Randomized clinical trial of adenosine 5'-triphosphate in patients with advanced non-small-cell lung cancer
Extracellular adenosine 5'-triphosphate (ATP) is involved in the regulation of a variety of biologic processes, including neurotransmission, muscle contraction, and liver glucose metabolism, via purinergic receptors. In nonrandomized studies involving patients with different tumor types includi...
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description | Extracellular adenosine 5'-triphosphate (ATP) is involved in the regulation of a variety of biologic processes, including neurotransmission, muscle contraction, and liver glucose metabolism, via purinergic receptors. In nonrandomized studies involving patients with different tumor types including non-small-cell lung cancer (NSCLC), ATP infusion appeared to inhibit loss of weight and deterioration of quality of life (QOL) and performance status. We conducted a randomized clinical trial to evaluate the effects of ATP in patients with advanced NSCLC (stage IIIB or IV).
Fifty-eight patients were randomly assigned to receive either 10 intravenous 30-hour ATP infusions, with the infusions given at 2- to 4-week intervals, or no ATP. Outcome parameters were assessed every 4 weeks until 28 weeks. Between-group differences were tested for statistical significance by use of repeated-measures analysis, and reported P values are two-sided.
Twenty-eight patients were allocated to receive ATP treatment and 30 received no ATP. Mean weight changes per 4-week period were -1.0 kg (95% confidence interval [CI] = -1.5 to -0.5) in the control group and 0.2 kg (95% CI = -0.2 to +0.6) in the ATP group (P =.002). Serum albumin concentration declined by -1.2 g/L (95% CI= -2.0 to -0.4) per 4 weeks in the control group but remained stable (0.0 g/L; 95% CI = -0.3 to +0.3) in the ATP group (P =.006). Elbow flexor muscle strength declined by -5.5% (95% CI = -9.6% to -1. 4%) per 4 weeks in the control group but remained stable (0.0%; 95% CI= -1.4% to +1.4%) in the ATP group (P =.01). A similar pattern was observed for knee extensor muscles (P =.02). The effects of ATP on body weight, muscle strength, and albumin concentration were especially marked in cachectic patients (P =.0002, P =.0001, and P =. 0001, respectively, for ATP versus no ATP). QOL score changes per 4-week period in the ATP group showed overall less deterioration than in the control group-physical scores (-0.2% versus -2.4%; P =. 0002); functional scores (+0.4% versus -5.5%; P =.02); psychologic scores (-0.7% versus -2.4%; P =.11); overall QOL score (+0.1% versus -3.5%; P =.0001).
This randomized trial demonstrates that ATP has beneficial effects on weight, muscle strength, and QOL in patients with advanced NSCLC. |
doi_str_mv | 10.1093/jnci/92.4.321 |
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Fifty-eight patients were randomly assigned to receive either 10 intravenous 30-hour ATP infusions, with the infusions given at 2- to 4-week intervals, or no ATP. Outcome parameters were assessed every 4 weeks until 28 weeks. Between-group differences were tested for statistical significance by use of repeated-measures analysis, and reported P values are two-sided.
Twenty-eight patients were allocated to receive ATP treatment and 30 received no ATP. Mean weight changes per 4-week period were -1.0 kg (95% confidence interval [CI] = -1.5 to -0.5) in the control group and 0.2 kg (95% CI = -0.2 to +0.6) in the ATP group (P =.002). Serum albumin concentration declined by -1.2 g/L (95% CI= -2.0 to -0.4) per 4 weeks in the control group but remained stable (0.0 g/L; 95% CI = -0.3 to +0.3) in the ATP group (P =.006). Elbow flexor muscle strength declined by -5.5% (95% CI = -9.6% to -1. 4%) per 4 weeks in the control group but remained stable (0.0%; 95% CI= -1.4% to +1.4%) in the ATP group (P =.01). A similar pattern was observed for knee extensor muscles (P =.02). The effects of ATP on body weight, muscle strength, and albumin concentration were especially marked in cachectic patients (P =.0002, P =.0001, and P =. 0001, respectively, for ATP versus no ATP). QOL score changes per 4-week period in the ATP group showed overall less deterioration than in the control group-physical scores (-0.2% versus -2.4%; P =. 0002); functional scores (+0.4% versus -5.5%; P =.02); psychologic scores (-0.7% versus -2.4%; P =.11); overall QOL score (+0.1% versus -3.5%; P =.0001).
