Evidence map›Paper›PMID 28204981›Full record

ArticleInvestigational new drugs2017

Phase 1b trial of proteasome inhibitor carfilzomib with irinotecan in lung cancer and other irinotecan-sensitive malignancies that have progressed on prior therapy (Onyx IST reference number: CAR-IST-553).

Susanne M Arnold, Kari Chansky, Markos Leggas, Michael A Thompson, John L Villano, John Hamm, Rachel E Sanborn, Glen J Weiss, Gurkamal Chatta, Maria Q Baggstrom

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

Article in Investigational new drugs, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Proteasome: Role in T Cell Function Regulation.International journal of biological sciences · 2025
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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

10 authors at 9 institutions in 1 country.

Susanne M ArnoldUniversity of Kentucky Markey Cancer Center, 800 Rose Street CC445, Lexington, KY, 40536, USA. susanne.arnold@uky.edu.
Kari ChanskyCancer Research and Biostatistics (CRAB), Seattle, WA, USA.
Markos LeggasUniversity of Kentucky Markey Cancer Center, 800 Rose Street CC445, Lexington, KY, 40536, USA.
Michael A ThompsonAurora Research Institute, Milwaukee, WI, USA.
John L VillanoUniversity of Kentucky Markey Cancer Center, 800 Rose Street CC445, Lexington, KY, 40536, USA.
John HammNorton Cancer Institute, Louisville, KY, 40202, USA.
Rachel E SanbornProvidence Cancer Center, Portland, OR, USA.
Glen J WeissCancer Treatment Centers of America At Western Regional Medical Center, Goodyear, AZ, USA.
Gurkamal ChattaRoswell Park Cancer Institute, Buffalo, NY, USA.
Maria Q BaggstromWashington University School of Medicine Department of Internal Medicine, St. Louis, MO, USA.
Markey Cancer Center · USAurora Health Care · USCancer Research And Biostatistics · USNorton Healthcare · USProvidence Portland Medical Center · USRoswell Park Comprehensive Cancer Center · USUniversity of Kentucky · USWashington University in St. Louis · USWestern Regional Medical Center · US

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI KATHLEEN L. O'CONNOR · 2013 to 2026
$38.3M
NCI NIH HHS P30 CA177558
6 · The paper itself

Abstract

Introduction Proteasome inhibition is an established therapy for many malignancies. Carfilzomib, a novel proteasome inhibitor, was combined with irinotecan to provide a synergistic approach in relapsed, irinotecan-sensitive cancers. Materials and Methods Patients with relapsed irinotecan-sensitive cancers received carfilzomib (Day 1, 2, 8, 9, 15, and 16) at three dose levels (20/27 mg/m2, 20/36 mg/m2 and 20/45 mg/m2/day) in combination with irinotecan (Days 1, 8 and 15) at 125 mg/m2/day. Key eligibility criteria included measurable disease, a Zubrod PS of 0 or 1, and acceptable organ function. Patients with stable asymptomatic brain metastases were eligible. Dose escalation utilized a standard 3 + 3 design. Results Overall, 16 patients were enrolled to three dose levels, with four patients replaced. Three patients experienced dose limiting toxicity (DLT) and the maximum tolerated dose (MTD) was exceeded in Cohort 3. The RP2 dose was carfilzomib 20/36 mg/m

Indexed as

AdolescentAntineoplastic Combined Chemotherapy ProtocolsCamptothecinDose-Response Relationship, DrugDrug Administration ScheduleFemaleHumansIrinotecanLung NeoplasmsMaleMaximum Tolerated DoseNeoplasm Recurrence, LocalOligopeptidesProteasome InhibitorsCamptothecincarfilzomibIrinotecanOligopeptidesProteasome InhibitorsCarfilzomibIrinotecanLung cancerPhase I

Identifiers

PMID28204981
PMCPMC5577369
OpenAlexW2587792628

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.