Clinical Trial Details
— Status: Withdrawn
Administrative data
| NCT number |
NCT05331131 |
| Other study ID # |
22-0292 |
| Secondary ID |
|
| Status |
Withdrawn |
| Phase |
Phase 2
|
| First received |
|
| Last updated |
|
| Start date |
September 19, 2022 |
| Est. completion date |
November 14, 2025 |
Study information
| Verified date |
January 2024 |
| Source |
Northwell Health |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
Patients with head and neck cancer generally receive a standard of care of 7 weeks of daily
radiation therapy given alongside an aggressive chemotherapy drug called cisplatin. While
rates of cure are often strong for patients who are able to complete treatment without any
unscheduled breaks, the rates of high grade toxicity associated with this treatment are high
even with the use of the most modern techniques of treatment. Pain, swallowing dysfunction,
loss of taste sensation, and ulceration of the mouth and throat are ubiquitous and often
contribute to a nutritional breakdown requiring feeding tube placement. Unfortunately, even
with aggressive use of opioids and other conventional palliation methods, breakthrough pain
and other toxicities are very common. In addition to the quality of life burdens of these
side effects, patients who are unable to complete treatment on schedule have worse control of
their cancer and worse overall survival.
Clearly, there is a clinical need for better management of these toxicities. The
investigators hypothesize that ketamine mouthwash may effectively reduce both pain and the
need for opioid drugs in this patient population. There is a large body of literature
supporting the use of ketamine for pain control in diseases other than cancer, and a smaller
but growing body of literature showing the effectiveness of ketamine for control of
cancer-associated pain. Additionally, by providing ketamine in mouthwash form, the evidence
shows that one can avoid the side effects associated with giving ketamine throughout the
body, and in fact no significant side effects have been reported so far with this treatment.
In this study, the investigators will provide ketamine mouthwash to patients undergoing the
standard treatment for this disease over a two week period, and measure their response in
terms of both pain and need for opioids, as well as other measurements of quality of life.
The investigators will also measure unscheduled interruptions in treatment. In years to come,
the data from this study may show an impact on cancer control and survival.
Description:
There is an unmet need for improvement in pain control among patients with cancer and
undergoing anti-neoplastic therapies, with by one recent estimate 59% of patients on
treatment and 33% of patients who completed curative treatment reporting inadequate pain
control (1).
This burden is especially grave in the setting of curative treatment for head and neck
cancer, in which rates of severe acute pain and other toxicities with major impact on quality
of life are known to be high among radiotherapy and chemoradiotherapy patients.
In RTOG 9003, a randomized controlled trial evaluating altered fractionation in the setting
of definitive radiotherapy in locally advanced head and neck cancer, acute grade 3-4 oral
mucositis was seen in 25% of standard fractionation and 41% of hyperfractionation patients,
and acute grade 3-4 pharyngeal/esophageal toxicity was seen in 11% of standard fractionation
and 26% of hyperfractionation patients. In RTOG 0129, a randomized controlled trial
evaluating accelerated fractionation in the setting of definitive cisplatin-based
chemotherapy concurrent with radiotherapy in stage III-IV head and neck cancer, acute grade
3-4 dysphagia was seen in 23% of standard fractionation and 21% of accelerated fractionation
patients, and acute grade 3-4 oral/pharyngeal mucositis was seen in 39% of standard
fractionation and 33% of accelerated fractionation patients. Additionally, in RTOG 0129, 69%
of standard and 67% of accelerated fractionation patients received nutritional support via
feeding tube by treatment end (2,3).
The above landmark RTOG studies did not use modern intensity-modulated radiation therapy
(IMRT) techniques which have since become standard in head and neck radiotherapy, and data do
exist suggesting reduced acute toxicities through the use of IMRT such as in RTOG 0022 (4).
Nevertheless, the burden is still significant, particularly when concurrent cisplatin is
given. For example, in RTOG 1016, a randomized controlled trial which demonstrated the
inferiority of cetuximab given concurrently with IMRT vs. concurrent cisplatin and IMRT in
HPV-positive oropharyngeal cancers, the IMRT plus cisplatin arm showed an acute grade 3-4
dysphagia rate of 37.4%, an acute grade 3-4 oral mucositis rate of 41.5%, an acute grade 3-4
pharyngeal mucositis rate of 13.6%, an acute grade 3-4 anorexia rate (which is likely due at
least in part to pain and swallowing dysfunction) of 22.4%, and a rate of feeding tube
nutritional support at treatment end of 62% (5).
