Results
Patient and Treatment Characteristics
A total of 300 patients were presented to the HNMDTB during the study period. Of these, 14 refused treatment and 33 opted for treatment at another institution, leaving 253 who received treatment at the MEDVAMC. Of these, 6 patients died prior to or during treatment delivery, 10 opted for observation, and 15 opted for palliative systemic treatment.
A total of 212 patients received curative intent treatment during the study period. For these patients, the interval from referral to treatment initiation averaged 63 days (median = 50 days), while the interval from diagnosis to treatment initiation averaged 47 days (median = 40 days)
(Table 1). One hundred thirty patients were treated surgically of which 57 patients (44%) received PORT. For this group of patients, which received multimodality treatment, time from surgery to PORT initiation averaged 43 days (median = 41 days). A majority (47/55; 85%) patients were treated within a 100-day treatment package time (TPT) and 37/57 (65%) initiated PORT within 6 weeks of surgery.
HNSCC Treatment Delivery
A total of 142 patients were diagnosed with HNSCC; 121 (85%) patients were compliant with treatment recommendations for treatment selection, intensity and timeframe (Table 2). Among new, previously not evaluated patients, the most common reason for referral was a mass or abnormal imaging (n=63), followed by hoarseness (n=25), and dysphagia/odynophagia (n=16). Only 3 patients had a known cancer diagnosis at the time of referral to Oto-HNS. Compliance was defined as: (1) agreeing to one of the HNMDTB treatment options presented to the patient and (2) compliance with diagnostic and therapeutic appointments designed to initiate timely care. Among all HNSCC patients, time from diagnosis to treatment initiation averaged 46 days (median = 41 days); for compliant patients, time from diagnosis to treatment initiation decreased to 44 days (median = 40 days). Among compliant HNSCC patients, 54 were treated surgically, followed by PORT in 24 patients. Of these 21/24 had a TPT of 100 days, and 18/24 initiated PORT within 6 weeks of surgery. For the 3 patients whose TPT extended past 100 days, 1 patient required unexpected extractions postoperatively, 1 had an acute episode of cholecystitis that required treatment at an outside hospital, and 1 presented with a concomitant visual stroke that required intervention prior to adjuvant treatment initiation. With the exception of these 3 patients, all other patients, 21/24 initiated PORT within 7 weeks of surgery.
A majority of all compliant HNSCC (67/121) patients were treated nonsurgically, and most (n = 52) were treated with concurrent chemo-radiation. Among these patients, time from referral to treatment initiation averaged 64 days (median = 63 days), and time from diagnosis to treatment initiation averaged 52 days (median = 49 days). For patients with early stage disease who underwent radiation alone, time from diagnosis to treatment initiation was substantially reduced (mean = 38 days, median = 33 days). Overall, patients who underwent surgical treatment were able to initiate treatment faster compared to patients who underwent radiation-based treatment (diagnosis – treatment mean = 36 days vs 49 days; P < .05). This effect was maintained even for patients who required PORT (40 days vs 49 days; P < .05).
We next evaluated treatment initiation and delivery parameters as a function of disease site and stage. Patients with a diagnosis of laryngeal/hypopharyngeal SCC had mean time from referral to treatment of 65 days (median= 62 days) and mean time from diagnosis to treatment of 34 days (median= 33 days). Patients with a diagnosis of oropharyngeal cancer had a mean time from referral to treatment for 60 days (median= 56 days) and time from diagnosis to treatment of 49 days (median= 48 days). Patients who required radiation alone had a shorter diagnosis to treatment time compared with patients who required chemo-radiation (P < .01). Nodal status (N0 vs N+) was associated with increased diagnosis to treatment time (P < .01), but site (larynx/hypopharynx vs oropharynx) and T-classification were not (P = .48, P = 0.11, respectively). For patients which underwent surgical treatment, site (larynx/hypopharynx vs oral cavity/oropharynx) was associated with shorter time from diagnosis to treatment (24 vs 43 days; P = .02). Need for adjuvant treatment, nodal status, and T classification were not associated to differential time from diagnosis to treatment intervals (P = 0.39, P = .82, P = .73, respectively).
Data were available from 11 HNSCC patients (2 nasopharynx, 8 oropharynx, 1 larynx) which received chemo-radiation with curative intent at a non-MEDVAMC facility during the study period arranged through the Veteran Choice Program (VCP) during the study period. For these patients, mean time from diagnosis to treatment was 70 days (median= 73 days), and time from HNMDTB to treatment initiation was 65 days (median= 64 days).
Discussion
In our study, utilization of the tracking tool and closed-loop communication facilitated rapid treatment initiation (diagnosis-treatment mean=44 days) and delivery. Compliance with treatment package time <100 days was 88%; compliance with initiation of adjuvant radiation within 6 weeks of surgery was 75%. Timely initiation and delivery of multimodality cancer treatment can be facilitated by integration among participating services and by the presence of a fully integrated health care delivery system.
