Evidence map›Paper›PMID 36792187›Full record

Trial reportInternal medicine (Tokyo, Japan)2023

Efficacy and Safety of Synbiotics in Patients Undergoing Autologous Hematopoietic Stem Cell Transplantation: A Randomized, Double-blinded, Placebo-controlled Pilot Study.

Yu Mizutani, Shinichiro Kawamoto, Michiko Takahashi, Hisayo Doi, Kumiko Wakida, Satoko Tabuchi, Masaaki Tanda, Akihiro Soga, Ruri Chijiki, Hidetomo Takakura and 16 more

Open access · diamondAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Internal medicine (Tokyo, Japan), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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

26 authors at 1 institution in 1 country.

Yu MizutaniDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Shinichiro KawamotoDepartment of Transfusion Medicine and Cell Therapy, Kobe University Hospital, Japan.
Michiko TakahashiDivision of Nutrition, Kobe University Hospital, Japan.
Hisayo DoiDivision of Nursing, Kobe University Hospital, Japan.
Kumiko WakidaDivision of Nutrition, Kobe University Hospital, Japan.
Satoko TabuchiDivision of Nutrition, Kobe University Hospital, Japan.
Masaaki TandaDepartment of Pharmacy, Kobe University Hospital, Japan.
Akihiro SogaDepartment of Pharmacy, Kobe University Hospital, Japan.
Ruri ChijikiDepartment of Medical Oncology/Hematology, Kobe University Hospital, Japan.
Hidetomo TakakuraDepartment of Medical Oncology/Hematology, Kobe University Hospital, Japan.
Koji KawaguchiDepartment of Medical Oncology/Hematology, Kobe University Hospital, Japan.
Ako HigashimeDepartment of Medical Oncology/Hematology, Kobe University Hospital, Japan.
Marika WatanabeDepartment of Medical Oncology/Hematology, Kobe University Hospital, Japan.
Hiroya IchikawaDepartment of Medical Oncology/Hematology, Kobe University Hospital, Japan.
Sakuya MatsumotoDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Rina SakaiDepartment of Medical Oncology/Hematology, Kobe University Hospital, Japan.
Hideaki GotoDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Keiji KurataDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Seiji KakiuchiDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Yoshiharu MiyataDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Kiyoaki UryuDepartment of Medical Oncology/Hematology, Kobe University Hospital, Japan.
Yumiko InuiDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Akihito KitaoDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Kimikazu YakushijinDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Hiroshi MatsuokaDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Hironobu MinamiDivision of Medical Oncology/Hematology, Kobe University Graduate School of Medicine and Hospital, Japan.
Kobe University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective High-dose chemotherapy with autologous hematopoietic stem cell transplantation (auto-HSCT) is an effective treatment option for relapsed and refractory aggressive malignant lymphoma. However, patients frequently experience treatment-induced gastrointestinal symptoms. Synbiotics, including live microorganisms and nondigestible food ingredients, reportedly ameliorate chemotherapy-induced mucosal damage. In this study, we assessed the efficacy and safety of synbiotics in patients undergoing auto-HSCT. Methods This randomized, double-blinded study included patients with malignant lymphoma eligible for auto-HSCT. The patients were randomly assigned to either a synbiotic group receiving Bifidobacterium longum (BB536) and guar gum or a placebo group receiving a placebo containing dextrin. The supplements were administered twice daily from the start of conditioning chemotherapy up to 28 days after auto-HSCT. The primary endpoint was the duration of total parenteral nutrition (TPN). Results In total, 12 patients were included and randomized. The median duration of TPN was 15 (range, 12-33) days in the synbiotic group and 17.5 (range, 0-32) days in the placebo group. The median duration of grade ≥3 diarrhea was shorter in the synbiotic group than in then placebo group (2.5 vs. 6.5 days), as was the duration of hospital stay (31.5 vs. 43 days). The oral intake and quality of life regarding diarrhea and anorexia improved in the synbiotic group after engraftment. Synbiotic infections, including bacteremia, were not observed. Conclusion Synbiotics may reduce gastrointestinal toxicity, thereby reducing nutritional problems and improving the quality of life of patients undergoing auto-HSCT, without severe adverse events.

Indexed as

Gastrointestinal DiseasesHematopoietic Stem Cell TransplantationLymphomaSynbioticsDiarrheaHumansPilot ProjectsQuality of LifeTransplantation, Autologousautologous hematopoietic stem cell transplantationBifidobacterium longumdiarrheaguar gumquality of lifesynbiotics

Identifiers

PMID36792187
PMCPMC10641206
OpenAlexW4320717516

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.