Evidence map›Paper›PMID 27053499›Full record

ArticleClinical genitourinary cancer2016

Radium-223 in Heavily Pretreated Metastatic Castrate-Resistant Prostate Cancer.

Dipenkumar Modi, Clara Hwang, Hirva Mamdani, Seongho Kim, Hesham Gayar, Ulka Vaishampayan, Richard Joyrich, Elisabeth I Heath

Abstract read
In one paragraph

Article in Clinical genitourinary cancer, 2016. 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
–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

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.

  1. Article
  2. Interim and end-treatmentScientific reports · 2021
    Article
  3. Review
  4. Article
  5. Article
  6. Prostate-specific antigen flare induced byEuropean journal of nuclear medicine and molecular imaging · 2018
    Article
  7. Selection and monitoring of patients with metastatic castration-resistant prostate cancer for treatment with radium-223.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2018
    Review
  8. Delayed response after repeatedEuropean journal of nuclear medicine and molecular imaging · 2018
    Article
  9. Article
  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

8 authors.

Dipenkumar ModiDepartment of Internal Medicine, University Health Center, Wayne State University/Detroit Medical Center, Detroit, MI.
Clara HwangDepartment of Hematology-Oncology, Henry Ford Health System, Detroit, MI.
Hirva MamdaniDepartment of Hematology-Oncology, Indiana University, Indianapolis, IN.
Seongho KimBiostatistics Core, Department of Oncology, Karmanos Cancer Institute, School of Medicine, Wayne State University, Detroit, MI.
Hesham GayarDepartment of Radiation Oncology, McLaren Cancer Institute, Flint, MI.
Ulka VaishampayanDepartment of Hematology-Oncology, Karmanos Cancer Institute/Wayne State University, Detroit, MI.
Richard JoyrichDepartment of Nuclear Medicine, Wayne State University, Detroit, MI.
Elisabeth I HeathDepartment of Hematology-Oncology, Karmanos Cancer Institute/Wayne State University, Detroit, MI. Electronic address: heathe@karmanos.org.

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
NCI NIH HHS P30 CA022453
6 · The paper itself

Abstract

backgroundRadium-223 is a bone-targeting radiopharmaceutical that extends survival in mCRPC. Postapproval data are limited, and the value of biochemical and radiologic monitoring during radium therapy is unknown. PATIENTS AND

methodsWe conducted a retrospective study of 29 patients with mCRPC who received radium-223 at 1 of 3 participating institutions between August 2013 and December 2014. Trend of PSA, radiographic changes, and association of biochemical and clinical variables with PSA trend were measured.

resultsThe median age of patients was 70 years, 79% of patients (N = 23) were European Americans, and 17% of patients (N = 5) were African Americans. Twenty patients (69%) had received at least 3 lines of prior therapies. Some 38% of patients (N = 11) received all 6 cycles of radium-223. Twenty patients (69%) had an increase in PSA during radium therapy, and 4 patients (14%) had a decline in PSA levels. Five patients had visceral metastases on computed tomography imaging performed during the course of radium-223.

conclusionsRadium therapy in mCRPC was associated with an increase in PSA in the majority of these heavily pretreated patients. The development of visceral disease was not uncommon, suggesting a need for follow-up computed tomography monitoring during radium-223 therapy. The significance of early increases in PSA and pain with radium-223 is still uncertain. Although pain and PSA flare have been reported in patients who subsequently have a dramatic response to therapy, we observed that a PSA increase or pain flare correlates to an improvement in bone scans only in a minority of patients.

Indexed as

AgedAntineoplastic AgentsBlack or African AmericanHumansMaleMiddle AgedNeoplasm MetastasisProstate-Specific AntigenProstatic Neoplasms, Castration-ResistantRadioisotopesRadiumRetrospective StudiesTreatment OutcomeUnited StatesWhite PeopleAntineoplastic AgentsProstate-Specific AntigenRadioisotopesRadiumradium Ra 223 dichlorideAlpha-emitterBone scanBone-targeting radiopharmaceuticalPain flare-upProstate-specific antigen

Identifiers

PMID27053499
PMCPMC6849387

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.