Low Serum Vitamin D Levels Are Associated With Inferior Survival in Follicular Lymphoma: A Prospective Evaluation in SWOG and LYSA Studies
Recent literature reports a potential association between high vitamin D and improved lymphoma prognosis. We evaluated the impact of pretreatment vitamin D on follicular lymphoma (FL) outcome. SWOG participants were previously untreated patients with FL enrolled onto SWOG clinical trials (S9800, S99...
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creator | Kelly, Jennifer L Salles, Gilles Goldman, Bryan Fisher, Richard I Brice, Pauline Press, Oliver Casasnovas, Olivier Maloney, David G Soubeyran, Pierre Rimsza, Lisa Haioun, Corinne Xerri, Luc LeBlanc, Michael Tilly, Hervé Friedberg, Jonathan W |
description | Recent literature reports a potential association between high vitamin D and improved lymphoma prognosis. We evaluated the impact of pretreatment vitamin D on follicular lymphoma (FL) outcome.
SWOG participants were previously untreated patients with FL enrolled onto SWOG clinical trials (S9800, S9911, or S0016) involving CHOP chemotherapy plus an anti-CD20 antibody (rituximab or iodine-131 tositumomab) between 1998 and 2008. Participants included in our second independent cohort were also previously untreated patients with FL enrolled onto the Lymphoma Study Association (LYSA) PRIMA trial of rituximab plus chemotherapy (randomly assigned to rituximab maintenance v observation) between 2004 and 2007. Using the gold-standard liquid chromatography-tandem mass spectrometry method, 25-hydroxyvitamin D was measured in stored baseline serum samples. The primary end point was progression-free survival (PFS).
After a median follow-up of 5.4 years, the adjusted PFS and overall survival hazard ratios for the SWOG cohort were 1.97 (95% CI, 1.10 to 3.53) and 4.16 (95% CI, 1.66 to 10.44), respectively, for those who were vitamin D deficient (< 20 ng/mL; 15% of cohort). After a median follow-up of 6.6 years, the adjusted PFS and overall survival hazard ratios for the LYSA cohort were 1.50 (95% CI, 0.93 to 2.42) and 1.92 (95% CI, 0.72 to 5.13), respectively, for those who were vitamin D deficient (< 10 ng/mL; 25% of cohort).
Although statistical significance was not reached in the LYSA cohort, the consistent estimates of association between low vitamin D levels and FL outcomes in two independent cohorts suggests that serum vitamin D might be the first potentially modifiable factor to be associated with FL survival. Further investigation is needed to determine the effects of vitamin D supplementation in this clinical setting. |
doi_str_mv | 10.1200/JCO.2014.57.5092 |
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SWOG participants were previously untreated patients with FL enrolled onto SWOG clinical trials (S9800, S9911, or S0016) involving CHOP chemotherapy plus an anti-CD20 antibody (rituximab or iodine-131 tositumomab) between 1998 and 2008. Participants included in our second independent cohort were also previously untreated patients with FL enrolled onto the Lymphoma Study Association (LYSA) PRIMA trial of rituximab plus chemotherapy (randomly assigned to rituximab maintenance v observation) between 2004 and 2007. Using the gold-standard liquid chromatography-tandem mass spectrometry method, 25-hydroxyvitamin D was measured in stored baseline serum samples. The primary end point was progression-free survival (PFS).
After a median follow-up of 5.4 years, the adjusted PFS and overall survival hazard ratios for the SWOG cohort were 1.97 (95% CI, 1.10 to 3.53) and 4.16 (95% CI, 1.66 to 10.44), respectively, for those who were vitamin D deficient (< 20 ng/mL; 15% of cohort). After a median follow-up of 6.6 years, the adjusted PFS and overall survival hazard ratios for the LYSA cohort were 1.50 (95% CI, 0.93 to 2.42) and 1.92 (95% CI, 0.72 to 5.13), respectively, for those who were vitamin D deficient (< 10 ng/mL; 25% of cohort).
