Real‐world experience of tyrosine kinase inhibitors in children, adolescents and adults with relapsed or refractory bone tumours: A Canadian Sarcoma Research and Clinical Collaboration (CanSaRCC) study

Author:

Peretz Soroka Hagit1,Vora Tushar2,Noujaim Jonathan3,Marcoux Nicolas4,Cohen‐Gogo Sarah2,Alcindor Thierry5,Holloway Caroline6,Rodrigues Caroline1,Karachiwala Hatim7,Alvi Saima8,Lee Ursula9,Cheng Sylvia10,Banerji Shantanu11,Oberoi Sapna11ORCID,Feng Xiaolan9,Smrke Alannah9,Simmons Christine9,Razak Albiruni Abdul112,Gupta Abha A.12ORCID

Affiliation:

1. Division of Medical Oncology, Princess Margaret Cancer Centre University of Toronto Toronto Ontario Canada

2. Division of Hematology/Oncology, Hospital for Sick Children University of Toronto Toronto Ontario Canada

3. Division of Medical Oncology, Hôpital Maisonneuve Rosemont University of Montreal Montreal Quebec Canada

4. Division of Hematology‐Oncology Centre Hospitalier Universitaire de Québec Quebec Canada

5. Division of Medical Oncology McGill University Health Centre Montreal Quebec Canada

6. Division of Radiation Oncology, BC Cancer University of British Columbia Vancouver British Columbia Canada

7. Division of Medical Oncology, Cross Cancer Institute Alberta Health Services Edmonton Alberta Canada

8. Division of Pediatric Hematology/Oncology Jim Pattison Children's Hospital Saskatoon Saskatoon Saskatchewan Canada

9. Division of Medical Oncology, BC Cancer University of British Columbia Vancouver British Columbia Canada

10. Division of Pediatric Hematology/Oncology/BMT B.C. Children's Hospital, BC Cancer Vancouver British Columbia Canada

11. Department of Pediatric Hematology‐Oncology, CancerCare Manitoba Research Institute, Rady Faculty of Health Sciences University of Manitoba Winnipeg Manitoba Canada

12. Division of Medical Oncology, Mount Sinai Hospital University of Toronto Toronto Ontario Canada

Abstract

AbstractObjectivesWe conducted a retrospective multi‐centre study to assess the real‐world outcome of regorafenib (REGO) and cabozantinib (CABO) in recurrent/refractory bone tumours (BTs) including osteosarcoma (OST), Ewing sarcoma (EWS) and chondrosarcoma (CS)/extra‐skeletal mesenchymal CS (ESMC).MethodsAfter regulatory approval, data from patients with recurrent BT (11 institutions) were extracted from CanSaRCC (Canadian Sarcoma Research and Clinical Collaboration) database. Patient characteristics, treatment and outcomes were collected. Progression‐free survival (PFS) and overall survival (OS) were estimated using the Kaplan–Meier method.ResultsFrom July 2018 to May 2022, 66 patients received REGO or CABO; 39 OST, 18 EWS, 4 CS and 5 ESMC. Median age was 27.8 years (range 12–76); median starting dose was 60 mg for CABO (n = 37, range 40–60) and 120 mg for REGO (n = 29, range 40–160). Twenty‐eight (42.4%) patients required dose reduction: hand‐foot syndrome 7 (10.6%), nausea/vomiting 1 (1.5%), diarrhoea 1 (1.5%), 2 elevated LFTs (3%), elevated bilirubin 1 (1.5%) and mucositis 1 (1.5%). The median OS for patients with OST, EWS, CS and ESMC was 8.5 months (n = 39, 95% CI 7–13.1); 13.4 months (n = 18, 95% CI 3.4–27.2), 8.1 (n = 4, 95% CI 4.1–9.3) and 18.2 (n = 5, 95% CI (10.4–na), respectively. Median PFS for OST, EWS, CS and ECMS was 3.5 (n = 39, 95% CI 2.8–5), 3.9 (n = 18, 95% CI 2.1–5.9), 5.53 (n = 4. 95% CI 2.13–NA) and 11.4 (n = 5, 95% CI 1.83–14.7), respectively. Age, line of therapy, REGO versus CABO, or time from diagnosis to initiation of TKI were not associated with PFS on univariable analysis.ConclusionOur real‐world data show that TKIs have meaningful activity in recurrent BT with acceptable toxicities when started at modified dosing. Inclusion of TKIs in earlier lines of treatment and/or maintenance therapy could be questions for future research.

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Cabozantinib/regorafenib;Reactions Weekly;2023-11-04

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