Sena Valcarcel1, Javier Gallego2, Paula Jimenez-Fonseca3, Marc Diez4, Eva Martínez de Castro5, Raquel Hernandez6, Virginia Arrazubi7, Ana Custodio8, Juana María Cano9, Ana Fernández Montes10, Ismael Macias11, Laura Visa12, Aitana Calvo13, Rosario Vidal Tocino14, Nieves Martínez Lago15, María Luisa Limón16, Mónica Granja17, Mireia Gil18, Paola Pimentel19, Lola Macia-Rivas20, Carolina Hernández Pérez21, Montserrat Mangas22, Alfonso Martín Carnicero23, Paula Cerdà24, Lucía Gomez Gonzalez25, Francisco Garcia Navalon26, Mª Dolores Mediano Rambla27, Marta Martin Richard28, Alberto Carmona-Bayonas29. 1. Medical Oncology Department, Hospital Universitario Central de Asturias, ISPA, Avenida Roma Sn., CP 33011, Oviedo, Spain. senavg@gmail.com. 2. Medical Oncology Department, Hospital General Universitario de Elche, Elche, Spain. 3. Medical Oncology Department, Hospital Universitario Central de Asturias, ISPA, Oviedo, Spain. 4. Medical Oncology Department, Hospital Universitario Vall d'Hebron, Barcelona, Spain. 5. Medical Oncology Department, Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain. 6. Medical Oncology Department, Hospital Universitario de Canarias, Tenerife, Spain. 7. Medical Oncology Department, Hospital Universitario de Navarra, Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain. 8. Medical Oncology Department, Hospital Universitario La Paz, CIBERONC CB16/12/00398, Madrid, Spain. 9. Medical Oncology Department, Hospital General Universitario de Ciudad Real, Ciudad Real, Spain. 10. Medical Oncology Department, Complejo Hospitalario Universitario de Ourense, Orense, Spain. 11. Medical Oncology Department, Hospital Universitario Parc Tauli, Sabadell, Spain. 12. Medical Oncology Department, Hospital Universitario El Mar, Barcelona, Spain. 13. Medical Oncology Department, Hospital Universitario Gregorio Marañón, Madrid, Spain. 14. Medical Oncology Department, Complejo Asistencial Universitario de Salamanca - IBSAL, Salamanca, Spain. 15. Medical Oncology Department, Complejo Hospitalario Universitario de A Coruña, Coruña, Spain. 16. Medical Oncology Department, Hospital Universitario Virgen del Rocío, Seville, Spain. 17. Medical Oncology Department, Hospital Universitario Clínico San Carlos Madrid, Madrid, Spain. 18. Medical Oncology Department, Hospital General Universitario de Valencia, Ciberonc CB16/12/0035, Valencia, Spain. 19. Medical Oncology Department, Hospital Santa Lucía, Cartagena, Spain. 20. Pharmacy Department, Hospital Universitario Central de Asturias, Oviedo, Spain. 21. Medical Oncology Department, Hospital Universitario Nuestra Señora de La Candelaria, Tenerife, Spain. 22. Medical Oncology Department, Hospital Galdakao-Usansolo, Galdakao-Usansolo, Spain. 23. Medical Oncology Department, Hospital San Pedro, Logroño, Spain. 24. Medical Oncology Department, Hospital Santa Creu I Sant Pau, Barcelona, Spain. 25. Medical Oncology Department, Hospital General Universitario de Alicante, Alicante, Spain. 26. Medical Oncology Department, Hospital Universitario Son Llatzer, Mallorca, Spain. 27. Medical Oncology Department, Hospital Universitario Virgen de La Macarena, Seville, Spain. 28. Medical Oncology Department, Catalan Institute of Oncology (ICO), L'Hospitalet, Spain. 29. Hematology and Medical Oncology Department, Hospital Universitario Morales Meseguer, University of Murcia, IMIB, CP13/00126, PI17/0050 (ISCIII& FEDER), Murcia, Spain.
