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This phase II component of a multi-institutional phase II/III randomized trial assessed the feasibility and preliminary efficacy of acupuncture-like transcutaneous electrical nerve stimulation (ALTENS) in reducing radiation-induced xerostomia.
Head and neck cancer patients who were 3–24 months from completing radiotherapy ± chemotherapy (RT±C) and experiencing xerostomia symptoms with basal whole saliva production ≥0.1 ml/min and without recurrence were eligible. Patients received twice weekly ALTENS sessions (24 over 12 weeks) using a Codetron™ unit. The primary objective assessed the feasibility of ALTENS treatment. A patient was considered compliant if 19/24 ALTENS were delivered, with a targeted 85% compliance rate. Secondary objectives measured treatment-related toxicities and ALTENS effect on overall radiation-induced xerostomia burden using the University of Michigan Xerostomia-Related Quality of Life Scale (XeQOLS).
Of 48 accrued patients, 47 were evaluable. Median age was 60 years; 84% were male, 70% completed RT±C for > 12 months and 21% had received prior pilocarpine. All ALTENS sessions were completed in 34 patients, but 9 and 1 completed 20–23 and 19 sessions respectively, representing a 94% total compliance rate. 6-month XeQOLS scores were available for 35 patients; 30 (86%) achieved a positive treatment response with a mean reduction of 35.9% (SD 36.1). Five patients developed grade 1–2 gastrointestinal toxicity and one had grade 1 pain event.
ALTENS treatment for radiation-induced xerostomia can be uniformly delivered in a cooperative multicenter setting and has possible beneficial treatment response. Given these results, the phase III component of this study was initiated.
Xerostomia remains a common complication of radiation treatment for head and neck cancers, despite the introduction of newer radiation treatment techniques such as intensity-modulated radiation therapy (IMRT). In one prospective study, over 30% of patients treated with IMRT still reported RTOG grade 2 or higher xerostomia symptoms at six months after completion of treatment 1. The presence of xerostomia continues to adversely affect patients’ quality of life and, as such, the optimum management of this complication is under active investigation. Treatment with saliva substitutes and stimulation of salivary flow by pharmacological methods provides some symptomatic relief but no long lasting effect once active treatment is discontinued. Moreover, the administration of pharmacological methods is sometimes limited by associated adverse cholinergic side effects rendering treatments intolerable for the patient 2.
A single institutional phase II trial conducted at McMaster University (Hamilton, Ontario, Canada) suggested that non-invasive acupuncture-like transcutaneous nerve stimulation (ALTENS) on selected sets of acupuncture points increases whole salivary production and reduces radiation-induced xerostomia symptoms, with the benefits sustained for more than 6 months to one year 3. Patients reported an improvement in tongue dryness, speech, swallowing and overall comfort of the mouth. Consistency of saliva and oral mucous was also improved and associated with an improvement in taste. These positive results support the hypothesis that ALTENS treatment of selected acupuncture points based on traditional Chinese medicine principles may be effective in managing radiation-induced xerostomia symptoms. Ideally, a phase III placebo-controlled trial should be undertaken to further evaluate this hypothesis. However, the use of sham ALTENS treatment as a placebo is not possible since ALTENS treatment necessitates the induction of a strong, but subnoxious sensation. The use of low intensity stimulation, or stimulating locations that are not acupuncture points, may still induce an increase in endorphin release that may indirectly affect salivary function. Therefore, a randomized trial that compares ALTENS treatment with the current standard pharmaceutical intervention, that is oral pilocarpine, was considered acceptable to evaluate the comparative effectiveness and adverse effects of ALTENS treatment for radiation-induced xerostomia.
Since there was no data regarding the feasibility of ALTENS delivery in a multicenter setting, a phase II trial component aimed to evaluate this feasibility issue was deemed necessary prior to the start of the phase III component. This report summarizes the phase II results of this ongoing trial assessing the feasibility and potential utility of ALTENS in reducing radiation-induced xerostomia in a cooperative group setting.
This study was coordinated by the Radiation Therapy Oncology Group (RTOG) and performed with the approval of the institutional review board for human research at each participating institution.
The primary objective of this phase II study was to evaluate the feasibility of ALTENS treatments in a cooperative group setting. The secondary objectives were to determine ALTENS toxicities, and to assess preliminary efficacy of ALTENS by assessing xerostomia-related quality of life.
