Although, historically, the definition of active multiple myeloma required treatment to be initiated at the first sign of end-organ damage (per the CRAB criteria),1 the majority of the patients did not receive treatment to prevent this damage from setting in. This may have been acceptable when the therapeutic options were limited and there was no apparent benefit from early intervention, but in an era when 5-year survival from myeloma is quoted at approximately 50%2 and some patients are living with this disease for 10 years or longer, the need to prevent end-organ damage rather than merely treating it has become imperative in ensuring improved survivorship and better tolerability to subsequent therapies.Considering this, the International Myeloma Working Group (IMWG) recently updated its definition of active multiple myeloma by adding cases that do not meet the classic CRAB criteria, but that have clonal bone marrow plasma cell percentage ≥60%, an involved:uninvolved serum free light-chain ratio ≥100 with the involved serum free light-chain ≥10 mg/dL, or more than 1 focal lesion on magnetic resonance imaging (MRI) studies.3 Furthermore, the widespread utilization and availability of serum and urine free light-chain analyses has decreased the number of truly nonsecretory cases of multiple myeloma, providing measurable markers of disease assessment and response in a larger number of patients. It is also accepted that patients with a biopsy-proven bony or extramedullary plasmacytoma and meeting any of the CRAB criteria, even without ≥10% clonal bone marrow plasma cells, are treated as active myeloma.3 While all of this certainly will increase the prevalence of active multiple myeloma, it also will affect clinical trial eligibility and outcomes by introducing a subgroup of patients to treatment before the morbidity from the diagnosis affects them.
Our understanding of the pathophysiology of multiple myeloma has gone beyond the traditional view of it as a malignant monoclonal plasma cell disorder that eventually becomes refractory to treatment. With genomic and epigenetic analyses, a clearer picture is emerging of the various factors at play as the disease course progresses. Studies consistently show that in every patient with multiple myeloma, several parallel malignant clones are present at the time of diagnosis, with the clonal characteristics changing over time and in relation to therapy.4 In patients known to have high-risk disease by cytogenetics, significantly more genomic changes occur over time compared with patients with standard-risk myeloma, suggesting genetic instability in the former.4 Thus, while effective treatment may reduce or eliminate the dominant clone, other clones can still exist and gain a survival and/or growth advantage. This may provide a basis for the deeper and more durable responses being seen with combination regimens in the frontline as well as the relapsed myeloma setting.5,6
Several reports over the past few years have focused on the interaction of genetic alterations in multiple myeloma with epigenetic changes, such as aberrant DNA and histone methylation or abnormal microRNA expression that are found to contribute to the pathobiology of the disease.7-9 The interaction of the malignant clone with its microenvironment, as well as mechanisms that lead to the malignant plasma cell evading such interactions in advanced disease, is also being better understood, leading to the development of newer, distinct classes of drugs.10
The role of biologic characteristics of the plasma cell beyond risk stratification in determining therapeutic options is emerging. Mutations in the cereblon gene leading to lower expression have been associated with resistance to immunomodulatory drugs (IMiDs) and poorer response rates and overall survival (OS) in patients treated with pomalidomide.24 This may seem to be the first biomarker in multiple myeloma with therapeutic implications, but it is not yet being used in routine practice. More standardization and calibration is needed before this may be widely available and used to direct therapeutic choices in routine patient care. Similar biomarkers, which may be helpful in predicting a response to proteasome inhibitor treatment in patients with multiple myeloma are IRE1/XBP1, the suppression of which confers resistance to bortezomib, although this has only been reported mostly in preclinical models with sparse patient-level data.25
Another group of biomarkers being tested to determine therapeutic eligibility is the expression of surface antigens on plasma cells, against which monoclonal antibodies (mAbs) are in clinical development (eg, CD38, CD138, CD56). One of the tools that should be available soon for commercial use is a molecular profiling panel called MMprofiler (SkylineDx), which would have the capability of providing the SKY92 prognostic gene signature, cytogenetic markers, GEP clusters, single-geneexpression, and patient-level customized genome-wide data.
From 1998 until 2006, the clinical responses in patients with multiple myeloma, as well as determining disease relapse, were based on the European Group for Blood and Marrow Transplantation criteria.26 The IMWG updated these criteria in 2006, when some older definitions were clarified, new response categories were added, and the free light-chain criteria for measurable disease and response were defined.27,28 This update went beyond just a state of complete response (CR) to further categorize it into molecular CR, immunophenotypic CR, andstringent CR.27 These refinements of the CR category have been validated in various clinical settings and are achievable therapeutic goals to improve patient outcomes.29 Because the recently reported and currently used treatment regimens for multiple myeloma have been showing better responses than ever noted before, there has been work to further refine the depth of response by determining minimal residual disease (MRD) status of patients. This can be done by utilizing flow cytometry or high-throughput sequencing. Studies have shown that among patients achieving a biochemical CR, MRD-negative status is associated with superior outcomes, including progression-free survival (PFS) and OS.30-32 Recent data show that high-throughput sequencing–based MRD testing has at least a 10-fold higher sensitivity than the flow cytometry–based methodology.16 These techniques are being employed commonly in clinical trials, but uniform criteria for routine clinical practice are yet to be established.