This randomized trial demonstrates that ATP has beneficial effects on weight, muscle strength, and QOL in patients with advanced NSCLC.</description><identifier>ISSN: 0027-8874</identifier><identifier>ISSN: 1460-2105</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/92.4.321</identifier><identifier>PMID: 10675381</identifier><identifier>CODEN: JNCIEQ</identifier><language>eng</language><publisher>Cary, NC: Oxford University Press</publisher><subject>Adenosine Triphosphate - therapeutic use ; Aged ; Biological and medical sciences ; Body Weight ; Cachexia - drug therapy ; Cachexia - etiology ; Cachexia - prevention & control ; Carcinoma, Non-Small-Cell Lung - complications ; Clinical trials ; Drug therapy ; Female ; Humans ; Lung cancer ; Lung Neoplasms - complications ; Male ; Medical sciences ; Middle Aged ; Muscle Contraction - drug effects ; Muscle Weakness - drug therapy ; Muscle Weakness - etiology ; Palliative Care - methods ; Pneumology ; Quality of Life ; Serum Albumin - metabolism ; Treatment Outcome ; Tumors of the respiratory system and mediastinum ; Wasting Syndrome - drug therapy ; Wasting Syndrome - etiology ; Wasting Syndrome - prevention & control</subject><ispartof>JNCI : Journal of the National Cancer Institute, 2000-02, Vol.92 (4), p.321-328</ispartof><rights>2000 INIST-CNRS</rights><rights>Copyright Superintendent of Documents Feb 16, 2000</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-3fe02eda359e27900f940d06fadcdf3261ff3c8c15aa1f4ec60a8f2661181b023</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1315761$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10675381$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>AGTERESCH, H. J</creatorcontrib><creatorcontrib>DAGNELIE, P. C</creatorcontrib><creatorcontrib>VAN DER GAAST, A</creatorcontrib><creatorcontrib>STIJNEN, T</creatorcontrib><creatorcontrib>WILSON, J. H. P</creatorcontrib><title>Randomized clinical trial of adenosine 5'-triphosphate in patients with advanced non-small-cell lung cancer</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>J Natl Cancer Inst</addtitle><description>Extracellular adenosine 5'-triphosphate (ATP) is involved in the regulation of a variety of biologic processes, including neurotransmission, muscle contraction, and liver glucose metabolism, via purinergic receptors. In nonrandomized studies involving patients with different tumor types including non-small-cell lung cancer (NSCLC), ATP infusion appeared to inhibit loss of weight and deterioration of quality of life (QOL) and performance status. We conducted a randomized clinical trial to evaluate the effects of ATP in patients with advanced NSCLC (stage IIIB or IV).
Fifty-eight patients were randomly assigned to receive either 10 intravenous 30-hour ATP infusions, with the infusions given at 2- to 4-week intervals, or no ATP. Outcome parameters were assessed every 4 weeks until 28 weeks. Between-group differences were tested for statistical significance by use of repeated-measures analysis, and reported P values are two-sided.
Twenty-eight patients were allocated to receive ATP treatment and 30 received no ATP. Mean weight changes per 4-week period were -1.0 kg (95% confidence interval [CI] = -1.5 to -0.5) in the control group and 0.2 kg (95% CI = -0.2 to +0.6) in the ATP group (P =.002). Serum albumin concentration declined by -1.2 g/L (95% CI= -2.0 to -0.4) per 4 weeks in the control group but remained stable (0.0 g/L; 95% CI = -0.3 to +0.3) in the ATP group (P =.006). Elbow flexor muscle strength declined by -5.5% (95% CI = -9.6% to -1. 4%) per 4 weeks in the control group but remained stable (0.0%; 95% CI= -1.4% to +1.4%) in the ATP group (P =.01). A similar pattern was observed for knee extensor muscles (P =.02). The effects of ATP on body weight, muscle strength, and albumin concentration were especially marked in cachectic patients (P =.0002, P =.0001, and P =. 0001, respectively, for ATP versus no ATP). QOL score changes per 4-week period in the ATP group showed overall less deterioration than in the control group-physical scores (-0.2% versus -2.4%; P =. 0002); functional scores (+0.4% versus -5.5%; P =.02); psychologic scores (-0.7% versus -2.4%; P =.11); overall QOL score (+0.1% versus -3.5%; P =.0001).
