Evidence map›Paper›PMID 28244407›Full record

Trial reportInternational journal of radiation oncology, biology, physics2017

Long-Term Patient-Reported Outcomes From a Phase 3 Randomized Prospective Trial of Conventional Versus Hypofractionated Radiation Therapy for Localized Prostate Cancer.

Talha Shaikh, Tianyu Li, Elizabeth A Handorf, Matthew E Johnson, Lora S Wang, Mark A Hallman, Richard E Greenberg, Robert A Price, Robert G Uzzo, Charlie Ma and 4 more

Registry-linked trialAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in International journal of radiation oncology, biology, physics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03388619 (A Phase I Trial of Highly Conformal, Hypofractionated, Focally Dose Escalated Post-Prostatectomy Radiotherapy), which is not on this map. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 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.

NCT03388619 phase1completednot on this mapstarted 2018, after this paper: background citation

A Phase I Trial of Highly Conformal, Hypofractionated, Focally Dose Escalated Post-Prostatectomy Radiotherapy

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2018 to 2025Enrolled30ConditionsCancer Of Prostate, Prostate Neoplasms, Prostate Cancer, Neoplasms of ProstateArmsProstate bed with integrated boost, Prostate bed irradiation only, Whole Body Bone Scan, 18F-NaF PET Imaging, CT
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. A systematic review of minimum important changes for generic multi-attribute utility instruments and recommendations for their estimation.The European journal of health economics : HEPAC : health economics in prevention and care · 2025
    Pooled it
  2. Hypofractionation for clinically localized prostate cancer.The Cochrane database of systematic reviews · 2019
    Pooled it
  3. Hypofractionated radiotherapy for localized prostate cancer.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2017
    Pooled it
  4. Trial
  5. Quality of life outcomes from a dose-per-fraction escalation trial of hypofractionation in prostate cancer.Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology · 2016
    Trial
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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

14 authors.

Talha ShaikhDepartment of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Tianyu LiDepartment of Biostatistics, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Elizabeth A HandorfDepartment of Biostatistics, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Matthew E JohnsonDepartment of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Lora S WangDepartment of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Mark A HallmanDepartment of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Richard E GreenbergDepartment of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Robert A PriceDepartment of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Robert G UzzoDepartment of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Charlie MaDepartment of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
David ChenDepartment of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Daniel M GeynismanDepartment of Medical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Alan PollackDepartment of Radiation Oncology, University of Miami, Miami, Florida.
Eric M HorwitzDepartment of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania. Electronic address: eric.horwitz@fccc.edu.

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
Radiation, Hormones &Antisense Prostate Cancer TherapyR01CA101984 · NCI · FOX CHASE CANCER CENTER · PI POLLACK, ALAN · 2003 to 2007
$2.7M
NCI NIH HHS P30 CA006927NCI NIH HHS R01 CA101984
6 · The paper itself

Abstract

purposeTo assess the long-term quality of life (QoL) outcomes from a phase 3 trial comparing 2 modes of intensity modulated radiation therapy (IMRT): conventional IMRT (CIMRT) versus hypofractionated IMRT (HIMRT) in patients with localized prostate cancer. METHODS AND MATERIALS: Between 2002 and 2006, 303 men with low-risk to high-risk prostate cancer were randomized to 76 Gy in 38 fractions (CIMRT) versus 70.2 Gy in 26 fractions (HIMRT). QoL was compared by use of the Expanded Prostate Cancer Index Composite (EPIC), the International Prostate Symptom Score (IPSS), and EuroQoL (EQ5D) questionnaires. The primary outcome of the QoL analysis was a minimum clinically important difference defined as a 0.5 standard deviation change from baseline for each respective QoL parameter. Treatment effects were evaluated with the use of logistic mixed effects regression models.

resultsA total of 286, 299, and 218 patients had baseline EPIC, IPSS, or EQ5D data available and were included in the analysis. Overall, there was no statistically significant difference between the 2 treatment arms in terms of EPIC, IPSS, or EQ5D scores over time, although there was a trend toward lower EPIC urinary incontinence scores in the HIMRT arm. More patients in the HIMRT arm had a lower EPIC urinary incontinence score relative to baseline versus patients in the CIMRT arm with long-term follow-up. On multivariable analysis, there was no association between radiation fractionation scheme and any QoL parameter. When other clinical factors were examined, lymph node radiation was associated with worse EPIC hormonal scores versus patients receiving no lymph node radiation. In general, QoL outcomes were generally stable over time, with the exception of EPIC hormonal and EQ5D scores.

conclusionsIn this randomized prospective study, there were stable QoL changes in patients receiving HIMRT or CIMRT. Our results add to the growing body of literature suggesting that HIMRT may be an acceptable treatment modality in clinically localized prostate cancer.

Indexed as

AgedAged, 80 and overCausalityComorbidityHumansLongitudinal StudiesMaleMiddle AgedPrevalenceProstatic NeoplasmsQuality of LifeRadiation Dose HypofractionationRadiation InjuriesRadiotherapy, ConformalRisk FactorsSelf Report

Identifiers

PMID28244407
PMCPMC5331910

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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.