Elective Neck Dissection in Patients Undergoing Salvage Laryngectomy: Outcomes, Complications, and Considerations (2024)

  • Journal List
  • Cureus
  • v.16(5); 2024 May
  • PMC11168787

As a library, NLM provides access to scientific literature. Inclusion in an NLM database does not imply endorsem*nt of, or agreement with, the contents by NLM or the National Institutes of Health.
Learn more: PMC Disclaimer | PMC Copyright Notice

Elective Neck Dissection in Patients Undergoing Salvage Laryngectomy: Outcomes, Complications, and Considerations (1)

Link to Publisher's site

Cureus. 2024 May; 16(5): e60222.

Published online 2024 May 13. doi:10.7759/cureus.60222

PMCID: PMC11168787

PMID: 38868267

Monitoring Editor: Alexander Muacevic and John R Adler

Nickolas A Alsup,1 Soroush Farsi,1 Sydney K Blevins,1 Rachel Giese,2 Deanne King,1 Jumin Sunde,1 Emre Vural,1 and Mauricio MorenoElective Neck Dissection in Patients Undergoing Salvage Laryngectomy: Outcomes, Complications, and Considerations (2)1

Author information Article notes Copyright and License information PMC Disclaimer

Abstract

Objective

In this study, we sought to identify the predictors for occult nodal disease (OND) and compare oncologic outcomes in patients undergoing elective neck dissection (END)at the time of salvage laryngectomy (SLE) versus the observation group.

Methods

A retrospective chart review was conducted involving all patients with clinically node-negative (cN0) necks who underwent SLE at atertiary academic center over 12 years. A total of 58 patients met the inclusion criteria and were divided into two groups: END (n=39) and observation (n=19). Primary endpoints were OND, regional recurrence-free survival (RRFS), and disease-specific survival (DSS). Univariate analysis was performed to establish the association between variables with Fisher’s exact test and Mann-Whitney U test. Survival analysis was performed with the log-rank test.

Results

The cohort comprised 46 (79.3%) males and 12 (20.7%) females, with a mean age of 60 years. Pathological nodal disease was identified in five of 71 (7%) examined neck dissection specimens, with positive nodes found in levels II through IV. The only statistically significant predictor of OND was the rT3/rT4 stage (p=0.017). There were no differences in perioperative complications, RRFS (p=0.216), or DSS (p=0.298) between the END and observation groups.

Conclusions

In cN0 necks, the advanced recurrent T-stage (rT3-rT4) is a predictor for OND. As OND was found involving levels II, III, and IV in this study's specimens,formal lateral neck dissection should be the procedure of choice if END is to be performed alongside SLE. While END did not show a significantly higher morbidity profile versus conservative management in this cohort, the procedure did not improve loco-regional control or survival, even when stratifying by tumor stage.

Keywords: outcomes, survival, recurrence, occult nodal disease, elective neck dissection, salvage total laryngectomy

Introduction

In the setting of advanced laryngeal cancer, salvage laryngectomy (SLE) is generally considered the best available treatment with curative intent for residuals and recurrences, especially for patients without cervical metastasis [1]. There is a wide consensus regarding the role of therapeutic neck dissection for those presenting with node-positive status. Still, whether an elective neck dissection (END) is indicated in the clinically and radiologically node-negative (cN0) patient is unclear. While this procedure is frequentlyperformed as part of routine salvage surgery, a growing body of evidence questions its rationale and oncologic impact.

Among patients undergoing END alone with SLE, the rate of occult nodal disease (OND) varies, reported to range from as low as 0% to as high as 28% [2,3].Although different strategies have been proposed in the literature, there is no consensus on when END is appropriate [4,5].Several studies have concluded that END should not be performed at all, in light of the low rates of OND and high morbidity associated with the procedure [6,7].