This randomized trial demonstrates that ATP has beneficial effects on weight, muscle strength, and QOL in patients with advanced NSCLC.</description><subject>Adenosine Triphosphate - therapeutic use</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Body Weight</subject><subject>Cachexia - drug therapy</subject><subject>Cachexia - etiology</subject><subject>Cachexia - prevention & control</subject><subject>Carcinoma, Non-Small-Cell Lung - complications</subject><subject>Clinical trials</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - complications</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle Weakness - drug therapy</subject><subject>Muscle Weakness - etiology</subject><subject>Palliative Care - methods</subject><subject>Pneumology</subject><subject>Quality of Life</subject><subject>Serum Albumin - metabolism</subject><subject>Treatment Outcome</subject><subject>Tumors of the respiratory system and mediastinum</subject><subject>Wasting Syndrome - drug therapy</subject><subject>Wasting Syndrome - etiology</subject><subject>Wasting Syndrome - prevention & control</subject><issn>0027-8874</issn><issn>1460-2105</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUGLFDEQhYMo7uzq0asEET1lNpWk08lRFl2FBUH0HLLpxMnYnbRJt6K_3jQzoFiHKqj6eBTvIfQM6B6o5tfH5OK1Znux5wweoB0ISQkD2j1EO0pZT5TqxQW6rPVIW2kmHqMLoLLvuIId-vbJpiFP8bcfsBtjis6OeCmx9RywHXzKNSaPu9ekbedDrvPBLh7HhGe7RJ-Win_G5dDQHza5ppJyInWy40icH0c8rukrdtupPEGPgh2rf3qeV-jLu7efb96Tu4-3H27e3BHHlVgID54yP1jeac96TWnQgg5UBju4IXAmIQTulIPOWgjCO0mtCkxKAAX3lPEr9OqkO5f8ffV1MVOs2zM2-bxW01MNTAlo4Iv_wGNeS2q_Gcao7qXqNoicIFdyrcUHM5c42fLLADVbBGaLwGhmhGkRNP75WXS9n_zwD33yvAEvz4Ctze1Qmjmx_uU4dL0E_gek2Y99</recordid><startdate>20000216</startdate><enddate>20000216</enddate><creator>AGTERESCH, H. J</creator><creator>DAGNELIE, P. C</creator><creator>VAN DER GAAST, A</creator><creator>STIJNEN, T</creator><creator>WILSON, J. H. P</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>IQODW</scope><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>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20000216</creationdate><title>Randomized clinical trial of adenosine 5'-triphosphate in patients with advanced non-small-cell lung cancer</title><author>AGTERESCH, H. J ; DAGNELIE, P. C ; VAN DER GAAST, A ; STIJNEN, T ; WILSON, J. H. P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-3fe02eda359e27900f940d06fadcdf3261ff3c8c15aa1f4ec60a8f2661181b023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adenosine Triphosphate - therapeutic use</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Body Weight</topic><topic>Cachexia - drug therapy</topic><topic>Cachexia - etiology</topic><topic>Cachexia - prevention & control</topic><topic>Carcinoma, Non-Small-Cell Lung - complications</topic><topic>Clinical trials</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Lung cancer</topic><topic>Lung Neoplasms - complications</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle Weakness - drug therapy</topic><topic>Muscle Weakness - etiology</topic><topic>Palliative Care - methods</topic><topic>Pneumology</topic><topic>Quality of Life</topic><topic>Serum Albumin - metabolism</topic><topic>Treatment Outcome</topic><topic>Tumors of the respiratory system and mediastinum</topic><topic>Wasting Syndrome - drug therapy</topic><topic>Wasting Syndrome - etiology</topic><topic>Wasting Syndrome - prevention & control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>AGTERESCH, H. 