Evidence map›Paper›PMID 38028262›Full record

ArticleYonago acta medica2023

Clinical Outcomes of Switching from Zoledronic Acid to Denosumab for the Management of Severe Bone Metastasis from Hepatocellular Carcinoma: A Single-Center, Open-Label, Prospective Intervention Trial.

Kensuke Naruto, Tomokazu Kawaoka, Shintaro Yamasaki, Masanari Kosaka, Yuki Shirane, Yusuke Johira, Shigeki Yano, Kei Amioka, Yutaro Ogawa, Yuki Yoshikawa and 10 more

Open access · diamondAbstract read
In one paragraph

Article in Yonago acta medica, 2023. 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, top 50% 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, 0 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

20 authors at 1 institution in 1 country.

Kensuke NarutoDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Tomokazu KawaokaDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Shintaro YamasakiDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Masanari KosakaDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Yuki ShiraneDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Yusuke JohiraDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Shigeki YanoDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Kei AmiokaDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Yutaro OgawaDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Yuki YoshikawaDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Kenji YamaokaDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Shinsuke UchikawaDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Hatsue FujinoDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Atsushi OnoDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Yasutomo FujiiDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Takashi NakaharaDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Eisuke MurakamiDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Daiki MikiDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Masataka TsugeDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Shiro OkaDepartment of Gastroenterology, Hiroshima University Hospital, Hiroshima 734-8551, Japan.
Hiroshima University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Zoledronic acid reduces the risk of bone metastasis, but denosumab is a better option for treating bone metastases. However, few studies have evaluated the use of denosumab to treat bone metastasis originating from hepatocellular carcinoma. This study aimed to assess the clinical outcomes of switching from zoledronic acid to denosumab for treating bone metastasis in patients with hepatocellular carcinoma. Methods: This prospective study enrolled 10 patients with HCC and bone metastases. The levels of type 1 collagen cross-linked N-telopeptide (NTx) and tumor growth remained abnormal in these patients despite administration of zoledronic acid for over 3 months. We switched from zoledronic acid to 120 mg denosumab every 4 weeks and evaluated the clinical outcomes, including changes in the NTx level, pain level, and activities of daily living, as well as adverse events, after each administration. Results: Urinary NTx clearance was normal in all patients. The average urinary NTx clearance increased from 13.2 to 21.2 nmol BCE/nmol · Cre ( Conclusion: Switching to denosumab did not show a significant change of the pain and activity of daily living for the patients with severe bone metastasis from hepatocellular carcinoma, in whom the efficacy of zoledronic acid was limited.

Indexed as

bone metastasisdenosumabhepatocellular carcinomazoledronic acid

Identifiers

PMID38028262
PMCPMC10674054
OpenAlexW4388406243

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.