Evidence map›Paper›PMID 29299358›Full record

ArticleJournal of gastrointestinal oncology2017

Pacritinib to inhibit JAK/STAT signaling in refractory metastatic colon and rectal cancer.

Thomas Regenbogen, Ling Chen, Kathryn Trinkaus, Andrea Wang-Gillam, Benjamin R Tan, Manik Amin, Katrina S Pedersen, Haeseong Park, Rama Suresh, Kian-Huat Lim and 3 more

Abstract read
In one paragraph

Article in Journal of gastrointestinal oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. The JAK/STAT signaling pathway: from bench to clinic.Signal transduction and targeted therapy · 2021
    Review
  6. Review
  7. Review
  8. Targeting the JAK/STAT pathway in solid tumors.Journal of cancer metastasis and treatment · 2020
    Article
  9. 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

13 authors.

Thomas RegenbogenDivision of Oncology, Washington University, St. Louis, MO, USA.
Ling Chen
Kathryn Trinkaus
Andrea Wang-GillamDivision of Oncology, Washington University, St. Louis, MO, USA.
Benjamin R TanDivision of Oncology, Washington University, St. Louis, MO, USA.
Manik AminDivision of Oncology, Washington University, St. Louis, MO, USA.
Katrina S PedersenDivision of Oncology, Washington University, St. Louis, MO, USA.
Haeseong ParkDivision of Oncology, Washington University, St. Louis, MO, USA.
Rama SureshDivision of Oncology, Washington University, St. Louis, MO, USA.
Kian-Huat LimDivision of Oncology, Washington University, St. Louis, MO, USA.
Emily RatchfordDivision of Oncology, Washington University, St. Louis, MO, USA.
Amberly BrownDivision of Oncology, Washington University, St. Louis, MO, USA.
A Craig LockhartDivision of Oncology, University of Miami, Miami, FL, USA.

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
NCATS NIH HHS UL1 TR002345
6 · The paper itself

Abstract

backgroundTreatment options for patients with refractory colorectal cancer are limited and typically provide a chance of only modest benefit. The goal of this study was to evaluate the benefit of inhibiting the JAK/STAT inflammatory pathway with single agent pacritinib in patients with metastatic refractory colorectal adenocarcinoma.

methodsA single arm institutional trial was initiated and enrolled patients with metastatic colorectal cancer refractory to at least two standard lines of treatment. Pacritinib 400 mg daily was administered orally continuously in 28 day cycles.

resultsThe trial was discontinued prior to reaching the planned accrual due to an FDA hold on pacritinib and a lack of treatment benefit. Eleven patients were enrolled and seven were evaluated for response. Median baseline C-reactive protein level was 12.1 (2.1-147) mg/L. One patient had stable disease at eight weeks by RECIST criteria and six progressed. There were no grade 4 or 5 adverse events while patients were on study. The grade 2 and lower AE events experienced were consistent with prior pacritinib trials.

conclusionsIn seven evaluable patients there were no objective responses. The trial was discontinued prior to completing planned accrual based on a low likelihood that the progression free survival goal of 4 months would be met.

Indexed as

colorectal cancerPacritinibrefractory

Identifiers

PMID29299358
PMCPMC5750170

What Socratic holds

Textmetadata
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 Socratic graph.