Patients were eligible if they had a histologically confirmed diagnosis of head and neck cancer and had received radical radiation therapy, standard or IMRT, plus or minus chemotherapy, 3 months or more but less than 2 years from the time of study enrollment; no evidence of disease recurrence based on clinical examination, nasolaryngopharyngeal scope evaluation and imaging studies 8 weeks prior to enrollment; residual salivary function with unstimulated (basal) whole saliva production (WSP) equal or greater than 0.1 ml/min (having refrained from eating or drinking oral fluid for 2 hours prior to assessment); and had provided informed written consent. Use of pilocarpine or cevimeline was discontinued at least 2 weeks prior to enrollment. Patients were excluded if they were females who were pregnant, or had unstable cardiac disease, a pacemaker, or a Zubrod performance status greater than 2.
ALTENS treatments were administered with a Codetron™ (model 902-C, EHM Rehabilitation Technologies Ltd., Ontario, Canada) TENS units and Karaya electrode pads. This particular TENS device allows user to change stimulation parameters including frequency, wave form and intensity of stimulation. It also differs from conventional TENS units that it embeds a random circuit that enables random switching among six electrodes to prevent brain habituation to continuous stimulation 4. A pre-selected group of acupuncture points including live electrodes on bilateral SP6, ST36, LI4, and the ground electrode on CV24, was stimulated, Figure 1 and Photo 1. Locations of the acupuncture points were based on previous literature, Table 1 3,5. Square pulses of 250 millisecond duration were delivered in trains with a 4 Hz repetition rate. One acupuncture point was stimulated for 10 seconds at a time. CV24, as the site for the ground electrode, was stimulated throughout the whole treatment session. Intensity of stimulation (between level 3 to 6 on the machine) was adjusted to produce a deep strong, mild aching sensation at each acupuncture point. Random switching among electrodes was employed. ALTENS treatment was commenced within 14 days after study registration. All patients received twice weekly ALTENS sessions (20 minutes stimulation per session) for a total of 24 sessions given in 12 weeks, and no further sessions were allowed after 12 weeks. A maximum of 2 weeks without treatment was allowed and all outstanding sessions were administered in the remainder of the 12 week period, not to exceed 3 sessions per week. All treatment sessions were delivered at RTOG participating academic and community-based institutions.
Staff who administered the ALTENS at each institution for this study received training in ALTENS treatment delivery at the biannual RTOG meetings prior to study recruitment. Slides of training materials and a training video were posted on the RTOG website for easy access online. For each enrolled patient, electrode pad positions on the acupuncture points were recorded using digital photographs that were sent electronically to the principal investigator (R. Wong) for rapid approval before the third treatment session.
Preliminary efficacy of ALTENS treatment was assessed using the self-reported University of Michigan Xerostomia-Related Quality of Life Scale (XeQOLS). This scale contains 15 items covering four major domains of oral health-related quality of life including physical (4 items), personal/psychological (4 items), social functioning (3 items) and pain/discomfort issues (4 items) 6. Each item is scored on a 5 point (0–4) Likert-like scale with higher scores indicating increased xerostomia burden. An overall score is the average of the average scores of each domain and can range from 0 to 4. High reproducibility and sensitivity in using this scale were validated in previous trials, and strong correlation with salivary flow was demonstrated 7, 8, 9, 10, 11. The XeQOLS was administered at baseline (study registration) and 6 months after study enrollment.
Acute adverse events (AEs) were assessed per the National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 [NCI-CTCAE v3], (MedDRA version 6) at each treatment session and follow up assessment. The incidence of the worst grade toxicity sustained up to 90 days from treatment initiation was recorded as an acute toxicity event. In the event of a grade 3 skin reaction occurring at a acupuncture point (except CV24), the point would not be treated until reaction became grade 1. If CV24 developed grade 3 skin reaction, ALTENS was held until the reaction became grade 1.
The primary objective of the phase II component of this study was to evaluate the feasibility of ALTENS treatments in a cooperative group setting. Feasibility of ALTENS treatment was determined by patient compliance. A patient was considered compliant if 19 out of 24 treatment sessions were successfully delivered within the 12 week period. Fleming’s two-stage design was used to evaluate treatment compliance to allow early evaluation 12. Using a successful target compliance rate of 80%, statistical power of 0.87 and a type I error rate of 0.13, it was determined that 13 patients were needed for the first stage analysis. If there were less than 9 compliant patients, ALTENS treatment would be deemed not feasible. If all 13 patients were compliant, treatment would be immediately accepted as feasible. If there were between 9 to 12 compliant patients, a second stage analysis with 39 evaluable patients would be required. If 31 or more patients were compliant in the second stage analysis, the treatment would be deemed feasible. Forty-five patients were targeted to allow for an 8% ineligibility/lost rate.
