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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.
Peretz Soroka, Hagit; Vora, Tushar; Noujaim, Jonathan; Marcoux, Nicolas; Cohen-Gogo, Sarah; Alcindor, Thierry; Holloway, Caroline; Rodrigues, Caroline; Karachiwala, Hatim; Alvi, Saima; Lee, Ursula; Cheng, Sylvia; Banerji, Shantanu; Oberoi, Sapna; Feng, Xiaolan; Smrke, Alannah; Simmons, Christine; Razak, Albiruni Abdul; Gupta, Abha A.
Affiliation
  • Peretz Soroka H; Division of Medical Oncology, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.
  • Vora T; Division of Hematology/Oncology, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Noujaim J; Division of Medical Oncology, Hôpital Maisonneuve Rosemont, University of Montreal, Montreal, Quebec, Canada.
  • Marcoux N; Division of Hematology-Oncology, Centre Hospitalier Universitaire de Québec, Quebec, Canada.
  • Cohen-Gogo S; Division of Hematology/Oncology, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Alcindor T; Division of Medical Oncology, McGill University Health Centre, Montreal, Quebec, Canada.
  • Holloway C; Division of Radiation Oncology, BC Cancer, University of British Columbia, Vancouver, British Columbia, Canada.
  • Rodrigues C; Division of Medical Oncology, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.
  • Karachiwala H; Division of Medical Oncology, Cross Cancer Institute, Alberta Health Services, Edmonton, Alberta, Canada.
  • Alvi S; Division of Pediatric Hematology/Oncology, Jim Pattison Children's Hospital Saskatoon, Saskatoon, Saskatchewan, Canada.
  • Lee U; Division of Medical Oncology, BC Cancer, University of British Columbia, Vancouver, British Columbia, Canada.
  • Cheng S; Division of Pediatric Hematology/Oncology/BMT, B.C. Children's Hospital, BC Cancer, Vancouver, British Columbia, Canada.
  • Banerji S; Department of Pediatric Hematology-Oncology, CancerCare Manitoba Research Institute, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Oberoi S; Department of Pediatric Hematology-Oncology, CancerCare Manitoba Research Institute, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Feng X; Division of Medical Oncology, BC Cancer, University of British Columbia, Vancouver, British Columbia, Canada.
  • Smrke A; Division of Medical Oncology, BC Cancer, University of British Columbia, Vancouver, British Columbia, Canada.
  • Simmons C; Division of Medical Oncology, BC Cancer, University of British Columbia, Vancouver, British Columbia, Canada.
  • Razak AA; Division of Medical Oncology, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.
  • Gupta AA; Division of Medical Oncology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.
Cancer Med ; 12(18): 18872-18881, 2023 09.
Article in En | MEDLINE | ID: mdl-37724607
ABSTRACT

OBJECTIVES:

We 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).

METHODS:

After 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.

RESULTS:

From 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.

CONCLUSION:

Our 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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma / Sarcoma, Ewing / Soft Tissue Neoplasms / Bone Neoplasms / Osteosarcoma / Chondrosarcoma Type of study: Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Child / Humans / Middle aged Country/Region as subject: America do norte Language: En Journal: Cancer Med Year: 2023 Document type: Article Affiliation country: Canadá

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma / Sarcoma, Ewing / Soft Tissue Neoplasms / Bone Neoplasms / Osteosarcoma / Chondrosarcoma Type of study: Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Child / Humans / Middle aged Country/Region as subject: America do norte Language: En Journal: Cancer Med Year: 2023 Document type: Article Affiliation country: Canadá