Favorable role of IDH1/2 mutations aided with MGMT promoter gene methylation in the outcome of patients with malignant glioma
The implications of molecular biomarkers IDH1/2 mutations and MGMT gene promoter methylation were evaluated for prognostic outcome of glioma patients. Methods: Glioma cases were analyzed for IDH1/2 mutations and MGMT promoter methylation by DNA sequencing and MS-PCR, respectively. Results: Mutations...
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creator | Pandith, Arshad A. Qasim, Iqbal Baba, Shahid M. Koul, Aabid Zahoor, Wani Afroze, Dil Lateef, Adil Manzoor, Usma Bhat, Ina A. Sanadhya, Dheera R. Bhat, Abdul Ramzan, Altaf U. |
description | The
implications of molecular biomarkers IDH1/2 mutations and MGMT gene promoter
methylation were evaluated for prognostic outcome of glioma patients.
Methods:
Glioma cases were analyzed for IDH1/2 mutations and MGMT promoter methylation
by DNA sequencing and MS-PCR, respectively.
Results:
Mutations found in IDH1/2 genes totalled 63.4% (N=40) wherein IDH1 mutations
were significantly associated with oligidendrioglioma (p=0.005) and
astrocytoma (p=0.0002). IDH1mutants presented more, 60.5% in MGMT promoter
methylated cases (p=0.03). IDH1 mutant cases had better survival for GBM and oligodendrioglioma
(log rank p=0.01). Multivariate
analysis confirmed better survival in MGMT methylation carriers (HR: 0.59,
p=0.031). Combination of both biomarkers showed better prognosis on
temozolomide (p |
doi_str_mv | 10.25402/fsg.13372904 |
format | Dataset |
fullrecord | <record><control><sourceid>datacite_PQ8</sourceid><recordid>TN_cdi_datacite_primary_10_25402_fsg_13372904</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_25402_fsg_13372904</sourcerecordid><originalsourceid>FETCH-datacite_primary_10_25402_fsg_133729043</originalsourceid><addsrcrecordid>eNqVjrkOgkAURaexMGpp_35AWY2xdsOCzn7yhAdMMgsZHhoL_12C-gE29xZ3yRFiGYXreJOGcVB19TpKkm28C9OpeJ3w7jzeNIF3g7gKLocsCmIwPSMrZztAVVIJD8UN5Of8Cq13xjF5qMkSGOLmqccqKAvcDCc9F86MZ-0QkOXuMzeoVW3RMtRaOYNzMalQd7T4-kysTsfrPluVyFgoJtl6ZdA_ZRTKEV8O-PKHn_zbfwNdElPj</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>dataset</recordtype></control><display><type>dataset</type><title>Favorable role of IDH1/2 mutations aided with MGMT promoter gene methylation in the outcome of patients with malignant glioma</title><source>DataCite</source><creator>Pandith, Arshad A. ; Qasim, Iqbal ; Baba, Shahid M. ; Koul, Aabid ; Zahoor, Wani ; Afroze, Dil ; Lateef, Adil ; Manzoor, Usma ; Bhat, Ina A. ; Sanadhya, Dheera ; R. Bhat, Abdul ; Ramzan, Altaf U.</creator><creatorcontrib>Pandith, Arshad A. ; Qasim, Iqbal ; Baba, Shahid M. ; Koul, Aabid ; Zahoor, Wani ; Afroze, Dil ; Lateef, Adil ; Manzoor, Usma ; Bhat, Ina A. ; Sanadhya, Dheera ; R. Bhat, Abdul ; Ramzan, Altaf U.</creatorcontrib><description>The
implications of molecular biomarkers IDH1/2 mutations and MGMT gene promoter
methylation were evaluated for prognostic outcome of glioma patients.
Methods:
Glioma cases were analyzed for IDH1/2 mutations and MGMT promoter methylation
by DNA sequencing and MS-PCR, respectively.
Results:
Mutations found in IDH1/2 genes totalled 63.4% (N=40) wherein IDH1 mutations
were significantly associated with oligidendrioglioma (p=0.005) and
astrocytoma (p=0.0002). IDH1mutants presented more, 60.5% in MGMT promoter
methylated cases (p=0.03). IDH1 mutant cases had better survival for GBM and oligodendrioglioma
(log rank p=0.01). Multivariate
analysis confirmed better survival in MGMT methylation carriers (HR: 0.59,
p=0.031). Combination of both biomarkers showed better prognosis on
temozolomide (p<0.05).
Conclusions: IDH1/2 mutations proved independent
prognostic factors in glioma and associated with MGMT methylation for better
survival.</description><identifier>DOI: 10.25402/fsg.13372904</identifier><language>eng</language><publisher>Taylor & Francis</publisher><creationdate>2020</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,1888</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.25402/fsg.13372904$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Pandith, Arshad A.</creatorcontrib><creatorcontrib>Qasim, Iqbal</creatorcontrib><creatorcontrib>Baba, Shahid M.</creatorcontrib><creatorcontrib>Koul, Aabid</creatorcontrib><creatorcontrib>Zahoor, Wani</creatorcontrib><creatorcontrib>Afroze, Dil</creatorcontrib><creatorcontrib>Lateef, Adil</creatorcontrib><creatorcontrib>Manzoor, Usma</creatorcontrib><creatorcontrib>Bhat, Ina A.</creatorcontrib><creatorcontrib>Sanadhya, Dheera</creatorcontrib><creatorcontrib>R. Bhat, Abdul</creatorcontrib><creatorcontrib>Ramzan, Altaf U.</creatorcontrib><title>Favorable role of IDH1/2 mutations aided with MGMT promoter gene methylation in the outcome of patients with malignant glioma</title><description>The
implications of molecular biomarkers IDH1/2 mutations and MGMT gene promoter
methylation were evaluated for prognostic outcome of glioma patients.