Secondary objectives were to assess treatment-related toxicities and to evaluate the preliminary efficacy of ALTENS as measured by the XeQOLS 6. In terms of patient-reported xerostomia, a positive treatment response was defined as a reduction of at least 20% from baseline to 6 months in the XeQOLS. Four and 10 patients in the first and second stage analysis, respectively, had to show positive treatment response to proceed to the phase III component of the study.
From September 2008 to October 2009, nine RTOG member institutions recruited 48 patients into the phase II component of this study. Forty-seven patients were evaluable as one patient was excluded for registration errors. Patient characteristics are described in Table 2. Median age was 60 years (range: 24–80). Eighty-four percent (40) were male. The majority (87%) had grade 0 Zubrod performance status. Seventy percent completed radiation +/− chemotherapy treatment at least 12 months prior to study registration. Eighty-one percent of patients had prior chemotherapy and 21% had history of prior pilocarpine use.
In the first stage feasibility analysis, 12 out of 13 patients (92%) were compliant with treatment. Of these, 10 patients completed all 24 treatment sessions, one patient completed 23 sessions and another completed 22 sessions. The patient who was not compliant completed 10 ALTENS sessions and had to discontinue for lack of transportation. The high compliance rates of the first stage analysis allowed for the implementation of second stage phase II recruitment.
For the second stage feasibility analysis, all 47 patients recruited were included. Forty-four of these 47 patients (94%) were successful in complying with ALTENS treatments. Of these, 34 patients (72%) completed all treatment sessions. There were 3 patients who missed only 1 session, 5 patients 2 sessions, 1patient 4 sessions, and 1 who missed 5 sessions. Reasons for non-compliance with ALTENS treatment among the 3 patients included the lack of transportation for 1 patient (described in the first stage analysis) and device malfunction for the other 2 patients. Taken in totality, the two-stage analysis results demonstrate the feasibility of ALTENS treatment delivery in a multicenter cooperative group setting.
At the time of this report, XeQOLS scores at 6 months from registration were available for 35 out of 47 patients to evaluate ALTENS treatment response. Positive treatment response was achieved in 30 patients (86%). The median percent of XeQOLS scores reduction, indicating an improvement of symptoms, was 42.9%: results ranged from a 100% reduction to a 111% increase. The mean reduction was 35.9% (standard deviation = 36.1), Table 4. These results met the required response rate to proceed with the phase III component of this study. Of the 30 XeQOLS responders, 28 were compliant, completing at least 19 ALTENS sessions and 2 were not compliant.
There were no significant acute side effects associated with ALTENS treatment. Acute adverse events (NCI-CTCAE v3) reported as definitely, probably, or possibly related to ALTENS treatment included grade 1 and 2 gastrointestinal symptoms in 5 patients and one grade 1 pain event, Table 5.
Needle acupuncture has been shown to have promising positive effects on radiation-induced xerostomia in several non-randomized studies and one small randomized controlled study 13–18. However, the general reluctance of patients to have needle insertions and the requirement of trained expertise for treatment delivery may render needle acupuncture difficult to offer at conventional clinics 19. Non-invasive alternatives to needle acupuncture have been explored using transcutaneous nerve stimulators with selected treatment parameters, such as the acupuncture-like transcutaneous nerve stimulator (ALTENS). A-delta and C nerve fibres that are involved in needle acupuncture treatment with the typical ‘De qi’ response (experienced as a mild ache by the subject) can be activated by ALTENS using high intensity and low frequency stimulation 20, 21, 22. The use of electrode pads that are 3 to 4 cm in size also make the precise localization of acupuncture points (usually 0.5 to 2 cm in size) less important. Without needle insertion, the risk of deep tissue injury is eliminated. Thus, ALTENS treatments can be administered with minimal training in operating the device and with knowledge of simple anatomical information to local relevant acupuncture points. Studies have shown that ALTENS gives comparable treatment results to needle acupuncture treatment for multiple clinical indications, such as musculoskeletal pain disorders 23,24, 25. The Codetron™ units utilized in this study have an additional advantage in having a unique randomization circuitry that minimizes brain habituation to the continuous electrical stimulation and may improve treatment effectiveness 4. A randomized study comparing Codetron® to electroacupuncture (needle acupuncture with electrical stimulation) in chronic musculoskeletal pain also demonstrated that Codetron™ exerts comparable or better results than electroacupuncture 26.
