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Poster Display session

59P - Delay in diagnosis of soft tissue sarcoma (STS): Contributing factors and their impact on overall survival - Experience from a tertiary care hospital

Date

21 Mar 2025

Session

Poster Display session

Presenters

Eluska Iruarrizaga

Citation

Annals of Oncology (2025) 10 (suppl_3): 1-2. 10.1016/esmoop/esmoop104368

Authors

E. Iruarrizaga1, E. Iza Rodriguez2, J.M. Mane2, E. Novo3, R. Fernandez-Rodriguez4

Author affiliations

  • 1 Medical Oncology Dept., Hospital Universitario Cruces, 48903 - Barakaldo/ES
  • 2 Oncologia Médica, Hospital Universitario Cruces, 48903 - Barakaldo/ES
  • 3 Medical Oncology Department, Hospital Universitario Cruces, 48903 - Barakaldo/ES
  • 4 Medical Oncology, Hospital Universitario Cruces, 48903 - Barakaldo/ES

Resources

This content is available to ESMO members and event participants.

Abstract 59P

Background

STS are a rare and heterogeneous group of tumors often associated with diagnostic delays. Published studies have not clarified the reasons for these delays or their impact on patient OS. This retrospective study analyzed high-risk STS patients evaluated at our center between October 2018-October 2022. The study aimed to explore correlations between diagnostic intervals and survival outcomes.

Methods

The following intervals were analyzed: Total interval (TI): From first symptom (FS) to histological diagnosis (HD). Diagnostic interval (DI): From first medical consultation (FMC) to HD. Patient interval (PI): From FS to FMC. Primary care interval (PCI): From FMC to evaluation by a specialist (S) or sarcoma specialist (SS). Secondary care interval (SCI): From S evaluation to SS evaluation. Tertiary care interval TCI): From SS evaluation to histological diagnosis. Statistical analysis included chi-square tests and Cox regression models. Kaplan-Meier curves were used for survival analysis.

Results

52 pts were included. Descriptive analyses and collected characteristics are detailed in the table. Median intervals (in weeks) were: IT 33 (0.43–162), DI 9.4 (0.14–35.14), PI 23.6 (0–142.7), PCI 5.2 (0.14–21.14), SCI 6.96 (0–35), and TCI -1.4 (-22.4–7.14). The TI is prolonged primarily due to the PI. Pts with DI ≤6 months demonstrated longer OS compared to those with >6 months (58.5 ± 5.34 months vs. 47.19 ± 5.64 months), although the difference was not statistically significant (p = 0.123). DI were shorter when pts were directly referred to a SS from the FMC, bypassing intermediate S (median DI: 4.5 weeks [0.14–18] vs. 11 weeks [0.29–35.1]). No statistically significant correlations were found between the studied variables and diagnostic intervals. Table: 59P

% Correlation with longer TI (> 6 months)
Male/Female 65.4 / 34.6 p=0.244
Extremities/trunk wall 71.2 / 28.8 p=0.310
Firts symptom: Growth/pain/other 82.7 / 15.4 / 1.9 p=0.714
First imaging test: ultrasound / CT / NMR/ none 67.5 / 11.5 / 9.6 / 1.9 p=0.898
Localized/metastatic at diagnosis 92.3 / 7.7 p=0.5
Surgery: Yes/No 86.5 / 13.5 p=0.685
Size <5/>5 cm 28.8 / 23.2 p=0.358

Conclusions

Raising global awareness about the symptoms and diagnosis of STS among primary care providers and the general public is essential to reduce diagnostic delays and potentially improve patient survival outcomes.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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