Evidence map›Paper›PMID 30318513›Full record

ArticleBritish journal of cancer2018

Phase 1 study of ARQ 761, a β-lapachone analogue that promotes NQO1-mediated programmed cancer cell necrosis.

David E Gerber, M Shaalan Beg, Farjana Fattah, Arthur E Frankel, Oluwatomilade Fatunde, Yull Arriaga, Jonathan E Dowell, Ajit Bisen, Richard D Leff, Claudia C Meek and 10 more

Open access · hybridAbstract readClinical Trial, Phase I
In one paragraph

Article in British journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
5.1field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
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  6. Review
  7. Review
  8. Controlled Self-Immolative Release of β-Lapachone via an OptimizedJournal of the American Chemical Society · 2025
    Article
  9. Article
  10. Article
  11. β-Lapachone encapsulated into stealth liposomes: inhibition of biofilm and cell wall thickness of MRSA.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2025
    Article
  12. Article
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  14. Article
  15. Article
  16. Review
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  18. Article
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  20. 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

20 authors at 4 institutions in 1 country.

David E GerberDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA. david.gerber@utsouthwestern.edu.
M Shaalan BegDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Farjana FattahHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Arthur E FrankelDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Oluwatomilade FatundeHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Yull ArriagaDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Jonathan E DowellDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Ajit BisenDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Richard D LeffTexas Tech University Health Sciences Center School of Pharmacy, Dallas, TX, 75390, USA.
Claudia C MeekTexas Tech University Health Sciences Center School of Pharmacy, Dallas, TX, 75390, USA.
William C PutnamTexas Tech University Health Sciences Center School of Pharmacy, Dallas, TX, 75390, USA.
Raja Reddy KallemTexas Tech University Health Sciences Center School of Pharmacy, Dallas, TX, 75390, USA.
Indhumathy SubramaniyanTexas Tech University Health Sciences Center School of Pharmacy, Dallas, TX, 75390, USA.
Ying DongHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Joyce BolluytHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Venetia SarodeDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Xin LuoDepartment of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Yang XieDepartment of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Brian SchwartzArQule, Inc., Burlington, MA, 01803, USA.
David A BoothmanHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
The University of Texas Southwestern Medical Center · USTexas Tech University · USArqule (United States) · USTexas Tech University Health Sciences Center · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MELANIE H. COBB · 2010 to 2026
$53.7M
Development of New Cancer Treatments and InvestigatorsK24CA201543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GERBER, DAVID ERIC · 2016 to 2020
$737k
NCI NIH HHS K24 CA201543NCI NIH HHS P30 CA142543
6 · The paper itself

Abstract

backgroundNAD(P)H:quinone oxidoreductase 1 (NQO1) is a two-electron oxidoreductase expressed in multiple tumour types. ARQ 761 is a β-lapachone (β-lap) analogue that exploits the unique elevation of NQO1 found in solid tumours to cause tumour-specific cell death.

methodsWe performed a 3+3 dose escalation study of 3 schedules (weekly, every other week, 2/3 weeks) of ARQ 761 in patients with refractory advanced solid tumours. Tumour tissue was analysed for NQO1 expression. After 20 patients were analysed, enrolment was restricted to patients with NQO1-high tumours (H-score ≥ 200).

resultsA total of 42 patients were treated. Median number of prior lines of therapy was 4. Maximum tolerated dose was 390 mg/m

conclusionsARQ 761 has modest single-agent activity, which appears associated with tumour NQO1 expression. Principal toxicities include anaemia and possible methemoglobinaemia.

Indexed as

AdultAgedAged, 80 and overApoptosisCell Line, TumorDNA DamageFemaleHumansMaleMiddle AgedNAD(P)H Dehydrogenase (Quinone)NaphthoquinonesNecrosisNeoplasmsReactive Oxygen Speciesbeta-lapachoneNAD(P)H Dehydrogenase (Quinone)NaphthoquinonesNQO1 protein, humanReactive Oxygen Species

Identifiers

PMID30318513
PMCPMC6203852
OpenAlexW2897152103

What OpenQuestion holds

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LicenceCC BY
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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.