U.S. flag

An official website of the United States government

NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.

Cover of Radiotherapy Treatments for Head and Neck Cancer Update

Radiotherapy Treatments for Head and Neck Cancer Update

Comparative Effectiveness Review, No. 144

Investigators: , PhD, , MS, MPH, , MD, , PhD, MPH, and , PhD.

Author Information and Affiliations
Rockville (MD): Agency for Healthcare Research and Quality (US); .
Report No.: 15-EHC001-EF

Structured Abstract

Objectives:

This report is an update of a Comparative Effectiveness Review (CER) published in final form in May 2010 on the benefits and harms of radiotherapy (RT) to treat patients with head and neck cancer (CER No. 20). RT modalities included two-dimensional RT (2DRT), three-dimensional conformal RT (3DCRT), intensity-modulated RT (IMRT), and proton-beam RT (PBT).

In this CER update we included 3DCRT, IMRT, PBT, and stereotactic body RT (SBRT). We used the same Key Questions as for CER No. 20, asking whether any of these modalities is more effective than the others (1) in reducing normal tissue toxicity and adverse events, and improving quality of life (QOL); (2) in improving local tumor control, time to disease progression, and survival; or (3) when used in certain anatomic locations or patient subpopulations; and, finally, whether (4) there is more variation in patient outcomes with any modality secondary to user experience, treatment planning, or target volumes.

The main finding of CER No. 20 was that late xerostomia was reduced and QOL domains related to xerostomia were improved in patients treated with IMRT compared with those who received either 3DCRT or 2DRT. Evidence was insufficient to draw conclusions on survival or tumor control, adverse events other than late xerostomia (e.g., mucositis, dysphagia, skin toxicities, or osteoradionecrosis of the jaw), whether patient and tumor characteristics affected relative outcomes, or whether physician experience and treatment characteristics affected relative clinical outcomes such as survival or treatment-associated adverse events.

Data sources:

A medical librarian searched MEDLINE®, Embase®, and the Cochrane Controlled Trials Registry for English-language articles. The overall search was performed for a period dating 12 months before the final literature search in CER No. 20 (September 28, 2009) through April 2013. For SBRT, the literature was searched for the period January 1, 1990, through April 2013. The search was updated May 1, 2014. A search of the gray literature included clinical trial registries and information from manufacturers if available.

Review methods:

We sought only comparative studies that reported clinical outcomes and QOL among our populations of interest. In preparing CER No. 20, we found noncomparative studies to be uninformative due to substantial heterogeneity in methods and populations, so we excluded them from the update. Data were abstracted for each Key Question by one reviewer, with independent data verification. The study limitations of randomized controlled trials (RCTs) and other comparative studies were assessed using the U.S. Preventive Services Task Force (USPSTF) criteria. The strength of the body of evidence for specific outcomes was assessed according to the latest guidance in the Agency for Healthcare Research and Quality “Methods Guide for Effectiveness and Comparative Effectiveness Reviews.”

Results:

In two searches, we identified 7,130 unique titles and screened 284 in full text. Of the latter, 14 unique studies (N=1,781) in 15 reports met the inclusion criteria, including one RCT (N=60). In the updated search, we identified a second citation to an RCT. However, the latter included the same patients as the previously identified RCT. Therefore, it was not double-counted in the total number of patients; however, because it reported additional, different outcomes, it was reviewed. In 13 unique studies (14 reports, including the RCT), 3DCRT and IMRT were compared. One study compared 3DCRT and SBRT; none compared IMRT and SBRT. As in CER No. 20, no evidence was identified on PBT. Key outcomes of therapy included overall survival, local control, adverse effects, and QOL. According to USPSTF criteria, the RCT was deemed fair quality, whereas the other 13 studies were graded as poor quality.

Conclusions:

New evidence on the comparative effectiveness of RT modalities for head and neck cancer is limited and heterogeneous for each comparison of 3DCRT versus IMRT or SBRT. We did not identify any evidence for PBT. New moderate-strength evidence enhances the CER No. 20 finding of reduced late xerostomia with IMRT compared with 3DCRT, with no relative change in other conclusions on adverse events or QOL. New evidence was insufficient to draw conclusions about the relative effects of IMRT and 3DCRT on overall survival or locoregional tumor control. New evidence is insufficient to draw conclusions on the comparative effectiveness of 3DCRT or IMRT versus SBRT or PBT.

Contents

Prepared for: Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services1, Contract No. 290-2007-10058, Prepared by: Blue Cross and Blue Shield Association, Evidence-based Practice Center, Chicago, IL

Suggested citation:

Ratko TA, Douglas GW, de Souza JA, Belinson SE, Aronson N. Radiotherapy Treatments for Head and Neck Cancer Update. Comparative Effectiveness Review No. 144. (Prepared by Blue Cross and Blue Shield Association Evidence-based Practice Center under Contract No. 290-2007-10058.) AHRQ Publication No. 15-EHC001-EF. Rockville, MD: Agency for Healthcare Research and Quality; December 2014. www.effectivehealthcare.ahrq.gov/reports/final.cfm.

This report is based on research conducted by the Blue Cross and Blue Shield Association Evidence-based Practice Center (EPC) under contract to the Agency for Healthcare Research and Quality (AHRQ), Rockville, MD (Contract No. 290-2007-10058). The findings and conclusions in this document are those of the authors, who are responsible for its contents; the findings and conclusions do not necessarily represent the views of AHRQ. Therefore, no statement in this report should be construed as an official position of AHRQ or of the U.S. Department of Health and Human Services.

The information in this report is intended to help health care decisionmakers—patients and clinicians, health system leaders, and policymakers, among others—make well-informed decisions and thereby improve the quality of health care services. This report is not intended to be a substitute for the application of clinical judgment. Anyone who makes decisions concerning the provision of clinical care should consider this report in the same way as any medical reference and in conjunction with all other pertinent information, i.e., in the context of available resources and circumstances presented by individual patients.

AHRQ or U.S. Department of Health and Human Services endorsement of any derivative products that may be developed from this report, such as clinical practice guidelines, other quality enhancement tools, or reimbursement or coverage policies, may not be stated or implied.

This report may periodically be assessed for currency. If an assessment is done, the resulting surveillance report describing the methodology and findings will be found on the Effective Health Care Program Web site at www.effectivehealthcare.ahrq.gov. Search on the title of the report.

None of the investigators have any affiliations or financial involvement that conflicts with the material presented in this report.

1

540 Gaither Road, Rockville, MD 20850; www​.ahrq.gov

Bookshelf ID: NBK269018PMID: 25590120

Views

  • PubReader
  • Print View
  • Cite this Page
  • PDF version of this title (1.4M)

Related information

Similar articles in PubMed

See reviews...See all...

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...