Exploratory Study on the Use of Pregabalin for the Treatment of Taxol Related Arthralgia-Myalgia
NCT ID: NCT02024568
Last Updated: 2013-12-31
Study Results
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Basic Information
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UNKNOWN
PHASE2
38 participants
INTERVENTIONAL
2013-12-31
2015-05-31
Brief Summary
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Sporadic reports suggest that a drug called gabapentin may be effective in the management of this adverse effect. Observations from our practice indicate that pregabalin, which possesses similar biological activity to that of gabapentin, may also be useful in preventing and treating paclitaxel associated myalgia - arthralgia.
The current study represents an initial evaluation of the hypothesis that pregabalin may be beneficial in the management of the symptoms due to the "Arthralgia-Myalgia Syndrome". The investigation will be carried out in the format of a small scale, randomized, placebo controlled trial with patients receiving paclitaxel in the course of standard treatment for breast cancer.
Detailed Description
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Paclitaxel and docetaxel are the major representatives of the drug class of taxanes, agents commonly used in the treatment of a variety of solid tumors. They interfere with the mitotic process of dividing cells by stabilizing the microtubules and are the mainstay of treatment in lung, breast, and ovarian cancer, among others. The adverse side effects associated with taxane treatment frequently impair the quality of life of cancer patients and occasionally impose discontinuation of the oncological treatment of choice (Forsyth, Balmaceda et al. 1997; Saibil, Fitzgerald et al. 2010).
The phenomenon of diffuse pain involving joints and muscles in the wake of treatment with taxanes commonly referred to as Taxane related Arthralgia-Myalgia Syndrome (from here on noted as TAMS) is well known and documented (Rowinsky, Chaudhry et al. 1993). It is common, as apparent from a recent retrospective study of patients treated with regimens used for breast cancer which revealed an 80% incidence of taxane related pain (Saibil, Fitzgerald et al. 2010).
The pain may be localized, regional or diffuse, most commonly in the back, hips, shoulders, thighs, legs and feet (Loprinzi, Maddocks-Christianson et al. 2007). It is usually depicted as arthralgia-myalgia due to the difficulty to associate it clearly with either the joints or the muscles (Loprinzi, Maddocks-Christianson et al. 2007). The nature of the sensation is described as aching, deep pain, often with associated radiating, shooting, stabbing, pulsating elements (Loprinzi, Maddocks-Christianson et al. 2007). The sensation is of unique quality previously unencountered by those experiencing it, the description of which is not compatible with established reports of neuropathic pain.
The syndrome may be of incapacitating intensity, capable of imposing days of bed restriction on those suffering from it. This burden is often extended to significant others who have to remain and care for the daily needs of those handicapped by the pain. Attempts of treatment with steroids, non-steroid anti-inflammatory drugs and opioid analgesics frequently fail to produce satisfactory results (Garrison, McCune et al. 2003).
Pregabalin - Basic Pharmacology and Potential for Treatment of TAMS:
Pregabalin is a small molecule with an established efficacy in the treatment of neuropathic pain (Gajraj 2007). It is known to interact with the α2-δ subunit of voltage gated calcium channels present in multiple tissues, most prominently in brain and muscle (Taylor, Angelotti et al. 2007).
Pregabalin is rapidly absorbed via a specialized transport system, reaching a peak concentration in the serum circa one hour after oral ingestion (Gajraj 2005). Bioavailability exceeds 90% and the pharmacokinetic profile is linear throughout the clinically relevant concentrations (Gajraj 2005). It does not bind significantly to proteins in the blood stream, does not undergo any modification during its passage through the organism, and is eliminated unchanged in the urine (Gajraj 2005). No significant pharmacokinetic interactions have been reported to date (Gajraj 2007).
Currently pregabalin is being used in the treatment of neuropathic pain and as an anti-epileptic agent (Gajraj 2007). Accumulated evidence is supportive of a high degree of safety in its use, with the most common side effects constituting of mild to moderate degree dizziness, somnolence, feeling drunk, fatigue and increased weight (Harmark, van Puijenbroek et al. 2011).
Sporadic reports suggest that gabapentin may be effective in alleviating Taxol related arthralgia-myalgia symptoms (Nguyen and Lawrence 2004). On grounds of similar pharmacodynamics (Bryans and Wustrow 1999) it may be hypothesized that pregabalin also has potential to alleviate the paclitaxel related arthralgia-myalgia. Furthermore, observations from our clinical oncology service are supportive of this hypothesis.
Evaluation of the Taxane Related Arthralgia-Myalgia Syndrome:
Pain constitutes a major component of the Taxane related Arthralgia-Myalgia Syndrome (from here on referred to as TAMS) (Garrison, McCune et al. 2003). We propose that pregabalin may have a significantly beneficial effect on the pain secondary to this syndrome. Consequently, evaluation of the pain before and after treatment with the study drug by means of a well established pain scoring method is required.
Modern pain research acknowledges the subjective and complex nature of pain that complicates its assessment. Furthermore, ethical imperatives place constraints on the comparative control to serve the in evaluation of a novel analgesic intervention (Silverman, O'Connor et al. 1993). One of the solutions to this issue, using normalized ordinal evaluations of pain and analgesic drug consumption around a central value in a manner that also accounts for changes in analgesic drug requirements (Silverman, O'Connor et al. 1993) will serve for direct assessment of the study hypothesis.
The Integrated Assessment of Pain Score and Rescue Analgesic Treatment evaluation according to Silverman et al will be augmented by raw pain assessment by means of a well established pain scoring method (Farrar, Portenoy et al. 2000).
Bed restriction is a direct result of the TAMS that is often described by those suffering from it. It is hereby proposed to monitor bed restriction by recording the number of hours spent in horizontal position between the time of getting up from the night's sleep and the hour of going to bed at the end of the day. The proposed measure will compare the number of hours spent in the horizontal position on the day preceding the taxane treatment, and the number of hours spent in that position on the day with the highest score of pain during the week following treatment. The sample size is not calculated to serve the validation of this novel measure, but an effort to assess its association with established quality-of-life scores will be made.
The current proposal is focused on evaluating an intervention with potential to have a positive impact on the quality of life of individuals receiving chemotherapy with taxanes. The FACT-Taxane scale is a psychometric tool specifically developed to assess the impact of taxane based treatment (Cella, Peterman et al. 2003). However, quality of life is a composite measure, and requires a larger sample size to determine efficacy, and therefore it will only serve as a secondary endpoint.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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Pregabalin
Includes 19 out of 38 subjects reporting athralgia-myalgia in the wake of paclitaxel infusion in the course of breast cancer treatment.
Pregabalin started on the evening before receiving infusion of paclitaxel and 5 day thereafter. Initial dosing of 75mg twice daily (morning + evening). Option for dose increase with additional 75mg in case of inadequate pain control. A minimal interval of 2 hours is required between doses.
In case of poorly tolerated side effects a reduction to 50mg doses is available.
Access to additional analgesic interventions is open as required for patient wellbeing.
Pregabalin
See arm description
Placebo
Includes 19 out of 38 subjects reporting athralgia-myalgia in the wake of paclitaxel infusion in the course of breast cancer treatment.
Placebo externally identical to the pregabalin 75mg capsules will be started on the evening before receiving infusion of paclitaxel and 5 day thereafter. Initial dosing of 1 capsule twice daily (morning + evening). Option for dose increase with additional capsule in case of inadequate pain control. A minimal interval of 2 hours is required between doses.
In case of poorly tolerated side effects a reduction to capsules with the appearance of 50mg pregabalin capsules is available.
Access to additional analgesic interventions is open as required for patient wellbeing.
Placebo
See arm description
Interventions
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Pregabalin
See arm description
Placebo
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Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Experience of myalgia-arthralgia related pain of moderate or worse degree of severity after a course of paclitaxel containing chemotherapy.
Exclusion Criteria
* Known restricting adverse events related to treatment with pregabalin or gabapentin.
* Renal failure with GFR less than 30ml/min.
* Participation in clinical trial 3 weeks or less prior to screening.
* Confounding myalgia and / or arthralgia unrelated to chemotherapy.
* Medical condition compromising the likelihood of completing the trial.
18 Years
FEMALE
No
Sponsors
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Assaf-Harofeh Medical Center
OTHER_GOV
Responsible Party
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Principal Investigators
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Jonathan Grunfeld, M.D.
Role: PRINCIPAL_INVESTIGATOR
Employee of Asaf Harofeh M.C.
