Evidence map›Paper›PMID 31170574›Full record

ReviewCritical reviews in oncology/hematology2019

The evolution and understanding of skeletal complication endpoints in clinical trials of tumors with metastasis to the bone.

A Hussain, R J Lee, J N Graff, S Halabi

Open access · hybridAbstract readReview
In one paragraph

Review in Critical reviews in oncology/hematology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
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  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Risk factors for skeletal-related events in non-small cell lung cancer patients treated with bone-modifying agents.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2021
    Article
  13. Review
  14. Bone Metastasis: Current State of Play.Translational oncology · 2020
    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

4 authors at 4 institutions in 1 country.

A HussainUniversity of Maryland, School of Medicine, Marlene and Stuart Greenebaum Cancer Center, and Baltimore VA Medical Center, Baltimore, MD, USA. Electronic address: ahussain@som.umaryland.edu.
R J LeeMassachusetts General Hospital Cancer Center, Boston, MA, USA.
J N GraffKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
S HalabiDuke University Medical Center, Durham, NC, USA.
Duke Medical Center · USMassachusetts General Hospital · USOregon Health & Science University · USUniversity of Maryland, Baltimore · US

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
Serum Androgens as Predictors of Survival in Metastatic Prostate CancerR21CA195424 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HALABI, SUSAN, RYAN, CHARLES JAMES · 2015 to 2016
$398k
Optimization of Multi-Modal Therapies in Pre-clinical models of Prostate CancerI01BX000545 · VA · BALTIMORE VA MEDICAL CENTER · PI HUSSAIN, ARIF · 2009 to 2021
–
BLRD VA I01 BX000545NCI NIH HHS P30 CA014236NCI NIH HHS R21 CA195424
6 · The paper itself

Abstract

Bone metastases are a frequent complication of solid tumors, leading to significant skeletal sequelae that negatively impact quality of life and survival. Prevention and management of skeletal-related complications are critical treatment goals in oncology. Endpoints used in clinical trials to evaluate skeletal-related complications have evolved. In contrast to single measures of bone health, contemporary clinical trial endpoints reflect composite measures of skeletal-related complications, and increasingly also survival. In addition, key symptomatic components, which are more reflective of quality of life and the patient experience, are being incorporated. Given the evolution and resulting diversity of the endpoints being used in pivotal trials, it is becoming increasingly relevant to clarify the utility and the potential clinical impact of these measures not only within the context of trials but also in the real-world setting. Here, we describe the development and evolution of skeletal endpoints used in trials, and discuss their clinical relevance.

Indexed as

Quality of LifeBone NeoplasmsClinical Trials as TopicFractures, BoneHumansIncidenceNeoplasmsBoneBone metastasesEndpointSkeletal-related eventSymptomatic skeletal event

Identifiers

PMID31170574
PMCPMC6609290
OpenAlexW2943344648

What OpenQuestion holds

Textmetadata
LicenceTDM
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.