Abstract
Background:
We analysed the outcomes of 726 cases of primary head and neck cancer patients managed between 1996 and 2008, including those managed in the multidisciplinary clinic or team setting (MDT) and those managed outside of an MDT by individual disciplines (non-MDT) in the same institution.
Methods:
Data were collected from the Hospital Based Cancer Registry and a database within the Head and Neck Cancer Clinic. Univariable comparisons and multivariable analyses were performed using a logistic regression model. Survival by staging was analysed. Comparisons of management and outcomes were made between MDT and non-MDT patients.
Results:
395 patients (54%) had been managed in the MDT vs 331 patients (46%) non-MDT. MDT patients were more likely to have advanced disease (likelihood ratio χ2=44.7, P<0.001). Stage IV MDT patients had significantly improved 5-year survival compared with non-MDT patients (hazard ratio=0.69, 95% CI=0.51–0.88, P=0.004) and more synchronous chemotherapy and radiotherapy (P=0.004), and the non-MDT group had more radiotherapy as a single modality (P=0.002).
Conclusions:
The improved survival of MDT-managed stage IV patients probably represents both the selection of multimodality treatment and chemotherapeutic advances that these patients received in a multidisciplinary team setting by head and neck cancer specialists as opposed to cancer generalists in a non-MDT setting.
Keywords: multidisciplinary clinic, primary head and neck cancer, survival, cancer management
Head and neck (H&N) cancers are a complex, heterogeneous group of malignancies, which require multifaceted treatment strategies and the input of a number of specialities. To facilitate timely and appropriate evidence-based management of H&N cancer cases, most centres have now established multidisciplinary team meetings (MDT) in which each of the medical and allied health specialities are represented so that accurate tumour staging and treatment plans can be best tailored to individuals (Expert Advisory Group on Cancer, 1995; Taylor et al, 2010).
A challenge for service providers is the lack of level I evidence in H&N cancer management. An MDT provides a combination of evidence-based management, local experience and availability of treatment modalities. The assumed benefits of the MDT include improvements in communication between health professionals, coordination and continuity of care and better clinical outcomes (Westin and Stalfors, 2008). Despite this, MDTs are costly, and their benefits in improving outcomes in the management of H&N cancer have not been widely studied (Westin and Stalfors, 2008; Taylor et al, 2010).
The Sir Charles Gairdner Hospital Based Cancer Registry (HBCR) was started in 1996 for systematic collection of data on patients with certain primary cancers, including H&N malignancies. A weekly H&N Cancer MDT is attended by otolaryngologists, plastic surgeons, radiation and medical oncologists, dentists, dieticians, speech pathologists, radiologists and a nurse cancer care coordinator. The MDT reviews each new patient's diagnosis, imaging, medical and social factors, confirms staging and formulates a management plan. After initial treatment, cases are reviewed again at the MDT whenever further treatment is planned. The MDT follows the National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology.
Despite the availability of the MDT at SCGH, we recognised that a large proportion of newly diagnosed patients are still managed by individual disciplines outside of the MDT, which included clinicians who were in fact generalists with an interest in H&N cancer but also clinicians who were members of the MDT.
The primary aim of our study was to analyse the differences in outcome and survival data between these two groups of H&N cancer patients managed at SCGH.
Materials and methods
A retrospective 12-year analysis was undertaken, involving data from the SCGH HBCR and SCGH MDT. This study was approved by the Sir Charles Gairdner Human Research Ethics Committee (QI no 2444). Patients attending the MDT were entered into a Microsoft Access database and were also included in the HBCR. Newly diagnosed primary H&N cancer patients presenting to the hospital for treatment (MDT and non-MDT) from 1 January 1996 until 1 February 2009, whose complete hospital and HBCR records were obtainable, were included.
Patient demographics, cancer site, staging, treatment and outcomes of different modalities and combinations of therapies were compared. All cases were followed-up for death by the Registrar General of Western Australia. Statistical methods for analysis included Cox proportional hazards regression and likelihood ratio χ2-tests (LRχ2). Analysis of survival was used to estimate the hazard ratio (HR), with associated 95% confidence intervals and P-values. For all analyses, a P-value <0.05 was interpreted as statistically significant, but for univariable Cox regression results, the sequential rejection method of Holm was used to correct the critical significance level for multiple comparisons (Holm, 1979). Data analysis was conducted using the Stata package (StataCorp, 2009. Stata Statistical Software Release 11; StataCorp LP, College Station, TX, USA).