Abstract
PURPOSE: This study aimed to compare ramucirumab-paclitaxel versus chemotherapy in second-line (2L) advanced gastroesophageal cancer (aGEC) based on HER2 status and analyze prognostic factors. METHODS: The study includes patients from the AGAMENON-SEOM registry with aGEC and known HER2 status who received 2L between 2016 and 2021. The Kaplan-Meier method was used to calculate progression-free survival (PFS) and overall survival (OS) and multivariable Cox regression analysis was done to adjust for confounding variables. RESULTS: Of the 552 patients who met the selection criteria, 149 (26.9%) had HER2-positive aGEC, 89 were treated with chemotherapy, and 60 with ramucirumab-paclitaxel, and 403 had an HER2-negative aGEC, 259 were treated with chemotherapy, and 144 with ramucirumab-paclitaxel. In the whole sample, 2L PFS was 3.0 months (95% CI 2.8-3.2), 2L OS, 5.7 months (5.2-6.3), and ramucirumab-paclitaxel versus chemotherapy was associated with increased PFS (HR 0.64, 95% CI 0.53-0.78, p < 0.0001) and OS (HR 0.68, 0.55-0.83, p = 0.0002). Median PFS of ramucirumab- paclitaxel versus chemotherapy was 3.5 vs 2.8 months (HR 0.67, 0.54-0.83, p = 0.0004) in HER2-negative, and 4.7 vs 2.7 months (HR 0.57, 0.40-0.82, p = 0.0031) in HER2-positive aGEC, respectively. Median OS for ramucirumab-paclitaxel versus chemotherapy was 6.6 vs 5 months (HR 0.67, 0.53-0.85, p = 0.0007) in HER2-negative, and 7.4 vs 5.6 months (HR 0.70, 0.53-1.04, p = 0.083) in HER2-positive aGEC, respectively. ECOG-PS, tumor burden, Lauren subtype, and neutrophil-lymphocyte ratio were prognostic factors. CONCLUSIONS: In patients with an aGEC from the AGAMENON-SEOM registry, 2L treatment with ramucirumab-paclitaxel was superior to chemotherapy in PFS, OS and response rate, independent of HER2 status.
PURPOSE: This study aimed to compare ramucirumab-paclitaxel versus chemotherapy in second-line (2L) advanced gastroesophageal cancer (aGEC) based on HER2 status and analyze prognostic factors. METHODS: The study includes patients from the AGAMENON-SEOM registry with aGEC and known HER2 status who received 2L between 2016 and 2021. The Kaplan-Meier method was used to calculate progression-free survival (PFS) and overall survival (OS) and multivariable Cox regression analysis was done to adjust for confounding variables. RESULTS: Of the 552 patients who met the selection criteria, 149 (26.9%) had HER2-positive aGEC, 89 were treated with chemotherapy, and 60 with ramucirumab-paclitaxel, and 403 had an HER2-negative aGEC, 259 were treated with chemotherapy, and 144 with ramucirumab-paclitaxel. In the whole sample, 2L PFS was 3.0 months (95% CI 2.8-3.2), 2L OS, 5.7 months (5.2-6.3), and ramucirumab-paclitaxel versus chemotherapy was associated with increased PFS (HR 0.64, 95% CI 0.53-0.78, p < 0.0001) and OS (HR 0.68, 0.55-0.83, p = 0.0002). Median PFS of ramucirumab- paclitaxel versus chemotherapy was 3.5 vs 2.8 months (HR 0.67, 0.54-0.83, p = 0.0004) in HER2-negative, and 4.7 vs 2.7 months (HR 0.57, 0.40-0.82, p = 0.0031) in HER2-positive aGEC, respectively. Median OS for ramucirumab-paclitaxel versus chemotherapy was 6.6 vs 5 months (HR 0.67, 0.53-0.85, p = 0.0007) in HER2-negative, and 7.4 vs 5.6 months (HR 0.70, 0.53-1.04, p = 0.083) in HER2-positive aGEC, respectively. ECOG-PS, tumor burden, Lauren subtype, and neutrophil-lymphocyte ratio were prognostic factors. CONCLUSIONS: In patients with an aGEC from the AGAMENON-SEOM registry, 2L treatment with ramucirumab-paclitaxel was superior to chemotherapy in PFS, OS and response rate, independent of HER2 status.
Authors: Rupert Bartsch; Catharina Wenzel; Gabriela Altorjai; Ursula Pluschnig; Margaretha Rudas; Robert M Mader; Michael Gnant; Christoph C Zielinski; Guenther G Steger Journal: J Clin Oncol Date: 2007-08-06 Impact factor: 44.544
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Authors: Almudena Cotes Sanchís; Javier Gallego; Raquel Hernandez; Virginia Arrazubi; Ana Custodio; Juana María Cano; Gema Aguado; Ismael Macias; Carlos Lopez; Flora López; Laura Visa; Marcelo Garrido; Nieves Martínez Lago; Ana Fernández Montes; María Luisa Limón; Aitor Azkárate; Paola Pimentel; Pablo Reguera; Avinash Ramchandani; Juan Diego Cacho; Alfonso Martín Carnicero; Mónica Granja; Marta Martín Richard; Carolina Hernández Pérez; Alicia Hurtado; Olbia Serra; Elvira Buxo; Rosario Vidal Tocino; Paula Jimenez-Fonseca; Alberto Carmona-Bayonas Journal: PLoS One Date: 2020-07-31 Impact factor: 3.240
Authors: In Sil Choi; Jee Hyun Kim; Ju Hyun Lee; Koung Jin Suh; Ji Yun Lee; Ji-Won Kim; Se-Hyun Kim; Jin Won Kim; Jeong-Ok Lee; Yu Jung Kim; Soo-Mee Bang; Jong Seok Lee; Keun-Wook Lee Journal: PLoS One Date: 2018-10-22 Impact factor: 3.240