Radiotherapy for Post-Chemotherapy Residual Mass in Advanced Seminoma: A Fluorodeoxyglucose Positron Emission
V Murthy1, S Karmakar1, J Carlton1
1Department of Radiation Oncology, Tata Memorial Hospital, Parel, Mumbai, India.
Summary
Fluorodeoxyglucose positron emission tomography-computed tomography (FDG PET-CT) can identify patients with classical seminoma who may benefit from radiotherapy for post-chemotherapy residual masses. A risk-adapted approach using FDG PET-CT SUVmax values refines treatment decisions for improved locoregional control.
Area of Science:
- Oncology
- Nuclear Medicine
- Radiotherapy
Background:
- Management of post-chemotherapy residual masses in classical seminoma lacks consensus.
- Fluorodeoxyglucose positron emission tomography-computed tomography (FDG PET-CT) can detect viable disease in residual masses.
- FDG PET-CT may help tailor therapy for seminoma patients.
Purpose of the Study:
- To evaluate if FDG PET-CT can identify patients who benefit from locoregional radiotherapy.
- To assess the diagnostic accuracy of FDG PET-CT in detecting viable disease.
- To compare survival outcomes between different risk groups based on FDG PET-CT findings.
Main Methods:
- Retrospective analysis of advanced classical seminoma patients treated with chemotherapy.
- Stratification into low risk (SUVmax <3) and high risk (SUVmax ≥3) groups based on FDG PET-CT.
- Subgroup analysis for a very high risk group (residual nodal size ≥3 cm and SUVmax ≥3).
Main Results:
- Sixty-nine patients were analyzed; 48 observed, 21 received radiotherapy.
- Locoregional failure rates were 0% in the radiotherapy group vs. 30% in the observation group for the very high risk subgroup (P=0.059).
- Benefit in locoregional control did not translate to improved overall survival.
Conclusions:
- A tailored, FDG PET-based risk-adapted treatment approach refines management of post-chemotherapy residual masses in seminoma.
- Radiotherapy appears beneficial for patients with post-chemotherapy residual mass SUVmax ≥3.
- FDG PET-CT aids in selecting seminoma patients for risk-adapted radiotherapy.