Successful diagnosis and treatment of a single advanced stage HNSCC patient generally requires between 12 and 15 specialty trained individuals (physicians, speech pathologists, radiation physicists, registered dietitians, etc) generating an extremely complex clinical challenge. In a fragmented health care system, such as that encountered by the majority of the US population, this process can sometimes become an insurmountable challenge. Published literature demonstrates an escalating crisis for a majority of HNSCC patients treated in the United States as it relates to treatment-related metrics.1,8,10,11 This is particularly problematic given the proven impact of treatment delays, treatment breaks, and incomplete treatment delivery on HNSCC outcomes.10,12-14 Most recent datasets indicate that the effect sizes associated with these parameters easily dwarf gains in HNSCC survival obtained from technological and scientific advances in surgical techniques, radiation techniques, and development of novel systemic therapeutic strategies for this disease.9,15-18
Fragmentation of cancer care has been associated with substandard HNSCC treatment delivery and remains common even in the United States.19-21 However, we have found that diagnosis and timely treatment of HNSCC, even within an integrated health delivery system with all components of a multidisciplinary team and a single EMR within a physical plant, still remains challenging.1 However, integrated health systems provide a unique opportunity, both for study and to improve treatment-related metrics. Over the study period, delivery of multimodality treatment within 100 day TPT occurred in 88% of patients compared with our historical comparator of 68%.1 Compliance with a 6-week interval between surgery and PORT of 75% was substantially higher than our historical comparator of 42%.1 These numbers also compare favorably to data from national US databases, but remain significantly below our expectations as a multidisciplinary treatment group.11,22,23 In addition to these basic metrics, we observed several patterns of treatment delivery that can be used to further refine and improve diagnostic and therapeutic strategies.
Surgical patients consistently demonstrate the fastest time from referral to treatment and diagnosis to treatment of any group of patients. This pattern remains consistent even when patients present with advanced stage disease that require adjuvant treatment. Several factors likely contribute to this. First, HNSCC cancer referrals at our institution are initiated through the surgical team (Oto-HNS). Second, surgical teams (Oto-HNS ablative, Oto-HNS reconstructive, OMFS) are able to coordinate surgical care in an expeditious manner. Third, planning associated with patient disposition and nutritional requirements (ie, gastrostomy placement) can be facilitated during the inpatient postoperative period. In contrast, for patients receiving nonsurgical treatment, there are multiple interventions that all must occur prior to treatment initiation (ie, dental extractions, gastrostomy placement). This can be particularly difficult in patients with advanced stage disease who require chemo-radiation. Despite our efforts to date, we have been unable to reduce mean time from diagnosis to treatment for this group to under 45 days, which is our current goal. Patients which require single modality radiation treatment can generally initiate treatment rapidly; this is particularly true for patients with early stage laryngeal disease who do not generally require dental extractions or evaluation for gastrostomy placement.
Utilization of the VCP can play an important role for patients that live far away from their primary VHA institution, but it does not improve treatment metrics and may actually delay treatment initiation, since it requires additional work-up and evaluation at the secondary institution. This is to be expected since utilization of VCP will often lead to fragmentation of care, particularly for chemo-radiation based regimens that are resource and facility intensive. We contend that, rather than relying on VCP, additional efforts and resources within the VHA should be dedicated toward facilitating transportation, coordination of care delivery, and housing for patients who are otherwise VCP candidates.
Moreover, utilization of a real-time tracking tool and closed-loop communication allows for rapid interventions for individual patients, coordination of appointments, and minimization of diagnostic and treatment delays. At an institutional level, utilization of the tracking tool allows us to generate quarterly and yearly reports for the entire multidisciplinary treatment team, track progress in real time, and discuss performance with institutional administration to optimize resource utilization and allocation.
There are 2 natural follow-up questions regarding implementation of such an approach. First, what are the relative costs associated with implementation? Implementation of the described approach was specifically designed to obviate the need for additional personnel (ie, dedicated patient navigator) since manpower is a significant cost generator and notoriously difficult to secure across various medical care delivery systems. No additional testing was implemented as part of the described approach, which could impact cost. Second, what are the benefits with regard to oncologic outcomes secondary to implementation? Our data are not mature enough (we do not have 2-year follow-up on the entire patient cohort) and our dataset large is not yet large enough to definitively answer this question. Since oncologic outcomes are site and stage specific, we will need to acquire a substantially larger patient dataset prior to measuring improvements in outcomes compared with our historical controls. However, the published datasets for head and neck cancer from other groups have shown a very substantial gain in survival as a function of treatment package time.23
Across all patient subsets, time from referral to diagnosis ranges from 10 to 14 days. Our institutional goal is to reduce this time frame to 5 working days, through additional coordination of in-clinic and same-day biopsy via sampling of primary tumor and/or fine needle aspiration of cervical nodes. In addition, streamlined referral patterns are essential to expediting evaluation through development of clinical pathways designed to identify cancer patients among the wide variety of etiologies which present with similar initial symptoms.24-27 Further coordination of treatment can incorporate development of true multidisciplinary clinics, which have been shown to impact both care delivery and survival.28 However, this requires significant buy-in and coordination of multiple distinct services, which can remain difficult in the current clinical environment. These processes will require dedicated Lean Six Sigma methodology to be incorporated into our tracking tool and development of a parallel resource utilization and cost analysis designed to provide systemic optimization.
Conclusion
We developed a prospective tracking tool available to providers and clinic staff to track patients from initial referral through diagnosis and treatment completion and used it to evaluate clinical care delivery. This resulted in timely initiation and delivery of multimodality cancer treatment via integration among participating services and by the presence of a fully integrated health care delivery system.
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