More studies in the past few years have suggested that at the cohort level, END in itself confers no discernible survival advantage versus observation alone after SLE; individual tumor characteristics such as staging and location along with other considerations such as lifestyle factors and comorbidities need to be assessed on a case-by-case basis to determine whether END is desirable for a particular patient [8-10].For instance, some studies have identified distinct risk factors for higher rates of OND such as recurrent T3/T4 stage and supraglottic location, concluding that END might only be indicated in the presence of these clinical findings [11,12]. Given the small number of studies on survival rates and the challenges the studies have encountered with regardto meta-analyses, we decided to review our institutional experience, with the objectives of assessing the impact of END on oncologic outcomes, identifying clinicopathological predictors for OND, and establishing a morbidity profile for the procedure [8].

Materials and methods

This study was conducted at the University of Arkansas for Medical Sciences, a tertiary academic center in Little Rock, Arkansas, USA. The study design received approval from the university's Institutional Review Board (IRB# 228942). Patient selection for the study was based on a retrospective chart review of individuals who had undergone total laryngectomy over 12 years. The inclusion criteriawere defined as follows: 1) biopsy-proven recurrent squamous cell carcinoma of the larynx or hypopharynx, including all subsites and stages, 2) prior definitive radiation or concomitant chemoradiation with curative intent, and 3) cN0 neck, based on axial imaging with contrast CT or MRI at the time of re-staging. The exclusion criteria were as follows: 1) primary laryngectomy, 2) partial laryngectomy, 3) clinically or radiologically node-positive neck, 4) functional laryngectomy (aspiration, chondritis), 5) incomplete course of radiation therapy, and 6) elective neck dissection of levels less than II-IV (lateral neck dissection).

Of the 180 potentially eligible patients, 58 were ultimately included in the study, with the most common cause for exclusion being primary laryngectomy. The study group was then divided into END and observation-only cohorts for comparison. Data retrieved from the charts included the following parameters: demographic information, initial and recurrent cancer staging, radiation data, risk factors, tumor characteristics, postoperative course, complications, and oncologic outcomes. Histopathological data included the following aspects: tumor size, margin status, number of lymph nodes, presence and location of pathologically positive nodes, perineural invasion, lymphovascular invasion, and degree of differentiation.

The data analysis was performed using IBM SPSS® Statistics for Windows, Version 22.0. (IBM Corp., Armonk, NY). The primary endpoints were OND, regional recurrence-free survival (RRFS), and disease-specific survival (DSS). Univariate analysis was performed to establish the association between variables with Fisher’s exact test and Mann-Whitney U test. Survival analysis was performed with the log-rank test. A recurrence event was defined as clinical or radiological evidence of disease, with censoring at the last follow-up if no recurrence event occurred by then.For all statistical purposes, significance was set at ap-value less than or equal to 0.05.

Results

Of the 58 patients with a cN0 neck and receiving SLE, 39 (67.2%) underwent END, while 19 (32.8%) had observation only. These two groups were mostly comparable in terms of demographics, tumor staging, and histopathological features, as shown in Table ​Table1.1. However, a larger proportion of patients completed a chemoradiation course in the END group (p=0.013). The study group comprised 46 males and 12 females, with a mean age of 60 years at the time of salvage surgery. The mean radiation dose was 65.7 Gy (range: 51-70.2; SD=4.5), and the average disease-free interval to the diagnosis of the recurrence was 17.8 months. Overall, the mean postoperative follow-up durationfor the group was 25 months.

