Evidence map›Paper›PMID 29713488›Full record

ArticleOxford medical case reports2018

Progressive renal insufficiency related to ALK inhibitor, alectinib.

Kojiro Nagai, Hiroyuki Ono, Motokazu Matsuura, Michael Hann, Sayo Ueda, Sakiya Yoshimoto, Masanori Tamaki, Taichi Murakami, Hideharu Abe, Hisashi Ishikura and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Oxford medical case reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. 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

11 authors at 3 institutions in 1 country.

Kojiro NagaiDepartment of Nephrology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Hiroyuki OnoDepartment of Nephrology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Motokazu MatsuuraDepartment of Nephrology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Michael HannDepartment of the Directorate for Medical Services, US Navy Hospital, Yokosuka, Japan.
Sayo UedaDepartment of Nephrology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Sakiya YoshimotoDepartment of Nephrology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Masanori TamakiDepartment of Nephrology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Taichi MurakamiDepartment of Nephrology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Hideharu AbeDepartment of Nephrology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Hisashi IshikuraDepartment of Surgery, Division of Thoracic Surgery, Tokushima Red Cross Hospital, Tokushima, Japan.
Toshio DoiDepartment of Nephrology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Tokushima University · JPNaval Hospital Yokosuka Japan · JPTokushima Red Cross Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alectinib is a second generation anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitor and is generally effective and tolerated in patients who have demonstrated disease progression or adverse effects while on the first generation inhibitor, crizotinib. ALK inhibitors can cause a reversible chronic increase of serum creatinine concentration; however, they rarely induce progressive renal insufficiency. We herein report a case of a 68-year-old woman diagnosed with ALK-positive advanced non-small cell lung cancer and who received ALK inhibitors. Due to dysgeusia and transaminitis, her medication was switched from crizotinib to alectinib. Rapid progressive glomerulonephritis developed 1 year after the initiation of alectinib treatment. A renal biopsy revealed unique kidney lesions in both tubules and glomeruli. Glucocorticoid therapy partially reversed kidney impairment. However, re-administration of alectinib caused kidney dysfunction, which was improved by the cessation of alectinib. Our case suggests that much attention should be paid to kidney function when using ALK inhibitors.

Indexed as

nephrologyoncologypharmacology and pharmacy

Identifiers

PMID29713488
PMCPMC5915949
OpenAlexW2800638039

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.