Evidence map›Paper›PMID 36627672›Full record

ArticleJournal of pharmaceutical health care and sciences2023

Higher incidence of pegfilgrastim-induced bone pain in younger patients receiving myelosuppressive chemotherapy: a real-world experience.

Shinya Tsuboi, Tatsuya Hayama, Katsuhiro Miura, Akihiro Uchiike, Daisuke Tsutsumi, Takashi Yamauchi, Yoshihiro Hatta, Susumu Ootsuka

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of pharmaceutical health care and sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Shinya TsuboiDepartment of Pharmacy, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan.
Tatsuya HayamaDepartment of Pharmacy, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan.
Katsuhiro MiuraTumor Center, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan. miura.katsuhiro@nihon-u.ac.jp.ORCID http://orcid.org/0000-0002-1538-3804
Akihiro UchiikeDepartment of Pharmacy, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan.
Daisuke TsutsumiDepartment of Pharmacy, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan.
Takashi YamauchiDepartment of Pharmacy, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan.
Yoshihiro HattaDepartment of Medicine, Division of Hematology and Rheumatology, Nihon University School of Medicine, 30-1, Oyaguchikamicho, Itabashi City, Tokyo, 173-3610, Japan.
Susumu OotsukaDepartment of Pharmacy, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan.
Nihon University Itabashi Hospital · JPNihon University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPegfilgrastim is widely used for the prevention of febrile neutropenia (FN) in patients receiving myelosuppressive chemotherapy for various types of cancer. However, pegfilgrastim-induced bone pain (PIBP) is a relevant adverse event occurring during cancer treatment. Thus, we aimed to determine the risk factors for PIBP in real-world clinical practice. MAIN BODY: We retrospectively collected the clinical records of patients who received pegfilgrastim to support myelosuppressive chemotherapy with at least a 10% risk of FN between 2015 and 2018 at our center. Patients received pegfilgrastim 3.6 mg between days 2 and 7 after chemotherapy administration (day 1) for primary or secondary prophylaxis against FN. All adverse events were recorded according to the Common Terminology Criteria for Adverse Events. Patients who experienced intermittent bone pain in the back, femur, or other anatomic sites after the pegfilgrastim administration were considered to have PIBP. To evaluate the relationship between PIBP incidence and patient characteristics, we performed univariate and multivariate logistic regression analyses to calculate the odds ratios (ORs) of possible risk factors for PIBP. We analyzed the data of 305 patients (median age: 63 years), who underwent 1220 chemotherapy cycles with pegfilgrastim per cycle. Univariate analysis revealed that female sex (vs. male sex), younger age (< 55 years vs. ≥ 55 years), and solid cancers (vs. hematologic cancers) had significantly higher ORs (p < 0.05). However, only younger age (< 55 years) was an independent risk factor for PIBP on multivariate analysis (OR 3.62, 95% confidence interval 1.51-8.69, p = 0.004).

conclusionsYounger age (< 55 years) was significantly associated with a higher risk of PIBP among patients receiving chemotherapy with a ≥ 10% risk of FN. Therefore, oncologists should meticulously formulate management plan for PIBP in younger patients after administering pegfilgrastim.

Indexed as

AgeBone painChemotherapyFebrile neutropeniaPegfilgrastim

Identifiers

PMID36627672
PMCPMC9832663
OpenAlexW4314434838

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LicenceCC BY
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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.