Results
A total of 726 newly diagnosed patients fulfilled the inclusion criteria (see Figure 1). MDT patients were younger by about 2 years of age on average (P=0.046), which is a potential source of bias, as increasing age at diagnosis is associated with a significant increase in risk of death (HR=1.04, P<0.001). Survival times were further analysed for stage I–IV groups individually, and there was no significant difference in outcomes for stages I–III between MDT- and non-MDT-treated patients (see Table 1). The numbers in each of these stages were too small to provide adequate statistical power. There was, however, a statistically significant difference in survival for stage-IV patients who were managed by the MDT (HR=0.69, 95% CI=0.51–0.88, P=0.004; see Figure 2). Furthermore, patients seen in the multidisciplinary clinic were more likely to have advanced disease (LRχ2=44.7, P<0.001), which would produce bias, suggesting greater risk for that subset of patients, if stage was not controlled for in the analysis.
Table 1. H&N cancers, 1996–2008.
Seen at MDT
|
Difference between MDT and non-MDT | Difference in survival | ||
---|---|---|---|---|
No (%) | Yes (%) | P | P | |
Tumour site | ||||
Oral cavity | 49 (14.8) | 92 (23.3) | 0.003 | 0.761 |
Oropharynx | 74 (22.3) | 116 (29.4) | 0.03 | 0.665 |
Nasopharynx | 17 (5.12) | 11 (2.78) | 0.103 | 0.044 |
Hypopharynx | 16 (4.82) | 13 (3.29) | 0.295 | <0.001 |
Larynx | 93 (28.0) | 90 (22.8) | 0.106 | 0.048 |
Nasal cavity/sinus | 42 (12.7) | 39 (9.87) | 0.237 | 0.01 |
Salivary glands | 36 (10.8) | 25 (6.33) | 0.029 | 0.012 |
Other | 5 (1.51) | 9 (2.28) | 0.446 | 0.174 |
Total | 332 (100) | 395 (100) | ||
Treatment modality | <0.001 | |||
Chemotherapy only | 2 (0.87) | 2 (0.76) | 0.862 | 0.009 |
Surgery only | 31 (13.4) | 42 (16.0) | 0.562 | 0.08 |
Radiotherapy only | 120 (52.0) | 83 (31.7) | <0.001 | 0.028 |
Radiotherapy+ chemotherapy | 27 (11.7) | 28 (10.7) | 0.002 | 0.572 |
Radiotherapy+ chemotherapy+surgery | 16 (6.9) | 18 (6.9) | 0.868 | 0.189 |
Synchronous chemotherapy | 35 (15.2) | 89 (34.0) | <0.001 | 0.039 |
Total | 231 (100) | 262 (100) |
Abbreviations: H&N=head and neck; MDT=multidisciplinary team.
Grouping according to the UICC (Union for International Cancer Control) TNM version 6 and treatment pattern overall.
Analysis of therapy variables suggests that the multidisciplinary clinic has a substantial influence on treatment decisions. Patients seen in the multidisciplinary clinic were significantly less likely to receive radiotherapy alone for positive nodes (LRχ2=16.08, P<0.001), significantly less likely to receive surgical treatment alone for their cancer (LRχ2=10.74, P<0.001) and positive nodes (LRχ2=19.42, P<0.0001). There was an increasing incidence in the use of combination chemotherapy and radiotherapy from 12.5% in 1996 to 45% in 2008 (Cuzick test for trend, P<0.001; Cuzick, 1985) and a concomitant decline in the use of radiotherapy alone from 27.1% in 1996 to 15% in 2008 (Cuzick test for trend, P<0.001). Synchronous chemotherapy and radiotherapy increased from 2.1% in 1996 to 42.5% in 2008 (Cuzick test for trend, P<0.001). Combination surgery, chemotherapy and radiotherapy increased from 6.3% in 1996 to 12.5% in 2008. There was a clear difference in treatment modalities in the MDT vs non-MDT group. The MDT has more synchronous chemotherapy and radiotherapy (P=0.004) and the non-MDT group has significantly more radiotherapy as a single modality (P=0.002).
