Evidence map›Paper›PMID 24782655›Full record

ArticleInternational journal of medical sciences2014

Serum lactate dehydrogenase levels as a predictive marker of oxaliplatin-induced hypersensitivity reactions in Japanese patients with advanced colorectal cancer.

Kyoko Seki, Yasuo Tsuduki, Takeshi Ioroi, Michiko Yamane, Hiroko Yamauchi, Yukinari Shiraishi, Tadaaki Ogawa, Izumi Nakata, Kohshi Nishiguchi, Teruhisa Matsubayashi and 5 more

Abstract read
In one paragraph

Article in International journal of medical sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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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

15 authors.

Kyoko Seki1. Department of Pharmacy, Japan Labour Health and Welfare Organization, Kobe Rosai Hospital, Kobe 651-0053, Japan.
Yasuo Tsuduki2. Department of Pharmacy, National Hospital Organization Kobe Medical Center, Kobe 654-0155, Japan.
Takeshi Ioroi3. Department of Pharmacy, Kobe University Hospital, Kobe 650-0017, Japan.
Michiko Yamane4. Department of Pharmacy, Japanese Red Cross Kobe Hospital, Kobe 651-0073, Japan.
Hiroko Yamauchi5. Department of Pharmacy, Shinko Hospital, Kobe 651-0072, Japan.
Yukinari Shiraishi1. Department of Pharmacy, Japan Labour Health and Welfare Organization, Kobe Rosai Hospital, Kobe 651-0053, Japan.
Tadaaki Ogawa1. Department of Pharmacy, Japan Labour Health and Welfare Organization, Kobe Rosai Hospital, Kobe 651-0053, Japan.
Izumi Nakata2. Department of Pharmacy, National Hospital Organization Kobe Medical Center, Kobe 654-0155, Japan.
Kohshi Nishiguchi3. Department of Pharmacy, Kobe University Hospital, Kobe 650-0017, Japan.
Teruhisa Matsubayashi4. Department of Pharmacy, Japanese Red Cross Kobe Hospital, Kobe 651-0073, Japan.
Yoshihide Takakubo5. Department of Pharmacy, Shinko Hospital, Kobe 651-0072, Japan.
Motohiro Yamamori6. School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya 663-8179, Japan.
Akiko Kuwahara6. School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya 663-8179, Japan.
Noboru Okamura6. School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya 663-8179, Japan.
Toshiyuki Sakaeda3. Department of Pharmacy, Kobe University Hospital, Kobe 650-0017, Japan ; 7. Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 606-8501, Japan ; 8. Department of Pharmacokinetics, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveClinical laboratory test data obtained prior to treatments were previously analyzed from the standpoint of susceptibility to hypersensitivity reactions in patients treated with the platimun anticancer agent, oxaliplatin (L-OHP). In the present study, the time course from the first to last cycle of the treatment was additionally analyzed to determine a better predictor of these reactions.

methodsA total of 20 laboratory test data were obtained from 108 Japanese patients with advanced colorectal cancer who were treated with the L-OHP-containing regimens, FOLFOX4 and/or mFOLFOX6. The averages and variation coefficients (CV%) of the data until the last cycle of the treatment were compared between patients with hypersensitivity reactions and those without.

resultsThe average serum lactate dehydrogenase (LDH) level was lower in patients with grade 1/2 reactions (P=0.016), whereas its CV% value was higher in patients with grade 3/4 reactions (P=0.005) than in those without reactions. An increase in serum LDH levels was observed in some patients with grade 3/4 reactions as the cycle number increased, and thereafter hypersensitivity reactions occurred. This phenomenon was not always observed, but was never detected in patients with grade 1/2 reactions.

conclusionsSerum LDH levels may be a predictive marker of hypersensitivity reactions in patients treated with L-OHP. Further extensive examinations with a larger number of patients are needed to establish a patient management strategy.

Indexed as

AdultAgedAsian PeopleBiomarkers, TumorColorectal NeoplasmsDrug HypersensitivityDrug-Related Side Effects and Adverse ReactionsFemaleHumansL-Lactate DehydrogenaseMaleMiddle AgedOrganoplatinum CompoundsOxaliplatinPrognosisBiomarkers, TumorL-Lactate DehydrogenaseOrganoplatinum CompoundsOxaliplatincolorectal cancerFOLFOXhypersensitivity reactionsoxaliplatinserum lactate dehydrogenase level

Identifiers

PMID24782655
PMCPMC4003551

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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.