Evidence map›Paper›PMID 28211889›Full record

ArticleBlood cancer journal2017

Clinical utility of the Revised International Staging System in unselected patients with newly diagnosed and relapsed multiple myeloma.

N Tandon, S V Rajkumar, B LaPlant, A Pettinger, M Q Lacy, A Dispenzieri, F K Buadi, M A Gertz, S R Hayman, N Leung and 12 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. European journal of nuclear medicine and molecular imaging · 2019
    Article
  17. Review
  18. Article
  19. The Role ofContrast media & molecular imaging · 2018
    Article
  20. The effect of novel therapies in high-molecular-risk multiple myeloma.Clinical advances in hematology & oncology : H&O · 2017
    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

22 authors at 1 institution in 1 country.

N TandonDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
S V RajkumarDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
B LaPlantDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
A PettingerDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
M Q LacyDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
A DispenzieriDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
F K BuadiDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
M A GertzDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
S R HaymanDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
N LeungDivision of Hematology, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0002-5651-1411
R S GoDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
D DingliDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
P KapoorDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Y LinDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Y L HwaDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
A L FonderDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
M A HobbsDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
S R ZeldenrustDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
J A LustDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
W I GonsalvesDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
S J RussellDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
S K KumarDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic in Arizona · US

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Rafael Fonseca · 2015 to 2026
$25.5M
NCATS NIH HHS UL1 TR000135NCI NIH HHS P50 CA186781
6 · The paper itself

Abstract

We analyzed the utility of Revised International staging system (RISS) in an unselected cohort of newly diagnosed multiple myeloma (NDMM; cohort 1), and relapsed/refractory multiple myeloma (RRMM; cohort 2) patients. Cohort 1 included 1900 patients seen within 90 days of diagnosis, from 2005 to 2015, while cohort 2 had 887 patients enrolled in 23 clinical trials at Mayo Clinic. The overall survival (OS) and progression-free survival (PFS) was calculated from the time since diagnosis or trial registration. The median estimated follow up was 5 and 2.3 years for Cohorts 1 and 2, respectively. Among 1067 patients evaluable in Cohort 1, the median OS and PFS was 10 and 2.8 years for RISS stage I, 6 and 2.7 years for RISS stage II and 2.6 and 1.3 years for RISS stage III (P<0.0001). Among 456 patients evaluable in Cohort 2, the median OS and PFS was 4.3 and 1.1 years for RISS stage I, 2 and 0.5 years for RISS stage II and 0.8 and 0.2 years for RISS stage III (P<0.0001). In conclusions, RISS gives a better differentiation of NDMM as well as RRMM patients into three survival subgroups and should be used to stratify patients in future clinical trials.

Indexed as

AdultAgedAged, 80 and overCohort StudiesFemaleHumansMaleMiddle AgedMultiple MyelomaNeoplasm StagingPrognosisYoung Adult

Identifiers

PMID28211889
PMCPMC5386331
OpenAlexW2588224757

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.