Multiple Myeloma
Conditions
Keywords
Multiple Myeloma, Cancer, Velcade, Bortezomib, Chinese patients
Brief summary
The purpose of this study is to acquire information on the usage, effectiveness, safety, and levels of health care resource utilization associated with Velcade therapy in recurrent and refractory multiple myeloma patients who are initiating Velcade and various combination therapies within the approved indication in a naturalistic setting.
Detailed description
This is a national, multi-center (study conducted in multiple sites), non-interventional (a scientific study where one or more investigators monitor one or more patients being treated with the same medication), observational study (a scientific study to make a clear and easy understanding of the cause and effect relationship) of Chinese Multiple Myeloma patients treated with Velcade. The study consists of 3 phases, including, screening phase, treatment phase, and follow up phase. In the screening phase, data will be collected on the basis of patient's demographic status, components of disease severity assessment, and potential prognostic factors. Data on prior cancer treatments will be collected retrospectively at baseline for patients receiving cancer treatment prior to receiving Velcade. In the treatment phase, Velcade is administered intravenously for a 2-week treatment period followed by a 10-day rest period. Each treatment cycle consists of 21 days. Prospective (in which the participants are first identified and then followed forward as time passes) observational data will be collected during treatment with Velcade. In the follow up phase, patients will be followed for up to three years to document long-term survival data. For patients who reinitiate Velcade, data collection should follow Velcade treatment period documentation process. Safety evaluations will be based on the incidence, intensity, and types of adverse events. The total duration of the study is set prospectively for three years from the date of the patients' initiation of Velcade.
Interventions
DRUGNo intervention
This is an observational study. Velcade will be administered as per the recommended regimen. (Velcade, 1.3 mg/m2/dose, administered intravenously on days 1, 4, 8 and 11, for 2 weeks)
Sponsors
Xian-Janssen Pharmaceutical Ltd.
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
No
Inclusion criteria
* Must give informed consent in agreement with local legislation * Must not have any contraindication listed in package insert
Exclusion criteria
* Patients currently participating in another investigational study of Velcade or any other medication * Patients with severe hepatic or renal impairment * Patients with platelet count below 25000/μl * Patients who are considered disqualified for the study by the investigators
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of patients on concomitant medications | Up to 3 years | Concomitant medications will be considered as a measure of health care resource utilization associated with Velcade therapy. Concomitant medications include over-the-counter as well as prescription medications, start and stop dates, dosages, and indication. The compliance of concomitant medications will be evaluated by the percentage of patient reported dose over prescribed dose. |
| Bone marrow puncture and biopsy | Up to 3 years | — |
| β2-microglobulin | Up to 3 years | — |
| C-reactive protein | Up to 3 years | — |
| Serum electrolytes | Up to 3 years | — |
| Information on dosage of Velcade | Baseline to Day 21 | Dosage of Velcade will be considered on Velcade utilization. The unit of dosage will be milligram per square meter body surface area. |
| Lactate dehydrogenase | Up to 3 years | — |
| Routine blood examination | Up to 3 years | — |
| Liver function test | Up to 3 years | — |
| Information on treatment sequence for Velcade therapy | Baseline (Day -1) to Day 21 | Treatment sequence or the line of therapy will be considered on Velcade utilization. |
| Renal function test | Up to 3 years | — |
| Information on duration of Velcade therapy | Baseline to Day 21 | Duration of Velcade therapy will be measured on Velcade utilization. The unit of duration will be number of days or the length of the course of therapy. |
| Information on patient diagnosis for Velcade therapy | Baseline to Day 21 | Diagnosis of patients will be considered on Velcade utilization. |
| Number of patients with disease response or progression | Up to 3 years | Complete response (CR), near complete response (complete response with positive immunofixation; nCR), partial response (PR), minimal response (MR), stable disease (SD), progressive disease (PD), or relapse from CR (RCR); the methods and criteria used to evaluate the responses will be chosen by the physician and recorded. |
| Time to response | Up to 3 years | Time to response is calculated from the start date of the cycle of Velcade therapy. |
| Duration of response | Up to 3 years | Duration of response is calculated from the date on which response is documented until PD, RCR, death, or study termination occurs. |
| Time to progression | Up to 3 years | Time to progression is calculated from the date on which response is documented until PD or RCR occurs. |
| Survival status | Up to 3 years | Survival status is calculated from the start of Velcade therapy until death; to be monitored, to the extent possible, beyond the end of Velcade therapy, up to the end of the study period. |
| Number of patients with adverse events | Up to 3 years | Safety criteria will be considered for new skeletal events (fractures, radiotherapy of bone, operation on the bone, spinal cord compression), infection and haematological toxicity (with greater than or equal to grade 3 using WHO Common Toxicity Criteria \[WHO CTC\]), and any neurotoxic events by WHO CTC. |
| Number of emergency room visits while using Velcade therapy | Up to 3 years | Emergency room visits will be considered as a measure of health care resource utilization associated with Velcade therapy. |
| Number of inpatient hospital stays while using Velcade therapy | Up to 3 years | Inpatient hospital stays and the reasons for hospitalization will be considered as a measure of health care resource utilization associated with Velcade therapy. |
| Number of days for each hospital stay | Up to 3 years | Days for each hospital stay will be considered as a measure of health care resource utilization associated with Velcade therapy. |
| Number of patients on whom therapeutic therapies will be conducted | Up to 3 years | Therapeutic therapies (eg: surgery) will be considered as a measure of health care resource utilization associated with Velcade therapy. |
| Number of patients on whom chest radiograph will be conducted | Up to 3 years | — |
| Number of patients on whom whole-body bone scan will be conducted | Up to 3 years | — |
| Number of patients on whom radiograph for designated area will be conducted | Up to 3 years | — |
| Serum immunoglobin and M-protein | Up to 3 years | — |
| M-protein detected by immunofixation electrophoresis | Up to 3 years | — |
| Urine light chain M-protein | Up to 3 years | — |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Sociodemographics for Velcade therapy | Baseline | Sociodemographics of patients will be assessed, at the initiation of Velcade therapy, such as: gender, date of birth, height, weight, highest degree, and career information. |
| Number of chronic concomitant disease | Baseline | Chronic concomitant disease will be assessed at the initiation of Velcade therapy. |
| Treatment history | Baseline | Treatment history will be assessed at the initiation of Velcade therapy. Treatment history includes: confirmation date of diagnosis of multiple myeloma patients or other patients receiving Velcade therapy; names of diseases for patient receiving Velcade therapy; prior treatments for multiple myeloma; outcomes of prior treatments for multiple myeloma. |
| Indications for Velcade therapy | Baseline (Day -1) | Multiple myeloma patients who receive two or more prior treatments and demonstrate disease progression on the most recent treatment will be indicated for Velcade therapy. |
Outcome results
None listed