Evidence map›Paper›PMID 38055127›Full record

Trial reportInvestigational new drugs2024

A multicenter phase II trial of the triplet antiemetic therapy with palonosetron, aprepitant, and olanzapine for a cisplatin-containing regimen. - PATROL-I.

Daiki Tsuji, Shigeru Nakagaki, Itsuki Yonezawa, Kenichi Suzuki, Takashi Yokokawa, Yohei Kawasaki, Takumi Yamaguchi, Takashi Kawaguchi, Masahiro Hatori, Takuma Matsumoto and 8 more

Abstract readClinical Trial, Phase IIMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Investigational new drugs, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

18 authors at 11 institutions in 1 country.

Daiki TsujiDepartment of Clinical Pharmacology & Genetics, School of Pharmaceutical Sciences, University of Shizuoka, Suruga-ku, Shizuoka, Japan. d-tsuji@u-shizuoka-ken.ac.jp.ORCID 0000-0001-8894-2841
Shigeru NakagakiDepartment of Pharmacy, Shizuoka General Hospital, Shizuoka, Japan.
Itsuki YonezawaDepartment of Clinical Pharmacology & Genetics, School of Pharmaceutical Sciences, University of Shizuoka, Suruga-ku, Shizuoka, Japan.
Kenichi SuzukiDepartment of Clinical Pharmacology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.
Takashi YokokawaDepartment of Pharmacy, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Yohei KawasakiFaculty of Nursing, Japanese Red Cross College of Nursing, Tokyo, Japan.
Takumi YamaguchiInstitute for Assistance of Academic and Education, IAAE, Kanagawa, Japan.
Takashi KawaguchiDepartment of Practical Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.
Masahiro HatoriDepartment of Pharmacy, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Takuma MatsumotoPharmaceutical Department, National Hospital Organization Iwakuni Clinical Center, Yamaguchi, Japan.
Yukio SakataDepartment of Pharmacy, Hakodate Municipal Hospital, Hokkaido, Japan.
Keisuke YamamotoDepartment of Pharmacy, Seirei Hamamatsu General Hospital, Shizuoka, Japan.
Tomoyasu NishimuraDepartment of Pharmacy, Wakayama Medical University Hospital, Wakayama, Japan.
Yuki KogureDepartment of Pharmacy, National Hospital Organization Higashihiroshima Medical Center, Hiroshima, Japan.
Toshinobu HayashiDepartment of Pharmaceutical and Health Care Management, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Misa OsawaDepartment of Pharmacy, Shizuoka General Hospital, Shizuoka, Japan.
Kunihiko ItohDepartment of Clinical Pharmacology & Genetics, School of Pharmaceutical Sciences, University of Shizuoka, Suruga-ku, Shizuoka, Japan.
Masaya WatanabeDepartment of Gastroenterological Surgery, Shizuoka General Hospital, Shizuoka, Japan.
Shizuoka General Hospital · JPUniversity of Shizuoka · JPJapanese Foundation For Cancer Research · JPTokyo University of Pharmacy and Life Sciences · JPFukuoka University · JPHakodate National Hospital · JPHigashihiroshima Medical Center · JPIwakuni Medical Center · JPJapanese Red Cross College of Nursing · JPSeirei Hamamatsu General Hospital · JPWakayama Medical University · JP

Funding

Japan Society for the Promotion of Science 20K07179
6 · The paper itself

Abstract

Dexamethasone is one of the key antiemetic agents and is widely used even now. However, dexamethasone has been associated with several adverse reactions even after short-term administration. Therefore, developing a steroid-free antiemetic regimen is an important issue to consider. Thus, the purpose of this study was to investigate the efficacy and safety of palonosetron, aprepitant, and olanzapine in a multi-institutional phase II study. Chemotherapy-naive patients scheduled to receive cisplatin were enrolled and evaluated for the occurrence of chemotherapy-induced nausea and vomiting during 120 h after chemotherapy. The primary endpoint of the study was total control (TC) in the overall phase. The key secondary endpoint was complete response (CR), which was assessed in the acute, delayed, and overall phase, respectively. Adverse events were evaluated according to the Common Terminology Criteria for Adverse Events. Eighty-five patients were enrolled from 8 centers in Japan, of which 83 were evaluable for analyses. The percentage of patients who achieved TC during the overall phase was 31.3%. CR was achieved in 61.4%, 84.3%, and 65.1% of patients during the overall, acute, and delayed phases, respectively. The most frequently reported adverse event was anorexia. The primary endpoint was below the threshold and we could not find benefit in the dexamethasone-free regimen, but CR during the overall phase was similar to that of the conventional three-drug regimen. This antiemetic regimen without dexamethasone might be an option for patients for whom corticosteroids should not be an active application.

Indexed as

AntiemeticsAprepitantCisplatinDexamethasoneHumansOlanzapinePalonosetronPathologic Complete ResponseAntiemeticsAprepitantCisplatinDexamethasoneOlanzapinePalonosetronAprepitantChemotherapy-induced nausea and vomiting (CINV)Fos-aprepitantOlanzapinePalonosetron

Identifiers

PMID38055127
OpenAlexW4389395676

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.