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Multiple myeloma, gammopathies

Improving prognostic assignment in older adults with multiple myeloma using acquired genetic features, clonal hemopoiesis and telomere length

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Fig. 1: The outcome of a range of molecular and clinical features as a function of age.
Fig. 2: The distribution and nature of the mutations used to define clonal hematopoiesis.

References

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Acknowledgements

We thank all the patients and their families for their contributions to this study. The authors acknowledge continued support from Multiple Myeloma Research Foundation and the Perelman Family Foundation. BAW and GJM received grant support through a Translational Research Program award from the Leukemia & Lymphoma Society (6020-20). EMB received funding from the Fédération Française de Recherche sur le Myélome et les Gammapathies under the aegis of the Fondation de France.

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Correspondence to Gareth J. Morgan.

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Boyle, E.M., Williams, L., Blaney, P. et al. Improving prognostic assignment in older adults with multiple myeloma using acquired genetic features, clonal hemopoiesis and telomere length. Leukemia 36, 221–224 (2022). https://doi.org/10.1038/s41375-021-01320-3

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