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Poster Display session

12P - Do retroperitoneal extragonadal germ cell tumours (pR-GCT) exist? Evaluation of treatment outcomes of an international retrospective collaboration (PRIMERE study-IGG05)

Date

15 Mar 2024

Session

Poster Display session

Presenters

Chiara Cavalli

Citation

Annals of Oncology (2024) 9 (suppl_2): 1-2. 10.1016/esmoop/esmoop102404

Authors

C. Cavalli1, E. Gusmaroli1, I. Taglialatela1, M. Mego2, D. Bimbatti3, S. Secondino4, D. Biasoni1, M. Catanzaro5, M. Claps1, M. Zimatore5, T. Torelli1, S. Stagni1, A. Macchi6, A. Tesone6, P. Pedrazzoli7, U. Basso8, G. Procopio9, N. Nicolai6, P. Giannatempo1

Author affiliations

  • 1 Medical Oncology Department, Fondazione IRCCS - Istituto Nazionale dei Tumori, 20133 - Milan/IT
  • 2 Department Of Oncology, National Cancer Institute of Slovakia, 833 10 - Bratislava/SK
  • 3 Medical Oncology 1 Department, IOV - Istituto Oncologico Veneto IRCCS, 35128 - Padova/IT
  • 4 Medical Oncology Department, Fondazione IRCCS Policlinico San Matteo, 27100 - Pavia/IT
  • 5 Department Of Urology, Fondazione IRCCS - Istituto Nazionale dei Tumori, 20133 - Milan/IT
  • 6 Urology, Fondazione IRCCS - Istituto Nazionale dei Tumori, 20133 - Milan/IT
  • 7 Oncology Department, Fondazione IRCCS Policlinico San Matteo, 27100 - Pavia/IT
  • 8 Medical Oncology Unit 1, Department Of Oncology, ISTITUTO ONCOLOGICO VENETO IOV - IRCCS, 35128 - PADOVA/IT
  • 9 Medical Oncology Dept., Fondazione IRCCS - Istituto Nazionale dei Tumori, 20133 - Milan/IT

Resources

This content is available to ESMO members and event participants.

Abstract 12P

Background

Primitive Retroperitoneal Germinal Cell Tumors (pR-GCT) corresponds to the clinical case of retroperitoneal ascertained GCT without evidence of primary testicular tumor and accounts for up to 40 % of extragonadal GCTs. An occult primary testicular tumor is often missed at diagnosis. Treatment modalities and outcomes have not been specifically addressed, preventing robust recommendations. We performed an international call to assess prognosis of treatment outcomes of these pts.

Methods

Clinical, pathological and treatment data pts with pR-GCT between April 1988 and January 2022 were retrospectively collected across four referral centers. Kaplan Meier methods, univariable and multivariable Cox regression models (MCRMs) were used.

Results

Ninety-nine pts (median age 37 years - IQR: 29-45) were collected. Ninety-three (94%) had histological diagnosis by biopsy or primary retroperitoneal lymph-node dissection: 60 (62.5%) had non-seminomatous (pR-NSGCTs) and 33 (34.4%) had seminomatous (pR-SGCTs). IGCCCG prognostic allocation was possible in 91 pts: 34 (35.8%) were good, 23 (24.2%) intermediate and 34 (35.8%) poor-risk, respectively. All pts underwent cisplatin-based chemotherapy, usually BEP (94.9%). After chemotherapy, 25 (25.3%) pts underwent orchiectomy: viable tumor was present in 8 (32%), burn-out lesions in 6 (24%) and no lesion in 11 (44%). After a median FUP of 45 m (IQR:15-90), the 5-yrs OS was 58%, being 85% in case of pR-SGCT and 46% in case of pR-NSGCT. According to IGCCCG classification 5-yrs OS was 83.3% for good, 57% for intermediate, 42% for poor-risk pts, respectively. No difference in term of OS (60% vs 56%, p-value 0.81) was observed between patient who had or not radical orchiectomy. At MCRMs only IGCCCG poor risk category (HR 3.2, CI: 1.18-8.84, p-value 0.02) was independent predictor of a worse OS.

Conclusions

Eventually, a significant proportion of patients with pR-GCT had a misclassified primary testicular tumor. 5 years-OS according to IGCCCG-classification is worse than expected. The role of a surgical exploration of the suspected primary tumor remains controversial and the existence of a real category of p-RGCT cannot be excluded.

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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