Discussion
Despite widespread implementation of MDTs in cancer management in a number of countries, robust evidence to suggest improvement in outcomes in patients with H&N cancer is lacking, which contributes to scepticism regarding MDT patient management. The literature suggests that MDT time delays and expense are some potential reasons why treating doctors believe that early-stage H&N cancers can be successfully managed outside of an MDT, principally referring patients with advanced malignancy (Taylor and Ramirez, 2009). Apart from influencing treatment decisions, MDTs have also been shown to improve cancer staging and subsequently patient outcomes (Stephens et al, 2006). Consequences of non-MDT management include the possibility of less accurate staging, lack of allied health input and loss to follow-up, due to the lack of coordinated care, as is available in MDT settings. A search of the medical literature reveals a number of cohort studies from single centres or regions that have demonstrated survival benefits linking MDT management in a range of malignancies. (Junor et al, 1994; Birchall et al, 2004; Morris et al, 2006; Stephens et al, 2006). However, they are subject to bias and therefore it is difficult to say whether results from one centre can be extrapolated to another centre (Expert Advisory Group on Cancer, 1995). Nevertheless, in the absence of level I or II data, these studies form the basis of clinical guideline formulation and inform current best practice.
A surprisingly high proportion of H&N cancer patients at SCGH were managed independently of the MDT by various disciplines, including otolaryngology, plastic surgery, general surgery, radiation oncology and medical oncology. This presented a unique opportunity to analyse the potential differences in management and outcomes between the two cohorts of patients. Investigating the reasons why some of our colleagues never referred or inconsistently referred all H&N cancer patients to the MDT was beyond the scope of this study. However, we do acknowledge that this may be a potential source of bias in reporting our results.
Our results indicate two principal findings. First, there is a significant increase in survival for patients managed through the MDT when stage, age at diagnosis and year of diagnosis are controlled for in the analysis. Second, the use of a selection of multimodality therapy treatment options is significantly associated with management of patients by the MDT and it seems likely that this is also the cause of the reduced risk of death for MDT. These findings may be explained by the fact that H&N cancer specialists (MDT) as opposed to cancer generalists (non-MDT) are involved in management and that a large proportion of the non-MDT patients were treated more than 10 years ago when advances in chemotherapeutic therapies were not yet present. The adoption of these recent chemotherapeutic advances in the MDT may account for increased survival of stage-IV MDT-treated patients.
The results of this study have been openly discussed with all our colleagues in our institution and we have recommended adherence to evidence-based guidelines and management of all H&N cancer cases in an MDT irrespective of staging. In the last 12 months since the release and discussion of these findings, opinions and viewpoints regarding the H&N cancer MDT have shifted to an increase in patient referrals of all cancer stages. A repeat audit of patient outcomes in the future is recommended.
References
- Birchall M, Bailey D, King P (2004) Effect of process standards on survival of patients with head and neck cancer in the south and west of England. Br J Cancer 91: 1477–1481 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cuzick J (1985) A Wilcoxon-type test for trend. Stat Med 4: 87–90 [DOI] [PubMed] [Google Scholar]
- Expert Advisory Group on Cancer (1995) A Report by the Expert Advisory Group on Cancer to the Chief Medical Officers of England and Wales. A Policy Framework for Commissioning Cancer Services – the Calman-Hine Report. Department of Health: London [Google Scholar]
- Holm S (1979) A simple sequentially rejective multiple test procedure. Scand Stat Theory Appl 6: 65–70 [Google Scholar]
- Junor EJ, Hole DJ, Gillis CR (1994) Management of ovarian cancer: referral to a multidisciplinary team matters. Br J Cancer 70: 363–370 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morris E, Haward RA, Gilthorpe MS, Craigs C, Forman D (2006) The impact of the Calman-Hine report on the processes and outcomes of care for Yorkshire's colorectal cancer patients. Br J Cancer 95: 979–985 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stephens MR, Lewis WG, Brewster AE, Lord I, Blackshaw GR, Hodzovic I, Thomas GV, Roberts SA, Crosby TD, Gent C, Allison MC, Shute K (2006) Multidisciplinary team management is associated with improved outcomes after surgery for esophageal cancer. Dis Esophagus 19: 164–171 [DOI] [PubMed] [Google Scholar]
- Taylor C, Munro AJ, Glynne-Jones R, Griffith C, Trevatt P, Richards M, Ramirez AJ (2010) Multidisciplinary team working in cancer: what is the evidence? Br Med J 340: 743–745 [DOI] [PubMed] [Google Scholar]
- Taylor C, Ramirez AJ, on behalf of the Cancer Research UK Promoting Early Presentation Group (2009) Multidisciplinary Team Members' Views about MDT Working: Results from a Survey Commissioned by the National Cancer Action Team. National Health Service: London [Google Scholar]
- Westin T, Stalfors J (2008) Tumour boards/multidisciplinary head and neck cancer meetings: are they of value to patients, treating staff or a political additional drain on healthcare resources? Curr Opin Otolaryngol Head Neck Surg 16: 103–107 [DOI] [PubMed] [Google Scholar]