Acupuncture points utilized in this study were selected based on Traditional Chinese Medicine principles and on the positive results of the single institutional phase II trial mentioned above 3. In Traditional Chinese acupuncture practice, selection of acupuncture points for treating a disease largely depends on the particular meridian/s involved in the disease process, the energetic nature and the traditionally identified functions of individual acupuncture points. The trajectories of the Large Intestine, Stomach, Spleen and Conception meridians pass through the mandible area where major salivary glands are located, and the oral cavity where minor salivary glands are located. Acupuncture points along these four meridians have been used in previous positive studies for xersotomia treatment 13–18. For example, the Large Intestine meridian was commonly utilized in these reported studies. In one study, LI2, an acupuncture points on the radial side of the distal phalanx of the index finger, used together with three auricular points, was shown to produce sustained relief of xerostomia symptoms 17. In this study protocol, an acupuncture point from each of these four meridians was chosen for stimulation. LI4 on the Large Intestine meridian, is commonly used for parotitis treatment and is postulated to have a direct effect on the parotid glands. ST36 on the Stomach meridian, was selected for its traditionally recognized “tonification” effect that improves overall energy of the meridian and promotes its flow through all meridians. Since Stomach and Large intestine meridians are in the same energetic group, YangMing, ST36 stimulation can also potentiate the treatment effect of LI4. On the Spleen meridian, SP6 is an acupuncture point situated on the confluence of three Ying meridians that, when stimulated, promotes body fluid, including salivary production. CV24 on the Conception meridian, stimulates salivary flow and is commonly indicated for treating xerostomia caused by various pathological conditions 5.
Although the underlying mechanisms by which acupuncture treatment may improve salivary function are still unclear, recent evidence suggests that acupuncture treatment may work through differential stimulation of the autonomic nervous system 27. Activation of the parasympathetic component increases overall volume of salivary production and deactivation of sympathetic component stimulation reduces salivary viscosity 28. Parasympathetic stimulation also enhances the release of specific neuropeptides including calcitonin gene-related peptide (C-GRP), a potent vasodilator that also promotes salivary secretion 29, 30, 31, 32. A brain functional magnetic resonance study also demonstrated that needling LI2, compared to a sham acupuncture point, can activate the insular and the operculum that overlap brain areas known to be involved in gustation and salivation 33. ALTENS treatment may act via similar mechanisms to acupuncture in alleviating symptoms due to radiation-induced xerostomia.
The use of electrical stimulation may have additional advantages. In two clinical studies of patients with xerostomia resulting from various causes, there was significant improvement in salivary production and symptoms associated with xerostomia after electrical stimulation using a device applied to the tongue and hard palate 34, 35. Laboratory studies have shown that electrical stimulation of the parasympathetic nerve to the parotid and submandibular glands in rats causes a mitogenic response as indicated by an increase in tritiated thymidine uptake of the glands 36. This implies the regeneration of salivary gland acinar cells may be possible after initial interventions and may explain the long-term benefits of acupuncture and ALTENS treatments demonstrated in several clinical studies 3,37, 38. Other mechanisms include direct stimulation of minor salivary glands that may not have suffered as much radiation damage to increase salivary output.
A multi-center setting, including both academic and non-academic cancer centers, was selected in conducting this investigation to ensure that the study results reflect how well the interventions being examined work in a conventional clinical environment. Since there were no previous RTOG trials using ALTENS, and no published data regarding the feasibility of ALTENS treatment in a multi-center setting, a phase II component was added to the designed phase III randomized trial to demonstrate the feasibility of ALTENS treatment and a potential positive treatment response. The high percentage of patients complying with protocol therapy clearly demonstrates that ALTENS is feasible in a conventional treatment setting. The rapid patient recruitment rate, averaging 6 patients per month, also reflects the ease of implementation of this device and the high level of patient’s acceptance of this treatment modality. The device malfunction that led to the non-compliance of two patients was found to be users’ errors. All devices were rechecked by the manufacturer and were shown to have functioned properly. The subjects must have had evidence of residual salivary function and have completed radical radiation treatment longer than 3 months, but no longer than 2 years, prior to entering the study. These criteria were included with the anticipation that patients with some residual functional salivary tissue would have a higher chance of response. This was also the study population examined in previous trials 3. Although some reports have suggested a slight recovery of salivary function after radical radiation to the salivary glands, most studies demonstrated irreversible salivary dysfunction. Progressive salivary acinar necrosis and gland atrophy with associated salivary functional decline have been shown to occur until 6 to 8 months after radiation therapy 39, 40. Early intervention may best be delivered during this period of functional decline to arrest deterioration of salivary function and to induce regeneration of salivary gland tissue.
