# Prediction Model for Brain Metastasis in Patients With Metastatic Germ‐Cell Tumors

**Authors:** Tareq Salous, Ryan Ashkar, Sandra K. Althouse, Clint Cary, Timothy Masterson, Nasser H. Hanna, Jennifer King, Lawrence H. Einhorn, Nabil Adra

PMC · DOI: 10.1002/cam4.70649 · Cancer Medicine · 2025-02-06

## TL;DR

This study developed a prediction model to identify patients with metastatic germ cell tumors who are at high risk for brain metastasis.

## Contribution

The novel contribution is a practical and effective prediction model for brain metastasis in metastatic germ cell tumors.

## Key findings

- The model includes factors like age ≥40, choriocarcinoma histology, and metastasis characteristics to predict BM risk.
- Patients with higher scores on the model had significantly increased probabilities of having brain metastasis.
- The model showed strong discrimination capability in predicting brain metastasis occurrence.

## Abstract

Brain metastasis (BM) is an independent adverse prognostic factor in metastatic germ cell tumors (mGCT). We aimed to establish an effective and practical BM prediction model.

Between January 1990 and September 2017, 2291 patients with mGCT who were treated at Indiana University were identified. Patients were divided into two categories: BM present (N = 154) and BM absent (N = 2137). Kaplan–Meier methods were used to analyze progression free survival (PFS) and overall survival (OS). Logistic regression was used to determine a predictive model for whether BM was present. The data was separated into training and validation datasets with equal numbers of events in each.

The 2‐year PFS and OS for patients with versus without BM: 17% versus 65% (p < 0.001) and 62% versus 91% (p < 0.001) respectively. Among the 154 patients with BM, 64 (42%) had radiation only (whole‐brain radiotherapy or gamma knife), 22 (14%) had BM‐surgery only, 14 (9%) had both radiation and BM‐surgery. 54 patients (35%) did not receive local therapy for BM. Stepwise selection was used to determine the best model with p < 0.15 as the entry and staying criteria. The model with the largest ROC AUC was used moving forward. The model was tested in the validation dataset. A model was generated including age at diagnosis ≥ 40, choriocarcinoma predominant histology, pre‐chemotherapy hCG≥ 5000, presence of pulmonary metastases size < 3, or ≥ 3 cm, and presence of bone metastasis. Patients with score of 0, 1, 2, 3, 4, 5, 6, 7, 8 points had a 0.6%, 1.4%, 3.5%, 8.2%, 18.3%, 36%, 58%, 78%, 90% probability of having BM, respectively.

The prediction model developed in this study demonstrated discrimination capability of predicting BM occurrence in mGCT and can be used to identify high‐risk patients.

## Full-text entities

- **Genes:** HTC2 (hypertrichosis 2 (generalized, congenital)) [NCBI Gene 3342] {aka CGH, CXINSq27.1, HCG}
- **Diseases:** Germ-Cell Tumors (MESH:D009373), choriocarcinoma (MESH:D002822), BM (MESH:D009362)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC11800130/full.md

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Source: https://tomesphere.com/paper/PMC11800130