Table 1

Demographic and clinicopathological characteristics for the elective neck dissection and observation cohorts

Fisher’s exact test.§Mann-Whitney U test. *Denotes statistical significance

END: elective neck dissection

Patient characteristicsEND (n=39)Observation (n=19)Combined (n=58)p-value
Male,n (%)29 (74)17 (89)46 (79)0.301
Female,n (%)10 (26)2 (11)12 (21)0.301
Average time to recurrence, months16.420.617.8n/a
Smoking history, pack years4350450.430§
Age at laryngectomy, years5964600.184§
Race,n (%)
African-American5 (13)4 (21)9 (16)0.456
White, non-Hispanic34 (87)15 (79)49 (84)0.456
Tumor site,n (%)
Supraglottic17 (44)5 (26)22 (38)0.256
Glottic9 (23)9 (47)18 (31)0.075
Transglottic11 (28)5 (26)16 (28)n/a
Hypopharynx2 (5)0 (0)2 (3)n/a
Recurrent T-stage,n (%)
rT102 (11)2 (3)0.103
rT212 (31)1 (5)13 (22)0.042†*
rT315 (38)11 (58)26 (45)0.260
rT412 (31)5 (26)17 (29)n/a
Histopathological characteristics,n (%)
Well-moderately differentiated2 (5)1 (5)3 (5)n/a
Moderately differentiated25 (64)11 (58)36 (62)0.774
Moderate-poorly differentiated4 (10)04 (7)0.292
Poorly differentiated1 (3)2 (11)3 (5)0.247
Differentiation not specified04 (21)4 (7)0.009†*
Lymphovascular invasion8 (21)3 (16)11 (19)n/a
Perineural invasion13 (33)5 (26)18 (31)0.763
Previous treatment,n (%)
Radiotherapy17 (44)15 (79)32 (55)0.013†*
Chemoradiotherapy22 (56)4 (21)26 (45)0.013†*

Open in a separate window

There were only two cases of hypopharyngeal tumors; the vast majority of the patients presented with laryngeal primaries. Among these, glottic, supraglottic, and transglottic locations were similarly represented, as shown in Table ​Table1.1. On histopathology, extralaryngeal extension was identified in seven cases, and margins were negative (>1 mm) in all but three patients, one of whom had dysplasia at the margin.

Occult nodal disease

From the 39 patients who underwent neck dissection, a total of 71 neck dissection specimens were studied. Only five of these specimens (7%) were found to have microscopic nodal disease, with one patient having bilateral disease. Overall, a total of 1,202 lymph nodes were assessed, and only six of those (0.5%) were microscopically positive for the disease. The clinicopathological characteristics of these patients are summarized in Table ​Table2.The2.The only statistically significant predictor for OND was advanced recurrent T-stage (rT3 and rT4) (p=0.017), as shown in Table ​Table33.

Table 2

Clinical characteristics of patients with occult nodal disease

PatientNeck level (# nodes)Recurrent T-stageRecurrent locationInitial stageInitial tumor locationDifferentiation
AIV (1)T4GlotticT1N0GlotticModerate to poor
BII-IV (2)T3TransglotticT2N0GlotticWell
CII (2)T3SupraglotticT3NXSupraglotticModerate
DIII (1)T4TransglotticUnknownTransglotticWell

Open in a separate window

Table 3

Clinicopathological predictors for occult nodal disease

Fisher’s exact test.§Mann-Whitney U test. *Denotes statistical significance

Variablep-value
Age0.160§
Alcohol use (current)0.162
Smoking status0.424
Recurrent T-stage0.017†*
Glottic vs. supraglottic0.768
Positive margins (<1 mm)0.248

Open in a separate window

Oncologic outcomes

A comparative analysis of the oncologic outcomes between the groups is presented in Table ​Table4.Overall,4.Overall, at both two years and five years, there were no statistically significant differences in RRFS (p=0.216) or DSS (p=0.298) between the END and observation groups. Additionally, a subset analysis consideringonly patients with advanced disease (rT3/rT4) did not show any statistically significant differences in RRFS (p=0.942) or DSS (p=0.850) between the surgical and observation groups.

