Evidence map›Paper›PMID 30082475›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2018

Phase I Study of the Investigational Aurora A Kinase Inhibitor Alisertib plus Rituximab or Rituximab/Vincristine in Relapsed/Refractory Aggressive B-cell Lymphoma.

Kevin R Kelly, Jonathan W Friedberg, Steven I Park, Kevin McDonagh, John Hayslip, Daniel Persky, Jia Ruan, Soham Puvvada, Peter Rosen, Swaminathan Padmanabhan Iyer and 15 more

Open access · bronzeAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  8. The two sides of chromosomal instability: drivers and brakes in cancer.Signal transduction and targeted therapy · 2024
    Review
  9. Review
  10. Histone Modifications and Their Targeting in Lymphoid Malignancies.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Review
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  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. The role of Aurora-A in human cancers and future therapeutics.American journal of cancer research · 2020
    Review
  20. 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

25 authors at 1 institution in 1 country.

Kevin R KellyUSC Norris Comprehensive Cancer Center, Los Angeles, California (previously University of Texas Health Science Center at San Antonio, San Antonio, Texas). kevin.kelly@med.usc.edu.
Jonathan W FriedbergUniversity of Rochester Medical Center, Rochester, New York.
Steven I ParkLevine Cancer Institute and Carolinas Healthcare System, Charlotte, North Carolina.
Kevin McDonaghVanderbilt University, Nashville, Tennessee (previously University of Kentucky Markey Cancer Center, Lexington, Kentucky).
John HayslipUniversity of Kentucky Markey Cancer Center, Lexington, Kentucky.
Daniel PerskyUniversity of Arizona, Tucson, Arizona.
Jia RuanWeill Cornell Medical College, New York, New York.
Soham PuvvadaUniversity of Arizona, Tucson, Arizona.
Peter RosenProvidence St Joseph Medical Center, Disney Family Cancer Center, Burbank, California.
Swaminathan Padmanabhan IyerMethodist Hospital, Houston, Texas.
Alexandra StefanovicUniversity of Miami Miller School of Medicine, Sylvester Cancer Center, Miami, Florida.
Steven H BernsteinUniversity of Rochester Medical Center, Rochester, New York.
Steven WeitmanUniversity of Texas Health Science Center at San Antonio, San Antonio, Texas.
Anand KarnadUniversity of Texas Health Science Center at San Antonio, San Antonio, Texas.
Gregory MonohanUniversity of Kentucky Markey Cancer Center, Lexington, Kentucky.
Ari VanderWaldeUniversity of Tennessee Health Science Center and West Clinic, Memphis, Tennessee.
Raul MenaProvidence St Joseph Medical Center, Disney Family Cancer Center, Burbank, California.
Monika SchmelzDepartment of Pathology, College of Medicine, University of Arizona, Tucson, Arizona.
Catherine SpierDepartment of Pathology, College of Medicine, University of Arizona, Tucson, Arizona.
Susan GroshenUSC Norris Comprehensive Cancer Center, Los Angeles, California (previously University of Texas Health Science Center at San Antonio, San Antonio, Texas).
Karthik VenkatakrishnanMillennium Pharmaceuticals, Inc., Cambridge, Massachusetts, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited.
Xiaofei ZhouMillennium Pharmaceuticals, Inc., Cambridge, Massachusetts, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited.
Emily Sheldon-WanigaBluebird Bio, Cambridge, Massachusetts (previously Millennium Pharmaceuticals, Inc., Cambridge, Massachusetts, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited).
E Jane LeonardMillennium Pharmaceuticals, Inc., Cambridge, Massachusetts, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited.
Daruka MahadevanUniversity of Arizona, Tucson, Arizona.
University of Rochester Medical Center · US

Funding

USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Fumito Ito · 1985 to 2026
$181.4M
NCI NIH HHS P30 CA014089
6 · The paper itself

Abstract

purposeThe aurora A kinase inhibitor alisertib demonstrated single-agent clinical activity and preclinical synergy with vincristine/rituximab in B-cell non-Hodgkin lymphoma (B-NHL). This phase I study aimed to determine the safety and recommended phase II dose (RP2D) of alisertib in combination with rituximab ± vincristine in patients with relapsed/refractory aggressive B-NHL. PATIENTS AND

methodsPatients with relapsed/refractory, diffuse, large, or other aggressive B-NHL received oral alisertib 50 mg b.i.d. days 1 to 7, plus i.v. rituximab 375 mg/m

resultsForty-five patients participated. The alisertib RP2D for MR was 50 mg b.i.d. For MRV (

conclusionsThe combination of alisertib 50 mg b.i.d. plus rituximab or alisertib 40 mg b.i.d. plus rituximab and vincristine was well tolerated and demonstrated activity in non-GCB DLBCL.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsAurora Kinase AAzepinesDisease ProgressionDrug MonitoringDrug Resistance, NeoplasmFemaleHumansLymphoma, B-CellMaleMaximum Tolerated DoseMiddle AgedMolecular Targeted TherapyAurora Kinase AAzepinesMLN 8237PyrimidinesRituximabVincristine

Identifiers

PMID30082475
PMCPMC7731903
OpenAlexW2886677294

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.