A phase II study of guadecitabine combined with irinotecan vs regorafenib or TAS‐102 in irinotecan‐refractory metastatic colorectal cancer patients

Author:

Lee Valerie1ORCID,Parkinson Rose1,Zahurak Marianna1,Cope Leslie1,Cercek Andrea2,Verheul Henk3ORCID,Gootjes Elske3,Lenz Heinz Josef4,Iqbal Syma4,Jones Peter5,Baylin Stephen1,Rami Vandna1,Ahuja Nita1,El Khoueiry Anthony4,Azad Nilofer S.1

Affiliation:

1. School of Medicine Johns Hopkins University Baltimore Maryland USA

2. Memorial Sloan Kettering Cancer Center New York New York USA

3. Vrije Universiteit Amsterdam Amsterdam The Netherlands

4. School of Medicine University of Southern California Los Angeles California USA

5. Van Andel Institute Grand Rapids Michigan USA

Abstract

AbstractDNA methyltransferase inhibitors (DNMTi) have demonstrated benefit in reversing resistance to systemic therapies for several cancer types. In a phase II trial of guadecitabine and irinotecan compared to regorafenib or TAS‐102 in pts with advanced mCRC refractory to irinotecan. Patients with mCRC refractory to irinotecan were randomized 2:1 to guadecitabine and irinotecan (Arm A) vs standard of care regorafenib or TAS‐102 (Arm B) on a 28‐day cycle. Between January 15, 2016 and October 24, 2018, 104 pts were randomized at four international sites, with 96 pts undergoing treatment, 62 in Arm A and 34 in Arm B. Median overall survival was 7.15 months for Arm A and 7.66 months for Arm B (HR 0.93, 95% CI: 0.58–1.47, P = .75). The Kaplan–Meier rates of progression free survival at 4 months were 32% in Arm A and 26% in Arm B. Common ≥Grade 3 treatment related adverse events in Arm A were neutropenia (42%), anemia (18%), diarrhea (11%), compared to Arm B pts with neutropenia (12%), anemia (12%). Guadecitabine and irinotecan had similar OS compared to standard of care TAS‐102 or regorafenib, with evidence of target modulation. Clinical trial information: NCT01896856.

Funder

Stand Up To Cancer

Astex Pharmaceuticals

Publisher

Wiley

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