Table 4

Oncologic outcomes - elective neck dissection vs. observation cohorts

§Log-rank test

Regional recurrence-free survivalDisease-specific survival
2-year5-year2-year5-year
Elective neck dissection77.0%71.5%73.5%63.7%
Observation93.3%93.3%94.1%78.4%
p=0.216§p=0.298§

Open in a separate window

Postoperative course

Table ​Table55 summarizes the frequency of short- and long-term complications in both groups. The overall pharyngocutaneous (PC) fistula rate in this series was 22.4%, which aligns with the findings in the literature [13]. In the END group, 11 of 39 (28.2%) patients had a fistula postoperatively, while two of 19 (10.5%) presented with this condition in the observation group (p=0.186). A subset analysis was performedincludingonly patients with a primary pharyngeal closure. In this subset, six of 23 (26.1%) and two of 10 (20%) had a fistula in the END and observation groups, respectively (p=1.000). One patient in the END group died due tomyocardial infarction postoperatively. The length of hospital stay was similar in both groups (average of seven days with a median length of stay of 10 days).

Table 5

Postoperative complications in the observation and elective neck dissection cohorts

Fisher’s exact test

END: elective neck dissection group

ComplicationObservation (n=19), n (%)END (n=39), n (%)p-value
Pharyngocutaneous fistula2 (10.5)11 (28.2)0.186
Pneumonia2 (10.5)2 (5.1)0.446
Cardiovascular1 (5.3)3 (7.7)0.117
Fluid collection3 (15.8)3 (7.7)0.342
Pharyngeal stenosis1 (5.3)3 (7.7)0.732
Required blood transfusion1 (5.3)1 (2.6)0.579

Open in a separate window

Discussion

Organ preservation schemes with salvage surgery are the current standard of care for laryngeal cancer in the developed world. While there is little dispute on the need for neck dissection in patients with clinically positive necks, the role of this procedure in cN0 necks has been increasingly challenged. Advances in preoperative imaging continue to push the envelope for identifying low-volume disease in the neck, and such advances likely underlie the high variability in reported OND in surgical specimens [3,14].

In a study examining oral cavity, oropharyngeal, and hypopharyngeal DSS rates, Lee et al. suggested that salvage neck dissection is warranted when recurrence occurs within one year of treatment or if there was initial (pre-radiation) positive nodal disease [15]. Similarly, in a 2021 retrospective study of 171 salvage laryngectomies, Sharma et al. found that nodal positivity before a patient had started initial radiotherapy or chemoradiotherapy predicted occult metastasis on univariable and multivariable analysis [16]. The study suggested that initial nodal positivity warranted offering END to patients later undergoing SLE. Fritz et al. concluded that END improves tumor control in the setting of post-radiation failure andthe presence of two or more lymph nodes harboring occult metastatic disease portends a worse prognosis [17]. In a retrospective cohort study, Farlow et al. found that elective paratracheal node dissection at the time of SLE was associated with both improved overalland disease-free survival [12].

A few recent studies have compared survival rates for END versus observation only. A 2020 systematic review and meta-analysis by Gross et al. found no statistically significant difference in overall five-year survival for patients who had END versus observation alone [8]. The primary objective of this 18-study review was to determine rates of OND, and even though the review found 12 studies comparing outcomes between END and observation alone, only three studies could be included in the meta-analysis on survival outcomes. A subsequent cohort study involving 107 patients by Gross et al. found thatEND accompanying SLE in a cN0 neck was not associated with increased survival versus observation alone after surgery [18]. Two additional systematic reviews appeared in 2019 on this subject [9,10]. The studies agreed that no significant survival advantage had yet been shown in favor of END versus observation-only patients, yet supraglottic recurrence and locally advanced tumors are factors worthy of consideration when deciding whether to proceed with END. Rates of OND are higher in these groups, and END may offer some improved survival benefits in such cases.

