The Evolving Landscape: Exploring the Future of Myelodysplastic Syndrome Treatment with Dr. Rami Komrokji
This perspective delves into the evolving landscape of Myelodysplastic Syndrome (MDS) treatment. MDS presents a significant clinical challenge, often progressing to acute myeloid leukemia. For low-risk MDS, the emphasis is on personalized care through comprehensive risk assessment, clinical monitori...
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Veröffentlicht in: | Cancers 2023-11, Vol.15 (21), p.5170 |
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description | This perspective delves into the evolving landscape of Myelodysplastic Syndrome (MDS) treatment. MDS presents a significant clinical challenge, often progressing to acute myeloid leukemia. For low-risk MDS, the emphasis is on personalized care through comprehensive risk assessment, clinical monitoring, and tailored interventions, including promising agents like erythropoiesis-stimulating agents, lenalidomide, and luspatercept, with the anticipation of an expanding therapeutic arsenal and early intervention for improved outcomes. In contrast, high-risk MDS treatment is evolving towards upfront doublet or triplet therapies with a focus on minimal residual disease (MRD) monitoring. A holistic approach integrates various modalities, including stem cell transplant and post-transplant maintenance, all guided by individual patient circumstances. Risk-adapted strategies are crucial for enhancing patient outcomes. Precision medicine for MDS treatment is budding, largely driven by Next Generation Sequencing (NGS). NGS aids in early diagnosis, prognostication, and the targeting of specific mutations, with molecular data increasingly informing treatment responses and allowing for tailored interventions. Clinical trials within homogeneous patient groups with similar molecular profiles are becoming more common, enhancing treatment precision. In conclusion, the future of MDS treatment is moving towards personalized medicine, leveraging advanced technologies like NGS and molecular insights to improve outcomes in the realm of hematological malignancies. |
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MDS presents a significant clinical challenge, often progressing to acute myeloid leukemia. For low-risk MDS, the emphasis is on personalized care through comprehensive risk assessment, clinical monitoring, and tailored interventions, including promising agents like erythropoiesis-stimulating agents, lenalidomide, and luspatercept, with the anticipation of an expanding therapeutic arsenal and early intervention for improved outcomes. In contrast, high-risk MDS treatment is evolving towards upfront doublet or triplet therapies with a focus on minimal residual disease (MRD) monitoring. A holistic approach integrates various modalities, including stem cell transplant and post-transplant maintenance, all guided by individual patient circumstances. Risk-adapted strategies are crucial for enhancing patient outcomes. Precision medicine for MDS treatment is budding, largely driven by Next Generation Sequencing (NGS). NGS aids in early diagnosis, prognostication, and the targeting of specific mutations, with molecular data increasingly informing treatment responses and allowing for tailored interventions. Clinical trials within homogeneous patient groups with similar molecular profiles are becoming more common, enhancing treatment precision. In conclusion, the future of MDS treatment is moving towards personalized medicine, leveraging advanced technologies like NGS and molecular insights to improve outcomes in the realm of hematological malignancies.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15215170</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Acute myeloid leukemia ; Anemia ; Budding ; Clinical outcomes ; Clinical trials ; Diagnosis ; Disease ; Erythropoiesis ; Health aspects ; Hematology ; Leukemia ; Malignancy ; Medical colleges ; Minimal residual disease ; Mutation ; Myelodysplastic syndrome ; Myelodysplastic syndromes ; Neutropenia ; Next-generation sequencing ; Older people ; Patients ; Precision medicine ; Risk assessment ; Stem cell transplantation ; Stem cells ; Transplantation</subject><ispartof>Cancers, 2023-11, Vol.15 (21), p.5170</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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MDS presents a significant clinical challenge, often progressing to acute myeloid leukemia. For low-risk MDS, the emphasis is on personalized care through comprehensive risk assessment, clinical monitoring, and tailored interventions, including promising agents like erythropoiesis-stimulating agents, lenalidomide, and luspatercept, with the anticipation of an expanding therapeutic arsenal and early intervention for improved outcomes. In contrast, high-risk MDS treatment is evolving towards upfront doublet or triplet therapies with a focus on minimal residual disease (MRD) monitoring. A holistic approach integrates various modalities, including stem cell transplant and post-transplant maintenance, all guided by individual patient circumstances. Risk-adapted strategies are crucial for enhancing patient outcomes. Precision medicine for MDS treatment is budding, largely driven by Next Generation Sequencing (NGS). NGS aids in early diagnosis, prognostication, and the targeting of specific mutations, with molecular data increasingly informing treatment responses and allowing for tailored interventions. Clinical trials within homogeneous patient groups with similar molecular profiles are becoming more common, enhancing treatment precision. In conclusion, the future of MDS treatment is moving towards personalized medicine, leveraging advanced technologies like NGS and molecular insights to improve outcomes in the realm of hematological malignancies.