Evidence map›Paper›PMID 23492368›Full record

ArticleCancer research2013

Center of cancer systems biology second annual workshop--tumor metronomics: timing and dose level dynamics.

Philip Hahnfeldt, Lynn Hlatky, Giannoula Lakka Klement

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2013. 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
1.4field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Role of vascular normalization in benefit from metronomic chemotherapy.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Metronomics: towards personalized chemotherapy?Nature reviews. Clinical oncology · 2014
    Review
  7. Article
  8. Article
  9. Cyclophosphamide stimulates endoplasmic reticulum stress and induces apoptotic cell death in human glioblastoma cell lines.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

3 authors at 2 institutions in 1 country.

Philip HahnfeldtCenter of Cancer Systems Biology, Steward St. Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA, USA. Philip.Hahnfeldt@tufts.edu
Lynn Hlatky
Giannoula Lakka Klement
St. Elizabeth's Medical Center · USTufts University · US

Funding

Project 5 UC BerkleyU54CA149233 · NCI · STEWARD ST. ELIZABETH'S MEDICAL CENTER · PI HLATKY, LYNN · 2010 to 2014
$7.3M
The role of platelets in tumor growth, wound healing and other angiogenesis diseaR01GM093050 · NIGMS · TUFTS MEDICAL CENTER · PI KLEMENT, GIANNOULA LAKKA · 2010 to 2013
$1.3M
NCI NIH HHS U54 CA149233NCI NIH HHS U54-CA149233NIGMS NIH HHS R01 GM093050
6 · The paper itself

Abstract

Metronomic chemotherapy, the delivery of doses in a low, regular manner so as to avoid toxic side effects, was introduced over 12 years ago in the face of substantial clinical and preclinical evidence supporting its tumor-suppressive capability. It constituted a marked departure from the classic maximum-tolerated dose (MTD) strategy, which, given its goal of rapid eradication, uses dosing sufficiently intense to require rest periods between cycles to limit toxicity. Even so, upfront tumor eradication is frequently not achieved with MTD, whereupon a de facto goal of longer-term tumor control is often pursued. As metronomic dosing has shown tumor control capability, even for cancers that have become resistant to the same drug delivered under MTD, the question arises whether it may be a preferable alternative dosing approach from the outset. To date, however, our knowledge of the coupled dynamics underlying metronomic dosing is neither sufficiently well developed nor widely enough disseminated to establish its actual potential. Meeting organizers thus felt the time was right, armed with new quantitative approaches, to call a workshop on "Tumor Metronomics: Timing and Dose Level Dynamics" to explore prospects for gaining a deeper, systems-level appreciation of the metronomics concept. The workshop proved to be a forum in which experts from the clinical, biologic, mathematical, and computational realms could work together to clarify the principles and underpinnings of metronomics. Among other things, the need for significant shifts in thinking regarding endpoints to be used as clinical standards of therapeutic progress was recognized.

Indexed as

Systems BiologyAntineoplastic AgentsHumansMaximum Tolerated DoseNeoplasmsReceptors, Vascular Endothelial Growth FactorTime FactorsAntineoplastic AgentsReceptors, Vascular Endothelial Growth Factor

Identifiers

PMID23492368
PMCPMC3696500
OpenAlexW2126670898

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.