In a retrospective review of 125 patients with SLE, Freiser et al. reported no significant association between END and improved survival, though the study did find a significant difference in overall survival in patients with positive versus negative nodal pathology. The study suggested that END may offer prognostic information for approximately 10% of patients andthis should be discussed with the patient to decide whether to proceed with END [19]. Similarly, a retrospective study of 23 cases by Gouzos et al. found no significant survival advantage for END versus observation in cN0 necks undergoing SLE, yet END may result in a small percentage of patients being upstaged [20]. Bernard et al., in a retrospective review of 86 patients, found overall survival to be higher (p=0.037) for cN0 patients who had END accompanying SLE versus those who only had SLE and subsequent observation, but there was no significant benefit in terms of DSS or recurrence-free survival [21]. This interesting outcome may be attributable to comorbidities or unhealthy lifestyle factors leading to only fitter patients receiving END, and the study advised considering END for clinically node-negative necks.

In our study, OND was present in only 7% of pathological specimens and0.5% of the analyzed lymph nodes, which is within the range described in the literature. Advanced recurrent T-stage (rT3/rT4) was the only predictor for subclinical disease, which is consistent with previous reports [18]. We did not find tumor location to be a risk factor for OND, as has been suggested by other authors [3,18]. Of note, the surgical and observation groups had comparable oncologic outcomes in terms of RRFS and DSS. Thus, microscopic nodal disease, though present in a small percentage of patients, had limited overall impact and was unlikely the governing factor of the overall survival trends in our cohort. Along these lines, Gross et al. found that even though patients with supraglottic recurrence or advanced T classification tumors had a higher OND rate in their study, survival was not associated with END. Moreover, patients with recurrent hypopharyngeal subsites were at a higher risk for distant recurrence and death. Thus, the study concluded that survival outcomes likely hinged on underlying disease pathology, not surgical management [18].

Hilly et al. reported that END improved disease-free and overall survival in patients with locally advanced recurrent laryngeal squamous cell carcinoma (rT3 or rT4) and hypothesized that most series fail to show this advantage due to lack of stratification [22]. Our data donot support these findings as END did not confer significant survival advantages, even when properly stratifying by disease stage. However, considering the higher incidence of OND in patients with advanced stage (and the limited number of patients in most series), it is plausible to hypothesize that elective management of the neck might confer a survival advantage in this subset of patients.

Surgery in a radiated field carries an increased risk of postoperative wound complications [23,24]. Most authors agree that a modified radical neck dissection (levels I-V) is not warranted in such a setting, anda selective (lateral) neck dissection of levels II-IV is adequate according to the nodal drainage patterns described by Shah and Anderson [25]. Given the higher morbidity profile associated with formal lateral neck dissection in the salvage setting, it is certainly tempting to limit dissection to high-risk nodal basins. Indeed, several series suggest that a selective neck dissection of levels II-III, or even IIA and III, may be adequate for supraglottic carcinoma [5,26]. However, our findings do not support this approach, as microscopic nodal disease was found in all three levels of the lateral neck specimens. As such, we suggest that a formal lateral neck dissection should remain the procedure of choice for patients undergoing SLE.

Surgical manipulation of the neck may cause fibrosis or disruption of the vascular supply in the radiated neck, potentially resulting in impaired wound healing. In patients who undergo a primary pharyngeal closure without regional or free tissue transfer, END has been correlated with an increased risk of PC fistula in the post-radiation setting [27]. However, most series fail to establish this association, as the risk of disruption of the pharyngeal closure is likely multifactorial and not directly related to the neck. Our study found that PC fistula was more common in the END group, but this difference was not statistically significant, even when accounting for the type of reconstruction performed (p=0.186).

The impact of PET/CT was not thoroughly evaluated in our study. However, of the four patients with OND, only one had a preoperative PET/CT scan, which was negative for nodal disease (standardized uptake value <2). While this test has since become part of our preoperative workup, it is important to point out its relative lack of sensitivity (50%) for detecting OND [28]. Conversely, PET/CT is a valuable tool to assess clinically node-positive patients in the post-radiation setting, where it has demonstrated utility in preventing unnecessary surgical explorations [29]. Correlating with our pathological findings, we hypothesize that only one of the node-positive necks could have been identified preoperatively with a PET/CT scan as this neck had a 10 mm node. All remaining disease-positive lymph nodes were sub-centimeter and unlikely to be detected with this modality.

