Correction: Mancuso et al. Forcing Ahead: Second-Line Treatment Options for Lenalidomide-Refractory Multiple Myeloma. Cancers 2025, 17, 1168
Katia Mancuso, Simona Barbato, Francesco Di Raimondo, Francesca Gay, Pellegrino Musto, Massimo Offidani, Maria Teresa Petrucci, Elena Zamagni, Renato Zambello, Michele Cavo
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsMultiple Myeloma Research and Treatments · Chronic Myeloid Leukemia Treatments · Protein Degradation and Inhibitors
Affiliations
The authors have separated the affiliations originally listed in affiliation 4—this is so both affiliations can be organized from subordinate to superior.
Tables
In the original publication [1], the titles and contents of Tables 1 and 2 were not up-to-date with the final version of the manuscript, as requested by the Authors. The corrected tables “Table 1. Currently licensed treatment strategies in len-refractory MM: data on clinical efficacy” and “Table 2. ADC-based triplet treatments for len-refractory MM currently under EMA evaluation: data on clinical efficacy” appear below.
Text Correction
There was text correction made to the following sentence in Section 2—‘In a study aimed at gaining insights into the different patterns of len resistance, a longer exposure (≥1 year) to len and longer interval (≥18 months) from last len dose to subsequent start of pomalidomide were associated with higher response rates and longer PFS and OS, highlighting the importance of optimal sequencing to face the challenge of IMiD refractoriness [5]’.
The subheading for Section 4.1 has been updated to ‘PI-Based Doublets and Triplets Incorporating Either an Anti-CD38 MoAb or an Inhibitor of Exportin 1’.
In Section 4.2 there has been a text correction to paragraph 4—‘The combinations of Pd with MoAbs targeting CD38 and SLAMF7, like isa or elo (i.e., isa-Pd and elo-Pd, respectively), may be considered in heavily pretreated patients’.
There has been a text correction to Section 5, paragraph 5—‘Notably, at the second interim analysis, mOS was not yet reached in both arms, and 36-month estimations of OS were 74% in the BVd group and 60% in the DVd group, suggesting an early and statistically significant benefit with BVd (the HR was 0.58 [95% CI, 0.43–0.79]) [79]’.
The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.
The reference list from the paper itself. Each links out to its DOI / PubMed record.