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                  <mods:namePart>Corral, Jesus</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Paz Ares, Luis Gonzaga</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">funder</mods:roleTerm>
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                  <mods:namePart>ImmunoGen Inc</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2019-04-02T10:10:49Z</mods:dateAccessioned>
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               <mods:identifier type="citation">Clin Lung Cancer. 2017;18(1):68-76</mods:identifier>
               <mods:identifier type="doi">10.1016/j.cllc.2016.09.002</mods:identifier>
               <mods:identifier type="e-issn">1938-0690</mods:identifier>
               <mods:identifier type="issn">15257304</mods:identifier>
               <mods:identifier type="journal">Clinical lung cancer</mods:identifier>
               <mods:identifier type="pubmedID">28341109</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/7424</mods:identifier>
               <mods:abstract>INTRODUCTION: This trial assessed the safety and efficacy of LM in combination with carboplatin/etoposide therapy compared to carboplatin/etoposide treatment alone in patients with previously untreated extensive-disease small-cell lung cancer (ED-SCLC). PATIENTS AND METHODS: A run-in phase 1 stage was used to determine the recommended phase 2 dose and characterize the dose-limiting toxicities of LM in combination with carboplatin/etoposide followed by LM alone in patients with CD56-positive solid tumors. In phase 2, chemotherapy-naive ED-SCLC patients were randomized 2:1 to carboplatin AUC (area under the plasma concentration vs. time curve) of 5 day 1 + etoposide 100 mg/m2 days 1 to 3 plus LM (arm 1) or alone (arm 2). RESULTS: In the phase 1 study (n = 33), a dose of LM at 112 mg/m2 with carboplatin/etoposide was identified as the recommended phase 2 dose. However, because of an increased incidence of peripheral neuropathy events during early phase 2, this dose was reduced to 90 mg/m2. In phase 2, a total of 94 and 47 evaluable patients were assigned to arms 1 and 2, respectively. No difference in median progression-free survival was observed between arms 1 and 2 (6.2 vs. 6.7 months). The most common treatment-emergent adverse event leading to discontinuation was peripheral neuropathy (29%). A total of 21 patients had a treatment-emergent adverse event leading to death (18 in arm 1 and 3 in arm 2); for 10 individuals, this was an infection (pneumonia or sepsis) deemed to be related to the study drug. CONCLUSION: The combination of LM plus carboplatin/etoposide did not improve efficacy over standard carboplatin/etoposide doublet therapy in ED-SCLC patients and showed increased toxicity, including a higher incidence of serious infections with fatal outcomes.</mods:abstract>
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                  <mods:topic>Clinical trial</mods:topic>
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               <mods:subject>
                  <mods:topic>Combination therapy</mods:topic>
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               <mods:subject>
                  <mods:topic>SCLC</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Targeted drug delivery</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Tolerability</mods:topic>
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                  <mods:title>Phase 1/2 Study of the CD56-Targeting Antibody-Drug Conjugate Lorvotuzumab Mertansine (IMGN901) in Combination With Carboplatin/Etoposide in Small-Cell Lung Cancer Patients With Extensive-Stage Disease</mods:title>
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