Sex differences in toxicities among patients receiving regorafenib or trifluridine/tipiracil for refractory metastatic colorectal cancer: A subgroup analysis from the multicenter retrospective ReTrITA study.
Abstract
e15589 Background: A mounting body of evidence indicates the existence of sex disparities in the prevalence, severity, and prognosis of various cancers. In the context of metastatic colorectal cancer (mCRC), women are observed to exhibit a higher propensity for right-sided tumour development, a heightened frequency of microsatellite instability, and an increased prevalence of BRAF mutant tumours. These characteristics are commonly correlated with a poor prognosis when treated with conventional chemotherapeutic combination therapies. In this substudy, the impact of sex on the toxicity of treatment with regorafenib (R) or trifluridine/tipiracil (T) for refractory mCRC was investigated. Methods: A retrospective analysis of clinical data pertaining to patients treated with R and T between 2012 and 2023 was conducted at 17 Italian cancer centres. Results: A total of 1156 patients were retrospectively enrolled in the ReTrITA study. These patients had received sequential treatment with T and R (T/R, n = 261; R/T, n = 155) or T (n = 427) or R (n = 313) as monotherapy. The majority of patients were male (n = 674; 58.4% vs. n = 482; 41.6%). Within the safety set, an amount of 488 cases of grade (G) 3/4 toxicity were identified in patients treated with T (43,4% in women and 56,6% in men), compared to 343 G3/G4 toxicities observed in patients receiving R (47,6% in females vs. 52,4% observed in males), representing 58.7% and 41.3% of all toxicity events, respectively. Notably, male patients treated with T were observed to have a higher incidence of grade G3/G4 toxicities, with the most common being neutropenia (31.1%) and diarrhoea (2.2%), in comparison with women who reported 25.2% and 2%, respectively; it is noteworthy that both sexes presented with grade 3/4 anaemia (8.1%) (p = 0.6988). In R-treated patients, men showed a significant but slightly higher prevalence of the most common G3/G4 toxicities than women, such as fatigue (15.7% vs. 12.2%) and hand-foot syndrome (10.2% vs. 9.3%), while female patients had a higher incidence of hypertension than males (4.6% vs. 4.3%) (p = 0.0582). Finally, the occurrence of febrile neutropenia in only four males who received therapy with T, should not be underestimated. Conclusions: Our real-world analysis suggests that the prevalence of G3/G4 toxicities in response to R or T therapy is lower among female patients than male patients, with the exception of hypertension. In order to enhance comprehension of toxicities associated with sex in the future, the analysis of toxicity events could represent a valuable instrument to facilitate the collection of extensive datasets, thereby enabling a more in-depth comparison of male and female patients. Furthermore, using patient-reported outcomes may help us gain a better knowledge of the impact of anticancer treatment based on sex and gender.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Carlo Signorelli
Medical Oncology Unit, S.Rosa Hospital, ASL Viterbo, Viterbo, Italy
Michele Basso
Medical Oncology, Comprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy
Alessandro Passardi
Medical Oncology, IRST-IRCCS "Dino Amadori", Meldola, Italy
Jessica Lucchetti
Operative Research Unit of Medical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy
Ina Valeria Zurlo
Medical Oncology, 'Vito Fazzi' Hospital, Lecce, Italy
Cristina Morelli
Medical Oncology Unit, Department of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy
Emanuela Dell'Aquila
IRCCS Regina Elena National Cancer Institute, Rome, Italy
Donatello Gemma
Medical Oncology Department, Ospedale SS Trinità, Sora (FR), Italy
Alessandra Emiliani
Oncology Department, Isola Tiberina Hospital-Gemelli Isola, Rome, Italy
Federica Mazzuca
Department of Clinical and Molecular Medicine, Oncology Unit, Sant’ Andrea University Hospital, Sapienza University of Rome, Rome, Italy
Federica Zoratto
UOC Oncologia, Ospedale Santa Maria Goretti, ASL Latina, Latina, Italy
Mario Giovanni Chilelli
Medical Oncology Unit, Belcolle Hospital, ASL Viterbo, Viterbo, Italy
Maria Grazia Morandi
Medical Oncology Unit, San Camillo de Lellis Hospital, ASL Rieti, Rieti, Italy
Fiorenza Santamaria
Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy
Manuela Dettori
Medical Oncology Department, Ospedale Oncologico Armando Businco, Cagliari, Italy
Antonella Cosimati
Medical Oncology Department, UO Oncologia Universitaria della Casa della Salute di Aprilia, Aprilia (LT), Italy
Rosa Saltarelli
Medical Oncology Department, UOC Oncology, San Giovanni Evangelista Hospital, ASL RM5, Tivoli (RM), Italy
Alessandro Minelli
UO Oncologia, Ospedale San Paolo, ASL RM4, Civitavecchia (RM), Italy
Emanuela Lucci-Cordisco
UOC Genetica Medica, Dipartimento di Scienze della Vita e Sanità Pubblica, Fondazione Policlinico Universitario A.Gemelli, IRCCS; Medical Oncology Department, Comprehensive Cancer Center, Fondazione Policlinico Universitario A.Gemelli, Rome, Italy
Maria Alessandra Calegari
Medical Oncology, Comprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy