Evidence map›Paper›PMID 16416165›Full record

Trial reportDigestive diseases and sciences2005

A phase II trial of irinotecan in patients with previously untreated advanced esophageal and gastric adenocarcinoma.

Peter C Enzinger, Matthew H Kulke, Jeffrey W Clark, David P Ryan, Haesook Kim, Craig C Earle, Michele M Vincitore, Ann L Michelini, Robert J Mayer, Charles S Fuchs

Registry-linked trialAbstract readClinical Trial, Phase IIComparative Study
PubMed Publisher
In one paragraph

Trial report in Digestive diseases and sciences, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07126561 (Phase II Open Label Trial of Trastuzumab Deruxtecan), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 10% 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.

NCT07126561 phase2not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Phase II Open Label Trial of Trastuzumab Deruxtecan (Enhertu, DS-8210) in HER2 Positive Newly Diagnosed Metastatic Esophageal, Gastric, GEJ Cancer Patients With an ECOG Performance Status of 2

TypeinterventionalSponsorUniversity of ChicagoRan2026 to 2028Enrolled43ConditionsHER2 Positive Newly Diagnosed Metastatic Esophageal, Gastric, GEJ Cancer Patients With an ECOG Performance Status of 2ArmsTrastuzumab Deruxtecan
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 73 citations in OpenAlex.

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  3. Cetuximab plus cisplatin, irinotecan, and thoracic radiotherapy as definitive treatment for locally advanced, unresectable esophageal cancer: a phase-II study of the SWOG (S0414).Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2012
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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 5 institutions in 1 country.

Peter C EnzingerDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA. Peter_Enzinger@dfci.harvard.edu
Matthew H Kulke
Jeffrey W Clark
David P Ryan
Haesook Kim
Craig C Earle
Michele M Vincitore
Ann L Michelini
Robert J Mayer
Charles S Fuchs
Dana-Farber Cancer Institute · USHarvard University · USMassachusetts General Hospital · USBoston University · USBrigham and Women's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy options for esophagogastric adenocarcinoma remain limited. Irinotecan has demonstrated broad activity in a variety of epithelial malignancies. Forty-six patients with previously untreated, measurable, unresectable, or metastatic esophagogastric adenocarcinoma were enrolled. Patients received irinotecan (125 mg/m2 intravenously over 90 min weekly) for 4 consecutive weeks followed by a 2-week rest. Forty-three patients received at least one treatment and were evaluable for response and toxicity. One complete and five partial responses were observed, for an overall response rate of 14% (95% CI, 4-24%). Median survival for all 43 patients was 6.4 months (95% CI, 4.6-8.2 months). Grade 3 to 4 toxicity included 10 patients (23%) with neutropenia, 13 patients (30%) with late diarrhea, 6 patients (14%) with vomiting, and 6 patients (14%) with fatigue. We conclude that although single-agent irinotecan is an active agent for esophagogastric adenocarcinoma, the schedule utilized in this trial is associated with moderate toxicity. When used as a single-agent, a tri-weekly schedule may be preferable for this patient population.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overAntineoplastic Agents, PhytogenicCamptothecinDose-Response Relationship, DrugDrug Administration ScheduleEsophageal NeoplasmsEsophagogastric JunctionFemaleFollow-Up StudiesHumansIrinotecanMaleMaximum Tolerated DoseAntineoplastic Agents, PhytogenicCamptothecinIrinotecan

Identifiers

PMID16416165
OpenAlexW2024114545

What OpenQuestion holds

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Read underepoch 390

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.