Metronomic chemotherapy regimens and targeted therapies in non-Hodgkin lymphoma: The best of two worlds
Novel drugs are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs). Notwithstanding, especially in aggressive subtypes, chemotherapy remains the pillar of treatment. Indeed, the combination of highly effective Maximum-Tolerated-Dose Chemotherapy (MTD-CHEMO) + “novel drugs”...
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description | Novel drugs are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs). Notwithstanding, especially in aggressive subtypes, chemotherapy remains the pillar of treatment. Indeed, the combination of highly effective Maximum-Tolerated-Dose Chemotherapy (MTD-CHEMO) + “novel drugs”, has so far, fallen short from expectations, often because it caused excessive toxicity. Metronomic chemotherapy (mCHEMO), which is the frequent, long-term administration of low dose cytotoxic drugs, may allow more effective and tolerable combinations. mCHEMO pharmacodynamics, has been described as pleiotropic. In fact, it may have different cellular and molecular targets, when drugs or their schedules are modified. Although mCHEMO has been little explored in NHLs, pre-clinical studies - in lymphoma models - which addressed the activity of mCHEMO in combination with novel drugs, have shown very promising results. These included inhibitors of histone deacetylase, mTOR and PI3K/mTOR, as well as the immune checkpoint inhibitor anti-PD-L1. Moreover, a few impressive reports have recently shown all-oral mCHEMO schedules, with or without rituximab, can effectively shrink both B and T-cell aggressive NHLs. Indeed, these regimens allowed elderly-frail patients to achieve sustained remission, while toxicity proved manageable. In our opinion, all-oral mCHEMO, is an active, easy-to start, well-tolerated, and inexpensive therapeutic approach, which deserves further investigation. Most importantly, mCHEMO, holds promise to empower the activity of novel targeted therapies, without causing excessive toxicity.
•Targeted therapies are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs).•All-oral metronomic chemotherapy (mCHEMO) schedules have shown good activity and tolerability in elderly-frail NHL patients.•In NHLs, the combination of targeted therapies with mCHEMO schedules have shown promising pre-clinical and clinical results.•mCHEMO may be an ideal platform for further improving the armamentarium of NHLs therapies. |
doi_str_mv | 10.1016/j.canlet.2021.10.018 |
format | Article |
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•Targeted therapies are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs).•All-oral metronomic chemotherapy (mCHEMO) schedules have shown good activity and tolerability in elderly-frail NHL patients.•In NHLs, the combination of targeted therapies with mCHEMO schedules have shown promising pre-clinical and clinical results.•mCHEMO may be an ideal platform for further improving the armamentarium of NHLs therapies.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2021.10.018</identifier><identifier>PMID: 34673128</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>1-Phosphatidylinositol 3-kinase ; Administration, Metronomic ; Aged ; Apoptosis ; Cancer therapies ; Cell cycle ; Cell growth ; Chemotherapy ; Clinical studies ; Cytotoxicity ; Diffuse large B-Cell ; Dose-Response Relationship, Drug ; Drug dosages ; Elderly ; Frailty ; Geriatric Assessment ; Histone deacetylase ; Histone Deacetylase Inhibitors - therapeutic use ; Histone Deacetylases - genetics ; Humans ; Immune checkpoint inhibitors ; Immune Checkpoint Inhibitors - therapeutic use ; Immunosuppressive agents ; Lymphocytes T ; Lymphoma ; Lymphoma, Non-Hodgkin - drug therapy ; Lymphoma, Non-Hodgkin - genetics ; Lymphoma, Non-Hodgkin - pathology ; Lymphoma, T-Cell - drug therapy ; Lymphoma, T-Cell - pathology ; Metronomic chemotherapy ; Non-Hodgkin's lymphoma ; Non-Hodgkin-lymphoma ; PD-L1 protein ; Pharmaceutical industry ; Pharmacodynamics ; Phosphatidylinositol 3-Kinases - genetics ; Preclinical studies ; Remission ; Rituximab ; Rituximab - therapeutic use ; Schedules ; Signal Transduction - drug effects ; T-cell lymphoma ; TOR protein ; TOR Serine-Threonine Kinases - antagonists & inhibitors ; TOR Serine-Threonine Kinases - genetics</subject><ispartof>Cancer letters, 2022-01, Vol.524, p.144-150</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2021 Elsevier B.V. All rights reserved.