 vs 19). The difference in G ≥3 events between arms is reduced for AST and ALT (7 vs 1 and 8 vs 1). Conclusions: TUC with trastuzumab and capecitabine was well-tolerated. Rates of G ≥3 diarrhea and PPE were similar between tx arms. Elevated liver enzymes were higher on the TUC arm, but were transient and reversible. Discontinuation of TUC due to AEs was rare. Clinical trial information: NCT02614794.

Diarrhea
Elevated
AST/ALT/bilirubin
PPE
TUCCTUCCTUCC
Pts with any event, %80.953.321.3 / 20 / 18.611.2 / 6.6 / 10.263.452.8
    G ≥3 events12.98.64.5 / 5.4 / 0.70.5 / 0.5 / 2.513.19.1
Median days to onset122236323334.5
Events resolved, %79.684.183.768.854.258.3
Median days to resolution862226.562.551
Dose holds, %13.98.65.4 / 6.4 / 8.21.0 / 0.5 / 7.16.42
Dose reductions, %5.74.64.2 / 4.7 / 2.21.0 / 0.5 / 1.01.20.5
Dose discontinuations, %1.00.50.7 / 1.0 / 0.70.5 / 0.5 / 0.500

TUC = TUC arm; C = control arm

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Abstract Details

Meeting

2020 ASCO Virtual Scientific Program

Session Type

Poster Session

Session Title

Breast Cancer—Metastatic

Track

Breast Cancer

Sub Track

HER2-Positive

Clinical Trial Registration Number

NCT02614794

Citation

J Clin Oncol 38: 2020 (suppl; abstr 1043)

DOI

10.1200/JCO.2020.38.15_suppl.1043

Abstract #

1043

Poster Bd #

128

Abstract Disclosures