Poster Display session Poster Display session

101P - First evidence of antitumor activity of ITPP, a novel hypoxia-modifier: Results of a phase Ib trial (ID 353)

Presentation Number
101P
Lecture Time
12:30 - 12:30
Speakers
  • M. A. Schneider (Zurich, Switzerland)
Session Name
Poster Display session
Location
Room B, Geneva Palexpo, Geneva, Switzerland
Date
14.12.2018
Time
12:30 - 13:00
Authors
  • M. A. Schneider (Zurich, Switzerland)
  • P. Limani (Zurich, Switzerland)
  • M. Linecker (Zurich, Switzerland)
  • P. Kron (Zurich, Switzerland)
  • H. Petrosky (Zurich, Switzerland)
  • B. C. Pestalozzi (Zürich, Switzerland)
  • A. Jetter (Zurich, Switzerland)
  • R. Graf (Zurich, Switzerland)
  • B. Humar (Zurich, Switzerland)
  • J. Lehn (Strasbourg, France)
  • P. Clavien (Zurich, Switzerland)

Abstract

Background

Tumor hypoxia promotes the Warburg effect, decreases anti-tumor immune responses and increases malignant behavior, thereby fostering disease progression. The novel anti-hypoxic molecule myo-inositoltrispyrophosphate (ITPP) acts as an allosteric effector of hemoglobin and efficiently counteracts hypoxia. In preclinical models, ITPP normalized tumor-associated vasculature, enhanced chemotherapy efficacy, decreased tumor burden and increased survival.

Methods

The present study is a first in-human exploratory, prospective, open-labelled, mono-centric Phase IB study according to a classical 3 + 3 dose escalation scheme in patients with non-resectable hepatopancreatobiliary tumors. The study intervention consists of 9 infusions of ITPP over 3 weeks, followed by administration of conventional chemotherapy. Primary endpoints are the determination of safety and tolerability of ITPP, while secondary endpoints aim at assessing tumor responses via imaging.

Results

29 patients were included between 04/2015 and 07/2018, with 1 patient withdrawn from the study and 28 assessed for the primary endpoints. ITPP administration was safe and well tolerated. Dose limiting toxicity in the form of Hypercalcemia CTCAE grade 4 occured in the highest cohort tested (Cohort 8: 14’500mg/m2). 7 serious adverse events were recorded without relation to ITPP. 48 adverse events occurred, with 30 judged to be possibly or definitively related to ITPP. Hypercalcemia (19x), Hypomagnesemia (5x), Hypophosphatemia (4x) were the most freequently observed treatment emerged toxicities. Of the ITPP-treated patients, 10 had radiological disease stabilization, 4 experienced a decrease in tumor markers. 4 patients had stable disease with subsequent chemotherapy, while 5 benefited from a strong partial response.

Conclusions

Administration of ITPP before chemotherapy is safe and well tolerated with acceptable side-effects. Further exploration of ITPP's potential in phase II/III trials is warranted.

Clinical trial identification

NCT02528526.

Legal entity responsible for the study

Pierre-Alain Clavien.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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