Evidence map›Paper›PMID 39225556›Full record

SynthesisCancer medicine2024

Efficacy and safety of pharmacotherapy for cancer cachexia: A systematic review and network meta-analysis.

Hao Chen, Masashi Ishihara, Hiroki Kazahari, Ryusuke Ochiai, Shigeru Tanzawa, Takeshi Honda, Yasuko Ichikawa, Nobuyuki Horita, Hisashi Nagai, Kiyotaka Watanabe and 1 more

Abstract readSystematic ReviewNetwork Meta-Analysis
In one paragraph

Synthesis in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
–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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Practical prescribing in cancer cachexia.Current opinion in supportive and palliative care · 2026
    Review
  4. Observational
  5. Review
  6. Review
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

11 authors.

Hao ChenDepartment of Oncology, Teikyo University School of Medicine, Tokyo, Japan.ORCID 0000-0003-3074-2235
Masashi IshiharaDepartment of Oncology, Teikyo University School of Medicine, Tokyo, Japan.
Hiroki KazahariDepartment of Oncology, Teikyo University School of Medicine, Tokyo, Japan.
Ryusuke OchiaiDepartment of Oncology, Teikyo University School of Medicine, Tokyo, Japan.
Shigeru TanzawaDepartment of Oncology, Teikyo University School of Medicine, Tokyo, Japan.
Takeshi HondaDepartment of Oncology, Teikyo University School of Medicine, Tokyo, Japan.
Yasuko IchikawaDepartment of Oncology, Teikyo University School of Medicine, Tokyo, Japan.
Nobuyuki HoritaDepartment of Chemotherapy, Yokohama City University Hospital, Yokohama, Japan.ORCID 0000-0002-8200-0340
Hisashi NagaiGraduate School of Human and Environmental Studies, Tokai University, Tokyo, Japan.
Kiyotaka WatanabeDepartment of Oncology, Teikyo University School of Medicine, Tokyo, Japan.
Nobuhiko SekiDepartment of Oncology, Teikyo University School of Medicine, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer cachexia affects more than half of all cancer patients, reducing survival rates. Evidence-based approaches are urgently needed to optimize treatment.

methodsA systematic review and network meta-analysis were conducted to assess the effectiveness and safety of different pharmacotherapies for cancer cachexia. Three databases (PubMed, Cochrane Library, and Web of Science) were searched for the period from January 1, 2000, to March 20, 2024. The netmeta package in R software was used to calculate the pooled effect, employing a random effects model.

resultsSeven placebo-controlled randomized trials involving 1421 patients were analyzed. Pairwise analysis showed that body weight increases were 4.6 kg (95% confidence interval [CI] 0.83-8.37 kg) for olanzapine, 3.82 kg (95% CI 0.73-6.91 kg) for espindolol (20 mg), 2.36 kg (95% CI 1.84-2.89 kg) for anamorelin (100 mg), and 1.31 kg (95% CI 0.42-2.19 kg) for anamorelin (50 mg). In terms of safety profiles, olanzapine demonstrated the lowest odds ratio when compared to placebo, at 0.26 (95% CI 0.07-0.94), followed by anamorelin (50 mg) at 0.86 (95% CI 0.30-2.48), and anamorelin (100 mg) at 0.89 (95% CI 0.42-1.88). However, network meta-analysis could not confirm the superiority of olanzapine over anamorelin in terms of efficacy and safety.

conclusionBoth olanzapine and anamorelin are useful in improving body weight in patients with cancer cachexia. Personalization may be helpful for different patients.

Indexed as

CachexiaNeoplasmsOlanzapineHumansHydrazinesOligopeptidesRandomized Controlled Trials as TopicTreatment OutcomeanamorelinHydrazinesOlanzapineOligopeptidesanamorelinbody weightcancer cachexianetwork meta‐analysisolanzapine

Identifiers

PMID39225556
PMCPMC11369987

What OpenQuestion holds

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Registered trials

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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.