</rights><rights>2021. Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-42c648b32917f27fb1821f4b94d12d2dc50b86b4740a3b7dce38d6b0df42bd223</citedby><cites>FETCH-LOGICAL-c390t-42c648b32917f27fb1821f4b94d12d2dc50b86b4740a3b7dce38d6b0df42bd223</cites><orcidid>0000-0002-8597-8459 ; 0000-0001-7120-9141</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.canlet.2021.10.018$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34673128$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cox, Maria Christina</creatorcontrib><creatorcontrib>Bocci, Guido</creatorcontrib><title>Metronomic chemotherapy regimens and targeted therapies in non-Hodgkin lymphoma: The best of two worlds</title><title>Cancer letters</title><addtitle>Cancer Lett</addtitle><description>Novel drugs are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs). Notwithstanding, especially in aggressive subtypes, chemotherapy remains the pillar of treatment. Indeed, the combination of highly effective Maximum-Tolerated-Dose Chemotherapy (MTD-CHEMO) + “novel drugs”, has so far, fallen short from expectations, often because it caused excessive toxicity. Metronomic chemotherapy (mCHEMO), which is the frequent, long-term administration of low dose cytotoxic drugs, may allow more effective and tolerable combinations. mCHEMO pharmacodynamics, has been described as pleiotropic. In fact, it may have different cellular and molecular targets, when drugs or their schedules are modified. Although mCHEMO has been little explored in NHLs, pre-clinical studies - in lymphoma models - which addressed the activity of mCHEMO in combination with novel drugs, have shown very promising results. These included inhibitors of histone deacetylase, mTOR and PI3K/mTOR, as well as the immune checkpoint inhibitor anti-PD-L1. Moreover, a few impressive reports have recently shown all-oral mCHEMO schedules, with or without rituximab, can effectively shrink both B and T-cell aggressive NHLs. Indeed, these regimens allowed elderly-frail patients to achieve sustained remission, while toxicity proved manageable. In our opinion, all-oral mCHEMO, is an active, easy-to start, well-tolerated, and inexpensive therapeutic approach, which deserves further investigation. Most importantly, mCHEMO, holds promise to empower the activity of novel targeted therapies, without causing excessive toxicity.
•Targeted therapies are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs).•All-oral metronomic chemotherapy (mCHEMO) schedules have shown good activity and tolerability in elderly-frail NHL patients.•In NHLs, the combination of targeted therapies with mCHEMO schedules have shown promising pre-clinical and clinical results.•mCHEMO may be an ideal platform for further improving the armamentarium of NHLs therapies.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>Administration, Metronomic</subject><subject>Aged</subject><subject>Apoptosis</subject><subject>Cancer therapies</subject><subject>Cell cycle</subject><subject>Cell growth</subject><subject>Chemotherapy</subject><subject>Clinical studies</subject><subject>Cytotoxicity</subject><subject>Diffuse large B-Cell</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug dosages</subject><subject>Elderly</subject><subject>Frailty</subject><subject>Geriatric Assessment</subject><subject>Histone deacetylase</subject><subject>Histone Deacetylase Inhibitors - therapeutic use</subject><subject>Histone Deacetylases - genetics</subject><subject>Humans</subject><subject>Immune checkpoint inhibitors</subject><subject>Immune Checkpoint Inhibitors - therapeutic use</subject><subject>Immunosuppressive agents</subject><subject>Lymphocytes T</subject><subject>Lymphoma</subject><subject>Lymphoma, Non-Hodgkin - drug therapy</subject><subject>Lymphoma, Non-Hodgkin - genetics</subject><subject>Lymphoma, Non-Hodgkin - pathology</subject><subject>Lymphoma, T-Cell - drug therapy</subject><subject>Lymphoma, T-Cell - pathology</subject><subject>Metronomic chemotherapy</subject><subject>Non-Hodgkin's lymphoma</subject><subject>Non-Hodgkin-lymphoma</subject><subject>PD-L1 protein</subject><subject>Pharmaceutical industry</subject><subject>Pharmacodynamics</subject><subject>Phosphatidylinositol 3-Kinases - genetics</subject><subject>Preclinical studies</subject><subject>Remission</subject><subject>Rituximab</subject><subject>Rituximab - therapeutic use</subject><subject>Schedules</subject><subject>Signal Transduction - drug effects</subject><subject>T-cell lymphoma</subject><subject>TOR protein</subject><subject>TOR Serine-Threonine Kinases - antagonists & inhibitors</subject><subject>TOR Serine-Threonine Kinases - genetics</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1vEzEQhi1ERUPhHyBkiUsvG_y1u94ekKqqpUhFXMrZ8sds4rBrB9tplX9fh5QeOHCaVzPPfGhehD5QsqSEdp83S6vDBGXJCKM1tSRUvkILKnvW9IMkr9GCcCIaLnl7it7mvCGEtKJv36BTLrqeUyYXaPUdSoohzt5iu4Y5ljUkvd3jBCs_Q8hYB4eLTisoUMWfqoeMfcAhhuY2utWvqqf9vF3HWV_g-zVgA7ngOOLyGPFjTJPL79DJqKcM75_jGfp5c31_ddvc_fj67eryrrF8IKURzHZCGs4G2o-sHw2VjI7CDMJR5pizLTGyM6IXRHPTOwtcus4QNwpmHGP8DJ0f525T_L2rZ6jZZwvTpAPEXVaslUJw3g5dRT_9g27iLoV6XaUGLruOCVkpcaRsijknGNU2-VmnvaJEHYxQG3U0Qh2MOGSrEbXt4_PwnZnBvTT9_XwFvhwBqN948JBUth6CBecT2KJc9P_f8AQuBpuX</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Cox, Maria Christina</creator><creator>Bocci, Guido</creator><general>Elsevier B.V</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8597-8459</orcidid><orcidid>https://orcid.org/0000-0001-7120-9141</orcidid></search><sort><creationdate>20220101</creationdate><title>Metronomic chemotherapy regimens and targeted therapies in non-Hodgkin lymphoma: The best of two worlds</title><author>Cox, Maria Christina ; Bocci, Guido</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-42c648b32917f27fb1821f4b94d12d2dc50b86b4740a3b7dce38d6b0df42bd223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>Administration, Metronomic</topic><topic>Aged</topic><topic>Apoptosis</topic><topic>Cancer therapies</topic><topic>Cell cycle</topic><topic>Cell growth</topic><topic>Chemotherapy</topic><topic>Clinical studies</topic><topic>Cytotoxicity</topic><topic>Diffuse large B-Cell</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug dosages</topic><topic>Elderly</topic><topic>Frailty</topic><topic>Geriatric Assessment</topic><topic>Histone deacetylase</topic><topic>Histone Deacetylase Inhibitors - therapeutic use</topic><topic>Histone Deacetylases - genetics</topic><topic>Humans</topic><topic>Immune checkpoint inhibitors</topic><topic>Immune Checkpoint Inhibitors - therapeutic use</topic><topic>Immunosuppressive agents</topic><topic>Lymphocytes T</topic><topic>Lymphoma</topic><topic>Lymphoma, Non-Hodgkin - drug therapy</topic><topic>Lymphoma, Non-Hodgkin - genetics</topic><topic>Lymphoma, Non-Hodgkin - pathology</topic><topic>Lymphoma, T-Cell - drug therapy</topic><topic>Lymphoma, T-Cell - pathology</topic><topic>Metronomic chemotherapy</topic><topic>Non-Hodgkin's lymphoma</topic><topic>Non-Hodgkin-lymphoma</topic><topic>PD-L1 protein</topic><topic>Pharmaceutical industry</topic><topic>Pharmacodynamics</topic><topic>Phosphatidylinositol 3-Kinases - genetics</topic><topic>Preclinical studies</topic><topic>Remission</topic><topic>Rituximab</topic><topic>Rituximab - therapeutic use</topic><topic>Schedules</topic><topic>Signal Transduction - drug effects</topic><topic>T-cell lymphoma</topic><topic>TOR protein</topic><topic>TOR Serine-Threonine Kinases - antagonists & inhibitors</topic><topic>TOR Serine-Threonine Kinases - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cox, Maria Christina</creatorcontrib><creatorcontrib>Bocci, Guido</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cox, Maria