Evidence map›Paper›PMID 34278011›Full record

ArticleClinical and translational radiation oncology2021

A single-institution phase I feasibility study of dose-escalated IMRT for non-operative locally advanced esophageal carcinoma.

Gregory Vlacich, Andrew Ballard, Shahed N Badiyan, Matthew Spraker, Lauren Henke, Hyun Kim, A Craig Lockhart, Haeseong Park, Rama Suresh, Yi Huang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational radiation oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 2 institutions in 1 country.

Gregory VlacichDepartment of Radiation Oncology, Washington University, St. Louis, MO, United States.
Andrew BallardSouthern Illinois University-Edwardsville, Edwardsville, IL, United States.
Shahed N BadiyanDepartment of Radiation Oncology, Washington University, St. Louis, MO, United States.
Matthew SprakerDepartment of Radiation Oncology, Washington University, St. Louis, MO, United States.
Lauren HenkeDepartment of Radiation Oncology, Washington University, St. Louis, MO, United States.
Hyun KimDepartment of Radiation Oncology, Washington University, St. Louis, MO, United States.
A Craig LockhartDepartment of Medicine, Division of Oncology, Washington University, St. Louis, MO, United States.
Haeseong ParkDepartment of Medicine, Division of Oncology, Washington University, St. Louis, MO, United States.
Rama SureshDepartment of Medicine, Division of Oncology, Washington University, St. Louis, MO, United States.
Yi HuangDepartment of Radiation Oncology, Washington University, St. Louis, MO, United States.
Cliff G RobinsonDepartment of Radiation Oncology, Washington University, St. Louis, MO, United States.
Jeffrey D BradleyDepartment of Radiation Oncology, Washington University, St. Louis, MO, United States.
Pamela P SamsonDepartment of Radiation Oncology, Washington University, St. Louis, MO, United States.
Washington University in St. Louis · USSouthern Illinois University Edwardsville · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeRadiation dose escalation to improve poor outcomes with chemoradiation in locally advanced esophageal carcinoma is limited in part by increased toxicity. This Phase I study investigates the use of IMRT to improve tolerability of dose escalation. MATERIALS AND

methodsA single-institution, prospective study was conducted between 2007 and 2013 for individuals with inoperable esophageal carcinoma. Gross disease received 60 Gy in 30 fractions and at-risk sites received 54 Gy with simultaneous integrated boost. Concurrent chemotherapy primarily consisted of cisplatin/5-FU. The primary objective was to assess feasibility (<15% rate of grade 4-5 toxicity). Secondary objectives included assessment of overall survival (OS), progression free survival (PFS), and locoregional (LRR) and distant recurrence.

resultsTwenty-six patients were enrolled with median follow up of 17.6 months (range 0.1 to 152.0). The majority were AJCC 7th edition Stage III (54%), distal esophagus primary (81%), and adenocarcinoma histology (85%). Twenty-one patients (81%) completed their course of radiation therapy, while only 55% received 2 cycles of concurrent cisplatin/5-FU. One grade 5 and one grade 4 cardiac event occurred, both during chemoradiation and before receiving 50 Gy. The 3-year OS was 48.6% (95% CI: 32.5 to 72.2%) and PFS was 28.5% (95% CI: 14.6 to 55.5%). Half developed distant failure with LRR occurring in 10 patients (38%), isolated in 5 patients.

conclusionWhile feasibility was demonstrated, toxicity and compliance remained limiting factors with outcomes similar to historical controls. There remains an uncertain role for dose escalation in definitive management of locally advanced esophageal cancer.

Indexed as

ChemoradiationDose escalationEsophageal cancerPhase IRadiation therapy

Identifiers

PMID34278011
PMCPMC8267428
OpenAlexW3094610630

What OpenQuestion holds

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Registered trials

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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.