Evidence map›Paper›PMID 36498476›Full record

ArticleJournal of clinical medicine2022

Combination of Bone-Modifying Agents with Immunotarget Therapy for Hepatocellular Carcinoma with Bone Metastases.

Zhaoyu Chen, Zhilong Shen, Xiang Wang, Pengru Wang, Xiaofei Zhu, Jiefu Fan, Bo Li, Wei Xu, Jianru Xiao

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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

9 authors at 1 institution in 1 country.

Zhaoyu ChenDepartment of Orthopedic Oncology, Changzheng Hospital, Naval Medical University (Second Military Medical University), 415 Fengyang Road, Shanghai 200003, China.ORCID 0000-0002-3772-5780
Zhilong ShenDepartment of Orthopedic Oncology, Changzheng Hospital, Naval Medical University (Second Military Medical University), 415 Fengyang Road, Shanghai 200003, China.ORCID 0000-0002-8623-4996
Xiang WangDepartment of Orthopedic Oncology, Changzheng Hospital, Naval Medical University (Second Military Medical University), 415 Fengyang Road, Shanghai 200003, China.
Pengru WangDepartment of Orthopedic Oncology, Changzheng Hospital, Naval Medical University (Second Military Medical University), 415 Fengyang Road, Shanghai 200003, China.
Xiaofei ZhuDepartment of Radiation Oncology, Changhai Hospital, Naval Medical University (Second Military Medical University), 168 Changhai Road, Shanghai 200082, China.
Jiefu FanDepartment of Vascular Surgery, Changhai Hospital, Naval Medical University (Second Military Medical University), 168 Changhai Road, Shanghai 200082, China.
Bo LiDepartment of Orthopedic Oncology, Changzheng Hospital, Naval Medical University (Second Military Medical University), 415 Fengyang Road, Shanghai 200003, China.
Wei XuDepartment of Orthopedic Oncology, Changzheng Hospital, Naval Medical University (Second Military Medical University), 415 Fengyang Road, Shanghai 200003, China.
Jianru XiaoDepartment of Orthopedic Oncology, Changzheng Hospital, Naval Medical University (Second Military Medical University), 415 Fengyang Road, Shanghai 200003, China.
Second Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to limited investigations about efficacy of tyrosine kinase inhibitors (TKIs) plus immune-checkpoint inhibitors (ICIs) versus TKIs alone, and effects of durations of bone modifying agents (BMAs) on the survival of patients with hepatocellular carcinoma (HCC) and bone metastases (BoM), we aim to compare the efficacy of TKIs both alone and in combination with ICIs, as well as comparing long-term and no or perioperative use of BMAs for patients with HCC and BoM. Patients with pathologically confirmed HCC and BoM were included in the study. They were stratified into the TKIs group and the TKIs + ICIs group, and the perioperative and the long-term use of BMAs group. Overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and disease control rate (DCR) were calculated to assess the response to these regimes. The cumulative risk of initial skeletal-related events (SREs) was used to evaluate treatment efficacy for bone lesions. A total of 21 (33.9%) patients received TKIs (Sorafenib or Lenvatinib) alone and 41 (66.1%) received TKIs + ICIs. The combination group showed higher ORR than monotherapy group (1/21, 4.7% vs. 9/41, 22.0%;

Indexed as

bone metastasesdenosumabhepatocellular carcinomaimmunotarget therapyPD-1

Identifiers

PMID36498476
PMCPMC9738198
OpenAlexW4309729324

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.