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J Cancer. 2017; 8(10): 1801–1808.
Published online 2017 July 1. doi:  10.7150/jca.17999
PMCID: PMC5556643

Effect of pomalidomide on relapsed/refractory multiple myeloma: a systematic review and meta-analysis

Abstract

In this work, we aim to further analyze the effect of pomalidomide for relapsed and/or refractory multiple myeloma (RRMM). A systematic literature search of PubMed, MEDLINE and EMBASE was conducted on September 20, 2016. Pooled effect size (ES) with corresponding 95% confidence intervals (CIs) were calculated using random-effects model. STATA software (version 12.0; Stata Corporation; College Station, TX, USA) was employed to do all statistical analyses. A total of 8 studies were included for analysis. The combined results demonstrated that the pooled proportion of overall response rate (ORR) was 0.35 (95% CI 0.27 to 0.43, P=0.000), and the pooled proportion of complete response rate (CRR) was 0.02 (95% CI 0.01 to 0.03, P=0.541). Pomalidomide was generally well tolerated by patients reported in the studies. Further studies would be required to conduct more prospective randomized controlled trials (RCTs) with larger samples to assess the proper place of pomalidomide as single agent or combined with other agents for RRMM.

Keywords: pomalidomide, multiple myeloma, meta-analysis

Introduction

Multiple myeloma (MM) is a hematologic disorder characterized by the proliferation of malignant plasma cell clones in the bone marrow or/and extramedually sites 1. It is the second most common hematologic malignancy and accounts for as many as 20% of deaths from hematological malignancies and 2% of deaths from all cancers 2, 3. MM is a heterogeneous disease, with its wide spectrum of aggression and treatment resistance and a diverse array of malignant cellular malfunctions, which drive individual clones 4, 5. Although progresses have been made over the last few decades for the development of new and increasingly effective agents, the prognosis of MM still remains unfavorable and it is regarded as an incurable disease characterizing by rapid relapse and broad treatment refractoriness 6, 7. To overcome this drug resistance, a number of therapeutic approaches have been developed in recent years 8. The introduction of the immunomodulatory drugs (IMiDs) (eg. thalidomide and lenalidomide) and the proteasome inhibitors (eg. bortezomib and calfizomib), used either as single agent or combined with classic chemotherapy, have improved the outcome for patients with MM 9, 10. However, even in patients who achieve stringent complete response (sCR), the disease will inevitably relapse, highlighting the necessity for the development of novel agents in treating newly diagnosed and relapsed/refractory MM (RRMM) 1, 4, 11-16.

Pomalidomide is one of the potent IMiDs and has been tested with very encouraging results for MM patients in early investigations, especially in those who have been refractory to both lenalidomide- and bortezomib-based therapies 17, 18. It was approved by the Food and Drug Administration (FDA) in February 2013 and the European Medicines Agency (EMA) in August 2013 for use alone or in combination with dexamethasone for those patients with MM who have received at least two prior therapies including lenalidomide and bortezomib and have demonstrated disease progression on their last therapy 13, 17. Several clinical trials have shown that pomalidomide was effective for patients with RRMM 19. However, the overall response rate (ORR) of pomalidomide varies in these studies, and these published reports consisted of the clinical trials with small sample sizes which have no enough power to determine the efficacy of pomalidomide for RRMM 20. Also, there are no complete summary of the efficacy and toxicity of pomalidomide for updated published clinical trials. Here, we performed a systematic review and a meta-analysis of clinical trials to summarize the effect of pomalidomide for the treatment of patients with RRMM.

Methods

Study selection

We performed a literature search without language restrictions using the databases of PubMed, MEDLINE and EMBASE on September 20, 2016 according to the Preferred Reporting Items for Systematic Reviews and Meta Analysis (PRISMA) guidelines 21. The search strategy included the phase “pomalidomiade” pairing independently with “multiple myeloma” or “MM”. The reference lists were screened of all of the identified studies in the field. Prospective trials (randomized controlled trials or single-armed observational trials) examining pomalidomiade as the treatment for RRMM were included. We included full texts and did not apply any restriction on age, gender or ethnicity. Retrospective studies, case reports, review articles and studies with less than 5 patients were excluded. When multiple publications reported on the same population, only the most recent study was included.

