Evidence map›Paper›PMID 36581856›Full record

Observational studyBMC pulmonary medicine2022

Osteosclerotic change as a therapeutic response to gefitinib in symptomatic non-small cell lung cancer bone metastasis.

Michihito Miyagi, Hirohisa Katagiri, Hideki Murata, Junji Wasa, Toshiaki Takahashi, Haruyasu Murakami, Hideyuki Harada, Keita Mori, Mitsuru Takahashi

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in BMC pulmonary medicine, 2022. 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
0.6field-weighted citation impact, top 30% 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, 5 citations in OpenAlex.

  1. Trial
  2. Review
  3. Observational
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

9 authors at 1 institution in 1 country.

Michihito MiyagiDevision of Orthopedic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Hirohisa KatagiriDevision of Orthopedic Oncology, Shizuoka Cancer Center, Shizuoka, Japan. h.katagiri@scchr.jp.ORCID http://orcid.org/0000-0001-8449-3604
Hideki MurataDevision of Orthopedic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Junji WasaDevision of Orthopedic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Toshiaki TakahashiDevision of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Haruyasu MurakamiDevision of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Hideyuki HaradaDivision of Radiation Therapy, Radiation and Proton Therapy Center, Shizuoka Cancer Center, Shizuoka, Japan.
Keita MoriDepartment of Biostatistics, Clinical Research Center, Shizuoka Cancer Center, Shizuoka, Japan.
Mitsuru TakahashiDevision of Orthopedic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Shizuoka Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite improvement in the overall survival of patients with non-small cell lung cancer (NSCLC) harboring epidermal growth factor receptor (EGFR) mutation, the effects of EGFR tyrosine kinase inhibitor (EGFR-TKI) treatment on bone metastasis remain unclear. This study investigated radiological responses to gefitinib regarding bone metastasis in patients.

methodsWe treated 260 patients with NSCLC and symptomatic bone metastasis. Thirty-seven patients harboring EGFR mutation were treated with gefitinib for more than 30 days and followed up for more than 3 months (GEF group). We performed a retrospective observational study by selecting 36 cases without EGFR-TKI treatment, at least 3 months of follow-up, and at least two radiological evaluations as the control group. We assessed the best overall radiological response, interval from treatment initiation to appearance of a radiological response, and the local response maintenance rate.

resultsThe best effect in the GEF group was 98% partial response or better, which was significantly higher than the 57% observed in the control group (p < 0.001). The GEF and control groups maintained 83% and 42% local response maintenance rates at one year, respectively (p < 0.001). In the GEF with radiotherapy group, the local response maintenance rate was maintained at 92% at 1 year, while in the GEF without RT group, there was a decrease in the local response maintenance rate from 270 days.

conclusionGefitinib treatment for bone metastases in patients harboring EGFR mutation resulted in a beneficial osteosclerotic change in most patients. Combined gefitinib and radiotherapy provide long-lasting local control of bone metastases.

Indexed as

Antineoplastic AgentsBone NeoplasmsCarcinoma, Non-Small-Cell LungLung NeoplasmsErbB ReceptorsErlotinib HydrochlorideGefitinibHumansMutationProtein Kinase InhibitorsQuinazolinesAntineoplastic AgentsErbB ReceptorsErlotinib HydrochlorideGefitinibProtein Kinase InhibitorsQuinazolinesBone metastasesEpidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI)Non-small cell lung cancer (NSCLC)Osteosclerosis

Identifiers

PMID36581856
PMCPMC9801654
OpenAlexW4313263711

What OpenQuestion holds

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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.