Abstract 1931P
Background
Our understanding of the clinical characteristics, survival rate, and prognostic factors of ultra-rare sarcomas (URSs) is limited due to the low incidence. The aim of this study is to understand the clinical differences among URS, non-URS (NURS), and other non-sarcoma solid tumors (NSST).
Methods
Clinical demographics and survival of solid tumor patients(pts) of Taiwan Cancer Registry diagnosed between January 1, 2002, and December 31, 2019, were retrieved. URS included sarcoma histologies with an incidence < 1/1,000,000 persons. The annual percent change (APC) was computed to summarize the change in incidence for the recent years. Overall survival (OS) was estimated from the time of diagnosis to death or the last follow-up. The impact of gender, age, diagnosis period (2002-2010 vs. 2011-2019), and histology type on OS were estimated by Cox proportional hazard method.
Results
A total of 1,578,049 pts were included (URS [n=2,154], NURS [n=32,454], and NSST [n=1,543,441]). Among all sarcoma pts, 6.2% were URS; the top three most common histologies of URS were endometrial stromal sarcoma (n=292), pleomorphic liposarcoma (n=212), and epithelioid sarcoma (n=209). The APC of URS continued a surging trend from 2002 to 2019 (APC 3.81, p < 0.05) while the APC of NURS and NSST decelerated after 2010. URS pts are younger (p < 0.001) and more likely to be female (p < 0.001). In the multivariate analysis adjusted for gender, age, and diagnosis period, URS pts had worse OS than NURS pts (HR 1.70, 95% CI 1.59-1.81, p < 0.001). When all pts were divided into four age groups (0-18, 18-40, 40-70, and >70), the negative impact of URS on OS was most significant in adolescents and young adults (AYA, age 18-40) (HR:2.23; 95% CI, 1.94-2.55; p < 0.001). Unlike NSST, where the OS improved in the past decade (HR:0.84, 95% CI, 0.83-0.84, p < 0.001), OS of URS and NURS both worsened (URS: HR:1.14, 95% CI, 1.01-1.30; p <0.05; NURS: HR:1.05, 95% CI, 1.02-1.09, p < 0.005) in the period 2011 to 2019 compared to 2002 to 2010.
Conclusions
Our findings showed that the incidence of URS is increasing but the OS worsened. Among different age groups, the detrimental effect of URS was most prominent in the AYA pts. Awareness of URS and precision medicine-based therapies for URS are desperately needed.
Clinical trial identification
Editorial acknowledgement
This study was supported by the Health Promotion Administration, Ministry of Health and Welfare, grant no. A1111010: Tobacco Health and Welfare Taxation and Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Legal entity responsible for the study
The authors.
Funding
Health Promotion Administration, Ministry of Health and Welfare, Taiwan.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1971P - Metastatic osteosarcoma, patterns of care and outcomes of patients in a real-life setting: The Metabone national observational study
Presenter: Mathilde Reich
Session: Poster session 15
1972P - Molecular mechanism study of recurrence/metastasis for Enneking IIb osteosarcoma
Presenter: Junqiang Yin
Session: Poster session 15
1975P - Systemic therapy for KIT/PDGFRA wild-type GIST
Presenter: Mehdi Brahmi
Session: Poster session 15
1976P - Financial difficulties experienced by gastrointestinal stromal tumor (GIST) patients in the Netherlands: Data from a cross-sectional multicenter study
Presenter: Deborah van de Wal
Session: Poster session 15
1977P - A registry-based analysis of the projected genomic landscape among unclassified KIT/PDGFRA wildtype mutations in patients with gastrointestinal stromal tumors
Presenter: Jerry Call
Session: Poster session 15
1978P - Identification of SDH-deficient GIST increases after the implementation of diagnostic algorithm in Life Raft Group (LRG) patient registry data
Presenter: Denisse Evans
Session: Poster session 15
1979P - phase I trial of pembrolizumab in HIV-associated Kaposi sarcoma (KS)
Presenter: Kathryn Lurain
Session: Poster session 15
1980P - Artificial intelligence analysis shows enhanced CCNG1 expression in sarcoma tumors, a novel biomarker for DeltaRex-G tumor targeted retrovector encoding a CCNG1 inhibitor gene
Presenter: Sant Chawla
Session: Poster session 15
1981P - Histopathological diagnostic discrepancies in bone and soft tissue tumors referred to a specialist sarcoma center and its clinical impact
Presenter: Akira Kawai
Session: Poster session 15