Data extraction

Data from each study were independently extracted by two reviewers using a standardized data-extraction form. Any disagreements were resolved by consensus or by consultation with a third reviewer. The following information was extracted from each study: (1) the first author's last name, (2) year of publication, (3) study design, (4) number and characteristics of subjects included, (5) mean age of subjects, (6) definition of RRMM, (7) dosage and procedure of pomalidomiade treatment, (8) response of the treatment, (9) patients' survival of the treatment and (10) effect size (95% confidential interval (CI)). Qualities of included non-comparative cohort studies using the Newcastle-Ottawa scale 22 and randomized controlled trials (RCTs) using the Cochrane tool for assessment of bias were assessed 23.

Statistical analysis

Considering some of the inter-study variation, the random-effects model was chosen to increase power and precision of this analysis regardless of heterogeneity for the entire study. All statistical analyses were conducted by the STATA software (version 12.0; Stata Corporation; College Station, TX, USA). Test results were considered to be statistically significant at p<0.05. We estimated relative risk (RR) with their 95% CI using the standardized mean difference (SMD). Heterogeneity was evaluated by I2 values, and we considered significant heterogeneity to be present when the I2 statistic was >50%, and moderate heterogeneity when the I2 statistic was >30%.

Results

Literature search

A total of 398 publications were identified during the initial search. After removing of redundant duplicates, 334 studies were included and considered as potentially relevant studies. After screening the title or abstract, 107 studies were excluded for not involving MM. Of the remaining 227 records, 171 reports were further excluded. Afterwards, 56 reports were retrieved and evaluated in detail. 48 of these studies met the exclusion criteria with 43 not involving RRMM, 2 combining carfilzomib (another novel agent) with pomalidomiade, and 3 duplicate publications of included studies. Eventually, 8 complete papers met the selection criteria and were included in this meta-analysis (Figure Figure11).

Figure 1
Data flow chart of number of studies identified and included into the meta-analysis

Study characteristics and qualities

The design features and characteristics of the included studies were presented in Table Table11, including 4 non-comparative studies 24-27 and 4 RCTs 28-31. A total of 891 evaluable patients were enrolled in the included eight prospective studies. The overall quality of the four single-arm pilot studies was moderate according to Newcastle-Ottawa scale, and the overall quality of the four RCTs were adequate according to Cochrane tool for assessment of bias (Table Table22). Regimens and dosage of pomalidomiade in different studies were also different (Table Table33).

Table 1
Basic information and characteristics of included studies
Table 2
The quality of included studies
Table 3
Regimen and Dosage of the treatment

Response rate of pomalidomide treatment

Because there were three studies using different regimens of pomalidomide, we divided them into two parts when analyzed 26, 30, 31. Efficacy of the treatment was summarized in Table Table44, including ORR, complete response (CR), very good partial response (VGPR), partial response (PR), median time-to-response (TOR), median overall survival (OS), median progression-free survival (PFS) and median duration of response (DOR). Data on the ORR (the rate of CR plus VGPR and PR) were extracted from the eight studies selected (891 patients). The random-effects model was chosen, and a high heterogeneity between studies (I2 =83.4%) was observed. The pooled proportion of ORR was 0.35 (95% CI 0.27 to 0.43, P=0.000) (Figure Figure22). Data on the complete response rate (CRR) were also extracted, and no heterogeneity existed (I2 =0.0%). The pooled proportion of CRR was 0.02 (95% CI 0.01 to 0.03, P=0.541) (Figure Figure33).

