| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Stojanovic, Goran |
| dc.contributor.author | Spigel, David |
| dc.contributor.author | Dowlati, Afshin |
| dc.contributor.author | NAVARRO, ALEJANDRO |
| dc.contributor.author | Yang, James Chih-Hsin |
| dc.contributor.author | Chen, Yuanbin |
| dc.date.accessioned | 2024-07-02T09:28:08Z |
| dc.date.available | 2024-07-02T09:28:08Z |
| dc.date.issued | 2024-07-01 |
| dc.identifier.citation | Spigel DR, Dowlati A, Chen Y, Navarro A, Yang JCH, Stojanovic G, et al. RESILIENT Part 2: A Randomized, Open-Label Phase III Study of Liposomal Irinotecan Versus Topotecan in Adults With Relapsed Small Cell Lung Cancer. J Clin Oncol. 2024 Jul 1;42(19):2317–26. |
| dc.identifier.issn | 1527-7755 |
| dc.identifier.uri | https://hdl.handle.net/11351/11652 |
| dc.description | Liposomal Irinotecan; Topotecan; Small cell lung cancer |
| dc.description.abstract | Purpose
The phase III RESILIENT trial compared second-line liposomal irinotecan with topotecan in patients with small cell lung cancer (SCLC).
Patients and Methods
Patients with SCLC and progression on or after first-line platinum-based chemotherapy were randomly assigned (1:1) to intravenous (IV) liposomal irinotecan (70 mg/m2 every 2 weeks in a 6-week cycle) or IV topotecan (1.5 mg/m2 daily for 5 consecutive days, every 3 weeks in a 6-week cycle). The primary end point was overall survival (OS). Key secondary end points included progression-free survival (PFS) and objective response rate (ORR).
Results
Among 461 randomly assigned patients, 229 received liposomal irinotecan and 232 received topotecan. The median follow-up was 18.4 months. The median OS was 7.9 months with liposomal irinotecan versus 8.3 months with topotecan (hazard ratio [HR], 1.11 [95% CI, 0.90 to 1.37]; P = .31). The median PFS per blinded independent central review (BICR) was 4.0 months with liposomal irinotecan and 3.3 months with topotecan (HR, 0.96 [95% CI, 0.77 to 1.20]; nominal P = .71); ORR per BICR was 44.1% (95% CI, 37.6 to 50.8) and 21.6% (16.4 to 27.4), respectively. Overall, 42.0% and 83.4% of patients receiving liposomal irinotecan and topotecan, respectively, experienced grade ≥3 related treatment-emergent adverse events (TEAEs). The most common grade ≥3 related TEAEs were diarrhea (13.7%), neutropenia (8.0%), and decreased neutrophil count (4.4%) with liposomal irinotecan and neutropenia (51.6%), anemia (30.9%), and leukopenia (29.1%) with topotecan.
Conclusion
Liposomal irinotecan and topotecan demonstrated similar median OS and PFS in patients with relapsed SCLC. Although the primary end point of OS was not met, liposomal irinotecan demonstrated a higher ORR than topotecan. The safety profile of liposomal irinotecan was consistent with its known safety profile; no new safety concerns emerged. |
| dc.language.iso | eng |
| dc.publisher | American Society of Clinical Oncology |
| dc.relation.ispartofseries | Journal of Clinical Oncology;42(19) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Pulmons - Càncer - Tractament |
| dc.subject | Medicaments antineoplàstics - Ús terapèutic |
| dc.subject | Inhibidors enzimàtics - Ús terapèutic |
| dc.subject.mesh | Antineoplastic Agents |
| dc.subject.mesh | Topoisomerase I Inhibitors |
| dc.subject.mesh | Carcinoma, Non-Small-Cell Lung |
| dc.subject.mesh | /drug therapy |
| dc.title | RESILIENT Part 2: A Randomized, Open-Label Phase III Study of Liposomal Irinotecan Versus Topotecan in Adults With Relapsed Small Cell Lung Cancer |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1200/JCO.23.02110 |
| dc.subject.decs | antineoplásicos |
| dc.subject.decs | inhibidores de la topoisomerasa I |
| dc.subject.decs | carcinoma de pulmón de células no pequeñas |
| dc.subject.decs | /farmacoterapia |
| dc.relation.publishversion | https://doi.org/10.1200/JCO.23.02110 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Spigel DR] Sarah Cannon Research Institute/Tennessee Oncology, Nashville, TN. [Dowlati A] University Hospitals Seidman Cancer Center and Case Western Reserve University, Cleveland, OH. [Chen Y] Cancer and Hematology Centers of Western Michigan, Grand Rapids, MI. [Navarro A] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Chih-Hsin Yang J] National Taiwan University Hospital and National Taiwan University Cancer Center, Taipei, Taiwan. [Stojanovic G] Institute for Pulmonary Diseases of Vojvodina, Sremska Kamenica, Serbia |
| dc.identifier.pmid | 38648575 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |