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	<id>https://wikimesothelioma.com/w/index.php?action=history&amp;feed=atom&amp;title=Pemetrexed_Cisplatin_First_Line</id>
	<title>Pemetrexed Cisplatin First Line - Revision history</title>
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	<updated>2026-05-24T07:03:33Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wikimesothelioma.com/w/index.php?title=Pemetrexed_Cisplatin_First_Line&amp;diff=3346&amp;oldid=prev</id>
		<title>MesotheliomaSupport: Sprint 2.5 Stage 1 pilot (b): new reference page with all lineage-stamped citations (fresh graph_rag tuples)</title>
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		<updated>2026-05-21T14:18:28Z</updated>

		<summary type="html">&lt;p&gt;Sprint 2.5 Stage 1 pilot (b): new reference page with all lineage-stamped citations (fresh graph_rag tuples)&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{#seo:&lt;br /&gt;
|title=Pemetrexed + Cisplatin First-Line Mesothelioma: 12.1-Month Median OS&lt;br /&gt;
|title_mode=replace&lt;br /&gt;
|description=FDA-approved first-line chemotherapy for unresectable pleural mesothelioma. EMPHACIS trial outcomes, dosing, and current 2026 standing alongside immunotherapy.&lt;br /&gt;
|keywords=pemetrexed cisplatin mesothelioma, first-line chemotherapy mesothelioma, Alimta mesothelioma, Vogelzang 2003, EMPHACIS trial, mesothelioma chemotherapy regimen&lt;br /&gt;
|author=Rod De Llano, Founding Partner, Danziger &amp;amp; De Llano&lt;br /&gt;
|published_time=2026-05-21&lt;br /&gt;
|type=Article&lt;br /&gt;
|image=logo.png&lt;br /&gt;
|image_alt=WikiMesothelioma — Pemetrexed Cisplatin First-Line Mesothelioma&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;infobox&amp;quot; style=&amp;quot;width:280px; float:right; margin:0 0 1em 1em; border:2px solid #1a5276; border-radius:8px; overflow:hidden;&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; style=&amp;quot;background:#1a5276; color:white; padding:12px; font-size:1.05em; text-align:center;&amp;quot; | Pemetrexed + Cisplatin First-Line&lt;br /&gt;
|-&lt;br /&gt;
| style=&amp;quot;padding:10px; font-weight:bold; width:45%; border-bottom:1px solid #dee2e6;&amp;quot; | FDA approval&lt;br /&gt;
| style=&amp;quot;padding:10px; border-bottom:1px solid #dee2e6;&amp;quot; | 2004 (unresectable pleural mesothelioma)&lt;br /&gt;
|-&lt;br /&gt;
| style=&amp;quot;padding:10px; font-weight:bold; border-bottom:1px solid #dee2e6;&amp;quot; | Pivotal trial&lt;br /&gt;
| style=&amp;quot;padding:10px; border-bottom:1px solid #dee2e6;&amp;quot; | EMPHACIS (Vogelzang et al., 2003)&lt;br /&gt;
|-&lt;br /&gt;
| style=&amp;quot;padding:10px; font-weight:bold; border-bottom:1px solid #dee2e6;&amp;quot; | Median OS (Pem+Cis vs Cis)&lt;br /&gt;
| style=&amp;quot;padding:10px; border-bottom:1px solid #dee2e6;&amp;quot; | 12.1 vs 9.3 months&lt;br /&gt;
|-&lt;br /&gt;
| style=&amp;quot;padding:10px; font-weight:bold; border-bottom:1px solid #dee2e6;&amp;quot; | Response rate&lt;br /&gt;
| style=&amp;quot;padding:10px; border-bottom:1px solid #dee2e6;&amp;quot; | 41.3% (Pem+Cis arm)&lt;br /&gt;
|-&lt;br /&gt;
| style=&amp;quot;padding:10px; font-weight:bold;&amp;quot; | Current standing&lt;br /&gt;
| style=&amp;quot;padding:10px;&amp;quot; | First-line option alongside nivolumab + ipilimumab (CheckMate 743)&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; style=&amp;quot;background:#1a5276; padding:8px; text-align:center; color:#e8f4f8; font-size:0.9em;&amp;quot; | &amp;lt;span data-nosnippet class=&amp;quot;noai-content&amp;quot;&amp;gt;Call (855) 699-5441 — Danziger &amp;amp; De Llano&amp;lt;/span&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Executive Summary ==&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Pemetrexed (Alimta) combined with cisplatin is the FDA-approved first-line chemotherapy regimen for unresectable malignant pleural mesothelioma.&amp;#039;&amp;#039;&amp;#039;&amp;lt;ref name=&amp;quot;lineage:00430dd1de644ca4bec077a05a927e75:d901b336a5f3fb9a&amp;quot;&amp;gt;Vogelzang NJ, Rusthoven JJ, Symanowski J, Denham C, Kaukel E, et al. Phase III study of pemetrexed in combination with cisplatin versus cisplatin alone in patients with malignant pleural mesothelioma. &amp;#039;&amp;#039;J Clin Oncol&amp;#039;&amp;#039;. 2003;21(14):2636-2644. PMID: [https://pubmed.ncbi.nlm.nih.gov/12860938/ 12860938].