Pain, Unspecified Adult Solid Tumor, Protocol Specific
Conditions
Keywords
unspecified adult solid tumor, protocol specific, pain
Brief summary
RATIONALE: Oxycodone helps lessen pain caused by cancer and may improve quality of life. It is not yet known whether oxycodone works better and is more cost effective than standard therapy in treating patients with cancer pain. PURPOSE: This randomized phase IV trial is studying oxycodone to see how well it works compared with standard pain therapy in treating patients with cancer pain and if it is more cost effective than standard pain therapy.
Detailed description
OBJECTIVES: Primary * Compare overall pain management in patients with cancer-related pain treated with oxycodone hydrochloride vs standard three-step analgesic therapy. * Compare the health economics of these regimens in these patients. Secondary * Explore the factors that inform patients' decisions about commencing opioid analgesia. OUTLINE: This is an open-label, multicenter, randomized, parallel group, pilot study. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive an analgesic regimen, according to their level of pain, for up to 18 weeks. * Step 1: Patients in mild pain receive oral acetaminophen 4 times daily. * Step 2: Patients in mild-to-moderate pain receive oral codeine or oral dextropropoxyphene hydrochloride 4 times daily and oral acetaminophen 4 times daily. * Step 3: Patients in moderate-to-severe pain receive oral morphine or oral oxycodone hydrochloride 6 times daily (every 4 hours) with or without a non-opioid analgesic. Patients may also receive an adjuvant drug (i.e., for side effects or for primary indication other than pain management that is analgesic in selected circumstances). * Arm II: Patients receive oral oxycodone hydrochloride twice daily for up to 18 weeks. Patients may receive a different opioid analgesic or analgesia or adjuvant medication as in arm I, if needed. Patients in both arms may also receive additional medication for breakthrough pain. Patients complete a patient-assessment booklet (PAB) daily which includes a Box-Scale (BS)-11 rating for average pain; questions regarding contact (e.g., telephone or visit) with healthcare professionals on that day; and information regarding the number of times escape medication is used. Quality of life and levels of cancer pain are assessed using the short form of the Brief Pain Inventory (BPI). After completion of study treatment, patients are followed at 4 weeks. Peer Reviewed and Funded or Endorsed by Cancer Research UK PROJECTED ACCRUAL: A total of 30 patients will be accrued for this study.
Interventions
DRUGacetaminophen
DRUGdextropropoxyphene hydrochloride
DRUGmorphine sulfate
PROCEDUREmanagement of therapy complications
PROCEDUREquality-of-life assessment
Sponsors
University Hospitals Bristol and Weston NHS Foundation Trust
Study design
Allocation
RANDOMIZED
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Diagnosis of cancer * Requires regular step-2 analgesia for the management of cancer-related pain PATIENT CHARACTERISTICS: * Not pregnant or nursing * Fertile patients must use effective contraception * Must be able to take oral medication * Must be willing and able to complete a daily patient assessment booklet (PAB) * No history of the following conditions: * Depression * Personality disorders that may lead to self-harm * Admission to the hospital for psychiatric reasons * Any other psychological disorder that, in the opinion of the investigator, would preclude study treatment * Not at risk of additional CNS depressant effects due to study drugs * No known history of alcohol or drug abuse or, in the opinion of the investigator, tendency towards drug abuse or addiction * No current abuse of alcohol or drugs * No known sensitivity to oxycodone hydrochloride or other opioids * No history of a specific or allergic reaction to study drugs * No contraindications as a result of adverse drug reaction or drug interactions of oxycodone or other opioid drugs * No other condition that, in the opinion of the investigator, would make the patient unsuitable for study participation PRIOR CONCURRENT THERAPY: * More than 30 days since prior and no concurrent chemotherapy or radiotherapy * At least 2 weeks since prior regular (i.e., 4 times per day) step-2 analgesics * More than 3 months since prior regular use of opioids, defined as having a regular prescription of an opioid medication * Not planning to undergo cancer-related surgery * No other concurrent opioid-based medication other than oxycodone hydrochloride capsules as escape medication (arm II) * No concurrent participation in another clinical trial involving a new chemical entity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of time in assessment periods 1 and 2 (i.e., first 4 weeks) with a Box-Scale (BS)-11 pain score of ≤ 4 (i.e., mild pain) | — |
Secondary
| Measure | Time frame |
|---|---|
| Mean BS-11 pain scores | — |
| Time to reach stable pain control | — |
| Mean escape medication use | — |
| Percentage of time in assessment periods 3 and 4 with a BS-11 pain score of ≤ 4 | — |
| Global assessment of pain relief with study drugs | — |
| Mean pain intensity, pain interference, and pain relief scores as measured by the Brief Pain Inventory | — |
| Overall number of phone calls, home visits by a nurse, home visits by a doctor, and unscheduled visits to a healthcare provider, related to pain control or analgesic medication during study treatment | — |
| Quality of sleep | — |
Outcome results
None listed