Chemoradiotherapy with concurrent durvalumab for the palliative treatment of oligometastatic oesophageal and gastrooesophageal carcinoma with dysphagia: a single arm phase II clinical trial (PALEO, sponsored by the Australasian Gastro-Intestinal Trials Group)

Fiona Day(Hunter Medical Research Institute), Swetha Sridharan(Calvary Mater Newcastle Hospital), James Lynam(Calvary Mater Newcastle Hospital), Craig Gedye(Calvary Mater Newcastle Hospital), Catherine Johnson(Hunter Medical Research Institute), Allison Fraser(Calvary Mater Newcastle Hospital), Stephen R. Thompson(UNSW Sydney), Michael Michael(The University of Melbourne), Trevor Leong(The University of Melbourne), Amitesh Roy(Flinders Medical Centre), Mahesh Kumar(Calvary Mater Newcastle Hospital), André van der Westhuizen(Calvary Mater Newcastle Hospital), Gaik Tin Quah(Calvary Mater Newcastle Hospital), Hiren Mandaliya(Calvary Mater Newcastle Hospital), Girish Mallesara(Calvary Mater Newcastle Hospital), Joshua Sappiatzer(Flinders Private Hospital), Christopher Oldmeadow(Hunter Medical Research Institute), Jarad Martin(Calvary Mater Newcastle Hospital)
BMC Cancer
December 17, 2022
Cited by 6Open Access
Full Text

Abstract

Abstract Background Oesophageal and gastrooesophageal junction (GOJ) carcinoma frequently present with dysphagia and de novo metastatic disease. There is scope to improve treatment paradigms to both address symptoms and improve survival. One method is integrating immune checkpoint inhibition with novel treatment combinations. Methods PALEO is a single arm, phase II clinical trial in patients with previously untreated, oligometastatic or locoregionally advanced oesophageal or GOJ carcinoma and dysphagia. PALEO is sponsored by the Australasian Gastro-Intestinal Trials Group (AGITG). Participants receive 2 weeks of therapy with concurrent hypofractionated radiotherapy of 30Gy in 10 fractions to the primary tumour, weekly carboplatin AUC2, weekly paclitaxel 50 mg/m 2 and durvalumab 1500 mg q4 weekly, followed by durvalumab monotherapy continuing at 1500 mg q4weekly until disease progression, unacceptable toxicity or 24 months of therapy. A single metastasis is treated with stereotactic radiotherapy of 24Gy in 3 fractions in week 7. The trial primary endpoint is the progression free survival rate at 6 months. Secondary endpoints include duration of dysphagia relief, nutritional status change, quality of life, response rate, toxicity, progression free survival and overall survival. The tertiary endpoint is prediction of outcome based on biomarkers identified from patient serial blood samples collected pre- and post-radiotherapy. Discussion This unique investigator-initiated clinical trial is designed to simultaneously address the clinically relevant problems of dysphagia and distant disease control. The overarching aims are to improve patient nutrition, quality of life and survival with low toxicity therapy. AGITG PALEO is a multidisciplinary collaboration and will add to the understanding of the relationship between radiotherapy and the anti-tumour immune response. Trial registration Australian and New Zealand Clinical Trials Registry: ACTRN12619001371189 , registered 8 October 2019.


Related Papers

No related papers found

Powered by citation graph analysis