Figure 2
Overall response of pomalidomide treatment in patients with RRMM. (RRMM, relapsed/refractory multiple myeloma; ES, effect size)
Figure 3
Complete response of pomalidomide treatment in patients with RRMM. (RRMM, relapsed/refractory multiple myeloma; ES, effect size)
Table 4
Efficacy of the treatment

Potential side effects of pomalidomide treatment

The safety of pomalidomide was deemed good and no long-term complications were reported. In our included studies, common hematologic toxicities of the patients in different studies consisted of anemia, neutropenia and thrombocytopenia; nonhematologic toxicities included fatigue, dyspnea, bone pain, renal failure and pneumonia (Table Table55). Mortality of patients seldom occurred in the studies and no deaths were attributed to pomalidomide.

Table 5
Adverse effects of pomalidomide treatment

Discussion

Pomalidomide is a second generation IMiDs and has demonstrated effective even in MM patients who were refractory to lenalidomide and bortezomib 32. The reason why it was approved by FDA is that in several clinical trials it shows sustained and significant effects and great antitumor activity in RRMM 29, 33-35. In this meta-analysis, we summarized and evaluated the efficacy of pomalidomide in the treatment of RRMM. We identified eight studies, including four RCTs and four single-armed prospective studies with 891 patients. The qualities of the eight studies were adequate. The random-effects model was chosen, and a high heterogeneity between studies was observed.

Current treatment standards of RRMM include salvage chemotherapy, salvage autologous stem cell transplantation (auto-SCT), allogeneic stem cell transplantation (allo-SCT) and post-transplant consolidation/maintenance therapy 36-38. For those patients who received salvage chemotherapy, thalidomide, lenalidomide and bortezomib could be the treatments of choice. However, if the patients are still refractory to bortezomib or lenalidomide, it seemed it would be no good options for them. As a novel agent for RRMM, pomalidomide showed to have encouraging result for RRMM, as our analysis showed that the pooled proportion of ORR was 0.35 and CRR was 0.02 after pomalidomide therapy. This might better guide us the further use this agent. Of noted, ORR of pomalidomide as single agent was only 18% in the study conducted by Richardson et al 30, but ORR became 33% once combining pomalidomide with dexamethasone for RRMM patients. The effect of combination of pomalidomide with dexamethasone or cyclophosphamide were better than that of single agent was also seen in other studies included, but the severe toxicities resulted from combination treatment also needs our attention. It seems that the higher dosage of pomalidomide (4mg) is not correlated with better ORR and survival of RRMM patients compared to that of lower dosage (2mg) in our analysis, but we need further confirmation in case that it is the coincidence because only a small number of patients were included in the analysis. Given these findings, we may conclude that combination treatment would be better than that of the single agent therapy for RRMM.

Several limitations associated with this meta-analysis were recognized. Firstly, most of the studies we included had different treatment regimens and dosage, and it is hard to be uniformed. Also, the precision of pooled ES can be affected by the small sample size of some studies; therefore, we chose the random-effects model for the entire study to increase power and precision regardless of heterogeneity. Moreover, the effect of pomalidomide might vary by different ethnicities around the world, and it is difficult to summarize them.

Further studies would be required to address the more concrete mechanisms of pomalidomide for MM. Though the pooled ORR and CR in our analysis demonstrated some advantages of pomalidomide for those patients even refractory to bortezomib and lenalidomide, the sample size is small, so the conduction of more prospective RCTs with larger samples to assess the proper place of pomalidomide for single agent or combined with other agents in RRMM is necessary, and toxicities of pomalidomide should also be carefully monitored. What's more, whether pomalidomide can be extended to newly diagnosed or more advanced MM 39-41 or other hematological malignancies require further studying 42.

Author Contributions

RC and BC had the idea and designed this meta-analysis. RC and CL identified reports of trials and extracted data. XZ, YW and CG provided statistical advice and RC did all statistical analyses. RC, CL, YW and BC checked for statistical inconsistency and interpreted data. RC drafted the report and all other authors critically reviewed and approved final article. BC is guarantor of this article.

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