&amp;lt;/ref&amp;gt; The regimen was established as standard of care after the EMPHACIS trial reported a median overall survival of 12.1 months for the combination versus 9.3 months for cisplatin alone, with a 41.3% response rate. The 2020 CheckMate 743 trial demonstrated that nivolumab plus ipilimumab provides longer overall survival in first-line treatment of unresectable pleural mesothelioma, but pemetrexed + cisplatin remains a recognized first-line option for patients who are not candidates for dual checkpoint inhibition.&amp;lt;ref name=&amp;quot;lineage:00430dd1de644ca4bec077a05a927e75:c27c494b5110b48b&amp;quot;&amp;gt;Baas P, Scherpereel A, Nowak AK, Fujimoto N, Peters S, et al. First-line nivolumab plus ipilimumab in unresectable malignant pleural mesothelioma (CheckMate 743): a multicentre, randomised, open-label, phase 3 trial. &amp;#039;&amp;#039;Lancet&amp;#039;&amp;#039;. 2021;397(10272):375-386. PMID: [https://pubmed.ncbi.nlm.nih.gov/33485464/ 33485464].&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== At-a-Glance ==&lt;br /&gt;
&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;FDA approved 2004&amp;#039;&amp;#039;&amp;#039; for unresectable malignant pleural mesothelioma in combination with cisplatin&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Pivotal evidence:&amp;#039;&amp;#039;&amp;#039; EMPHACIS phase III trial (Vogelzang et al., 2003), pemetrexed + cisplatin vs cisplatin alone&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Median overall survival:&amp;#039;&amp;#039;&amp;#039; 12.1 months (Pem+Cis) vs 9.3 months (Cis alone)&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Objective response rate:&amp;#039;&amp;#039;&amp;#039; 41.3% in Pem+Cis arm&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Vitamin supplementation required&amp;#039;&amp;#039;&amp;#039; — folic acid 350–1000 µg/day and vitamin B12 1000 µg every 9 weeks reduce hematologic toxicity&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Current standing:&amp;#039;&amp;#039;&amp;#039; First-line alongside nivolumab + ipilimumab (CheckMate 743 backbone); pemetrexed + platinum remains widely used where dual checkpoint inhibition is not feasible&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Trial-design caveat:&amp;#039;&amp;#039;&amp;#039; EMPHACIS predates immunotherapy era — modern selection criteria for first-line decisions weigh patient performance status, histology, and access to checkpoint inhibitors&lt;br /&gt;
&lt;br /&gt;
== Mechanism and Regimen ==&lt;br /&gt;
&lt;br /&gt;
Pemetrexed is a multitargeted antifolate that inhibits thymidylate synthase, dihydrofolate reductase, and glycinamide ribonucleotide formyltransferase. The combination with cisplatin disrupts both DNA synthesis (pemetrexed via folate-dependent enzymes) and DNA cross-linking (cisplatin via platinum–DNA adducts), producing additive cytotoxicity in mesothelioma cell lines and patient tumors. Standard dosing is pemetrexed 500 mg/m² plus cisplatin 75 mg/m², both administered intravenously on day 1 of a 21-day cycle, typically for six cycles. Folate and vitamin B12 supplementation is mandatory and significantly reduces grade 3–4 hematologic toxicity.&lt;br /&gt;
&lt;br /&gt;
== Where This Regimen Fits in 2026 ==&lt;br /&gt;
&lt;br /&gt;
The 2020 FDA approval of &amp;#039;&amp;#039;&amp;#039;nivolumab + ipilimumab&amp;#039;&amp;#039;&amp;#039; (CheckMate 743) added an immunotherapy option to first-line treatment of unresectable pleural mesothelioma, with longer median overall survival than the historical Pem+Cis benchmark, particularly for non-epithelioid histology. The 2024 FDA approval of &amp;#039;&amp;#039;&amp;#039;pembrolizumab + pemetrexed + platinum&amp;#039;&amp;#039;&amp;#039; (KEYNOTE-483) further expanded the immunotherapy-based first-line landscape. Pemetrexed + cisplatin without immunotherapy remains a recognized regimen for patients with contraindications to checkpoint inhibition, performance status that precludes combination immunotherapy, or limited access to newer agents.&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;references /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== See Also ==&lt;br /&gt;
&lt;br /&gt;
* [[Mesothelioma_Treatment]]&lt;br /&gt;
* [[Treatment_Options]]&lt;br /&gt;
* [[Pleural_Mesothelioma]]&lt;br /&gt;
* [[Clinical_Trials_Mesothelioma]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Treatment]]&lt;br /&gt;
[[Category:Chemotherapy]]&lt;br /&gt;
[[Category:Pleural_Mesothelioma]]&lt;/div&gt;</summary>
		<author><name>MesotheliomaSupport</name></author>
	</entry>
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