Evidence map›Paper›PMID 42152044›Full record

ArticleBMC research notes2026

Feasibility of serial cfDNA measurement after perflubutane microbubble (Sonazoid

Hajime Imamura, Tomohiko Adachi, Daisuke Miyamoto, Takashi Hamada, Kazushige Migita, Ayaka Satoh, Yuki Nunoshita, Kouki Kurotaki, Shun Nakamura, Shinichiro Ogawa and 5 more

Abstract read
In one paragraph

Article in BMC research notes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Hajime ImamuraDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan. hajimeimamura0630@nagasaki-u.ac.jp.ORCID http://orcid.org/0000-0002-7205-7757
Tomohiko AdachiDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.ORCID http://orcid.org/0000-0001-7025-6173
Daisuke MiyamotoDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Takashi HamadaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.ORCID http://orcid.org/0000-0002-8438-750X
Kazushige MigitaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.ORCID http://orcid.org/0009-0003-7971-1621
Ayaka SatohDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Yuki NunoshitaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Kouki KurotakiDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Shun NakamuraDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Shinichiro OgawaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Baglan AskeyevDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.ORCID http://orcid.org/0000-0002-3695-7811
Hajime MatsushimaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.ORCID http://orcid.org/0000-0002-1577-6587
Ayaka KinoshitaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Akihiko SoyamaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.ORCID http://orcid.org/0000-0003-2932-4300
Susumu EguchiDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.ORCID http://orcid.org/0000-0002-7876-0152

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCirculating cell-free DNA (cfDNA) is a promising liquid biopsy biomarker in pancreatic ductal adenocarcinoma (PDAC), but clinical sensitivity remains limited, particularly in localized disease. Experimental studies suggest that transient modulation of hepatic clearance may increase recoverable cfDNA. Perflubutane microbubbles (Sonazoid

methodsThis single-center prospective pilot study enrolled patients with resectable or borderline-resectable PDAC scheduled for curative-intent surgery. Perflubutane microbubbles (Sonazoid

resultsFive patients were enrolled, and all completed the full protocol without deviations. Of these, four had resectable disease and one had borderline-resectable disease. Clinical stage at presentation ranged from IB to IIIA. Serial blood collection, plasma processing, cfDNA extraction, and fluorometric quantification were successfully performed for all 25 planned samples. Baseline cfDNA concentrations ranged from 0.564 to 0.946 ng/µL. Four patients showed a decrease in cfDNA concentration at 5 min followed by relative stability through 60 min, whereas one patient demonstrated a transient greater-than-two-fold increase at 5 min, followed by persistently higher-than-baseline values through 60 min. At the cohort level, no consistent increase in cfDNA concentration was observed. No adverse events related to Sonazoid

conclusionsSerial peri-procedural cfDNA measurement using standardized sampling and fluorometric quantification was feasible and safe in patients with resectable or borderline-resectable PDAC. Administration of perflubutane microbubbles at standard diagnostic doses did not induce a uniform or sustained increase in circulating cfDNA concentrations in this pilot cohort. These findings provide feasibility data and may inform the design of future studies evaluating cfDNA dynamics after clearance-modulating interventions in PDAC. Trial Registration This study is registered in the Japan Registry of Clinical Trials (jRCT) under the identifier jRCTs071240095, registered on January 10, 2025. Registration details are available at: https://jrct.mhlw.go.jp/latest-detail/jRCTs071240095.

Indexed as

Carcinoma, Pancreatic DuctalContrast MediaFerric CompoundsFluorocarbonsIronMicrobubblesOxidesPancreatic NeoplasmsAgedAged, 80 and overBiomarkers, TumorFeasibility StudiesFemaleHumansMaleMiddle AgedBiomarkers, TumorContrast MediaFerric CompoundsFluorocarbonsIronOxidesperfluorobutaneSonazoidCell-free DNAFeasibility studyKupffer cellsLiquid biopsyPancreatic ductal adenocarcinomaPilot studySonazoidUltrasound contrast agent

Identifiers

PMID42152044
PMCPMC13361787

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.