Another aspect of the change has been the newer imaging modalities, of which positron emission tomography (PET) and MRI scans have been included in disease assessment and progression criteria already, as as well as the IMWG and are now considered standard of care.3 Further refinement of these techniques has helped in predicting prognosis in various therapeutic settings. For example, the presence of more than 3 focal lesions or standardized uptake value >4.2 at diagnosis are predictors of shorter PFS, and PET-CT negativity 3 months after an autologous stem cell transplant (ASCT) predicts a superior PFS and OS.33
Historically, the treatment algorithm guidelines in multiple myeloma have been based on whether a patient is considered ASCT-eligible or not. This had dichotomized the treatment approach, with the major difference being that younger, transplant-eligible patients would not be given melphalan- based regimens.19 Although this is still true, the distinction between transplant-eligible and -ineligible patients become less defined in recent years. The combination therapeutic regimens being used widely with IMiDs and proteasome inhibitors, such as cyclophosphamide-bortezomib-dexamethasone, lenalidomide-bortezomib-dexamethasone, and carfilzomib- lenalidomide-dexamethoasone, are fairly well tolerated and have made the use of melphalan less frequent, at least in the United States.6,34
Since the response rates have been ever improving, achieving an objective response to induction treatment in nearly all patients has become the norm rather than the exception, at least in the newly diagnosed setting and in a significant proportion of patients with relapsed disease. Thus, the comparator arm in randomized, phase III clinical trials is no longer single-agent dexamethasone alone and novel combination regimens have to show further improvement over the benefit from IMiD and proteasome inhibitor–containing doublets—at the least. The goals of treatment and therapeutic decision making have, in turn, been broadened to address several previously overlooked questions, such as quality of life, survivorship, improving depth of response, managing long-term complications, refining the duration of treatment, and demonstrating improvement in OS.35-37
The first novel therapeutic agent for the treatment of multiple myeloma to be approved by the FDA was bortezomib in 2003. Since then, the 2 classes of drugs, proteasome inhibitors and IMiDs, have defined how we manage this disease and have resulted in significantly improved OS and PFS in patients. However, until recently, the only newer agents receiving FDA approval for the treatment of myeloma were more drugs within these 2 classes, with better side-effect profiles and an improvement in efficacy.38,39 In 2014, a novel category of targeted drugs, the histone-deacetylase inhibitors, became available, with panobinostat being the first agent in this category.40 Although these agents have been received with some debate around its efficacy and adverse-event profile, several combination trials are under way to better define its role in myeloma therapeutics. Nevertheless, the availability of a novel drug class, rather than just novel agents within the older classes, is an exciting development. Several more drug classes are undergoing rapid clinical development, including mAbs (eg, anti-CD38, anti-CD138, and anti-CS1), a kinesin spindle protein inhibitor (filanesib), a phosphatidylinositide-3-kinase (PI3K)-AKT-mammalian target of rapamycin (mTOR) pathway inhibitor (afuresertib), a PIM-kinase inhibitor (LGH447), and a nuclear protein exportin 1 (selinexor), among others.41 Alternative approaches, including vaccine therapy and chimeric antigen receptor (CAR) T cells, are also being explored for multiple myeloma in several ongoing clinical trials (Table 2).42,43 Availability of these and other truly novel therapeutic options will help take the next step toward improving outcomes in patients with multiple myeloma by hopefully affecting disease biology and deepening the response rates, as well as providing more longer lasting efficacy, potentially realizing an elusive cure in this disease.
Affiliation: Sikander Ailawadhi, MD, is from the Division of Hematology-Oncology, Mayo Clinic, Jacksonville, FL.
Disclosure: Dr Ailawadhi has been a consultant and on the advisory board for Takeda Oncology and Onyx Pharmaceuticals.
Address correspondence to: Sikander Ailawadhi, MD, Division of Hematology-Oncology, Mayo Clinic, 4500 San Pablo Rd, Jacksonville, FL 32256. Phone: 904 953 6468; email: ailawadhi. email@example.com
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- Rajkumar SV, Dimopoulos MA, Palumbo A, et al. International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma. Lancet Oncol. 2014;15(12):e538-548.
- Keats JJ, Chesi M, Egan JB, et al. Clonal competition with alternating dominance in multiple myeloma. Blood. 2012;120(5):1067-1076.
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- Stewart AK, Rajkumar SV, Dimopoulos MA, et al; ASPIRE Investigators. Carfilzomib, lenalidomide, and dexamethasone for relapsed multiple myeloma. N Engl J Med. 2015;372(2):142-152.
- Chapman MA, Lawrence MS, Keats JJ, et al. Initial genome sequencing and analysis of multiple myeloma. Nature. 2011;471(7339):467-472.
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- Sharma A, Heuck CJ, Fazzari MJ, et al. DNA methylation alterations in multiple myeloma as a model for epigenetic changes in cancer. Wiley Interdiscip Rev Syst Biol Med. 2010;2(6):654-669.
- Ocio EM, Richardson PG, Rajkumar SV, et al. New drugs and novel mechanisms of action in multiple myeloma in 2013: a report from the International Myeloma Working Group (IMWG). Leukemia. 2014;28(3):525-542.
- Ailawadhi S, Aldoss IT, Yang D, et al. Outcome disparities in multiple myeloma: a SEER-based comparative analysis of ethnic subgroups. Br J Haematol. 2012;158(1):91-98.
- Greipp PR, San Miguel J, Durie BG, et al. International staging system for multiple myeloma. J Clin Oncol. 2005;23(15):3412-3420.
- Dispenzieri A, Rajkumar SV, Gertz MA, et al. Treatment of newly diagnosed multiple myeloma based on Mayo Stratification of Myeloma and Risk-adapted Therapy (mSMART): consensus statement. Mayo Clin Proc. 2007;82(3):323-341.
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- Kortum KM, Langer C, Monge J, et al. Targeted sequencing using a 47 gene multiple myeloma mutation panel (M(3) P) in -17p high risk disease. Br J Haematol. 2015;168(4):507-510.
- Kortum KM, Langer C, Monge J, et al. Longitudinal analysis of 25 sequential sample-pairs using a custom multiple myeloma mutation sequencing panel (M(3)P). Ann Hematol. 2015;94(7):1205-1211.
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