High dose chemotherapy in male patients with germ cell cancer: A population-based study by the SWENOTECA group.

Authors

null

Anna Jansson

Department of Immunology, Genetics & Pathology, Uppsala University, Uppsala, Sweden

Anna Jansson , Gabriella Elisabeth Cohn-Cedermark , Helene F. S. Negaard , Torgrim Tandstad , Olof Stahl , Annika Hedlund , Asa Karlsdottir , Martin Hellström , Carl Wilhelm Langberg , Camilla Sköld , Hege Sagstuen Haugnes , Ingrid Glimelius

Organizations

Department of Immunology, Genetics & Pathology, Uppsala University, Uppsala, Sweden, Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden, Department of Oncology, Oslo University Hospital, Oslo, Norway, The Cancer Clinic, St. Olavs University Hospital, Trondheim, Norway, Department of Oncology, Skåne University Hospital, Lund, Sweden, Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden, Department of Oncology, Haukeland University Hospital, Bergen, Norway, Department of Radiation Sciences, Oncology, Umeå University, Umeå, Sweden, Department of Oncology, University Hospital of North Norway, Tromso, Norway

Research Funding

No funding sources reported

Background: Selected patients with advanced germ cell tumors have a poor prognosis. These include patients with brain, bone or liver metastases, very elevated tumor markers or primary mediastinal tumor. High-dose chemotherapy (HDCT) with autologous stem cell support is recommended in the Swedish and Norwegian Testicular Cancer Group (SWENOTECA) guidelines in selected poor risk patients with poor response to/relapse after intense primary treatment. From the year 2011, the HDCT-regimen consisted of two cycles of carboplatin and etoposide. Our aim of this study was to evaluate survival and toxicity in patients treated with HDCT within the population-based SWENOTECA cancer care program in 2011-2021. Methods: All patients treated with HDCT according to guidelines in Sweden and Norway between 2011-2021 were included, in total 80 patients (76 non-seminoma and 4 seminoma). This reflected approximately 3% of all non-seminoma patients. HDCT was administered in three different clinical situations: delayed tumor marker decline during primary or intensified primary treatment (n=26), progressive disease during primary treatment (n=29) (defined as progressive disease within <3 months from last cycle of chemotherapy), or relapse with poor prognosis (n=25). The overall survival (OS) and failure-free survival (FFS) were calculated, and the toxicity was described. Results: The 5-year overall survival (OS) and failure free survival (FFS) after HDCT was 55% and 43% respectively. HDCT due to delayed tumor marker decline had a more favorable outcome, 5-year OS of 75% and 5-year FFS of 53%. HDCT due to relapse resulted in a 5-year OS of 61% and 5-year FFS of 58%. Patients treated with HDCT due to progressive disease during primary treatment had a markedly less favorable 5-year OS of 29% and 5-year FFS of 18%. Four patients (5%) died due to treatment. The most common treatment-related grade 3-4 toxicities were infections (n=69, 86%). Conclusions: In this population-based study, we have shown that HDCT for patients with advanced germ cell cancer according to the SWENOTECA cancer care program is achievable and leads to favorable OS and FFS rates. Furthermore, even though patients that receive HDCT due to progressive disease have a relatively poor outcome, 20-30% of patients do achieve long-term survival.

High-dose chemotherapy in Sweden and Norway 2011-2021. Overall survival at 1, 2 and 5 years, all patients. Survival probability %; (95% CI).

Indication for HDCTPatients, nDeaths Overall, n1-Year Survival Probability2-Year Survival Probability5-Year Survival Probability
Overall8036*70; (60-81)62; (52-73)55; (44-68)
Delayed marker decline26888; (76-100)80; (66-97)75; (60-95)
Progression292048; (33-70)33; (19-56)29; (16-52)
Part of relapse treatment25876; (61-95)76; (61-95)61; (41-91)

*Mortality due to HDCT-treatment 4/80 (5%).

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Abstract Details

Meeting

2024 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Genitourinary Cancer—Prostate, Testicular, and Penile

Track

Genitourinary Cancer—Prostate, Testicular, and Penile

Sub Track

Germ Cell/Testicular Cancer

Citation

J Clin Oncol 42, 2024 (suppl 16; abstr 5040)

DOI

10.1200/JCO.2024.42.16_suppl.5040

Abstract #

5040

Poster Bd #

358

Abstract Disclosures