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Poster Display session

322P - The utility of tumour markers in detecting relapses in testicular seminoma: Largest experience from a comprehensive cancer centre in India

Date

07 Dec 2024

Session

Poster Display session

Presenters

Debdeep Samaddar

Citation

Annals of Oncology (2024) 35 (suppl_4): S1505-S1530. 10.1016/annonc/annonc1689

Authors

D. Samaddar, A. Dhanawat, B. Jadhav, A. Tiwari, K. Jobanputra, M.J. Shah, N.S. Menon, P. Maitre, M. Pal, A. Arora, A. Ringe, A. Agrawal, S. Menon, G. Prakash, V. Murthy, V. Noronha, K. Prabhash, A.P. Joshi

Author affiliations

  • Medical Oncology, ACTREC, Tata Memorial Centre, Homi Bhaba National Institute, 410210 - Mumbai/IN

Resources

This content is available to ESMO members and event participants.

Abstract 322P

Background

The tumour markers alpha-fetoprotein (AFP), beta human chorionic gonadotropin (bHCG), and lactate dehydrogenase (LDH) are essential for diagnosing, managing, and monitoring of testicular cancer. This study assesses the effectiveness of these markers in detecting relapses in seminoma patients.

Methods

This retrospective study analysed data from all testicular seminoma patients treated at our hospital from 2014 to 2022. Baseline characteristics, initial treatments (active surveillance, radiotherapy, chemotherapy), relapse patterns (clinical, radiological, biochemical), stages at relapse and patient survival (those with or without relapse) were documented.

Results

Data from 351 patients were analysed, with a median follow-up of 59 months. The median time to relapse was 12.36 months. Relapse occurred in 46 patients (13.1%), with clinical relapse in 29 patients (63%), radiological relapse in 45 patients (97.8%), and biochemical relapse in 15 patients (32.6%). No isolated biochemical relapse was observed. Locoregional relapses were more common than systemic relapses (65.30% vs. 34.78%). Stages at relapse were predominantly stage II and stage III (58.6% and 39.1%, respectively). AFP levels during relapse ranged from 6 to 20 ng/ml, while bHCG levels ranged from 10 to 6000 mIU/ml. Median overall survival (OS) was 182.3 months for patients without recurrence and 126.73 months for those with recurrence. Table: 322P

Baseline characteristics and recurrence details

Characteristics All patients (n = 351)
Age
Median 38 years
IQR 32-47 years
Baseline stage
I 119 (33.9%)
II 110 (31.3%)
III 122 (34.8%)
Baseline tumor markers
Elevated AFP or bHCG 140 (39.9%)
Isolated LDH elevation 171 (48.7%)
Normal 40 (11.4%)
Treatment modality
Active surveillance 48 (13.7%)
Chemotherapy 266 (75.8%)
Radiation therapy 37 (10.5%)
Recurrence (n = 46)
Clinical 29 (63.0%)
Radiological 45 (97.8%)
Serological (AFP / BhCG) 15 (32.6%)
Isolated LDH elevation 1 (2.2%)
Stage at recurrence
I 1 (2.2%)
II 18 (39.1%)
III 27 (58.7%)
Treatment at recurrence
Chemotherapy 36 (78.3%)
Radiation therapy 3 (6.5%)
Surgery 7 (15.2%)

Conclusions

Our study reaffirms the importance of tumour markers in detecting relapse in testicular seminoma patients, challenging some existing literature.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

D. Samaddar.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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