Evidence map›Paper›PMID 36099135›Full record

ArticleIn vivo (Athens, Greece)

Analysis of Risk Factors for High-dose Cisplatin-induced Renal Impairment in Head and Neck Cancer Patients.

Hiroyoshi Koide, Satoshi Noda, Yumi Okunuki, Shigehiro Owaki, Takeshi Shimizu, Tomohiro Terada, Shin-Ya Morita

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

7 authors at 2 institutions in 1 country.

Hiroyoshi KoideDepartment of Pharmacy, Shiga University of Medical Science Hospital, Shiga, Japan.
Satoshi NodaDepartment of Pharmacy, Shiga University of Medical Science Hospital, Shiga, Japan; snoda@belle.shiga-med.ac.jp.
Yumi OkunukiDepartment of Pharmacy, Shiga University of Medical Science Hospital, Shiga, Japan.
Shigehiro OwakiDepartment of Otorhinolaryngology, Shiga University of Medical Science, Shiga, Japan.
Takeshi ShimizuDepartment of Otorhinolaryngology, Shiga University of Medical Science, Shiga, Japan.
Tomohiro TeradaDepartment of Pharmacy, Shiga University of Medical Science Hospital, Shiga, Japan.
Shin-Ya MoritaDepartment of Pharmacy, Shiga University of Medical Science Hospital, Shiga, Japan.
Shiga University of Medical Science Hospital · JPShiga University of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimConcurrent chemoradiotherapy with high-dose cisplatin (CDDP-RT) is the standard therapy for advanced head and neck cancer; however, due to CDDP-induced renal impairment, dose reduction or discontinuation is frequently required. Therefore, the identification of risk factors for renal impairment is of importance to improve the efficacy and safety of CDDP-RT. PATIENTS AND

methodsWe retrospectively investigated risk factors for renal impairment in advanced head and neck cancer patients receiving CDDP-RT. Renal impairment was defined as a >25% decrease from baseline in estimated glomerular filtration rate within 14 days after CDDP administration in the first cycle.

resultsOf the 82 patients analyzed in this study, 21 (26%) patients developed renal impairment. Multivariate logistic regression analysis showed that concomitant use of a calcium channel blocker or lower hemoglobin levels significantly contributed to the increased risk of CDDP-induced renal impairment (odds ratio=3.60, 95% confidence interval=1.04-12.40; odds ratio=0.71, 95% confidence interval=0.50-0.99, respectively), while concomitant use of proton pump inhibitors was a factor associated with a decreased risk of CDDP-induced renal impairment (odds ratio=0.20, 95% confidence interval=0.04-0.86).

conclusionRenal function of patients receiving calcium channel blocker or patients with lower hemoglobin levels should be monitored cautiously when receiving CDDP-RT.

Indexed as

CisplatinHead and Neck NeoplasmsCalcium Channel BlockersHemoglobinsHumansRetrospective StudiesRisk FactorsCalcium Channel BlockersCisplatinHemoglobinschemoradiotherapyCisplatinhead and neck cancerrenal impairment

Identifiers

PMID36099135
PMCPMC9463891
OpenAlexW4294904064

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.