cfDNA-inferred putative clonal hematopoiesis during first-line platinum-to-PARP inhibitor maintenance in ovarian cancer

Objective: To describe cell-free DNA (cfDNA)-inferred putative clonal hematopoiesis (CH) candidates during first-line platinum-based chemotherapy followed by poly(ADP-ribose) polymerase inhibitor (PARPi) maintenance in ovarian cancer.Methods: In SCRUM-Japan MONSTAR-SCREEN-1, we analyzed clinically reported paired tumor tissue and plasma cfDNA profiling (324-gene assays).Baseline (B1) data were assessed in 35 treatment-naïve patients; longitudinal cfDNA was available at B1, after platinum without progression (B2), and during/after PARPi without progression (B3) in 8 patients.Putative CH candidates were defined as pathogenic variants (variant allele frequency <40%) in prespecified CH-related genes detected in plasma but not detected in matched tumor tissue at clinical reporting thresholds.

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Publication Details

Journal
Journal of Gynecologic Oncology
Published
2026-08-03
DOI
https://doi.org/10.3802/jgo.2027.38.e11
Primary Topic
Cancer Genomics and Diagnostics
Type
article
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article

cfDNA-inferred putative clonal hematopoiesis during first-line platinum-to-PARP inhibitor maintenance in ovarian cancer

Kenichi Harano, Daisuke Aoki, Yoshiaki Nakamura, Kiyoko Kato et al.
Journal of Gynecologic Oncology
Cancer Genomics and Diagnostics
article

cfDNA-inferred putative clonal hematopoiesis during first-line platinum-to-PARP inhibitor maintenance in ovarian cancer

Kenichi Harano, Daisuke Aoki, Yoshiaki Nakamura, Kiyoko Kato, Tatsuyuki Chiyoda, Kimihiko Ito, Hidemichi Watari, Kazuhiro Takehara, Hideaki Bando, Tomomi Egawa‐Takata, Takao Fujisawa, Shogen Boku, Takayuki Yoshino, Masanori Isobe, Daisuke Shintani, Kei Ihira, Kosei Hasegawa, Hiromichi Nakajima, Hiroshi Yagi, Mika Okazawa‐Sakai, Yoh Hayasaki, Ichinosuke Hyodo
article en

Abstract

Objective: To describe cell-free DNA (cfDNA)-inferred putative clonal hematopoiesis (CH) candidates during first-line platinum-based chemotherapy followed by poly(ADP-ribose) polymerase inhibitor (PARPi) maintenance in ovarian cancer.Methods: In SCRUM-Japan MONSTAR-SCREEN-1, we analyzed clinically reported paired tumor tissue and plasma cfDNA profiling (324-gene assays).Baseline (B1) data were assessed in 35 treatment-naïve patients; longitudinal cfDNA was available at B1, after platinum without progression (B2), and during/after PARPi without progression (B3) in 8 patients.Putative CH candidates were defined as pathogenic variants (variant allele frequency <40%) in prespecified CH-related genes detected in plasma but not detected in matched tumor tissue at clinical reporting thresholds.

Journal of Gynecologic OncologyVol. 38
Kansai Medical University (JP), Kyushu University (JP), Keio University (JP), Kansai Rosai Hospital (JP), Saitama International Medical Center (JP), Shikoku Cancer Center (JP), Hokkaido University Hospital (JP), National Cancer Center Hospital East (JP), Gifu University (JP), International University of Health and Welfare (JP), Saitama Medical University (JP)
Good health and well-being
Openalex Percentile: Top 12%
Cancer Genomics and Diagnostics
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