Related Experiment Videos
Managing patients with advanced soft tissue sarcoma: Evolving landscape from an Australian perspective
Susie Bae1,2, Alan Brnabic3, Philip Crowe4
1Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Aim:
Despite lack of advances in the first-line systemic therapy, the overall survival (OS) has continued to improve in patients with advanced soft tissue sarcoma (STS) with the recent estimation of median OS at 20 months. Several systemic therapy options are available now for the second-line and beyond, with more treatment tailored to histology and molecular subtype. The aim of this retrospective study was to characterize current patterns of care in managing patients with advanced STS (aSTS) in Australia.
Methods:
Sarcoma databases from 7 Australian sarcoma services were accessed to identify patients diagnosed with locally advanced inoperable and/or metastatic STS between January 1, 2010 and December 31, 2015. Baseline clinicopathological factors and initial treatment patterns were descriptively analyzed. For the Victorian cohort where treatment of aSTS and follow-up details were available, further exploratory analysis was conducted to determine the impact of patient and tumor characteristics and the use of palliative-intent treatment OS.
Results:
Of 2261 cases of STS, 671 were deemed as aSTS. Two thirds were relapsed disease with a mean 1.9 years from initial diagnosis. Median age at diagnosis of aSTS was 59 years (18-95 years) and 56.3% was male. Histology classification revealed four main subtypes: undifferentiated pleomorphic sarcoma (UPS) (23.1%), leiomyosarcoma (18.2%), liposarcoma (12.8%), synovial sarcoma (8.2%), and other comprising 14 STS subtypes. For the Victorian cohort (N = 361), approximately 80% of patients accessed palliative-intent treatment of various modalities. Nearly 40% of patients underwent tumor-debulking surgery or metastasectomy, of which lung wedge resection was the most common (N = 83, 47.7%). A total of 438 palliative-intent radiotherapy treatments were delivered to 259 patients (71.7%), with the majority in the form of external beam radiotherapy. Palliative-intent systemic therapy was delivered to 51.5% of patients (N = 186), mostly (73%). Anthracycline-based therapy was the most commonly delivered therapy (N = 135, 72.6%). Approximately half of the patients in each line of therapy failed to proceed to the subsequent line of systemic therapy with 29.4% receiving three or more lines of therapy (N = 55). A total of 18.3% of patient (N = 34) participated in clinical trials or accessed off-label drugs. The median OS for the Victoria cohort was 15.4 months (95% confidence interval: 12.1, 18.2). The UPS histology subtype was associated with poorer OS, whereas receiving any modality of palliative-intent treatment conferred survival benefit.
Conclusion:
In Australia, aSTS is managed with diverse treatment approaches comprising various therapy modalities. Further work is planned in describing healthcare resource utilization and estimating costs by this patient cohort.
Insights
This study characterizes advanced soft tissue sarcoma (aSTS) care in Australia, finding diverse palliative treatments improve survival. Undifferentiated pleomorphic sarcoma (UPS) showed poorer outcomes, highlighting the need for tailored aSTS management.
Area of Science:
- Medical Oncology
- Surgical Oncology
- Clinical Research
Background:
- Advanced soft tissue sarcoma (aSTS) management lacks first-line therapy advances, yet overall survival (OS) has improved to a median of 20 months.
- Multiple second-line and beyond systemic therapy options exist, with increasing tailoring to histology and molecular subtypes.
Purpose of the Study:
- To characterize current patterns of care for advanced soft tissue sarcoma (aSTS) patients in Australia.
- To analyze the impact of patient and tumor characteristics on OS in a Victorian cohort.
- To evaluate the effectiveness of palliative-intent treatments in aSTS management.
Main Methods:
- Retrospective analysis of 671 advanced soft tissue sarcoma (aSTS) cases from 7 Australian sarcoma services (2010-2015).
- Descriptive analysis of clinicopathological factors and initial treatment patterns.
- Exploratory analysis of palliative-intent treatment modalities (surgery, radiotherapy, systemic therapy) and their impact on OS in the Victorian cohort (N=361).
Main Results:
- Approximately 80% of patients received palliative-intent treatment, including debulking surgery/metastasectomy (40%) and radiotherapy (71.7%).
- Palliative-intent systemic therapy was given to 51.5% of patients, with anthracycline-based regimens being most common.
- Median OS in the Victorian cohort was 15.4 months; palliative treatment conferred survival benefit, while UPS histology was associated with poorer OS.
Conclusions:
- Advanced soft tissue sarcoma (aSTS) in Australia is managed with diverse therapeutic modalities.
- Palliative-intent treatments demonstrate a survival benefit in advanced soft tissue sarcoma (aSTS).
- Future research will focus on healthcare resource utilization and cost estimation for this patient cohort.
Related Concept Videos
Treatment Resistant Cancers
Cancer Survival Analysis