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P</creatorcontrib><collection>Pascal-Francis</collection><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>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</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>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>AGTERESCH, H. J</au><au>DAGNELIE, P. C</au><au>VAN DER GAAST, A</au><au>STIJNEN, T</au><au>WILSON, J. H. P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Randomized clinical trial of adenosine 5'-triphosphate in patients with advanced non-small-cell lung cancer</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>J Natl Cancer Inst</addtitle><date>2000-02-16</date><risdate>2000</risdate><volume>92</volume><issue>4</issue><spage>321</spage><epage>328</epage><pages>321-328</pages><issn>0027-8874</issn><issn>1460-2105</issn><eissn>1460-2105</eissn><coden>JNCIEQ</coden><abstract>Extracellular adenosine 5'-triphosphate (ATP) is involved in the regulation of a variety of biologic processes, including neurotransmission, muscle contraction, and liver glucose metabolism, via purinergic receptors. In nonrandomized studies involving patients with different tumor types including non-small-cell lung cancer (NSCLC), ATP infusion appeared to inhibit loss of weight and deterioration of quality of life (QOL) and performance status. We conducted a randomized clinical trial to evaluate the effects of ATP in patients with advanced NSCLC (stage IIIB or IV).
Fifty-eight patients were randomly assigned to receive either 10 intravenous 30-hour ATP infusions, with the infusions given at 2- to 4-week intervals, or no ATP. Outcome parameters were assessed every 4 weeks until 28 weeks. Between-group differences were tested for statistical significance by use of repeated-measures analysis, and reported P values are two-sided.
Twenty-eight patients were allocated to receive ATP treatment and 30 received no ATP. Mean weight changes per 4-week period were -1.0 kg (95% confidence interval [CI] = -1.5 to -0.5) in the control group and 0.2 kg (95% CI = -0.2 to +0.6) in the ATP group (P =.002). Serum albumin concentration declined by -1.2 g/L (95% CI= -2.0 to -0.4) per 4 weeks in the control group but remained stable (0.0 g/L; 95% CI = -0.3 to +0.3) in the ATP group (P =.006). Elbow flexor muscle strength declined by -5.5% (95% CI = -9.6% to -1. 4%) per 4 weeks in the control group but remained stable (0.0%; 95% CI= -1.4% to +1.4%) in the ATP group (P =.01). A similar pattern was observed for knee extensor muscles (P =.02). The effects of ATP on body weight, muscle strength, and albumin concentration were especially marked in cachectic patients (P =.0002, P =.0001, and P =. 0001, respectively, for ATP versus no ATP). QOL score changes per 4-week period in the ATP group showed overall less deterioration than in the control group-physical scores (-0.2% versus -2.4%; P =. 0002); functional scores (+0.4% versus -5.5%; P =.02); psychologic scores (-0.7% versus -2.4%; P =.11); overall QOL score (+0.1% versus -3.5%; P =.0001).
This randomized trial demonstrates that ATP has beneficial effects on weight, muscle strength, and QOL in patients with advanced NSCLC.</abstract><cop>Cary, NC</cop><pub>Oxford University Press</pub><pmid>10675381</pmid><doi>10.1093/jnci/92.4.321</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Triphosphate - therapeutic use Aged Biological and medical sciences Body Weight Cachexia - drug therapy Cachexia - etiology Cachexia - prevention & control Carcinoma, Non-Small-Cell Lung - complications Clinical trials Drug therapy Female Humans Lung cancer Lung Neoplasms - complications Male Medical sciences Middle Aged Muscle Contraction - drug effects Muscle Weakness - drug therapy Muscle Weakness - etiology Palliative Care - methods Pneumology Quality of Life Serum Albumin - metabolism Treatment Outcome Tumors of the respiratory system and mediastinum Wasting Syndrome - drug therapy Wasting Syndrome - etiology Wasting Syndrome - prevention & control |
title | Randomized clinical trial of adenosine 5'-triphosphate in patients with advanced non-small-cell lung cancer |
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