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               <dc:title>A Phase Ib Study of the DNA-PK Inhibitor Peposertib Combined with Neoadjuvant Chemoradiation in Patients with Locally Advanced Rectal Cancer</dc:title>
               <dc:creator>Romesser, Paul</dc:creator>
               <dc:creator>Philip, Tony</dc:creator>
               <dc:creator>Fernandez-Martos, Carlos</dc:creator>
               <dc:creator>Tuli, Rich</dc:creator>
               <dc:creator>Capdevila Castillon, Jaume</dc:creator>
               <dc:creator>Garcia-Carbonero, Rocio</dc:creator>
               <dc:subject>Proteïnes quinases - Inhibidors - Ús terapèutic</dc:subject>
               <dc:subject>Quimioteràpia combinada</dc:subject>
               <dc:subject>Recte - Càncer - Tractament</dc:subject>
               <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Therapeutics::Drug Therapy::Antineoplastic Protocols::Therapeutics::Drug Therapy::Antineoplastic Combined Chemotherapy Protocols</dc:subject>
               <dc:subject>DISEASES::Neoplasms::Neoplasms by Site::Digestive System Neoplasms::Gastrointestinal Neoplasms::Intestinal Neoplasms::Colorectal Neoplasms::Rectal Neoplasms</dc:subject>
               <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Combined Modality Therapy::Chemoradiotherapy</dc:subject>
               <dc:subject>CHEMICALS AND DRUGS::Chemical Actions and Uses::Pharmacologic Actions::Molecular Mechanisms of Pharmacological Action::Enzyme Inhibitors::Protein Kinase Inhibitors</dc:subject>
               <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::terapéutica::farmacoterapia::protocolos antineoplásicos::terapéutica::farmacoterapia::protocolos de quimioterapia antineoplásica combinada</dc:subject>
               <dc:subject>ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias del sistema digestivo::neoplasias gastrointestinales::neoplasias intestinales::neoplasias colorrectales::neoplasias del recto</dc:subject>
               <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::tratamiento combinado::quimiorradioterapia</dc:subject>
               <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::acciones y usos químicos::acciones farmacológicas::mecanismos moleculares de acción farmacológica::inhibidores enzimáticos::inhibidores de proteínas cinasas</dc:subject>
               <dc:description>DNA-PK inhibitor peposertib; Neoadjuvant chemoradiation; Rectal cancer</dc:description>
               <dc:description>Inhibidor de l'ADN-PK peposertib; Quimioradiació neoadjuvant; Càncer de recte</dc:description>
               <dc:description>Inhibidor de ADN-PK peposertib; Quimiorradiación neoadyuvante; Cáncer de recto</dc:description>
               <dc:description>Purpose:&#xd;
Peposertib—an orally administered DNA-dependent protein kinase inhibitor—has shown potent radiosensitization in preclinical models. This dose-escalation study (NCT03770689) aimed to define the maximum tolerated dose (MTD) and recommended phase II dose (RP2D) of peposertib plus capecitabine-based chemoradiotherapy (CRT) and assessed its safety and efficacy in locally advanced rectal cancer.&#xd;
Patients and Methods:&#xd;
Patients were treated for 5 to 5.5 weeks with 50- to 250-mg peposertib once daily, capecitabine 825 mg/m2 twice daily, and radiotherapy (RT), 5 days per week. Following clinical restaging (8 weeks after CRT completion), patients with clinical complete response (cCR) could opt for surveillance. Total mesorectal excision was recommended upon incomplete response (IR).&#xd;
Results:&#xd;
Nineteen patients were treated with peposertib at doses of 50 mg (n = 1), 100 mg, 150 mg, and 250 mg (n = 6 each). Dose-limiting toxicities occurred in one out of five (100 mg), one out of six (150 mg), and three out of six (250 mg) evaluable patients. Peposertib ≤150 mg once daily was tolerable in combination with CRT. After 8 weeks of treatment with peposertib and CRT, the cCR was 15.8% (n = 3). Among the three patients with cCR, two underwent surgery and had residual tumors. Among the 16 patients with IR, seven underwent surgery and had residual tumors; five of the remaining nine patients opted for consolidative chemotherapy. The combined cCR/pathologic complete response (pCR) rate was 5.3% (n = 1, 100 mg cohort).&#xd;
Conclusions:&#xd;
Peposertib did not improve complete response rates at tolerable dose levels. The study was closed without declaring the MTD/RP2D.</dc:description>
               <dc:date>2024-06-06T08:42:23Z</dc:date>
               <dc:date>2024-06-06T08:42:23Z</dc:date>
               <dc:date>2024-02-21T12:44:49Z</dc:date>
               <dc:date>2024-02-21T12:44:49Z</dc:date>
               <dc:date>2024-02-15</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:identifier>http://hdl.handle.net/11351/11098</dc:identifier>
               <dc:relation>Clinical Cancer Research;30(4)</dc:relation>
               <dc:relation>https://doi.org/10.1158/1078-0432.CCR-23-1129</dc:relation>
               <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>American Association for Cancer Research</dc:publisher>
               <dc:source>Scientia</dc:source>
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