Evidence map›Paper›PMID 41034823›Full record

Trial reportBMC cancer2025

Olanzapine plus triple antiemetic therapy for prevention of carboplatin-induced nausea: a pooled analysis of two clinical trials.

Suguru Kojima, Naoki Inui, Takahito Suzuki, Kazuki Tanaka, Masato Karayama, Yusuke Inoue, Hideki Yasui, Hironao Hozumi, Yuzo Suzuki, Kazuki Furuhashi and 8 more

Abstract readRandomized Controlled TrialClinical Trial, Phase IIIClinical Trial, Phase II
In one paragraph

Trial report in BMC cancer, 2025. 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

18 authors.

Suguru KojimaSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
Naoki InuiSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan. inui@hama-med.ac.jp.
Takahito SuzukiDepartment of Respiratory Medicine, Hamamatsu Medical Center, Hamamatsu, Japan.
Kazuki TanakaDepartment of Respiratory Medicine, Fujieda Municipal General Hospital, Fujieda, Japan.
Masato KarayamaSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
Yusuke InoueSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
Hideki YasuiSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
Hironao HozumiSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
Yuzo SuzukiSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
Kazuki FuruhashiSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
Tomoyuki FujisawaSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
Noriyuki EnomotoSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
Koji NishimotoDepartment of Respiratory Medicine, Iwata City Hospital, Iwata, Japan.
Shun MatsuuraDepartment of Respiratory Medicine, Fujieda Municipal General Hospital, Fujieda, Japan.
Dai HashimotoDepartment of Respiratory Medicine, Seirei Hamamatsu General Hospital, Hamamatsu, Japan.
Takashi MatsuiDepartment of Respiratory Medicine, Seirei Mikatahara General Hospital, Hamamatsu, Japan.
Kazuhiro AsadaDepartment of Respiratory Medicine, Shizuoka General Hospital, Shizuoka, Japan.
Takafumi SudaSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChemotherapy-induced nausea and vomiting is a common adverse event of cancer treatments. Despite prophylactic antiemetic treatment, nausea remains a particular problem. We aimed to identify risk factors and clarify the usefulness of olanzapine for the control of carboplatin-induced nausea.

methodsThis was a pooled analysis of data from a single-arm, open-label, phase II trial and a prospective, randomized, double-blind, placebo-controlled phase III trial. We combined data from two trials with similar inclusion and exclusion criteria and treatment schedules. Chemotherapy-naïve patients aged ≥ 20 years with solid cancers who were scheduled to receive a first course of carboplatin-containing chemotherapy were enrolled. Patients in the olanzapine and placebo groups received olanzapine 5 mg or placebo, respectively, in combination with the neurokinin-1 (NK

resultsA total of 388 patients were evaluated (79.4% male, median age 72 years), including 208 patients in the olanzapine group. Overall, 87.5% in the olanzapine group and 75.0% in the placebo group were free of nausea (intergroup difference 12.5%, 95% CI, 4.7-20.3, p = 0.002), and the difference in proportion of patients reporting no appetite loss was 20.6% (95% CI, 11.5-29.6, p < 0.001). The overall complete response rates were 88.0% in the olanzapine group and 80.6% in the placebo group (p = 0.049). Multivariable analysis only identified no olanzapine use as significantly associated with a decreased risk of nausea (adjusted OR, 0.45, 95% CI, 0.26-0.76).

conclusionsThis analysis revealed that adding olanzapine to triple antiemetic therapy was associated with improved control of carboplatin-induced nausea.

trial registrationThe trial was registered with the University Hospital Medical Information Network Clinical Trial Registry (UMIN) 000026739, registered on 1 April 2017 and 000037749, registered on 1 September 2019.

Indexed as

AntiemeticsAntineoplastic AgentsBenzodiazepinesCarboplatinNauseaNeoplasmsAdultAgedAprepitantDexamethasoneDouble-Blind MethodDrug Therapy, CombinationFemaleHumansMaleMiddle AgedAntiemeticsAntineoplastic AgentsAprepitantBenzodiazepinesCarboplatinDexamethasoneMorpholinesOlanzapineAntiemeticCarboplatinChemotherapy-induced nausea and vomitingNauseaOlanzapineRisk factor

Identifiers

PMID41034823
PMCPMC12486796

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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.