Although statistical significance was not reached in the LYSA cohort, the consistent estimates of association between low vitamin D levels and FL outcomes in two independent cohorts suggests that serum vitamin D might be the first potentially modifiable factor to be associated with FL survival. Further investigation is needed to determine the effects of vitamin D supplementation in this clinical setting.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2014.57.5092</identifier><identifier>PMID: 25823738</identifier><language>eng</language><publisher>United States: American Society of Clinical Oncology</publisher><subject><![CDATA[Antibodies, Monoclonal - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biomarkers - blood ; Chromatography, Liquid ; Cyclophosphamide - administration & dosage ; Disease Progression ; Disease-Free Survival ; Doxorubicin - administration & dosage ; Female ; Humans ; Kaplan-Meier Estimate ; Lymphoma, Follicular - blood ; Lymphoma, Follicular - diagnosis ; Lymphoma, Follicular - drug therapy ; Lymphoma, Follicular - mortality ; Male ; Middle Aged ; ORIGINAL REPORTS ; Prednisone - administration & dosage ; Proportional Hazards Models ; Prospective Studies ; Risk Factors ; Rituximab - administration & dosage ; Tandem Mass Spectrometry ; Time Factors ; Treatment Outcome ; Vincristine - administration & dosage ; Vitamin D - analogs & derivatives ; Vitamin D - blood ; Vitamin D Deficiency - blood ; Vitamin D Deficiency - diagnosis ; Vitamin D Deficiency - mortality]]></subject><ispartof>Journal of clinical oncology, 2015-05, Vol.33 (13), p.1482-1490</ispartof><rights>2015 by American Society of Clinical Oncology.</rights><rights>2015 by American Society of Clinical Oncology 2015 American Society of Clinical Oncology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-f9fc2131719337c65caf6cfa4a41cfd456d16387fa8f68585156be59eeff2e943</citedby><cites>FETCH-LOGICAL-c396t-f9fc2131719337c65caf6cfa4a41cfd456d16387fa8f68585156be59eeff2e943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3716,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25823738$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kelly, Jennifer L</creatorcontrib><creatorcontrib>Salles, Gilles</creatorcontrib><creatorcontrib>Goldman, Bryan</creatorcontrib><creatorcontrib>Fisher, Richard I</creatorcontrib><creatorcontrib>Brice, Pauline</creatorcontrib><creatorcontrib>Press, Oliver</creatorcontrib><creatorcontrib>Casasnovas, Olivier</creatorcontrib><creatorcontrib>Maloney, David G</creatorcontrib><creatorcontrib>Soubeyran, Pierre</creatorcontrib><creatorcontrib>Rimsza, Lisa</creatorcontrib><creatorcontrib>Haioun, Corinne</creatorcontrib><creatorcontrib>Xerri, Luc</creatorcontrib><creatorcontrib>LeBlanc, Michael</creatorcontrib><creatorcontrib>Tilly, Hervé</creatorcontrib><creatorcontrib>Friedberg, Jonathan W</creatorcontrib><title>Low Serum Vitamin D Levels Are Associated With Inferior Survival in Follicular Lymphoma: A Prospective Evaluation in SWOG and LYSA Studies</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>Recent literature reports a potential association between high vitamin D and improved lymphoma prognosis. We evaluated the impact of pretreatment vitamin D on follicular lymphoma (FL) outcome.
SWOG participants were previously untreated patients with FL enrolled onto SWOG clinical trials (S9800, S9911, or S0016) involving CHOP chemotherapy plus an anti-CD20 antibody (rituximab or iodine-131 tositumomab) between 1998 and 2008. Participants included in our second independent cohort were also previously untreated patients with FL enrolled onto the Lymphoma Study Association (LYSA) PRIMA trial of rituximab plus chemotherapy (randomly assigned to rituximab maintenance v observation) between 2004 and 2007. Using the gold-standard liquid chromatography-tandem mass spectrometry method, 25-hydroxyvitamin D was measured in stored baseline serum samples. The primary end point was progression-free survival (PFS).
After a median follow-up of 5.4 years, the adjusted PFS and overall survival hazard ratios for the SWOG cohort were 1.97 (95% CI, 1.10 to 3.53) and 4.16 (95% CI, 1.66 to 10.44), respectively, for those who were vitamin D deficient (< 20 ng/mL; 15% of cohort). After a median follow-up of 6.6 years, the adjusted PFS and overall survival hazard ratios for the LYSA cohort were 1.50 (95% CI, 0.93 to 2.42) and 1.92 (95% CI, 0.72 to 5.13), respectively, for those who were vitamin D deficient (< 10 ng/mL; 25% of cohort).