As a result of the above and other randomized studies, IMRT with concurrent cisplatin-based
chemotherapy, with its high rates of expected high grade toxicities, is the standard of care
for head and neck cancers except for those that are potentially operative and those that are
very early stage.
Early treatment termination is common in definitive head and neck cancer treatment, and oral
and pharyngeal toxicities are among the most significant factors associated with early
treatment termination. In our own institution, among the 5014 new treatment starts between
2017 and 2019, curative intent head and neck cases had a 7.9% treatment termination rate, the
second highest by percentage of new starts of any disease site after vulvar cancer (vs. an
overall institutional rate of 4.1%), and made up 38.2% of all treatment terminations in this
interval, the highest share of any disease site by far (6).
Patients who fail to complete treatment are well understood to have vastly poorer rates of
control and survival than patients who do complete treatment. Additionally, head and neck
patients with extended treatment package time due to unscheduled breaks have worse survival
than those completing treatment on time (7,8). Therefore, therapies which can ameliorate
these toxicities and thereby reduce treatment breaks, package time, and terminations, may not
only improve patient quality of life but may also have a downstream beneficial impact on
control and survival metrics in light of improved rates of treatment completion.
Ketamine is an anesthetic agent developed in the 1960s as a derivative of phencyclidine (PCP)
to be a less toxic alternative to the latter. It maintains its position on the WHO list of
essential medications and continues to see widespread use in anesthesia and is widely and
inexpensively available globally. Ketamine has numerous routes of administration to fit
specific clinical needs, including IV, IN, IM, SC, IT/epidural, PO, and multiple topical
formulations.
Ketamine's complex pharmacology illustrates its potential benefits in the oncologic setting.
Its primary mechanism of action is as a high affinity non-competitive antagonist to the NMDA
receptor, driving anesthetic and analgesic effects which include decreased central
sensitization to opioids. Additional mechanisms of action promoting analgesia include:
reduction of extracellular D-serine with the downstream effect of reduced NMDA receptor
activation; inhibition of hyperpolarization-activated cyclic nucleotide gated channels
(HCNs); both potentiation and inhibition of cholinergic receptors; activation of mu-, kappa-,
and delta-opioid receptors; activation of sigma receptors; inhibition of voltage gated sodium
channels; reduction in activity of pro-inflammatory cytokines; and decreased astrocyte and
microglial activation leading to decreased transmission of nociceptive inputs. Further
therapeutic effects of ketamine include potent anti-depressant pathways, which can indirectly
ameliorate pain and discomfort by altering a subject's perception of pain acuity and may also
marginally improve treatment completion rates to the extent that depression is associated
with treatment termination. Conversely, adverse effects of ketamine are generally transient
except in the setting of heavy chronic use and are generally limited to systemic routes of
administration as opposed to topical routes (9).
Clinical data support ketamine use in the oncologic setting as well. To date, five randomized
controlled trials have analyzed systemic administration of ketamine to cancer patients, of
which four detected either statistically significant pain reduction or reduction in opioid
analgesic burden, while the fifth trial was hampered by a dose escalation design which led to
study subject withdrawal due to severe psychotomimetic adverse effects (10).
Topical administration of ketamine for local pain control is a further area of active
investigation. A randomized controlled trial analyzed the use of 1% ketamine cream, 2%
amitriptyline cream, and combination ketamine-amitriptyline cream for control of neuropathic
pain and found reductions in pain scores in all groups, although non-significantly vs.
placebo. Plasma concentrations of ketamine were measured in this study and ranged from
undetectable to 30ng/ml, as against a serum threshold level of 2000ng/ml for induction of
psychoactive effects, indicating essentially negligible potential for systemic side effects
including the feared psychotomimetic adverse effects (11,12). More broadly, a systematic
review of 34 studies on topical ketamine for pain control including 13 randomized controlled
trials in diverse domains including postherpetic neuralgia, diabetic neuropathy,
chemotherapy-induced neuropathy, and pelvic pain found clinically and statistically
significant pain reduction in the overwhelming majority of studies, with zero reported
systemic side effects and maximum reported plasma levels of 33ng/ml and 20.9 ng/ml for
ketamine and norketamine, respectively. Pain response to the treatment appears to be dose
dependent but even at concentrations up to 20% ketamine, systemic absorption remains
clinically insignificant (13).
Of particular note, topical ketamine solution has been used in two randomized controlled
trials for controlling post-tonsillectomy pain in pediatric patients. One trial compared 5%
ketamine administered to the tonsillar fossae with soaked swabs to a tramadol arm and a
placebo, and found statistically significant improvements in pain with both interventions,
with neither performing better than the other. The other trial randomized patients to 1%
ketamine spray, morphine spray, lidocaine spray, or normal saline spray. Lidocaine
outperformed the other groups at 20 minutes post-administration but ketamine and morphine
were equally superior by 60 minutes post-administration. Neither study reported systemic or
other adverse effects (14, 15).
