Evidence map›Paper›PMID 27408839›Full record

ArticleAsia Oceania journal of nuclear medicine & biology2013

Treatment efficacy of (153)Sm-EDTMP for painful bone metastasis.

Narjess Ayati, Kamran Aryana, Amir Jalilian, Toktam Hoseinnejad, Ali Bahrami Samani, Zahra Ayati, Farzane Shariati, S Rasoul Zakavi

Open access · greenAbstract read
In one paragraph

Article in Asia Oceania journal of nuclear medicine & biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 25 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Narjess AyatiNuclear Medicine Research Center, Mashhad University of Medical Science, Faculty of Medicine, Mashhad, Iran.
Kamran AryanaNuclear Medicine Research Center, Mashhad University of Medical Science, Faculty of Medicine, Mashhad, Iran.
Amir JalilianRadiopharmaceutical Research & Development Laboratory (RRDL), Nuclear Science and Technology Research Institute (NSTRI), Tehran, Iran.
Toktam HoseinnejadNuclear Medicine Research Center, Mashhad University of Medical Science, Faculty of Medicine, Mashhad, Iran.
Ali Bahrami SamaniRadiopharmaceutical Research & Development Laboratory (RRDL), Nuclear Science and Technology Research Institute (NSTRI), Tehran, Iran.
Zahra AyatiSchool of pharmacy, Mashhad University of Medical Science, Mashhad, Iran.
Farzane ShariatiNuclear Medicine Research Center, Mashhad University of Medical Science, Faculty of Medicine, Mashhad, Iran.
S Rasoul ZakaviNuclear Medicine Research Center, Mashhad University of Medical Science, Faculty of Medicine, Mashhad, Iran.
Mashhad University of Medical Sciences · IRNuclear Science and Technology Research Institute

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionInvolvement of the skeleton can cause an excruciating pain in two-thirds of terminal patients with a history of malignancy. Due to several limitations of other therapies, such as analgesics, bisphosphonates, chemotherapy, hormonal therapy and external beam radiotherapy; bone-seeking radiopharmaceuticals have an important role in palliation of pain from bone metastases. Although these kinds of therapies have many advantages including the ability to treat multiple sites of tumoral involvement simultaneously, no significant confliction with other treatments, ease of administration and the potential to be used repetitively; in Iran using of this modality is not widely practiced. In this study we evaluated the clinical usefulness of Sm-153 lexidronamfor pain management of bone metastases.

methods28 patients (14 males and 14 females) aged 38-77 years with a history of painful bone metastases caused by different cancers, not responding to conventional treatments were included in the study. All patients had a recent whole body bone scan indicating multiple bone metastases. 1 mCi/Kg Sm-153 lexidronam was injected intravenously to the patients. Whole body scintigraphy was done 3 or 18 hours post injection. Pain relief and quality of life have been evaluated by analog pain scale and Karnofsky index every week, respectively. Also, all patients were evaluated for hematological toxicity every two weeks. Active follow ups were performed.

results43% of patients showed the presence of the flare phenomenon during the first three days after Sm injection with a mean duration of 2.2 days. The pain relief began between 2 and 16 days post injection and the duration of pain palliation was in the range of 4 to 32 weeks (mean±SD=15.22±7.8). 64.3% of patients showed complete relief of pain and 21.4% achieved partial response to therapy. (Over all response to therapy was 85.7%). The lowest amount of peripheral blood cells was detected in the fourth week for RBCs and in the 6th week for WBCs and PLTs. No one experienced hematological toxicity induced problems.

conclusionSm-153 lexidronam is an effective treatment for painful bone metastases. The complication rate is low and the quality of life of the patients after treatment would be significantly improved.

Indexed as

153Sm-EDTMPpainful bone metastasisRadionuclide TherapySamarium

Identifiers

PMID27408839
PMCPMC4937668
OpenAlexW2271278148

What OpenQuestion holds

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LicenceCC BY
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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.