Although statistical significance was not reached in the LYSA cohort, the consistent estimates of association between low vitamin D levels and FL outcomes in two independent cohorts suggests that serum vitamin D might be the first potentially modifiable factor to be associated with FL survival. Further investigation is needed to determine the effects of vitamin D supplementation in this clinical setting.</description><subject>Antibodies, Monoclonal - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biomarkers - blood</subject><subject>Chromatography, Liquid</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Disease Progression</subject><subject>Disease-Free Survival</subject><subject>Doxorubicin - administration & dosage</subject><subject>Female</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Lymphoma, Follicular - blood</subject><subject>Lymphoma, Follicular - diagnosis</subject><subject>Lymphoma, Follicular - drug therapy</subject><subject>Lymphoma, Follicular - mortality</subject><subject>Male</subject><subject>Middle Aged</subject><subject>ORIGINAL REPORTS</subject><subject>Prednisone - administration & dosage</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>Risk Factors</subject><subject>Rituximab - administration & dosage</subject><subject>Tandem Mass Spectrometry</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Vincristine - administration & dosage</subject><subject>Vitamin D - analogs & derivatives</subject><subject>Vitamin D - blood</subject><subject>Vitamin D Deficiency - blood</subject><subject>Vitamin D Deficiency - diagnosis</subject><subject>Vitamin D Deficiency - mortality</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc1u1DAURi0EokPLnhXykk0G_8SxwwIpGtpSFGmQ0lJYWa5zzRgl8dROgvoKPHUzaqlg5cX9znetexB6Q8maMkLef9ls14zQfC3kWpCSPUMrKpjMpBTiOVoRyVlGFf9-hF6l9IssScXFS3TEhGJccrVCf-rwGzcQpx5_86Pp_YA_4Rpm6BKuIuAqpWC9GaHF137c4YvBQfQh4maKs59NhxfiLHSdt1NnIq7v-v0u9OYDrvDXGNIe7OhnwKdLdDKjD8MBaK6359gMLa5_NBVuxqn1kE7QC2e6BK8f32N0dXZ6ufmc1dvzi01VZ5aXxZi50llGOZW05FzaQljjCutMbnJqXZuLoqUFV9IZ5QollKCiuAFRAjjHoMz5Mfr40LufbnpoLQxjNJ3eR9-beKeD8fr_yeB3-meYdZ6TPGdiKXj3WBDD7QRp1L1PFrrODBCmpGkhpVKMCbZEyUPULrdIEdzTGkr0QaFeFOqDQi2kPihckLf_fu8J-OuM3wMxmZkr</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Kelly, Jennifer L</creator><creator>Salles, Gilles</creator><creator>Goldman, Bryan</creator><creator>Fisher, Richard I</creator><creator>Brice, Pauline</creator><creator>Press, Oliver</creator><creator>Casasnovas, Olivier</creator><creator>Maloney, David G</creator><creator>Soubeyran, Pierre</creator><creator>Rimsza, Lisa</creator><creator>Haioun, Corinne</creator><creator>Xerri, Luc</creator><creator>LeBlanc, Michael</creator><creator>Tilly, Hervé</creator><creator>Friedberg, Jonathan W</creator><general>American Society of Clinical Oncology</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150501</creationdate><title>Low Serum Vitamin D Levels Are Associated With Inferior Survival in Follicular Lymphoma: A Prospective Evaluation in SWOG and LYSA Studies</title><author>Kelly, Jennifer L ; Salles, Gilles ; Goldman, Bryan ; Fisher, Richard I ; Brice, Pauline ; Press, Oliver ; Casasnovas, Olivier ; Maloney, David G ; Soubeyran, Pierre ; Rimsza, Lisa ; Haioun, Corinne ; Xerri, Luc ; LeBlanc, Michael ; Tilly, Hervé ; Friedberg, Jonathan W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-f9fc2131719337c65caf6cfa4a41cfd456d16387fa8f68585156be59eeff2e943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Antibodies, Monoclonal - administration & dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biomarkers - blood</topic><topic>Chromatography, Liquid</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Disease Progression</topic><topic>Disease-Free Survival</topic><topic>Doxorubicin - administration & dosage</topic><topic>Female</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Lymphoma, Follicular - blood</topic><topic>Lymphoma, Follicular - diagnosis</topic><topic>Lymphoma, Follicular - drug therapy</topic><topic>Lymphoma, Follicular - mortality</topic><topic>Male</topic><topic>Middle Aged</topic><topic>ORIGINAL REPORTS</topic><topic>Prednisone - administration & dosage</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Rituximab - administration & dosage</topic><topic>Tandem Mass Spectrometry</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Vincristine - administration & dosage</topic><topic>Vitamin D - analogs & derivatives</topic><topic>Vitamin D - blood</topic><topic>Vitamin D Deficiency - blood</topic><topic>Vitamin D Deficiency - diagnosis</topic><topic>Vitamin D Deficiency - mortality</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kelly, Jennifer