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Dual Erb B Inhibition in Oesophago-gastric Cancer (DEBIOC): A phase I dose escalating safety study and randomised dose expansion of AZD8931 in combination with oxaliplatin and capecitabine chemotherapy in patients with oesophagogastric adenocarcinoma

Version 2 2020-05-07, 08:22
Version 1 2020-05-07, 08:21
journal contribution
posted on 2020-05-07, 08:22 authored by Anne Thomas, Pradeep S Virdee, Martin Eatock, Simon R Lord, Stephen Falk, D Alan Anthoney, Richard C Turkington, Matthew Goff, Leena Elhussein, Linda Collins, Sharon Love, Joanna Moschandreas, Mark R Middleton
Background: AZD8931 has equipotent activity against epidermal growth factor receptor, erbB2, and erbB3. Primary objectives were to determine the recommended phase II dose (RP2D) of AZD8931 + chemotherapy, and subsequently assess safety/preliminary clinical activity in patients with operable oesophagogastric cancer (OGC). Methods: AZD8931 (20 mg, 40 mg or 60 mg bd) was given with Xelox (oxaliplatin + capecitabine) for eight 21-day cycles, continuously or with intermittent schedule (4 days on/3 off every week; 14 days on/7 off, per cycle) in a rolling-six design. Subsequently, patients with OGC were randomised 2:1 to AZD8931 + Xelox at RP2D or Xelox only for two cycles, followed by radical oesophagogastric surgery. Secondary outcomes were safety, complete resection (R0) rate, six-month progression-free survival (PFS) and overall survival. Results: During escalation, four dose-limiting toxicities were observed among 24 patients: skin rash (1) and failure to deliver 100% of Xelox because of treatment-associated grade III-IV adverse events (AEs) (3: diarrhoea and vomiting; vomiting; fatigue). Serious adverse events (SAE) occurred in 15 of 24 (63%) patients. RP2D was 20-mg bd with the 4/3 schedule. In the expansion phase, 2 of 20 (10%) patients in the Xelox + AZD8931 group and 5/10 (50%) patients in the Xelox group had grade III–IV AEs. Six-month PFS was 85% (90% CI: 66%–94%) in Xelox + AZD8931 and 100% in Xelox alone. Seven deaths (35%) occurred with Xelox + AZD8931 and one (10%) with Xelox. R0 rate was 45% (9/20) with Xelox + AZD8931 and 90% (9/10) with Xelox-alone (P = 0.024). Conclusion: Xelox + AZD8931 (20 mg bd 4/3 days) has an acceptable safety profile administered as neoadjuvant therapy in operable patients with OGC. (Trial registration: EudraCT 2011-003169-13, ISRCTN-68093791).

Funding

This work was supported by AstraZeneca, Cancer Research UK [C10604/A14112] the Experimental Cancer Medicine Centre (ECMC) and NIHR Clinical Research Network [UKCRN ID 11855]. Additional NHS clinical service support costs for patient care while on study were met by the hosting sites. This study was part of the NIHR portfolio.

History

Citation

European Journal of Cancer Volume 124, January 2020, Pages 131-141

Version

  • VoR (Version of Record)

Published in

EUROPEAN JOURNAL OF CANCER

Volume

124

Pagination

131 - 141 (11)

Publisher

ELSEVIER SCI LTD

issn

0959-8049

eissn

1879-0852

Acceptance date

2019-10-13

Copyright date

2019

Available date

2019-11-22

Publisher version

https://www.sciencedirect.com/science/article/pii/S0959804919307737

Language

English