Methods:
Glioma cases were analyzed for IDH1/2 mutations and MGMT promoter methylation
by DNA sequencing and MS-PCR, respectively.
Results:
Mutations found in IDH1/2 genes totalled 63.4% (N=40) wherein IDH1 mutations
were significantly associated with oligidendrioglioma (p=0.005) and
astrocytoma (p=0.0002). IDH1mutants presented more, 60.5% in MGMT promoter
methylated cases (p=0.03). IDH1 mutant cases had better survival for GBM and oligodendrioglioma
(log rank p=0.01). Multivariate
analysis confirmed better survival in MGMT methylation carriers (HR: 0.59,
p=0.031). Combination of both biomarkers showed better prognosis on
temozolomide (p<0.05).
Conclusions: IDH1/2 mutations proved independent
prognostic factors in glioma and associated with MGMT methylation for better
survival.</description><fulltext>true</fulltext><rsrctype>dataset</rsrctype><creationdate>2020</creationdate><recordtype>dataset</recordtype><sourceid>PQ8</sourceid><recordid>eNqVjrkOgkAURaexMGpp_35AWY2xdsOCzn7yhAdMMgsZHhoL_12C-gE29xZ3yRFiGYXreJOGcVB19TpKkm28C9OpeJ3w7jzeNIF3g7gKLocsCmIwPSMrZztAVVIJD8UN5Of8Cq13xjF5qMkSGOLmqccqKAvcDCc9F86MZ-0QkOXuMzeoVW3RMtRaOYNzMalQd7T4-kysTsfrPluVyFgoJtl6ZdA_ZRTKEV8O-PKHn_zbfwNdElPj</recordid><startdate>20201214</startdate><enddate>20201214</enddate><creator>Pandith, Arshad A.</creator><creator>Qasim, Iqbal</creator><creator>Baba, Shahid M.</creator><creator>Koul, Aabid</creator><creator>Zahoor, Wani</creator><creator>Afroze, Dil</creator><creator>Lateef, Adil</creator><creator>Manzoor, Usma</creator><creator>Bhat, Ina A.</creator><creator>Sanadhya, Dheera</creator><creator>R. Bhat, Abdul</creator><creator>Ramzan, Altaf U.</creator><general>Taylor & Francis</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20201214</creationdate><title>Favorable role of IDH1/2 mutations aided with MGMT promoter gene methylation in the outcome of patients with malignant glioma</title><author>Pandith, Arshad A. ; Qasim, Iqbal ; Baba, Shahid M. ; Koul, Aabid ; Zahoor, Wani ; Afroze, Dil ; Lateef, Adil ; Manzoor, Usma ; Bhat, Ina A. ; Sanadhya, Dheera ; R. Bhat, Abdul ; Ramzan, Altaf U.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_25402_fsg_133729043</frbrgroupid><rsrctype>datasets</rsrctype><prefilter>datasets</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Pandith, Arshad A.</creatorcontrib><creatorcontrib>Qasim, Iqbal</creatorcontrib><creatorcontrib>Baba, Shahid M.</creatorcontrib><creatorcontrib>Koul, Aabid</creatorcontrib><creatorcontrib>Zahoor, Wani</creatorcontrib><creatorcontrib>Afroze, Dil</creatorcontrib><creatorcontrib>Lateef, Adil</creatorcontrib><creatorcontrib>Manzoor, Usma</creatorcontrib><creatorcontrib>Bhat, Ina A.</creatorcontrib><creatorcontrib>Sanadhya, Dheera</creatorcontrib><creatorcontrib>R. Bhat, Abdul</creatorcontrib><creatorcontrib>Ramzan, Altaf U.</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Pandith, Arshad A.</au><au>Qasim, Iqbal</au><au>Baba, Shahid M.</au><au>Koul, Aabid</au><au>Zahoor, Wani</au><au>Afroze, Dil</au><au>Lateef, Adil</au><au>Manzoor, Usma</au><au>Bhat, Ina A.</au><au>Sanadhya, Dheera</au><au>R. Bhat, Abdul</au><au>Ramzan, Altaf U.</au><format>book</format><genre>unknown</genre><ristype>DATA</ristype><title>Favorable role of IDH1/2 mutations aided with MGMT promoter gene methylation in the outcome of patients with malignant glioma</title><date>2020-12-14</date><risdate>2020</risdate><abstract>The
implications of molecular biomarkers IDH1/2 mutations and MGMT gene promoter
methylation were evaluated for prognostic outcome of glioma patients.
Methods:
Glioma cases were analyzed for IDH1/2 mutations and MGMT promoter methylation
by DNA sequencing and MS-PCR, respectively.
Results:
Mutations found in IDH1/2 genes totalled 63.4% (N=40) wherein IDH1 mutations
were significantly associated with oligidendrioglioma (p=0.005) and
astrocytoma (p=0.0002). IDH1mutants presented more, 60.5% in MGMT promoter
methylated cases (p=0.03). IDH1 mutant cases had better survival for GBM and oligodendrioglioma
(log rank p=0.01). Multivariate
analysis confirmed better survival in MGMT methylation carriers (HR: 0.59,
p=0.031). Combination of both biomarkers showed better prognosis on
temozolomide (p<0.05).
Conclusions: IDH1/2 mutations proved independent
prognostic factors in glioma and associated with MGMT methylation for better
survival.</abstract><pub>Taylor & Francis</pub><doi>10.25402/fsg.13372904</doi><oa>free_for_read</oa></addata></record> |
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title | Favorable role of IDH1/2 mutations aided with MGMT promoter gene methylation in the outcome of patients with malignant glioma |
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