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During the XVII International Myeloma Workshop (IMW) meeting in Boston, US, Sonja Zweegman and Alessandra Larocca presented an educational session entitled: “Management of Elderly Patients with Multiple Myeloma (MM)”.1 The current treatment options for frail patients were discussed, along with classification systems, and potential future directions for therapies.1
Also, at the IMW meeting, Ho Sup Lee presented an analysis of the outcomes of patients treated with bortezomib (V)-based regimens, by frailty scoring systems. The group found that patients who were classified as frail by IMWG criteria, or high-risk by R-MCI criteria, had a shorter survival compared to patients who were not frail, or who were deemed low-risk. The R-MCI criteria was more accurately able to predict survival compared to IMWG, however R-MCI is less easy to implement, indicating a requirement for a more simplified and predictable frailty risk model to use in clinical practice. Read more about this study below.5
Elderly and frail patients are often excluded from clinical trials, therefore clinical data on this population is lacking.5 When treating elderly patients, several factors should be considered;1
The current treatment paradigm for elderly patients with MM is shown in Table 1.
Table 1. Frontline treatment of elderly patients with MM1
IMWG frailty index, despite its limitations, is the best method of detecting frailty in MM. Treatment of these patients should include a shorter induction duration, a lower dosage and less dense therapy, whilst aiming to achieve a long duration of response. Drugs that are intended for ‘non-frail’ patients, like the monoclonal antibodies should be investigated further in this population |
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For fit elderly patients |
|
---|---|
Transplant eligible; ASCT |
Non-transplant eligible; without ASCT |
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|
|
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Conclusion: consider transplant, in combination with a monoclonal antibody containing regimen. For transplant ineligible patients, consider the approved regimens in the country, e.g. the European Medicines Agency (EMA) prefer VRd or dara-VMP. For patients with renal failure or high-risk cytogenetics, V-based regimens should be considered. Additional benefit may be seen by adding a monoclonal antibody to a proteasome inhibitor plus immunomodulatory drug regimen e.g. elotuzumab-VRd or dara-VRd1 |
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For the unfit and frail patients |
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Other trials: HOVON 143 (EudraCT 2016-002600-90): investigating the concept of non-toxic drugs for frail patients using ixazomib + dara + d13 |
Ongoing trials: UK-MRA FiTNEss trial, Myeloma XIV (NCT03720041): frailty-adjusted dosing comparing standard reactive therapy to frailty adjusted adaptive therapy using ixazomib + Rd14 |
Also during the XVII IMW meeting, Ho Sup Lee, Kosin University College of Medicine, Busan, KR, presented an evaluation of the clinical impact of frailty on outcomes in transplant ineligible MM patients treated with V-based chemotherapy as frontline treatment. Additionally, the authors compared the IMWG and R-MCI frailty scoring systems.
This retrospective study analyzed the outcomes of 366 patients (median age: 69 years) treated in South Korea between 2007 and 2017. Patients received VMP as frontline therapy, and were classified according to the IWMG (fit, unfit, frail) or R-MCI (low-, intermediate- or high-risk) criteria. For the IMWG criteria, ADL/instrumental ADL was substituted for Eastern Cooperative Oncology (ECOG) scores. More patients were classified as frail by IMWG criteria (43.4%) compared to high-risk by R-MCI criteria (13.7%).
The median PFS and OS for the total cohort, and for each frailty group, are shown in Table 2. When comparing frailty classification for PFS and OS by IMWG or R-MCI criteria, all were statistically significant (p< 0.001).
Table 2. PFS and OS by frailty score
|
N |
Median PFS, months (range) |
Median OS, months (range) |
---|---|---|---|
Total cohort |
366 |
23.7 (18.62–28.84) |
56.2 (46.36–66.04) |
IMWG scoring |
|
|
|
Fit |
78 |
24.6 (15.8–33.4) |
80.7 (54.3–107.2) |
Unfit |
129 |
38 (26.5–49.5) |
118 (55.9–180.2) |
Frail |
159 |
16.7 (13.2–20.1) |
38.5 (28.7–48.2) |
R-MCI scoring |
|
|
|
Low risk |
136 |
31.9 (24.1–39.8) |
118 (57.1–178.9) |
Intermediate risk |
180 |
24.6 (17.5–31.6) |
58.1 (47.8–68.4) |
High-risk |
50 |
12.8 (5.3–20.3) |
26.9 (21.1–32.7) |
IMWG, International Myeloma Working Group; OS, overall survival; PFS, progression free survival; R-MCI, revised Myeloma Comorbidity Index |
Using a cox proportional hazard model for PFS and OS, this analysis found that only classification system was significantly associated with PFS (for both IMWG and R-MCI), whilst for OS, age was significant for both classification systems, though classification system was only significant for R-MCI.
Patients who were classified as frail by IMWG criteria, or high-risk by R-MCI criteria, had a shorter survival compared to patients who were not frail, or who were deemed low-risk. The R-MCI criteria was more accurately able to predict survival compared to IMWG, however, due to the number of variables measured, R-MCI is less easy to implement. Therefore, there is a requirement for a more simplified and predictable frailty risk model to use in clinical practice.
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