Immune checkpoint inhibitors and Carbon iON radiotherapy In solid Cancers with stable disease (ICONIC)

Author:

Cavalieri Stefano12ORCID,Vitolo Viviana3ORCID,Barcellini Amelia34,Ronchi Sara3ORCID,Facoetti Angelica5,Campo Chiara6,Klersy Catherine7,Molinelli Silvia8,Agustoni Francesco49,Ferretti Virginia Valeria7,Silvestri Annalisa De7,Platania Marco10,Vecchio Michele Del10,Durante Marco11,Helm Alexander11,Fournier Claudia11,Braud Filippo de210,Pedrazzoli Paolo49,Orlandi Ester3ORCID,Licitra Lisa126

Affiliation:

1. Department of Head & Neck Medical Oncology 3, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, Milan, 20133, Italy

2. Department of Oncology & Hemato-Oncology, University of Milan, Via Santa Sofia 9/1, Milan, 20122, Italy

3. Radiation Oncology Unit, Clinical Department, CNAO National Center for Oncological Hadrontherapy, Via E. Borloni 1, Pavia, 27100, Italy

4. Department of Internal Medicine & Medical Therapy, University of Pavia, Via Aselli 43/45, Pavia, 27100, Italy

5. Radiobiology Unit, Research and Development Department, CNAO National Center for Oncological Hadrontherapy, Via E. Borloni 1, Pavia, 27100, Italy

6. Scientific Direction, CNAO National Center for Oncological Hadrontherapy, Via E. Borloni 1, Pavia, 27100, Italy

7. SSD Biostatistica & Clinical Trial Center Service of Biometry and Statistics, Fondazione IRCCS Policlinico San Matteo, Viale Golgi 19, Pavia, 27100, Italy

8. Medical Physics, Clinical Department, CNAO National Center for Oncological Hadrontherapy, Via E. Borloni 1, Pavia, 27100, Italy

9. Department of Medical Oncology, Fondazione IRCCS Policlinico San Matteo, Viale Golgi 19, Pavia, 27100, Italy

10. Department of Medical Oncology 1, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, Milan, 20133, Italy

11. Department of Biophysics, GSI Helmholtz Center for Heavy Ion Research, Darmstadt, 64291, Germany

Abstract

ICONIC is a multicenter, open-label, nonrandomized phase II clinical trial aiming to assess the feasibility and clinical activity of the addition of carbon ion radiotherapy to immune checkpoint inhibitors in cancer patients who have obtained disease stability with pembrolizumab administered as per standard-of-care. The primary end point is objective response rate, and the secondary end points are safety, survival and disease control rate. Translational research is an exploratory aim. The planned sample size is 27 patients. The study combination will be considered worth investigating if at least four objective responses are observed. If the null hypothesis is rejected, ICONIC will be the first proof of concept of the feasibility and clinical activity of the addition of carbon ion radiotherapy to immune checkpoint inhibitors in oncology.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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