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Updated: Jul 13, 2026

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
Pazopanib in the real-world setting in soft tissue sarcomas: data from the Italian national registry
B Vincenzi1, P P Olimpieri2, S Celant2
1Department of Medical Oncology, Università Campus Bio-Medico di Roma, Rome, Italy; Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Background:
Pazopanib is part of the therapeutic armamentarium for the treatment of patients with advanced non-adipocytic soft tissue sarcomas (STS) who have received prior chemotherapy, but its optimal use in STS histologies is still left to be further defined.
Design And Methods:
Data on STS patients treated with pazopanib in Italy have been prospectively collected from July 2013 to December 2019 through a drug monitoring registry managed by the Italian Medicines Agency (AIFA). This nationwide observational cohort study included patients with advanced STS who received pazopanib. Clinicians were mandatorily requested to fill in the AIFA monitoring registry in order to prescribe pazopanib. Patients were recorded on the basis of their clinical characteristics, histological subtype captured at the time of treatment start, and clinical outcome. Primary outcome was time to treatment discontinuation (TTD). Secondary outcomes recorded were frequency of dose reduction and time to first dose reduction.
Results:
We analyzed data from 1964 sarcoma patients. The most represented histological subtypes were leiomyosarcoma (44.7%), undifferentiated sarcomas/not otherwise specified (11.5%), and synovial sarcoma (8.1%). Overall, the median TTD was 106 days. The variables significantly associated to shorter TTD were Eastern Cooperative Oncology Group performance status (1-2 versus 0), the number of previous lines of treatment (2-4 versus 0-1) and prescribed dose (200 mg or 400 mg versus 800 mg, all once daily). Among the most represented (>20 patients) histological subtypes, we also observed longer TTD in patients with histological diagnosis of malignant solitary fibrous tumor if compared with undifferentiated sarcoma not otherwise specified.
Conclusions:
In this nationwide observational real-world study, the outcomes are similar to those reported in the pivotal trial (PALETTE study). Our study includes a significant number of patients with rare/ultra-rare sarcoma subtypes and underlines possible differences in treatment duration among these histologies.
Insights
Pazopanib treatment duration in advanced soft tissue sarcomas (STS) varied by patient factors and histology. Outcomes in this real-world Italian study mirrored pivotal trial results, highlighting potential differences in rare subtypes.
Area of Science:
- Oncology
- Pharmacology
- Clinical Trials
Background:
- Pazopanib is a treatment for advanced non-adipocytic soft tissue sarcomas (STS) after prior chemotherapy.
- Optimal use of pazopanib across different STS histologies requires further definition.
Purpose of the Study:
- To evaluate the real-world effectiveness and treatment patterns of pazopanib in advanced STS patients in Italy.
- To identify factors influencing time to treatment discontinuation (TTD) and dose reductions.
Main Methods:
- A nationwide observational cohort study of advanced STS patients treated with pazopanib from July 2013 to December 2019.
- Data collected prospectively through the Italian Medicines Agency (AIFA) drug monitoring registry.
- Primary outcome: time to treatment discontinuation (TTD); Secondary outcomes: dose reduction frequency and timing.
Main Results:
- Analyzed data from 1964 STS patients; most common subtypes were leiomyosarcoma (44.7%) and undifferentiated sarcoma (11.5%).
- Median TTD was 106 days. Shorter TTD associated with poorer performance status, more prior treatments, and lower pazopanib doses.
- Malignant solitary fibrous tumors showed longer TTD compared to undifferentiated sarcomas.
Conclusions:
- Real-world outcomes for pazopanib in advanced STS are comparable to the pivotal PALETTE trial.
- The study included diverse STS subtypes, including rare ones, suggesting potential variations in treatment duration among histologies.
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