</description><subject>Acute myeloid leukemia</subject><subject>Anemia</subject><subject>Budding</subject><subject>Clinical outcomes</subject><subject>Clinical trials</subject><subject>Diagnosis</subject><subject>Disease</subject><subject>Erythropoiesis</subject><subject>Health aspects</subject><subject>Hematology</subject><subject>Leukemia</subject><subject>Malignancy</subject><subject>Medical colleges</subject><subject>Minimal residual disease</subject><subject>Mutation</subject><subject>Myelodysplastic syndrome</subject><subject>Myelodysplastic syndromes</subject><subject>Neutropenia</subject><subject>Next-generation sequencing</subject><subject>Older people</subject><subject>Patients</subject><subject>Precision medicine</subject><subject>Risk assessment</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Transplantation</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkcFvFCEUxonRxGbt2SuJFy-7hYEBxltTt2pc08RuzxOGebSsMzAC07r_vUxqojb9OPDy5fe-PHgIvaVkw1hDzoz2BmKidUVrKskLdFIRWa2FaPjLf-rX6DSlAylijEohT5Db3wHe3ofh3vlbvNO-T0ZP8AFvf01DiIuZC3E55zkCDhZ_O8IQ-mOaBp2yM_j66PsYRsD7CDqP4DN-cPkOf4wb_F2PDn8NYww_Du4NemX1kOD0z71CN5fb_cXn9e7q05eL893aMMHzWlXcWqoYIx1XWlshgBIqOmkb4NwIy7umXx7Zib6zUCkqOZFM9KxuimfYCr1_zJ1i-DlDyu3okoFh0B7CnNpKqaaIFa3QuyfoIczRl-kWShGuaqn-Urd6gNZ5G3LUZgltz6Ws6vKTvC7U5hmqnB5GZ4IH64r_X8PZY4OJIaUItp2iG3U8tpS0y1LbJ0tlvwHCnpQ4</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Jackewicz, Sean Henry</creator><creator>Coloma, Helena S.</creator><creator>Cortiana, Viviana</creator><creator>Joshi, Muskan</creator><creator>Menon, Gayathri P.</creator><creator>Balasubramanian, Maduri</creator><creator>Park, Chandler H.</creator><creator>Leyfman, Yan</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PKEHL</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0009-0002-8764-9218</orcidid><orcidid>https://orcid.org/0009-0002-0863-0800</orcidid><orcidid>https://orcid.org/0000-0002-9331-1857</orcidid></search><sort><creationdate>20231101</creationdate><title>The Evolving Landscape: Exploring the Future of Myelodysplastic Syndrome Treatment with Dr. Rami Komrokji</title><author>Jackewicz, Sean Henry ; 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MDS presents a significant clinical challenge, often progressing to acute myeloid leukemia. For low-risk MDS, the emphasis is on personalized care through comprehensive risk assessment, clinical monitoring, and tailored interventions, including promising agents like erythropoiesis-stimulating agents, lenalidomide, and luspatercept, with the anticipation of an expanding therapeutic arsenal and early intervention for improved outcomes. In contrast, high-risk MDS treatment is evolving towards upfront doublet or triplet therapies with a focus on minimal residual disease (MRD) monitoring. A holistic approach integrates various modalities, including stem cell transplant and post-transplant maintenance, all guided by individual patient circumstances. Risk-adapted strategies are crucial for enhancing patient outcomes. Precision medicine for MDS treatment is budding, largely driven by Next Generation Sequencing (NGS). NGS aids in early diagnosis, prognostication, and the targeting of specific mutations, with molecular data increasingly informing treatment responses and allowing for tailored interventions. Clinical trials within homogeneous patient groups with similar molecular profiles are becoming more common, enhancing treatment precision. In conclusion, the future of MDS treatment is moving towards personalized medicine, leveraging advanced technologies like NGS and molecular insights to improve outcomes in the realm of hematological malignancies.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/cancers15215170</doi><orcidid>https://orcid.org/0009-0002-8764-9218</orcidid><orcidid>https://orcid.org/0009-0002-0863-0800</orcidid><orcidid>https://orcid.org/0000-0002-9331-1857</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acute myeloid leukemia Anemia Budding Clinical outcomes Clinical trials Diagnosis Disease Erythropoiesis Health aspects Hematology Leukemia Malignancy Medical colleges Minimal residual disease Mutation Myelodysplastic syndrome Myelodysplastic syndromes Neutropenia Next-generation sequencing Older people Patients Precision medicine Risk assessment Stem cell transplantation Stem cells Transplantation |
title | The Evolving Landscape: Exploring the Future of Myelodysplastic Syndrome Treatment with Dr. Rami Komrokji |
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