L</creatorcontrib><creatorcontrib>Salles, Gilles</creatorcontrib><creatorcontrib>Goldman, Bryan</creatorcontrib><creatorcontrib>Fisher, Richard I</creatorcontrib><creatorcontrib>Brice, Pauline</creatorcontrib><creatorcontrib>Press, Oliver</creatorcontrib><creatorcontrib>Casasnovas, Olivier</creatorcontrib><creatorcontrib>Maloney, David G</creatorcontrib><creatorcontrib>Soubeyran, Pierre</creatorcontrib><creatorcontrib>Rimsza, Lisa</creatorcontrib><creatorcontrib>Haioun, Corinne</creatorcontrib><creatorcontrib>Xerri, Luc</creatorcontrib><creatorcontrib>LeBlanc, Michael</creatorcontrib><creatorcontrib>Tilly, Hervé</creatorcontrib><creatorcontrib>Friedberg, Jonathan W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kelly, Jennifer L</au><au>Salles, Gilles</au><au>Goldman, Bryan</au><au>Fisher, Richard I</au><au>Brice, Pauline</au><au>Press, Oliver</au><au>Casasnovas, Olivier</au><au>Maloney, David G</au><au>Soubeyran, Pierre</au><au>Rimsza, Lisa</au><au>Haioun, Corinne</au><au>Xerri, Luc</au><au>LeBlanc, Michael</au><au>Tilly, Hervé</au><au>Friedberg, Jonathan W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low Serum Vitamin D Levels Are Associated With Inferior Survival in Follicular Lymphoma: A Prospective Evaluation in SWOG and LYSA Studies</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>33</volume><issue>13</issue><spage>1482</spage><epage>1490</epage><pages>1482-1490</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>Recent literature reports a potential association between high vitamin D and improved lymphoma prognosis. We evaluated the impact of pretreatment vitamin D on follicular lymphoma (FL) outcome.
SWOG participants were previously untreated patients with FL enrolled onto SWOG clinical trials (S9800, S9911, or S0016) involving CHOP chemotherapy plus an anti-CD20 antibody (rituximab or iodine-131 tositumomab) between 1998 and 2008. Participants included in our second independent cohort were also previously untreated patients with FL enrolled onto the Lymphoma Study Association (LYSA) PRIMA trial of rituximab plus chemotherapy (randomly assigned to rituximab maintenance v observation) between 2004 and 2007. Using the gold-standard liquid chromatography-tandem mass spectrometry method, 25-hydroxyvitamin D was measured in stored baseline serum samples. The primary end point was progression-free survival (PFS).
After a median follow-up of 5.4 years, the adjusted PFS and overall survival hazard ratios for the SWOG cohort were 1.97 (95% CI, 1.10 to 3.53) and 4.16 (95% CI, 1.66 to 10.44), respectively, for those who were vitamin D deficient (< 20 ng/mL; 15% of cohort). After a median follow-up of 6.6 years, the adjusted PFS and overall survival hazard ratios for the LYSA cohort were 1.50 (95% CI, 0.93 to 2.42) and 1.92 (95% CI, 0.72 to 5.13), respectively, for those who were vitamin D deficient (< 10 ng/mL; 25% of cohort).
Although statistical significance was not reached in the LYSA cohort, the consistent estimates of association between low vitamin D levels and FL outcomes in two independent cohorts suggests that serum vitamin D might be the first potentially modifiable factor to be associated with FL survival. Further investigation is needed to determine the effects of vitamin D supplementation in this clinical setting.</abstract><cop>United States</cop><pub>American Society of Clinical Oncology</pub><pmid>25823738</pmid><doi>10.1200/JCO.2014.57.5092</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Society of Clinical Oncology Online Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Antibodies, Monoclonal - administration & dosage Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biomarkers - blood Chromatography, Liquid Cyclophosphamide - administration & dosage Disease Progression Disease-Free Survival Doxorubicin - administration & dosage Female Humans Kaplan-Meier Estimate Lymphoma, Follicular - blood Lymphoma, Follicular - diagnosis Lymphoma, Follicular - drug therapy Lymphoma, Follicular - mortality Male Middle Aged ORIGINAL REPORTS Prednisone - administration & dosage Proportional Hazards Models Prospective Studies Risk Factors Rituximab - administration & dosage Tandem Mass Spectrometry Time Factors Treatment Outcome Vincristine - administration & dosage Vitamin D - analogs & derivatives Vitamin D - blood Vitamin D Deficiency - blood Vitamin D Deficiency - diagnosis Vitamin D Deficiency - mortality |
title | Low Serum Vitamin D Levels Are Associated With Inferior Survival in Follicular Lymphoma: A Prospective Evaluation in SWOG and LYSA Studies |
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