Relapse-free and overall survival in patients with non-seminomatous testicular germ cell tumours with teratoma-free primaries.

Authors

null

Pia Paffenholz

Department of Urology, University Hospital of Cologne, Cologne, Germany

Pia Paffenholz , Georg Landwehr , Christoph Alexander Seidel , Annika Poch , Carsten Bokemeyer , Richard Cathomas , Pailin Pongratanakul , Andreas Hiester , Peter Albers , Martin Pichler , Susanne Krege , Isabella Syring , Julia Heinzelbecker , Tim Nestler , David Pfister , Axel Heidenreich

Organizations

Department of Urology, University Hospital of Cologne, Cologne, Germany, University Hospital Cologne, Cologne, Germany, University Medical Center Hamburg-Eppendorf, Hamburg, Germany, Department of Oncology, Hematology and Bone Marrow Transplantation with Division of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburhg, Germany, Kantonsspital Chur, Coire, Switzerland, 4)Department of Urology, University Hospital Düsseldorf, Duesseldorf, Germany, Department of Urology, University Hospital of Duesseldorf, Duesseldorf, Germany, Division of Oncology, Medical University of Graz, Graz, Austria, Kliniken Essen-Mitte, Evangelische Huyssens-Stiftung/Knappschaft GmbH, Essen, Germany, Department of Urology, University Hospital Bonn, Bonn, Germany, University Medical Center of Southern Nevada, Homburg, Germany, University Hospital of Cologne, Department of Urology, Koblenz, Germany, Dept. of Urology, University Hospital Cologne, Cologne, Germany

Research Funding

Other
KoKoeln Fortune Program, 2020, Faculty of Medicine, University of Cologne, Germany)

Background: Characteristics and outcome of non-seminomatous testicular germ cell tumours (NSGCT) with teratoma-containing primaries are still under debate. Methods: We performed a retrospective analysis including 557 patients with metastatic NSGCT as a registry study within the "German Testicular Cancer Study Group". Results: Of the eligible 557 patients with NSGCT, 237 (42%) of all orchiectomy specimens had teratoma-containing primaries, while 320 (58%) were teratoma-free. Teratoma-containing primaries had a significantly higher clinical stage (p=0.002) and worse prognosis (p=0.051) compared to teratoma-free specimens. Lymph node metastasis were significantly larger before (4.5 vs 2.5cm; p<0.001) and after chemotherapy (3.5 vs 2.5 cm; p<0.001) in teratoma-containing primaries. Post-chemotherapy retroperitoneal lymph node dissection was performed in 57% of all patients. As teratoma-containing specimens revealed a significantly lower number of complete responses after chemotherapy, PC-PRLND was more often performed, with teratomatous elements being more often present in the PC-RPLND specimens compared to non-teratoma containing primaries. Kaplan-Meier estimates revealed that 19% of all patients relapsed during a median follow-up of 56 months [29-112] with a median time to relapse of 10 months. Teratoma-containing had a significantly lower relapse-free survival (RFS) compared to teratoma-free NSGCT (relapse rate 24% vs 16%, p=0.020). 8% (45/533) of all patients died due to their disease. There was no difference regarding the tumour-specific survival between teratoma-containing NSGCT and teratoma-free NSGCT when looking at the entire cohort of patients (8% vs. 9%, p=0.563), however median overall survival was not reached. Conclusions: In our study, NSGCT patients with teratoma-containing primaries showed a significantly higher clinical stage and worse prognosis at time of presentation compared to teratoma-free primaries. Furthermore, patients with teratoma-containing primaries showed a significantly worse relapse-free survival. Consequently, treating physicians should be aware of these patients portending a dismal prognosis and the presence of teratomatous elements might act as a reliable stratification tool for treatment decision in TGCT patients.

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Abstract Details

Meeting

2023 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Renal Cell Cancer; Adrenal, Penile, Urethral and Testicular Cancers

Track

Renal Cell Cancer,Adrenal Cancer,Penile Cancer,Testicular Cancer,Urethral Cancer

Sub Track

Therapeutics

Citation

J Clin Oncol 41, 2023 (suppl 6; abstr 421)

DOI

10.1200/JCO.2023.41.6_suppl.421

Abstract #

421

Poster Bd #

M3

Abstract Disclosures