Literature DB >> 33766818

Interim Analysis of the Phase II Study: Noninferiority Study of Doxorubicin with Upfront Dexrazoxane plus Olaratumab for Advanced or Metastatic Soft-Tissue Sarcoma.

Brian A Van Tine1,2,3, Angela C Hirbe4,2,3, Peter Oppelt4,3, Ashley E Frith4,3, Richa Rathore4, Joshua D Mitchell3,5, Fei Wan6, Shellie Berry4, Michele Landeau4, George A Heberton7, John Gorcsan8, Peter R Huntjens8, Yoku Soyama8, Justin M Vader9, Jose A Alvarez-Cardona5, Kathleen W Zhang5, Daniel J Lenihan3,5, Ronald J Krone10.   

Abstract

PURPOSE: To report the interim analysis of the phase II single-arm noninferiority trial, testing the upfront use of dexrazoxane with doxorubicin on progression-free survival (PFS) and cardiac function in soft-tissue sarcoma (STS). PATIENTS AND METHODS: Patients with metastatic or unresectable STS who were candidates for first-line treatment with doxorubicin were deemed eligible. An interim analysis was initiated after 33 of 65 patients were enrolled. Using the historical control of 4.6 months PFS for doxorubicin in the front-line setting, we tested whether the addition of dexrazoxane affected the efficacy of doxorubicin in STS. The study was powered so that a decrease of PFS to 3.7 months would be considered noninferior. Secondary aims included cardiac-related mortality, incidence of heart failure/cardiomyopathy, and expansion of cardiac monitoring parameters including three-dimensional echocardiography. Patients were allowed to continue on doxorubicin beyond 600 mg/m2 if they were deriving benefit and were not demonstrating evidence of symptomatic cardiac dysfunction.
RESULTS: At interim analysis, upfront use of dexrazoxane with doxorubicin demonstrated a PFS of 8.4 months (95% confidence interval: 5.1-11.2 months). Only 3 patients were removed from study for cardiotoxicity, all on > 600 mg/m2 doxorubicin. No patients required cardiac hospitalization or had new, persistent cardiac dysfunction with left ventricular ejection fraction remaining below 50%. The median administered doxorubicin dose was 450 mg/m2 (interquartile range, 300-750 mg/m2).
CONCLUSIONS: At interim analysis, dexrazoxane did not reduce PFS in patients with STS treated with doxorubicin. Involvement of cardio-oncologists is beneficial for the monitoring and safe use of high-dose anthracyclines in STS.See related commentary by Benjamin and Minotti, p. 3809. ©2021 American Association for Cancer Research.

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Year:  2021        PMID: 33766818      PMCID: PMC8282681          DOI: 10.1158/1078-0432.CCR-20-4621

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  30 in total

1.  Pharmacokinetics of dexrazoxane in subjects with impaired kidney function.

Authors:  Michael E Brier; Shari K Gaylor; J Patrick McGovren; Paul Glue; Annie Fang; George R Aronoff
Journal:  J Clin Pharmacol       Date:  2010-05-19       Impact factor: 3.126

2.  Dexrazoxane as a cardioprotectant in children receiving anthracyclines.

Authors:  Dana M Sepe; Jill P Ginsberg; Frank M Balis
Journal:  Oncologist       Date:  2010-11-04

3.  Dexrazoxane for cardiac protection against doxorubicin.

Authors: 
Journal:  Med Lett Drugs Ther       Date:  1995-11-24       Impact factor: 1.909

4.  The catalytic topoisomerase II inhibitor dexrazoxane induces DNA breaks, ATF3 and the DNA damage response in cancer cells.

Authors:  Shiwei Deng; Tiandong Yan; Teodora Nikolova; Dominik Fuhrmann; Andrea Nemecek; Ute Gödtel-Armbrust; Bernd Kaina; Leszek Wojnowski
Journal:  Br J Pharmacol       Date:  2015-02-27       Impact factor: 8.739

5.  Late Mortality After Dexrazoxane Treatment: A Report From the Children's Oncology Group.

Authors:  Eric J Chow; Barbara L Asselin; Cindy L Schwartz; David R Doody; Wendy M Leisenring; Sanjeev Aggarwal; K Scott Baker; Smita Bhatia; Louis S Constine; David R Freyer; Steven E Lipshultz; Saro H Armenian
Journal:  J Clin Oncol       Date:  2015-05-26       Impact factor: 44.544

Review 6.  The current and future role of dexrazoxane as a cardioprotectant in anthracycline treatment: expert panel review.

Authors:  S M Swain; P Vici
Journal:  J Cancer Res Clin Oncol       Date:  2003-10-17       Impact factor: 4.553

7.  Olaratumab and doxorubicin versus doxorubicin alone for treatment of soft-tissue sarcoma: an open-label phase 1b and randomised phase 2 trial.

Authors:  William D Tap; Robin L Jones; Brian A Van Tine; Bartosz Chmielowski; Anthony D Elias; Douglas Adkins; Mark Agulnik; Matthew M Cooney; Michael B Livingston; Gregory Pennock; Meera R Hameed; Gaurav D Shah; Amy Qin; Ashwin Shahir; Damien M Cronier; Robert Ilaria; Ilaria Conti; Jan Cosaert; Gary K Schwartz
Journal:  Lancet       Date:  2016-06-09       Impact factor: 79.321

8.  Topoisomerase II{alpha}-dependent and -independent apoptotic effects of dexrazoxane and doxorubicin.

Authors:  Tiandong Yan; Shiwei Deng; Annegret Metzger; Ute Gödtel-Armbrust; Andrew C G Porter; Leszek Wojnowski
Journal:  Mol Cancer Ther       Date:  2009-05-05       Impact factor: 6.261

9.  Dexrazoxane may prevent doxorubicin-induced DNA damage via depleting both topoisomerase II isoforms.

Authors:  Shiwei Deng; Tiandong Yan; Cathleen Jendrny; Andrea Nemecek; Mladen Vincetic; Ute Gödtel-Armbrust; Leszek Wojnowski
Journal:  BMC Cancer       Date:  2014-11-18       Impact factor: 4.430

10.  Efficacy and safety of Dexrazoxane (DRZ) in sarcoma patients receiving high cumulative doses of anthracycline therapy - a retrospective study including 32 patients.

Authors:  Markus K Schuler; Sebastian Gerdes; Antje West; Stephan Richter; Christoph Busemann; Leopold Hentschel; Felicitas Lenz; Hans-Georg Kopp; Gerhard Ehninger; Peter Reichardt; Daniel Pink
Journal:  BMC Cancer       Date:  2016-08-09       Impact factor: 4.430

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