Evidence map›Paper›PMID 20130879›Full record

Trial reportCancer chemotherapy and pharmacology2010

Phase II study of pemetrexed in patients with advanced neuroendocrine tumors.

Jennifer A Chan, Andrew X Zhu, Keith Stuart, Pankaj Bhargava, Craig C Earle, Jeffrey W Clark, Carolyn Casey, Eileen Regan, Matthew H Kulke

Registry-linked trialAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Cancer chemotherapy and pharmacology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00424723 (A Phase II Study of Pemetrexed in Patients With Advanced Neuroendocrine Tumors), which is not on this map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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.

NCT00424723 phase2completednot on this map

A Phase II Study of Pemetrexed in Patients With Advanced Neuroendocrine Tumors

TypeinterventionalSponsorDana-Farber Cancer InstituteRan2005 to 2010Enrolled32ConditionsNeuroendocrine TumorsArmsPemetrexed
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Article
  3. Review
  4. Advances in the therapy of gastroenteropancreatic-neuroendocrine tumours (GEP-NETs).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2010
    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

9 authors.

Jennifer A ChanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Dana 1220, Boston, MA, 02115, USA. jang@partners.org
Andrew X Zhu
Keith Stuart
Pankaj Bhargava
Craig C Earle
Jeffrey W Clark
Carolyn Casey
Eileen Regan
Matthew H Kulke

Funding

Tissue and Pathology ResourcesP50CA127003 · NCI · DANA-FARBER CANCER INST · PI SICINSKA, · 2007 to 2023
$33.2M
Molecular Analysis of Esophageal Cancer SurvivalK23CA093401 · NCI · DANA-FARBER CANCER INSTITUTE · PI KULKE, MATTHEW H · 2003 to 2007
$679k
Proteoglycans Modulate Sonic Hedgehog RseponsesK08HD048595 · NICHD · DANA-FARBER CANCER INSTITUTE · PI CHAN, JENNIFER A · 2005 to 2006
$221k
NCI NIH HHS CA093401NCI NIH HHS K23 CA093401NCI NIH HHS P50 CA127003NICHD NIH HHS K08 HD048595
6 · The paper itself

Abstract

purposeIn some reports, 5-fluorouracil has been associated with modest activity in patients with neuroendocrine tumors. Pemetrexed is a multitargeted antifolate with activity in tumor types not significantly responsive to other antifolates. We evaluated the efficacy of pemetrexed in a phase II study of patients with advanced neuroendocrine tumors.

methodsPatients with metastatic neuroendocrine tumors (excluding small-cell carcinoma) were treated with pemetrexed administered intravenously at a dose of 500 mg/m(2) every 21 days. To reduce potential toxicity, patients also received folic acid, vitamin B12 supplementation, and peri-infusional treatment with dexamethasone. Patients were followed for response, toxicity, and survival.

resultsThe study was designed with a total accrual goal of 32 patients. Due to lack of radiographic responses in patients during the study period, accrual was terminated at 17. However, one patient achieved a delayed partial response following discontinuation of pemetrexed. Ten patients were evaluable for biochemical response; five (50%) experienced >50% decrease in plasma chromogranin A. Among the 17 patients, 5 (29%) discontinued therapy due to treatment-related toxicity. The median overall survival was 12.1 months.

conclusionPemetrexed does not appear to have significant antitumor activity in patients with advanced neuroendocrine tumors. The limited antitumor activity and potential toxicity associated with pemetrexed mirrors experience with the majority of other cytotoxic agents in patients with neuroendocrine tumors. Investigation of novel, molecularly targeted agents may offer more promise in this disease.

Indexed as

AdultAgedAntimetabolites, AntineoplasticDexamethasoneFemaleFolic AcidGlutamatesGuanineHumansMaleMiddle AgedNeoplasm MetastasisNeuroendocrine TumorsPemetrexedSurvivalTreatment OutcomeAntimetabolites, AntineoplasticDexamethasoneFolic AcidGlutamatesGuaninePemetrexedVitamin B 12Vitamin B Complex

Identifiers

PMID20130879
PMCPMC3755014

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Registered trials

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.