Evidence map›Paper›PMID 33569309›Full record

ArticleTranslational lung cancer research2021

A prospective phase II study of multimodal prophylactic treatment for afatinib-induced adverse events in advanced non-small cell lung cancer (Niigata Lung Cancer Treatment Group 1401).

Masaaki Okajima, Satoru Miura, Satoshi Watanabe, Hiroshi Tanaka, Kazuhiko Ito, Takashi Ishida, Masato Makino, Akira Iwashima, Naoya Matsumoto, Kazuhiro Sato and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Translational lung cancer research, 2021. 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
0.9field-weighted citation impact, top 26% 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, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

14 authors at 9 institutions in 1 country.

Masaaki OkajimaDepartment of Respiratory Medicine, Saiseikai Niigata Hospital, Niigata, Japan.
Satoru MiuraDepartment of Internal Medicine, Niigata Cancer Center Hospital, Niigata, Japan.
Satoshi WatanabeDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Hiroshi TanakaDepartment of Internal Medicine, Niigata Cancer Center Hospital, Niigata, Japan.
Kazuhiko ItoDepartment of Respiratory Medicine, Niigata City General Hospital, Niigata, Japan.
Takashi IshidaDepartment of Internal Medicine, Niigata Prefectural Central Hospital, Joetsu, Japan.
Masato MakinoDepartment of Internal Medicine, Niigata Prefectural Shibata Hospital, Shibata, Japan.
Akira IwashimaDepartment of Respiratory Medicine, Nagaoka Chuo General Hospital, Nagaoka, Japan.
Naoya MatsumotoDepartment of Respiratory Medicine, Nishi-Niigata Chuo National Hospital, Niigata, Japan.
Kazuhiro SatoDepartment of Respiratory Medicine, Nagaoka Red Cross Hospital, Nagaoka, Japan.
Kosuke IchikawaDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Tetsuya AbeDepartment of Respiratory Medicine, Niigata City General Hospital, Niigata, Japan.
Hirohisa YoshizawaDepartment of Respiratory Medicine, Niigata Medical Center Hospital, Niigata, Japan.
Toshiaki KikuchiDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Niigata University · JPNiigata Cancer Center Hospital · JPNiigata City General Hospital · JPNagaoka Red Cross Hospital · JPNagara Medical Center · JPNiigata Prefectural Central Hospital · JPNiigata Prefectural Shibata Hospital · JPNishi Niigata Chuo National Hospital · JPSaiseikai Niigata Daini Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAfatinib has shown clinical benefits in patients with non-small cell lung cancer (NSCLC) harboring epidermal growth factor receptor (

methodsThis single-arm prospective study was conducted to evaluate the efficacy of multimodal prophylactic treatment for afatinib-induced toxicity in patients with

resultsForty-six patients were enrolled. The primary endpoint analysis was performed in 35 patients as the per-protocol (PP) population. The 4-week successful prophylaxis rate for severe or intolerable diarrhea was 82.9% (90% confidence interval: 70.1-91.9%). In the total population, the incidences of grade 3 or higher rash, oral mucositis and paronychia within 4 weeks were 4%, 2% and 4%, respectively.

conclusionsProphylactic loperamide administration was not effective in preventing severe or intolerable diarrhea during afatinib treatment. Adequate dose reduction will be a better approach to manage afatinib-induced diarrhea. Multimodal prevention using minocycline, topical steroids and gargling with sodium azulene may be helpful to maintain compliance with afatinib treatment (UMIN000016167).

Indexed as

adverse event managementafatinibepidermal growth factor receptor (EGFR)Non-small cell lung cancer (NSCLC)

Identifiers

PMID33569309
PMCPMC7867768
OpenAlexW3111548837

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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.