ATTAIN: Phase III study of etirinotecan pegol versus treatment of physician's choice in patients with metastatic breast cancer and brain metastases

Author:

Tripathy Debu1,Tolaney Sara M2,Seidman Andrew D3,Anders Carey K4,Ibrahim Nuhad1,Rugo Hope S5,Twelves Chris67,Dieras Veronique8,Müller Volkmar9,Tagliaferri Mary10,Hannah Alison L10,Cortés Javier1112

Affiliation:

1. The University of Texas MD Anderson Cancer Center, Department of Breast Medical Oncology, Houston, TX 77030, USA

2. Dana-Farber Cancer Institute, Center for Women's Cancers, Boston, MA 02215, USA

3. Memorial Sloan-Kettering Cancer Center, Bobst International Center, New York, NY 10065, USA

4. University of North Carolina School of Medicine, Duke Cancer Center, Chapel Hill, NC 27710, USA

5. University of California San Francisco, Department of Medicine (Hematology/Oncology), San Francisco, CA 94115, USA

6. University of Leeds, Leeds Institute of Cancer and Pathology (LICAP), Leeds, LS2 9JT, UK

7. St James' University Hospital, Institute of Oncology, Leeds, LS9 7BE, UK

8. Institut Curie, Oncological Medicine Department, 75248, Paris, France

9. University Medical Center Hamburg-Eppendorf, Department of Obstetrics and Gynecology, 20246 Hamburg, Germany

10. Nektar Therapeutics, San Francisco, CA 94158, USA

11. IOB Institute of Oncology, Quironsalud Group, 28034 Madrid & 08023 Barcelona, Spain

12. Vall d'Hebron Institute of Oncology (VHIO), Breast Cancer and Melanoma Group, 08035 Barcelona, Spain

Abstract

The increasing incidence of breast cancer brain metastases is a major clinical problem with its associated poor prognosis and limited treatment options. The long-acting topoisomerase-1 inhibitor, etirinotecan pegol, was designed to preferentially accumulate in tumor tissue including brain metastases, providing sustained cytotoxic SN38 levels. Motivated by improved survival findings from subgroup analyses from the Phase III BEACON trial, this ongoing randomized, Phase III trial compares etirinotecan pegol to drugs commonly used for advanced breast cancer in patients with stable, treated breast cancer brain metastases who have been previously treated with an anthracycline, taxane and capecitabine. The primary end point is overall survival. Secondary end points include objective response rate, progression-free survival and time to CNS disease progression or recurrence in patients with/without CNS lesions present at study entry. Trial registration number: NCT02915744.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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