# Evaluation of RECIST v1.1 for predicting overall survival in sarcoma patients with pulmonary metastasis

**Authors:** Lukas Gold, Konstantin Klambauer, Christian Dascalescu, Luca Klinge, Michael Winkelmann, Nabeel Mansour, Dirk Mehrens, Jens Ricke, Michael von Bergwelt-Baildon, Dorit Di Gioia, Lars H. Lindner, Wolfgang G. Kunz

PMC · DOI: 10.1186/s40644-026-01012-0 · Cancer Imaging · 2026-02-26

## TL;DR

This study examines how well RECIST v1.1 predicts survival in sarcoma patients with lung metastases, finding that new metastases are a strong indicator of poor survival.

## Contribution

The study identifies new metastases as a more reliable predictor of survival than RECIST v1.1's standard criteria in sarcoma patients.

## Key findings

- Patients with new metastases had significantly shorter overall survival (7.8 months vs. 27.0 months).
- RECIST v1.1's 20% growth threshold did not reliably predict survival differences (p = 0.221).

## Abstract

Response assessment in the treatment of metastatic sarcoma primarily depends on imaging, as no established clinical or serological biomarkers reliably predict survival outcomes. This study evaluates the utility of Response Evaluation Criteria in Solid Tumors (RECIST v1.1) in predicting overall survival (OS) in sarcoma patients with pulmonary metastases.

We selected consecutive study subjects from a prospective registry based on the following criteria: (1) available CT imaging at first diagnosis of pulmonary metastases from sarcoma, (2) available follow-up CT imaging within 16 weeks of systemic therapy initiation, (3) documentation of OS. Volumetric segmentation of up to 5 lung metastases was performed over time. Progressive disease (PD) was defined as increase of the unidimensional sum of lesions ≥ 20% or appearance of new metastases according to RECIST v1.1. Kaplan-Meier survival analyses were performed. P values < 0.05 were considered statistically significant.

Ninety-two patients were included (median age: 58 years; 50% female). Average time of follow-up CT was 67 days after baseline imaging. Patients with PD on first follow-up imaging (n = 24; 26%) showed significantly shorter OS (13.9 months vs. 29.3 months; p = 0.014). The unidimensional growth threshold of 20% proposed by RECIST did not stratify OS (14.6 months vs. 26.8 months, p = 0.221). The appearance of new metastases (n = 16; 17%) indicated significantly shorter OS (7.8 months vs. 27.0 months; p < 0.001) and was frequently observed even in patients with decreasing size of existing metastases (n = 7; 8%).

Imaging progression patterns of pulmonary metastatic sarcoma demonstrate distinct associations with OS, highlighting the need for sarcoma-specific adaptations to established response criteria.

The online version contains supplementary material available at 10.1186/s40644-026-01012-0.

## Linked entities

- **Diseases:** sarcoma (MONDO:0005089)

## Full-text entities

- **Diseases:** GIST (MESH:D046152), Metastases (MESH:D009362), synovial sarcoma (MESH:D013584), OS (MESH:D011475), bone sarcoma (MESH:D001847), mesothelioma (MESH:D008654), PD (MESH:D018450), hepatocellular carcinoma (MESH:D006528), solid (MESH:D018250), prostate cancer (MESH:D011471), leiomyosarcoma (MESH:D007890), osteosarcoma (MESH:D012516), disease (MESH:D004194), liposarcoma (MESH:D008080), Retroperitoneal Sarcoma (MESH:D012186), RECIST (MESH:D009369), lung lesion (MESH:D008171), metastatic (MESH:D000092182), Soft tissue sarcomas (MESH:D012509)
- **Chemicals:** iomeprol (MESH:C057937)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12952042/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12952042/full.md

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Source: https://tomesphere.com/paper/PMC12952042