Loratadine for the Prevention of G-CSF-related Bone Pain

Phase 2

Not yet recruiting

Brief Summary: The research question for the current study is: Is loratadine more effective than placebo in preventing G-CSF-related bone pain during autologous hematopoetic stem cell transplant in patients with lymphoma or multiple myeloma? The hypothesis is that prophylaxis with loratadine will help prevent or reduce the severity of bone pain in this setting.

Recruitment & Eligibility

Inclusion Criteria

A histologically or cytologically documented lymphoma or multiple myeloma
Next line of therapy is autologous stem cell transplant
Adult ≥ 18 years old.
Eastern Cooperative Oncology Group (ECOG) Performance Status 0-2.
Life expectancy of at least 12 weeks.
The absence of any additional poorly controlled systemic disease that is directly contraindicated or places subject at significant risk, including but not limited to: congestive heart failure, diabetes mellitus, cirrhosis or liver failure, renal failure.
Able to adhere to study protocols and visit schedules

Exclusion Criteria

Hypersensitivity or intolerance to antihistamines
Use of antihistamines within two days prior to the study period, excepting the use of single dose antihistamines during chemotherapy or blood transfusion protocols.
Recent use of G-CSF or pegfilgrastim defined as within 12 weeks of study accrual.
New and continued regular use of analgesics within the four days prior to the first dose of G-CSF

Arm && Interventions

Group	Intervention	Description
Placebo Arm	Placebo	Placebo capsule, administered initially 3 hours before the first dose of G-CSF in the autologous stem cell mobilization protocol, and then daily for a minimum of 8 days.
Loratadine Arm	Loratadine	Loratadine 10mg, administered initially 3 hours before the first dose of G-CSF in the autologous stem cell mobilization protocol, and then daily for a minimum of 8 days.

Primary Outcome Measures

Name	Time	Method
Bone Pain Interference (Brief Pain Inventory)	Brief Pain Inventory will be completed at baseline, daily during treatment (up to 12 days) and at the end of treatment (max day 12).	Reduction on impact on daily life as a composite score out of 10 as measured on the Brief Pain Inventory (BPI). BPI pain interference will be compared as a composite score (sum of individual pain interference values divided by 7).
Bone pain severity (QLQ-BM22)	QLQ-BM22 will be completed at baseline and at the end of treatment (max day 12).	Change in bone pain measured pre and post G-CSF in EORTC QLQ-BM22. QLQ-BM22 questionnaires will be compared to the post vs pre-treatment values and calculated as a composite sum (i.e. pre-treatment total score subtracted from post-treatment total score).
Bone Pain Severity (Brief Pain Inventory)	Brief Pain Inventory will be completed at baseline, daily during treatment (up to 12 days) and at the end of treatment (max day 12).	Reduction in bone pain will be measured as a change from pre-G-CSF baseline in the Brief Pain Inventory (BPI), with median values compared for each trial arm. BPI pain severity will be compared as a composite score (sum of individual pain values divided by 4).

Secondary Outcome Measures

Name	Time	Method
Rate of pain control use	Single measurement after all patients complete mobilization (max day 8)	Proportion of patients in each study arm that require use of additional pain control methods while receiving G-CSF.
Qualitative breakthrough of pain control use	Qualitative description of analgesic type after all patients complete mobilization (max day 8)	Type of medication used to control additional pain while receiving G-CSF.
Mean time to stem cell re-engraftment	Single measurement during stem cell re-infusion (max day 8)	Time in days between stem cell re-infusion and the measurement on complete blood count (CBC) of an absolute neutrophil count of greater than 500/mm3 for 3 consecutive days.
Rate of plerixafor use during in each study arm	Single measurement after all patients have completed end of treatment.	Proportion of patients in each study arm that require use of plerixafor during stem cell mobilization
Progression free survival	Patients will be followed for 1 year after completion of the study treatment.	Time between the date of treatment initiation and the date of disease progression or death (whatever the cause), whichever occurs first)
Stem cell mobilization efficacy	Single measurement at the end of mobilization protocol (max day 8)	Normalized mean and absolute number number of stem cells collected at the end of the mobilization protocol