In this phase II study, response to ALTENS treatments was assessed using the University of Michigan XeQOLS at 6 months from randomization. From the study results, it was intriguing to observe that 30/35 (86%) of patients reported a positive response with a mean reduction in XeQOLS scores of 35.9%. The facts that this endpoint was assessed at almost three months after ALTENS treatment completion and that 89% of patients recruited had developed xerostomia for 6 or more months after radiation therapy suggest a sustained response, compared to the 3 to 5 hours duration of action of pilocarpine. This may also imply the occurrence of salivary tissue regeneration. These improved XeQOLS scores may, however, also be explained by the possible natural recovery of salivary function after parotid sparing radiation techniques as suggested in a previous study 41. The randomized phase III component of this study will help to define the full efficacy of ALTENS treatment in alleviating radiation-induced xerostomia. The 'dose-response ' relationship, i.e. the optimal number of treatment sessions and duration of each session, has not been established. The utilization of 24 sessions given twice weekly over 12 weeks was largely based on the phase II trial at McMaster University mentioned above. The results of this study contribute to the dose-response data that are needed to better define optimum ALTENS treatment sessions.
ALTENS appears to be well tolerated without significant toxicities. There were only five patients who reported grade 1 and 2 gastrointestinal toxicities and one with grade 1 facial pain (CTCAE v3) in this phase II component of RTOG 0537. Interestingly, increased dry mouth is the only gastrointestinal toxicity that was reported by the five patients during ALTENS delivery, and that none of these patients reported subsequent worsening of their XeQOLS scores in follow-up. The reasons for this transient complaint of increased mouth dryness are unclear although anxiety during treatment may be a contributing factor. There was one patient who reported worsened XeQOLS by 111% at 6 months follow-up. This patient finished his radiation therapy plus chemotherapy 3 to 6 months before having ALTENS treatment and had no prior oral pilocarpine treatment. The reasons for the worsening of this patient’s xerostomia symptoms, again are unclear. Further follow-up assessments of this patient and the availability of more patients’ data in the phase III component of the RTOG0537 trial may help to identify possible contributing factors.
Given the feasibility of delivering ALTENS treatment in a multicenter setting and positive patient-reported treatment responses, upon the approval of the United States National Cancer Institute, the phase III component of RTOG 0537 initiated enrollment of patients in August of 2010. One hundred and forty-four eligible patients will be accrued and stratified according to previous pilocarpine usage and time interval after radical radiation. Patients will be randomized to oral pilocarpine, 5 mg three times a day for 12 weeks, or ALTENS treatments (administered with the Codetron™) two times weekly for 12 weeks. The primary efficacy endpoint is the XeQOLS score at nine months from randomization. Secondary endpoints include basal and stimulated (citric acid-primed) whole salivary production as measured by sialometry and treatment toxicity profiles.
The results of this phase II component of RTOG 0537 demonstrate the feasibility of delivering quality-assured ALTENS treatments for radiation-induced xerostomia in a cooperative multicenter setting, and show that ALTENS treatments may reduce patient-reported xerostomia symptoms. With the approval of the United States National Cancer Institute, the phase III component of RTOG 0537, comparing the efficacy of ALTENS versus pilocarpine in reducing radiation-induced xerostomia symptoms, was opened for patient accrual in August, 2010.
This work was supported by RTOG U10 CA21661 and CCOP U10 CA37422 grants from the National Cancer Institute.
Presented at the 52nd Annual Meeting of the American Society for Therapeutic Radiology and Oncology, October 31st - November 4th, 2010, San Diego, CA. and at the Radiation Therapy Oncology Group Semiannual Meeting, January 13th–16th, 2011.
This contents of this manuscript are the sole responsibility of the authors and do not necessarily represent the official views of the National Cancer Institute.
The authors have no disclosure, financially and non-financially, relating to the products described in this manuscript and to the conduction of this study.