Evidence map›Paper›PMID 28152117›Full record

ArticleJAMA otolaryngology-- head & neck surgery2017

Survival Rates Using Individualized Bioselection Treatment Methods in Patients With Advanced Laryngeal Cancer.

Gregory T Wolf, Emily Bellile, Avraham Eisbruch, Susan Urba, Carol R Bradford, Lisa Peterson, Mark E Prince, Theodoros N Teknos, Douglas B Chepeha, Norman D Hogikyan and 4 more

Open access · greenAbstract read
In one paragraph

Article in JAMA otolaryngology-- head & neck surgery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Outcomes of the modern management approach for locally advanced (TThe Journal of laryngology and otology · 2024
    Article
  5. Article
  6. Chemoradiotherapy vs radiotherapy for non-surgical locally advanced laryngeal squamous cell carcinoma patients: a propensity score-matched study and practical nomogram construction.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Prognostic factors in laryngeal squamous cell carcinoma.Laryngoscope investigative otolaryngology · 2020
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Gregory T WolfDepartment of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor.
Emily BellileDepartment of Biostatistics, University of Michigan Health System, Ann Arbor.
Avraham EisbruchDepartment of Radiation Oncology, University of Michigan Health System, Ann Arbor.
Susan UrbaDepartment of Internal Medicine, University of Michigan Health System, Ann Arbor.
Carol R BradfordDepartment of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor.
Lisa PetersonDepartment of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor.
Mark E PrinceDepartment of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor.
Theodoros N TeknosDepartment of Otolaryngology-Head and Neck Surgery, The Ohio State University, Wexner Medical Center, Columbus.
Douglas B ChepehaDepartment of Otolaryngology, University of Toronto, Toronto, Ontario, Canada.
Norman D HogikyanDepartment of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor.
Scott A McLeanDepartment of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor.
Jeffery MoyerDepartment of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor.
Jeremy M G TaylorDepartment of Biostatistics, University of Michigan Health System, Ann Arbor.
Francis P WordenDepartment of Internal Medicine, University of Michigan Health System, Ann Arbor.
Michigan Medicine · USThe Ohio State University Wexner Medical Center · USUniversity of Michigan–Ann Arbor · USUniversity of Toronto · CA

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Therapeutic Potential and Mechanism of Action of Potent Small Molecule InhibitorsP50CA097248 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WOLF, GREGORY T · 2002 to 2013
$25.3M
NCI NIH HHS P30 CA046592NCI NIH HHS P50 CA097248
6 · The paper itself

Abstract

Importance: Use of chemoradiotherapy for advanced laryngeal cancer led to a major shift in treatment as an alternative to laryngectomy. Despite widespread adoption of chemoradiotherapy, survival rates have not improved and the original premise of matching neoadjuvant chemotherapy tumor response to determine subsequent treatment has not been followed. Objective: To determine whether improved survival could be achieved by incorporating a single cycle of neoadjuvant chemotherapy to select patients with advanced disease for either laryngectomy or concurrent chemoradiotherapy. Design, Setting, and Participants: An unselected cohort of 247 patients with laryngeal cancer in an academic institution between 2002 and 2012 was evaluated. Patients with limited disease (stages I and II) underwent endoscopic resection, radiotherapy, or chemoradiotherapy for deeply invasive T2 lesions. For patients with advanced disease (stages III and IV), neoadjuvant chemotherapy, concurrent chemoradiotherapy, or primary surgery was recommended. Overall survival (OS) and disease-specific survival (DSS) were analyzed. Median follow-up was 48 months. The study was conducted from January 1, 2002, to December 31, 2012; data analysis was completed December 1, 2015. Interventions: Endoscopic resection, radiotherapy, chemoradiotherapy, neoadjuvant chemotherapy, concurrent chemoradiotherapy, and primary surgery. Main Outcomes and Measures: Overall survival and DSS. Results: Of the 247 patients, 191 (77.3%) were male; mean (SD) age was 59.6 (10.4) years. Of 94 patients with limited disease, 33 (35.1%) underwent endoscopic resection; 50 (53.2%), radiotherapy alone; and 11 (11.7%), chemoradiotherapy for deeply invasive T2 lesions. Of 153 patients with advanced disease, 71 (46.4%) received neoadjuvant chemotherapy; 50 (32.7%), concurrent chemoradiotherapy; and 32 (20.9%), surgery. Five-year OS and DSS was 75% (95% CI, 68%-81%) and 83% (95% CI, 77%-88%), respectively, for the entire cohort. The DSS was 92% (95% CI, 83%-97%) for patients with stage I or II and 78% (95% CI, 69%-84%) for patients with stage III or IV disease. For patients with advanced disease, 5-year OS and DSS ranged from 78% (95% CI, 55%-90%) and 91% (95% CI, 67%-98%), respectively, for surgery; to 76% (95% CI, 63%-85%) and 79% (95% CI, 67%-88%), respectively, for neoadjuvant bioselection; and to 61% (95% CI, 44%-75%) and 66% (95% CI, 48%-79%), respectively, for primary chemoradiotherapy. Propensity-adjusted, multivariable controlling for known prognostic factors DSS was significantly improved in the neoadjuvant group compared with the chemoradiotherapy group (hazard ratio [HR], 0.48; 95% CI, 0.29-0.80). Conclusions and Relevance: Superior survival rates were achieved with a bioselective treatment approach using a single cycle of neoadjuvant chemotherapy. Good survival rates were also achieved in patients selected for primary surgery, and both neoadjuvant chemotherapy and primary surgery were better than survival rates with concurrent chemoradiotherapy, suggesting that the optimal individualized treatment approach for patients with advanced laryngeal cancer has not yet been defined.

Indexed as

AgedAntineoplastic AgentsCarcinoma, Squamous CellChemoradiotherapyDisease-Free SurvivalEndoscopyFemaleHumansLaryngeal NeoplasmsLaryngectomyMaleMiddle AgedNeoadjuvant TherapyNeoplasm StagingPatient SelectionRetrospective StudiesAntineoplastic Agents

Identifiers

PMID28152117
PMCPMC5439146
OpenAlexW2583482683

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.