Christina</au><au>Bocci, Guido</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metronomic chemotherapy regimens and targeted therapies in non-Hodgkin lymphoma: The best of two worlds</atitle><jtitle>Cancer letters</jtitle><addtitle>Cancer Lett</addtitle><date>2022-01-01</date><risdate>2022</risdate><volume>524</volume><spage>144</spage><epage>150</epage><pages>144-150</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>Novel drugs are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs). Notwithstanding, especially in aggressive subtypes, chemotherapy remains the pillar of treatment. Indeed, the combination of highly effective Maximum-Tolerated-Dose Chemotherapy (MTD-CHEMO) + “novel drugs”, has so far, fallen short from expectations, often because it caused excessive toxicity. Metronomic chemotherapy (mCHEMO), which is the frequent, long-term administration of low dose cytotoxic drugs, may allow more effective and tolerable combinations. mCHEMO pharmacodynamics, has been described as pleiotropic. In fact, it may have different cellular and molecular targets, when drugs or their schedules are modified. Although mCHEMO has been little explored in NHLs, pre-clinical studies - in lymphoma models - which addressed the activity of mCHEMO in combination with novel drugs, have shown very promising results. These included inhibitors of histone deacetylase, mTOR and PI3K/mTOR, as well as the immune checkpoint inhibitor anti-PD-L1. Moreover, a few impressive reports have recently shown all-oral mCHEMO schedules, with or without rituximab, can effectively shrink both B and T-cell aggressive NHLs. Indeed, these regimens allowed elderly-frail patients to achieve sustained remission, while toxicity proved manageable. In our opinion, all-oral mCHEMO, is an active, easy-to start, well-tolerated, and inexpensive therapeutic approach, which deserves further investigation. Most importantly, mCHEMO, holds promise to empower the activity of novel targeted therapies, without causing excessive toxicity.
•Targeted therapies are rapidly moving forward the treatment-paradigm of non-Hodgkin-lymphomas (NHLs).•All-oral metronomic chemotherapy (mCHEMO) schedules have shown good activity and tolerability in elderly-frail NHL patients.•In NHLs, the combination of targeted therapies with mCHEMO schedules have shown promising pre-clinical and clinical results.•mCHEMO may be an ideal platform for further improving the armamentarium of NHLs therapies.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>34673128</pmid><doi>10.1016/j.canlet.2021.10.018</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-8597-8459</orcidid><orcidid>https://orcid.org/0000-0001-7120-9141</orcidid></addata></record> |
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subjects | 1-Phosphatidylinositol 3-kinase Administration, Metronomic Aged Apoptosis Cancer therapies Cell cycle Cell growth Chemotherapy Clinical studies Cytotoxicity Diffuse large B-Cell Dose-Response Relationship, Drug Drug dosages Elderly Frailty Geriatric Assessment Histone deacetylase Histone Deacetylase Inhibitors - therapeutic use Histone Deacetylases - genetics Humans Immune checkpoint inhibitors Immune Checkpoint Inhibitors - therapeutic use Immunosuppressive agents Lymphocytes T Lymphoma Lymphoma, Non-Hodgkin - drug therapy Lymphoma, Non-Hodgkin - genetics Lymphoma, Non-Hodgkin - pathology Lymphoma, T-Cell - drug therapy Lymphoma, T-Cell - pathology Metronomic chemotherapy Non-Hodgkin's lymphoma Non-Hodgkin-lymphoma PD-L1 protein Pharmaceutical industry Pharmacodynamics Phosphatidylinositol 3-Kinases - genetics Preclinical studies Remission Rituximab Rituximab - therapeutic use Schedules Signal Transduction - drug effects T-cell lymphoma TOR protein TOR Serine-Threonine Kinases - antagonists & inhibitors TOR Serine-Threonine Kinases - genetics |
title | Metronomic chemotherapy regimens and targeted therapies in non-Hodgkin lymphoma: The best of two worlds |
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