Case Report: Influence of BRCA1 germline mutation on treatment-related morbidity of a non-seminomatous germ cell tumor patient

We present the case of a 47-year-old male with advanced non-seminomatous germ cell tumor, who was found to carry a heterozygous pathogenic <i>BRCA1</i> germline variant following molecular testing due to a positive family history. While tumor analysis did not confirm loss of heterozygosity, evidence suggests that BRCA1 haploinsufficiency also increases genomic instability and cancer risk. After pre-phase treatment and the first cycle of chemotherapy, the patient developed prolonged pancytopenia leading to neutropenic sepsis. Subsequent cycles showed a shorter duration of pancytopenia, though it remained significant. A literature review indicates that BRCA1 deficiency may impair bone marrow recovery after chemotherapy, as observed in breast cancer patients, which we hypothesize also applies in this case. After first-line treatment, the patient had a partial response. In case of recurrence, the use of PARP inhibitors should be considered due to the BRCA1 deficiency.

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Publication Details

Journal
Frontiers in Oncology
Published
2025-05-30
DOI
https://doi.org/10.3389/fonc.2025.1579574
Citations
1
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
0.81
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article

Case Report: Influence of BRCA1 germline mutation on treatment-related morbidity of a non-seminomatous germ cell tumor patient

Pablo Villavicencio‐Lorini, Susann Schulze, Christine Dierks, Thomas Kegel et al.
1 citations
Frontiers in Oncology
DNA Repair Mechanisms
0.81
article

Case Report: Influence of BRCA1 germline mutation on treatment-related morbidity of a non-seminomatous germ cell tumor patient

Pablo Villavicencio‐Lorini, Susann Schulze, Christine Dierks, Thomas Kegel, Bruno Griesler, Haifa Kathrin Al‐Ali, Markus Eszlinger, Nadja Jaekel
article en
1 citations

Abstract

We present the case of a 47-year-old male with advanced non-seminomatous germ cell tumor, who was found to carry a heterozygous pathogenic <i>BRCA1</i> germline variant following molecular testing due to a positive family history. While tumor analysis did not confirm loss of heterozygosity, evidence suggests that BRCA1 haploinsufficiency also increases genomic instability and cancer risk. After pre-phase treatment and the first cycle of chemotherapy, the patient developed prolonged pancytopenia leading to neutropenic sepsis. Subsequent cycles showed a shorter duration of pancytopenia, though it remained significant. A literature review indicates that BRCA1 deficiency may impair bone marrow recovery after chemotherapy, as observed in breast cancer patients, which we hypothesize also applies in this case. After first-line treatment, the patient had a partial response. In case of recurrence, the use of PARP inhibitors should be considered due to the BRCA1 deficiency.

Frontiers in OncologyVol. 15
Halle Institute for Economic Research (DE), Medizinische Hochschule Brandenburg Theodor Fontane (DE), University Hospital in Halle (DE), Martin Luther University Halle-Wittenberg (DE)
Good health and well-being
Openalex Percentile: Top 27%
DNA Repair Mechanisms
0.81
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