Evidence map›Paper›PMID 33562238›Full record

ArticleJournal of clinical medicine2021

Identification of the Response-Related Biomarker of Bimonthly Hepatic Arterial Infusion Chemotherapy.

Kei Moriya, Tadashi Namisaki, Hiroaki Takaya, Kosuke Kaji, Hideto Kawaratani, Naotaka Shimozato, Yasuhiko Sawada, Akitoshi Douhara, Shinya Sato, Masanori Furukawa and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2021. 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
0.1field-weighted citation impact, top 58% of its field
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, 1 citations in OpenAlex.

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

13 authors at 1 institution in 1 country.

Kei MoriyaDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.
Tadashi NamisakiDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.ORCID 0000-0002-3158-5318
Hiroaki TakayaDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.
Kosuke KajiDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.
Hideto KawarataniDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.ORCID 0000-0002-4361-0592
Naotaka ShimozatoDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.
Yasuhiko SawadaDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.
Akitoshi DouharaDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.
Shinya SatoDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.
Masanori FurukawaDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.ORCID 0000-0002-9317-9083
Koh KitagawaDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.
Takemi AkahaneDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.ORCID 0000-0002-6675-0475
Hitoshi YoshijiDepartment of Gastroenterology and Hepatology, Nara Medical University, Nara 634-8521, Japan.
Nara Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the availability of molecularly targeted agents for advanced hepatocellular carcinoma (aHCC), these are limited to compensated cirrhotic patients, and concerns about decreased hepatic functional reserve (HFR) and unknown adverse events, which may affect long-term survival, remain unaddressed. In this study, we enrolled 96 aHCC patients treated with bimonthly hepatic arterial infusion chemotherapy (B-HAIC) with cisplatin or sorafenib monotherapy (oral sorafenib 400 mg twice daily) not only to demonstrate its efficacy and significance but also to indicate preferable candidates by setting a response-related biomarker. Differences in treatment had no significant effect on overall survival (OS). The response rate in patients treated with B-HAIC was relatively higher than those treated with sorafenib. HFR was well maintained over the treatment course with B-HAIC, while it was significantly impaired with sorafenib. By employing multivariate analysis, we found negative trends between progression-free survival (PFS) periods and serum levels of alpha fetoprotein as well as des-gamma-carboxy prothrombin (DCP). In addition, a logistic regression analysis of the relationship between serum DCP levels and PFS periods over 420 days (14 months) showed that the PFS periods of patients with higher DCP was significantly shorter than those of patients with lower DCP (

Indexed as

des-gamma-carboxy prothrombinhepatic arterial infusion chemotherapyhepatic functional reservehepatocellular carcinomamolecularly targeted therapies

Identifiers

PMID33562238
PMCPMC7914951
OpenAlexW3127039901

What OpenQuestion holds

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Registered trials

None linked

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.