Paper Details 
Original Abstract of the Article :
There is increasing evidence regarding the role of various maintenance therapy (MT) strategies after initial induction to treat newly diagnosed transplant-ineligible patients with MM. We reviewed the literature on available regimens for patients with transplant-ineligible newly diagnosed multiple my...See full text at original site
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引用元:
https://doi.org/10.1016/j.critrevonc.2022.103744

データ提供:米国国立医学図書館(NLM)

Tackling Transplant-Ineligible Multiple Myeloma: A Desert of Hope

The [treatment of transplant-ineligible multiple myeloma (NDMM)] presents significant challenges. This study examines the evidence-based recommendations for [induction and maintenance treatment] of NDMM. Much like a desert explorer seeking the most effective route to a distant oasis, this research explores the best strategies for managing this challenging disease.

Navigating the Landscape of Multiple Myeloma Treatment

The study reveals that [lenalidomide (R)-based regimens are still the front-line therapy] for NDMM, with increasing use of [bortezomib-based regimens]. The study also highlights the importance of [maintenance therapy (MT)], demonstrating its [survival benefits] compared to patients without MT. This is akin to providing a well-stocked caravan with essential supplies for a long desert journey, ensuring the best possible chance of survival.

Hope for Transplant-Ineligible Multiple Myeloma Patients

The study offers a glimmer of hope for individuals with NDMM, suggesting that [MT strategies can significantly improve outcomes]. This is a crucial finding, particularly for those who are not candidates for [autologous stem cell transplantation]. Much like discovering a hidden oasis in the desert, this research offers a new avenue for managing this challenging disease.

Dr.Camel's Conclusion

This study highlights the importance of maintenance therapy in the treatment of transplant-ineligible multiple myeloma. The findings suggest that MT strategies can significantly improve survival outcomes and offer hope for individuals who are not candidates for autologous stem cell transplantation. This research underscores the need for continued efforts to optimize treatments for this challenging disease.

Date :
  1. Date Completed 2022-07-26
  2. Date Revised 2022-07-26
Further Info :

Pubmed ID

35717005

DOI: Digital Object Identifier

10.1016/j.critrevonc.2022.103744

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