While this study provides valuable insights, it is crucial to acknowledge its limitations, mostly related to its retrospective design and limited access to certain data points and quality records.Since most of these patients were primarily treated in the community, data regarding the initial clinical and radiological status of the neck at presentation were inconsistent and hence not included in the analysis. Similarly, it was difficult to account for the significant variability in terms of organ preservation approach, radiation techniques, and fractionation schemes. Also, the study's single-center design may limit the generalizability of the findings, as results may be influenced by institution-specific practices or patient populations.

Though this study's two cohorts were very comparable in most aspects, surgical selection bias may always play a role as a confounding factor in a study of this nature. Moreover, the rate of chemoradiotherapy was higher in the END group, conceivably lowering the OND burden and increasing survival rates in this group. We believe such limitationsreflect the challenges and complexities intrinsic to the management of patients with recurrent cancer. Whether END is “right” for a cN0 neck is still not an easy question to answer. Elective management of the neck must still be a shared decision with the individual patient - a decision weighing patient morbidity, lifestyle, frailty, age, and those factors commonly believed to put a patient at risk for OND. Moving forward, there is a critical need for future studies to enhance the quality of evidence in this field. This can be achieved through prospective studies with larger sample sizes to improve statistical power. Despite this study’s limitations, its findings should be a valuable addition to the growing body of evidence on the subject.

Conclusions

In cN0 patients undergoing SLE, OND was present in only 7% of specimens, but positive lymph nodes were located in levels II, III, and IV. Given this indiscriminate distribution of OND, formal lateral neck dissection should be the preferred type of END to accompany SLE. An advanced recurrent stage (rT3-rT4) was the only predictor of OND in this study. END was not associated with a higher morbidity profile versus conservative management of the neck, yet the procedure conferred no measurable advantage in terms of disease control or survival, even when stratifying by tumor stage. As both groups had comparable oncologic outcomes in terms of RRFS and DSS, it is unlikely that ONDhad a significantimpact on this cohort's overall survival trends.

Notes

The authors have declared that no competing interests exist.

Author Contributions

Acquisition, analysis, or interpretation of data: Nickolas A. Alsup, Soroush Farsi, Sydney K. Blevins, Rachel Giese, Deanne King, Jumin Sunde, Emre Vural, Mauricio Moreno

Drafting of the manuscript: Nickolas A. Alsup, Soroush Farsi, Sydney K. Blevins, Rachel Giese, Emre Vural, Mauricio Moreno

Critical review of the manuscript for important intellectual content: Nickolas A. Alsup, Soroush Farsi, Deanne King, Jumin Sunde, Emre Vural, Mauricio Moreno

Concept and design: Rachel Giese, Deanne King, Emre Vural, Mauricio Moreno

Supervision: Deanne King, Jumin Sunde, Emre Vural, Mauricio Moreno

Human Ethics

Consent was obtained or waived by all participants in this study. University of Arkansas for Medical Sciences IRB issued approval 228942

Animal Ethics

Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.

References

1. Salvage laryngectomy after primary radio- and radiochemotherapy: aretrospective study. Sievert M, Goncalves M, Binder B, et al. HNO. 2021;69:47–52. [PMC free article] [PubMed] [Google Scholar]

2. Is elective neck dissection necessary in cases of laryngeal recurrence after previous radiotherapy for early glottic cancer? Deganello A, Meccariello G, Bini B, Paiar F, Santoro R, Mannelli G, Gallo O. J Laryngol Otol. 2014;128:1089–1094. [PubMed] [Google Scholar]

3. Occult nodal disease in patients with failed laryngeal preservation undergoing surgical salvage. Koss SL, Russell MD, Leem TH, Schiff BA, Smith RV. Laryngoscope. 2014;124:421–428. [PubMed] [Google Scholar]

