Evidence map›Paper›PMID 42176039›Full record

Observational studyJournal of cancer research and clinical oncology2026

Ondansetron oral soluble pellicles vs. azasetron for preventing nausea and vomiting in patients receiving antitumor therapies: a comparative observational study.

Cheng Zhao, Haibao Cao, Shuowen Yan, Runsen Sun, Lina Hu, Hui Yu, Cui Bai, Kai Cheng, Xiaoping Wu, Xiaoyi Pan and 6 more

Abstract readObservational StudyComparative Study
In one paragraph

Observational study in Journal of cancer research and clinical oncology, 2026. 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

16 authors.

Cheng ZhaoDepartment of Medical Oncology, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Haibao CaoDepartment of General Surgery, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Shuowen YanDepartment of General Surgery, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Runsen SunDepartment of General Surgery, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Lina HuDepartment of Medical Oncology, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Hui YuDepartment of Medical Oncology, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Cui BaiDepartment of Medical Oncology, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Kai ChengDepartment of Medical Oncology, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Xiaoping WuDepartment of General Surgery, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Xiaoyi PanDepartment of General Surgery, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Qiang ZhangDepartment of Pharmacy, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Bin JiangDepartment of General Practice Medicine, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Huiqian LiuDepartment of Pharmacy, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Simin TaoDepartment of Medical Oncology, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Jianfeng ZhangDepartment of Medical Oncology, Anqing Petrochemical Hospital of Nanjing Drum Tower Hospital Group, Anqing, 246002, China.
Meng WangKey Laboratory of Xin'an Medicine, Anhui Province Key Laboratory of R&D of Chinese Medicine, Ministry of Education, Anhui University of Traditional Chinese Medicine, 103 Meishan Road, Shushan District, 230038, Hefei, China. wangmeng@ahtcm.edu.cn.

Funding

Anhui Province Key Laboratory of Cancer Translational Medicine, Bengbu Medical University KFKT202402Anqing City Science and Technology Bureau 2023Z6009Health Research Program of Anqing AQWJ2023015the Beijing Dadi Medical Charity Foundation DDYL-A-2023-KY-HRZLZT
6 · The paper itself

Abstract

objectiveOndansetron oral soluble pellicles (OSP) show satisfactory effects on preventing nausea and vomiting following antitumor therapies. This study aimed to compare the antiemetic efficacy and safety profiles of ondansetron OSP vs. azasetron in patients receiving antitumor therapies.

methodsA total of 110 patients who received antitumor therapies were included in this comparative observational study. According to patient willingness, disease status, and tolerance, 55 patients received ondansetron OSP, and the other 55 patients received intravenous azasetron. During acute and delayed phases, the function living index emesis (FLIE) scale score and degrees of nausea and vomiting [high (46-63 points), moderate (19-45 points), or low (0-18 points)] were assessed. Adverse reactions were collected.

resultsDuring the acute phase, FLIE-nausea (5.7 ± 8.9 vs. 17.9 ± 13.6) and vomiting (6.9 ± 7.8 vs. 17.6 ± 13.9) domain scores were lower in patients receiving ondansetron OSP than those receiving azasetron (both P < 0.001). The degrees of nausea and vomiting were lower in patients receiving ondansetron OSP than those receiving azasetron (both P < 0.05). During the delayed phase, FLIE-nausea (5.0 ± 7.9 vs. 10.8 ± 9.1) and vomiting (4.2 ± 6.6 vs. 9.2 ± 8.7) domain scores were lower in patients receiving ondansetron OSP than those receiving azasetron (both P < 0.001). Regarding adverse reactions, the incidence of constipation was lower in patients receiving ondansetron OSP than those receiving azasetron (7.3% vs. 30.9%) (P = 0.003), but the incidence of headache did not differ (P = 0.113).

conclusionOndansetron OSP possess superior antiemetic effects and safety profiles to azasetron in patients receiving antitumor therapies.

Indexed as

AntiemeticsAntineoplastic AgentsNauseaNeoplasmsOndansetronVomitingAdministration, OralAdultAgedBridged Bicyclo Compounds, HeterocyclicFemaleHumansMaleMiddle AgedOxazinesAntiemeticsAntineoplastic AgentsazasetronBridged Bicyclo Compounds, HeterocyclicOndansetronOxazinesAdverse reactionsAzasetronNauseaOndansetron oral soluble pelliclesVomiting

Identifiers

PMID42176039
PMCPMC13376086

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