Association of Disease Recurrence With Survival Outcomes in Patients With Cutaneous Squamous Cell Carcinoma of the Head and Neck Treated With Multimodality Therapy.
Academic Medical Centers
Adult
Aged
Aged, 80 and over
Carcinoma, Squamous Cell
/ mortality
Cohort Studies
Combined Modality Therapy
/ methods
Disease-Free Survival
Female
Head and Neck Neoplasms
/ mortality
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Neoplasm Invasiveness
/ pathology
Neoplasm Recurrence, Local
/ mortality
Neoplasm Staging
Prognosis
Proportional Hazards Models
Retrospective Studies
Risk Assessment
Salvage Therapy
Skin Neoplasms
/ mortality
Statistics, Nonparametric
Survival Analysis
Treatment Outcome
United States
Journal
JAMA dermatology
ISSN: 2168-6084
Titre abrégé: JAMA Dermatol
Pays: United States
ID NLM: 101589530
Informations de publication
Date de publication:
01 04 2019
01 04 2019
Historique:
pubmed:
28
2
2019
medline:
11
2
2020
entrez:
28
2
2019
Statut:
ppublish
Résumé
It has previously been demonstrated that immunosuppressed patients with cutaneous squamous cell cancer of the head and neck (cSCC-HN) treated with surgery and postoperative radiotherapy have significantly inferior disease-related outcomes compared with immunocompetent patients, but data on outcomes after disease recurrence are limited. To report survival outcomes in patients with cSCC-HN after disease recurrence after surgery and postoperative radiotherapy and to investigate the association of immune status with disease-related outcomes. A multi-institutional study of 205 patients treated at the Cleveland Clinic, Washington University in St Louis, and the University of California, San Francisco, in which patients who underwent surgical resection and postoperative radiotherapy for primary or recurrent stage I to IV (nonmetastatic) cSCC-HN between January 1, 1995, and December 31, 2014, were identified. Patients with any disease recurrence, defined as local, regional, and/or distant failure, were included. Patients were categorized as immunosuppressed if they received a diagnosis of chronic hematologic malignant neoplasm or HIV or AIDS, or were treated with immunosuppressive therapy for organ transplantation 6 months or more before diagnosis. Statistical analysis was conducted from January 1, 1995, to December 31, 2015. Overall survival calculated using the Kaplan-Meier method and compared using the log-rank test. Of the 205 patients in the original cohort, 72 patients (63 men and 9 women; median age, 71 years [range, 43-91 years]) developed disease recurrence after surgery and postoperative radiotherapy. Forty patients (55.6%) were immunosuppressed, and 32 patients (44.4%) were immunocompetent. Locoregional recurrence was the most common first pattern of failure for both groups (31 immunosuppressed patients [77.5%]; 21 immunocompetent patients [65.6%]). After any recurrence, 1-year overall survival was 43.2% (95% CI, 30.9%-55.4%), and median survival was 8.4 months. For patients for whom information on salvage treatment was available (n = 45), those not amenable to surgical salvage had significantly poorer median cumulative incidence of survival compared with those who were amenable to surgical salvage (4.7 months; 95% CI, 3.7-7.0 months vs 26.1 months; 95% CI, 6.6 months to not reached; P = .01), regardless of their immune status. Results of this study suggest that patients with cSCC-HN who experience disease recurrence after definitive treatment with surgery and postoperative radiotherapy have poor survival, irrespective of immune status. Survival rates are low for patients with recurrent disease that is not amenable to surgical salvage. The low rate of successful salvage underscores the importance of intensifying upfront treatment to prevent recurrence.
Identifiants
pubmed: 30810715
pii: 2724789
doi: 10.1001/jamadermatol.2018.5453
pmc: PMC6459094
doi:
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
442-447Références
Head Neck. 2016 Feb;38(2):175-82
pubmed: 26791005
Cancer. 2017 Jun 1;123(11):2054-2060
pubmed: 28171708
Head Neck. 2005 Oct;27(10):843-50
pubmed: 16161069
Cancer. 1990 Oct 15;66(8):1692-6
pubmed: 1698529
N Engl J Med. 2015 Nov 12;373(20):1984
pubmed: 26559592
Arch Dermatol. 2004 Jul;140(7):837-42
pubmed: 15262694
N Engl J Med. 2017 Nov 9;377(19):1824-1835
pubmed: 28891423
Head Neck. 2012 Nov;34(11):1524-8
pubmed: 22109745
Transplantation. 2010 Sep 27;90(6):683-7
pubmed: 20808266
J Am Acad Dermatol. 2015 Aug;73(2):221-7
pubmed: 26028524
N Engl J Med. 2016 Jun 30;374(26):2542-52
pubmed: 27093365
N Engl J Med. 2017 Oct 5;377(14):1345-1356
pubmed: 28889792
Cochrane Database Syst Rev. 2008 Apr 16;(2):CD004424
pubmed: 18425902
N Engl J Med. 2015 Jun 25;372(26):2521-32
pubmed: 25891173
Am J Physiol. 1998 Jul;275(1):C251-9
pubmed: 9688856
Lancet Oncol. 2008 Aug;9(8):713-20
pubmed: 18617440
J Clin Oncol. 2018 May 1;36(13):1275-1283
pubmed: 29537906
J Clin Oncol. 2011 Sep 1;29(25):3419-26
pubmed: 21810686
J Clin Oncol. 2002 Jan 15;20(2):364-70
pubmed: 11786562
J Am Acad Dermatol. 2017 Dec;77(6):1110-1113.e2
pubmed: 28964539
N Engl J Med. 2018 Jul 26;379(4):341-351
pubmed: 29863979
Int J Dermatol. 2011 Dec;50(12):1496-500
pubmed: 21790552
N Engl J Med. 2016 Nov 3;375(18):1767-1778
pubmed: 27806234