4. Elective neck dissection for no neck during salvage total laryngectomy: findings, complications, and oncological outcome. Basheeth N, O'Leary G, Sheahan P. JAMA Otolaryngol Head Neck Surg. 2013;139:790–796. [PubMed] [Google Scholar]

5. Efficacy of diagnostic upper node evaluation during (salvage) laryngectomy for supraglottic carcinoma. Pennings RJ, Marres HA, den Heeten A, van den Hoogen FJ. Head Neck. 2009;31:158–166. [PubMed] [Google Scholar]

6. Should elective neck dissection be routinely performed in patients undergoing salvage total laryngectomy? Pezier TF, Nixon IJ, Scotton W, et al. J Laryngol Otol. 2014;128:279–283. [PubMed] [Google Scholar]

7. Lymph node positive head and neck carcinoma after curative radiochemotherapy: a long lasting debate on elective post-therapeutic neck dissections comes to a conclusion. Hermann RM, Christiansen H, Rödel RM. Cancer Radiother. 2013;17:323–331. [PubMed] [Google Scholar]

8. Elective neck dissection during salvage laryngectomy: a systematic review and meta-analysis. Gross JH, Vila PM, Simon L, Rizvi ZH, Zenga J, Jackson RS, Pipkorn P. Laryngoscope. 2020;130:899–906. [PubMed] [Google Scholar]

9. Elective neck dissection in patients with radio-recurrent and radio-residual squamous cell carcinoma of the larynx undergoing salvage total laryngectomy: Systematic review and meta-analysis. Lin DJ, Lam A, Warner L, Paleri V. Head Neck. 2019;41:4026–4035. [PubMed] [Google Scholar]

10. Elective neck dissection for salvage laryngectomy: a systematic review and meta-analysis. Lin C, Puram SV, Bulbul MG, Sethi RK, Rocco JW, Old MO, Kang SY. Oral Oncol. 2019;96:97–104. [PubMed] [Google Scholar]

11. Elective neck dissection during salvage laryngectomy. Yao M, Roebuck JC, Holsinger FC, Myers JN. Am J Otolaryngol. 2005;26:388–392. [PubMed] [Google Scholar]

12. Elective paratracheal lymph node dissection in salvage laryngectomy. Farlow JL, Birkeland AC, Rosko AJ, et al. Ann Surg Oncol. 2019;26:2542–2548. [PMC free article] [PubMed] [Google Scholar]

13. Pharyngocutaneous fistula after total laryngectomy: a single-institution experience, 2001-2012. Benson EM, Hirata RM, Thompson CB, et al. Am J Otolaryngol. 2015;36:24–31. [PMC free article] [PubMed] [Google Scholar]

14. Management of the N0 neck in recurrent laryngeal squamous cell carcinoma. Bohannon IA, Desmond RA, Clemons L, Magnuson JS, Carroll WR, Rosenthal EL. Laryngoscope. 2010;120:58–61. [PubMed] [Google Scholar]

15. The role of elective neck dissection during salvage surgery in head and neck squamous cell carcinoma. Lee DJ, Kwon KH, Chung EJ, Park IS, Kim JH, Rho YS. Acta Otolaryngol. 2013;133:886–892. [PubMed] [Google Scholar]

16. Is routine neck dissection warranted at salvage laryngectomy? Sharma S, Chaukar DA, Bal M, D'Cruz AK. J Laryngol Otol. 2021;135:785–790. [PubMed] [Google Scholar]

17. Recurrence rates after selective neck dissection in the N0 irradiated neck. Fritz MA, Esclamado RM, Lorenz RR, Wood BG, Lavertu P, Strome M. Arch Otolaryngol Head Neck Surg. 2002;128:292–295. [PubMed] [Google Scholar]

18. Oncologic outcomes after clinically node-negative salvage laryngectomy. Gross JH, Patel MR, Switchenko JM, et al. JAMA Otolaryngol Head Neck Surg. 2023;149:24–33. [PMC free article] [PubMed] [Google Scholar]

19. Complications and oncologic outcomes following elective neck dissection with salvage laryngectomy for the N0 neck. Freiser ME, Ojo RB, Lo K, Saint-Victor S, Bollig C, Nayak CS, Sargi ZB. Am J Otolaryngol. 2016;37:186–194. [PubMed] [Google Scholar]

20. Elective neck dissection for the node-negative neck during salvage laryngectomy: an analysis of survival outcomes and complication rates. Gouzos M, Dale O, Sethi N, Foreman A, Krishnan S, Hodge JC. J Laryngol Otol. 2019;133:788–791. [PubMed] [Google Scholar]

21. Elective neck treatment during salvage (pharyngo) laryngectomy. Bernard SE, Wieringa MH, Meeuwis CA, Baatenburg de Jong RJ, Sewnaik A. Eur Arch Otorhinolaryngol. 2019;276:1127–1133. [PubMed] [Google Scholar]

22. Elective neck dissection during salvage total laryngectomy--a beneficial prognostic effect in locally advanced recurrent tumours. Hilly O, Gil Z, Goldhaber D, et al. Clin Otolaryngol. 2015;40:9–15. [PubMed] [Google Scholar]

23. Surgical complications of salvage total laryngectomy following concurrent chemoradiotherapy. Furuta Y, Homma A, Oridate N, et al. Int J Clin Oncol. 2008;13:521–527. [PubMed] [Google Scholar]

24. Neck dissection after chemoradiotherapy: timing and complications. Goguen LA, Chapuy CI, Li Y, Zhao SD, Annino DJ. Arch Otolaryngol Head Neck Surg. 2010;136:1071–1077. [PubMed] [Google Scholar]

25. The impact of patterns of nodal metastasis on modifications of neck dissection. Shah JP, Andersen PE. Ann Surg Oncol. 1994;1:521–532. [PubMed] [Google Scholar]

26. Superselective neck dissection: rationale, indications, and results. Suárez C, Rodrigo JP, Robbins KT, et al. Eur Arch Otorhinolaryngol. 2013;270:2815–2821. [PubMed] [Google Scholar]

27. Pharyngocutaneous fistula after total laryngectomy: systematic review of risk factors. Dedivitis RA, Aires FT, Cernea CR, Brandão LG. Head Neck. 2015;37:1691–1697. [PubMed] [Google Scholar]

28. 18F-fluorodeoxyglucose positron emission tomography to evaluate cervical node metastases in patients with head and neck squamous cell carcinoma: a meta-analysis. Kyzas PA, Evangelou E, Denaxa-Kyza D, Ioannidis JP. J Natl Cancer Inst. 2008;100:712–720. [PubMed] [Google Scholar]

29. Observation versus neck dissection for positron-emission tomography-negative lymphadenopathy after chemoradiotherapy. Khodayari B, Daly ME, Bobinski M, Farwell DG, Shelton DK, Chen AM. Laryngoscope. 2014;124:902–906. [PubMed] [Google Scholar]

Articles from Cureus are provided here courtesy of Cureus Inc.

Elective Neck Dissection in Patients Undergoing Salvage Laryngectomy: Outcomes, Complications, and Considerations (2024)

References

Top Articles
Latest Posts
Article information

Author: Greg O'Connell

Last Updated:

Views: 5688

Rating: 4.1 / 5 (62 voted)

Reviews: 93% of readers found this page helpful

Author information

Name: Greg O'Connell

Birthday: 1992-01-10

Address: Suite 517 2436 Jefferey Pass, Shanitaside, UT 27519

Phone: +2614651609714

Job: Education Developer

Hobby: Cooking, Gambling, Pottery, Shooting, Baseball, Singing, Snowboarding

Introduction: My name is Greg O'Connell, I am a delightful, colorful, talented, kind, lively, modern, tender person who loves writing and wants to share my knowledge and understanding with you.