In the oncologic setting, the NCCTG N06CA randomized controlled trial determined that a
topical regimen of ketamine, baclofen, and amitriptyline for patients with
chemotherapy-associated peripheral neuropathy found statistical significant improvement in
motor neuropathy and a trend towards improvement in sensory neuropathy after four weeks of
treatment vs. placebo, without psychoactive side effects and an overall side effect profile
equivalent to placebo (16). A phase I trial of topical ketamine, amitriptyline, and lidocaine
for radiation dermatitis found long-term improvement in pain and other dermatologic endpoints
(17). A published case study describes a 32 year old patient with oral tongue cancer
undergoing adjuvant radiation therapy to 66 Gy who had severe breakthrough pain despite
aggressive interventions including transdermal fentanyl, oxycodone/acetaminophen, morphine
suspension (which paradoxically exacerbated pain), "magic mouthwash," hydromorphone, and
sucralfate. The patient was treated with ketamine mouthwash at a strength of 20mg/5ml,
experienced significant pain relief within minutes of administration, continued regular use
of ketamine mouthwash and went on to have profound and durable symptomatic improvement which
additionally enabled her nutritional recovery (18).
As of this writing, one phase II trial has studied topical oropharyngeal (i.e. mouthwash)
administration of ketamine in the setting of grade 3 or 4 chemotherapy-associated oral
mucositis. That study found statistically significant improvements in patient-reported pain
scores both at rest and when swallowing at multiple time intervals following ketamine
administration, statistically significant improvement in patient reported sleep quality, and
a non-statistically significant trend towards reduced median opioid analgesic burden for
which the study was likely underpowered (19).
An NCT-registered randomized controlled trial is studying the analgesic efficacy of ketamine
mouthwash in addition to topical anesthetics versus placebo in a population of 19 patients
receiving head and neck radiation therapy or chemoradiation. This study has not yet reported
results (20).
Another recently published randomized controlled trial studied the efficacy of ketamine
mouthwash for chemotherapy-associated oral mucositis in the pediatric population in terms of
analgesic impact and need for rescue analgesics. Only a single dose of ketamine was
administered and its effects only monitored for several hours. Although differences were
observed in the ketamine and placebo groups, they did not meet significance thresholds (21).
The two foregoing RCTs of ketamine mouthwash are limited by sample size, by only capturing
analgesia outcomes in the former case, and by single dose administration with transient
follow-up in the latter case. Nevertheless, they testify to the potential therapeutic value
of ketamine mouthwash for cancer patients, and to a safety profile favorable enough for
consideration its use in children.
The investigators' contention is that the above basic and clinical data, and the clear
clinical need for better control of toxicity associated with anti-neoplastic therapy of head
and neck cancer, justify a prospective trial investigating the use of ketamine for toxicity
control in head and neck cancer patients and its attendant impact on pain control, opioid
analgesic burden, functional quality of life metrics, and on-schedule completion of curative
therapy as prescribed. The investigators aim to study ketamine intervention in the setting of
intensity-modulated radiation therapy with concurrent cisplatin-based chemotherapy, the
standard of care and most intensive current curative regimen for definitive treatment of head
and neck cancer. Adjuvant therapy may also be an appropriate indication for ketamine
intervention, but adjuvant cases are excluded from the present study on the grounds that
post-operative recovery and complications introduce unforeseeable potential confounders in a
relatively small study population.
The study agent is a mouthwash preparation of ketamine hydrochloride 20mg/5ml in NovaFilm
suspension with OraSweet flavoring agent, which will be administered via swish and spit
technique. Subjects will be instructed on correct administration prior to the first dose and
will be observed in clinic for 1 hour following the initial administration for monitoring of
AEs. Subjects will then self-administer the drug on a QID basis. They will record their
self-administration (including the time of administration) in a paper drug log included among
the study materials distributed to them. They will be encouraged to space administration of
the drug as evenly as possible throughout the day. In order to achieve this interval of
dosing, they will be encouraged to administer the drug with breakfast, lunch, dinner, and
once more at bedtime. They will also be instructed that perfect uniformity of dosing schedule
is not strictly necessary, and that the timing of drug administration with meals is not
advised due to medical need to co-administer the drug with food, but rather to assist in
adherence to the QID schedule of administration. Participants will be provided written
instructions for self administration of the IP and site contact information should they have
questions.
