CanSaRCC Publications

Browse published manuscripts from the Canadian Sarcoma Research and Clinical Collaboration.

Cancer, Jan 2026
Outcomes following definitive treatment of malignant peripheral nerve sheath tumor are significantly worse for patients with neurofibromatosis type 1
This study suggests that patients with NF1‐associated MPNSTs experience worse outcomes.
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Cancer Medicine, Jan 2026
A Real-World Analysis of Outcomes in CIC-Rearranged Sarcomas
Complete resection is critical in CIC-rearranged sarcomas (CRS). Chemotherapy benefit remains uncertain, underscoring the need for improved local control and novel, biology-driven therapies.
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European Journal of Cancer, Nov 2025
Incidence, prevalence and treatment of patients with Epithelioid Haemangioendothelioma (EHE) in Canada
This is the largest series of EHE patients describing sequential systemic therapies. The role of systemic therapy in EHE in improving survival remains unclear and prospective studies with comparative arms are needed to add further insight into this chronic disease
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Pediatric Blood & Cancer, Apr 2025
Whole Abdominal Radiotherapy Is Tolerable and Effective in Children and Young Adults With Intra-Abdominal Sarcoma
Whole abdominal radiotherapy (WART) is utilized in children, adolescents, and young adults with intra-abdominal sarcoma, but efficacy and toxicity are uncertain. This study suggests WART is well tolerated among young sarcoma patients and provides meaningful local disease control when utilized in front-line adjuvant therapy.
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Journal of Pediatric Surgery, Apr 2025
Local Control for Pediatric Rhabdomyosarcoma of the Extremities: Is Radiotherapy Always Required After Adequate Surgical Resection?
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children and young adults. Typically, treatment involves a multimodal approach. The long-term consequences of offering RT especially to the extremity in children can be significant including growth delay, contracture, arthritis, and secondary malignancy. By presenting this distinctive real-world data, our aim is to illustrate that in a select high volume pediatric sarcoma center, extremity RMS can potentially be effectively managed through surgery and chemotherapy alone.
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European Journal of Cancer, May 2024
Real-word experience of pazopanib and sorafenib in patients with desmoid tumors

Sorafenib and pazopanib, two tyrosine kinase inhibitors (TKI), are widely used in patients with progressive symptomatic desmoid tumors (DT). Limited real-word data is available on long-term outcomes of patients who progressed on, stopped, or continued TKIs. .This retrospective study represents the largest cohort of DT patients treated with sorafenib or pazopanib to date. Discontinuation of treatment in responders is safe. The optimal treatment duration in patients with stable disease remains to be defined.
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Cancer Medicine, Sep 2023
Real-world experience of tyrosine kinase inhibitors in children, adolescents and adults with relapsed or refractory bone tumours
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
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Therapeutic Advances in Medical Oncology, Aug 2023
Clinico-demographic characteristics and outcomes of radiation-induced sarcomas (RIS)
Surgery is standard, and neoadjuvant chemotherapy (NACT) might be useful to downsize large lesions, especially in breast angiosarcoma (BAS) patients. Raising Radiation-induced sarcomas (RIS) awareness is fundamental to promoting appropriate management and fostering research through multi-institutional collaborations.
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Oral Oncology, July 2023
The impact of surgical resection margins on outcomes for adults with head and neck osteosarcomas
Osteosarcomas of the head and neck are rare and local recurrence remains a concern. Surgical resection with negative resection margins may improve survival, and a 3 mm resection margin threshold may optimize survival. Radiotherapy and/or chemotherapy should be considered in a multidisciplinary setting based on risk-features.
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Cancer Reports, Apr 2023
Radiation-induced sarcomas following childhood cancer
RIS is a serious late effect of radiotherapy in childhood cancer; however, radiation remains an integral component of primary tumor management and requires participation from a specialized multi-disciplinary team, aiming to mitigate RIS and other potential late effects.
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Current Oncology, June 2022
Extra-Pleural Pneumonectomy (EPP) in Children and Adults with Locally Advanced Sarcoma
EPP offers a feasible and life-prolonging surgical consideration for patients with locally advanced sarcoma involving the pleura in combination with chemotherapy and radiation. Consequently, EPP should be considered during multi-disciplinary tumor board discussions at high-volume centers.
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Psycho-oncology, Nov 2019
High prevalence of persistent emotional distress in desmoid tumor
Clinical experience suggests a high prevalence of emotional distress in patients with desmoid tumor (DT). We examine longitudinal Distress Assessment and Response Tool (DART) scores to estimate prevalence and persistence of distress, and compare cross-sectional data between DT and malignant sarcoma cohorts, to identify predictors of distress.
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