Locations
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Assaf HaRofeh Medical Center
Be'er Ya'akov (Zerifin), , Israel
Countries
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Central Contacts
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References
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Bryans JS, Wustrow DJ. 3-substituted GABA analogs with central nervous system activity: a review. Med Res Rev. 1999 Mar;19(2):149-77. doi: 10.1002/(sici)1098-1128(199903)19:23.0.co;2-b.
Cella D, Peterman A, Hudgens S, Webster K, Socinski MA. Measuring the side effects of taxane therapy in oncology: the functional assesment of cancer therapy-taxane (FACT-taxane). Cancer. 2003 Aug 15;98(4):822-31. doi: 10.1002/cncr.11578.
Farrar JT, Portenoy RK, Berlin JA, Kinman JL, Strom BL. Defining the clinically important difference in pain outcome measures. Pain. 2000 Dec 1;88(3):287-294. doi: 10.1016/S0304-3959(00)00339-0.
Forsyth PA, Balmaceda C, Peterson K, Seidman AD, Brasher P, DeAngelis LM. Prospective study of paclitaxel-induced peripheral neuropathy with quantitative sensory testing. J Neurooncol. 1997 Oct;35(1):47-53. doi: 10.1023/a:1005805907311.
Gajraj NM. Pregabalin for pain management. Pain Pract. 2005 Jun;5(2):95-102. doi: 10.1111/j.1533-2500.2005.05205.x.
Gajraj NM. Pregabalin: its pharmacology and use in pain management. Anesth Analg. 2007 Dec;105(6):1805-15. doi: 10.1213/01.ane.0000287643.13410.5e.
Garrison JA, McCune JS, Livingston RB, Linden HM, Gralow JR, Ellis GK, West HL. Myalgias and arthralgias associated with paclitaxel. Oncology (Williston Park). 2003 Feb;17(2):271-7; discussion 281-2, 286-8.
Harmark L, van Puijenbroek E, Straus S, van Grootheest K. Intensive monitoring of pregabalin: results from an observational, Web-based, prospective cohort study in the Netherlands using patients as a source of information. Drug Saf. 2011 Mar 1;34(3):221-31. doi: 10.2165/11585030-000000000-00000.
Loprinzi CL, Maddocks-Christianson K, Wolf SL, Rao RD, Dyck PJ, Mantyh P, Dyck PJ. The Paclitaxel acute pain syndrome: sensitization of nociceptors as the putative mechanism. Cancer J. 2007 Nov-Dec;13(6):399-403. doi: 10.1097/PPO.0b013e31815a999b.
Nguyen VH, Lawrence HJ. Use of gabapentin in the prevention of taxane-induced arthralgias and myalgias. J Clin Oncol. 2004 May 1;22(9):1767-9. doi: 10.1200/JCO.2004.99.298. No abstract available.
Rowinsky EK, Chaudhry V, Forastiere AA, Sartorius SE, Ettinger DS, Grochow LB, Lubejko BG, Cornblath DR, Donehower RC. Phase I and pharmacologic study of paclitaxel and cisplatin with granulocyte colony-stimulating factor: neuromuscular toxicity is dose-limiting. J Clin Oncol. 1993 Oct;11(10):2010-20. doi: 10.1200/JCO.1993.11.10.2010.
Saibil S, Fitzgerald B, Freedman OC, Amir E, Napolskikh J, Salvo N, Dranitsaris G, Clemons M. Incidence of taxane-induced pain and distress in patients receiving chemotherapy for early-stage breast cancer: a retrospective, outcomes-based survey. Curr Oncol. 2010 Aug;17(4):42-7. doi: 10.3747/co.v17i4.562.
Silverman DG, O'Connor TZ, Brull SJ. Integrated assessment of pain scores and rescue morphine use during studies of analgesic efficacy. Anesth Analg. 1993 Jul;77(1):168-70. No abstract available.
Taylor CP, Angelotti T, Fauman E. Pharmacology and mechanism of action of pregabalin: the calcium channel alpha2-delta (alpha2-delta) subunit as a target for antiepileptic drug discovery. Epilepsy Res. 2007 Feb;73(2):137-50. doi: 10.1016/j.eplepsyres.2006.09.008. Epub 2006 Nov 28.
Other Identifiers
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WS1826148
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
105/13
Identifier Type: -
Identifier Source: org_study_id