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International Tailored Chemotherapy Adjuvant (ITACA) trial, a phase III multicenter randomized trial comparing adjuvant pharmacogenomic-driven chemotherapy versus standard adjuvant chemotherapy in completely resected stage II-IIIA non-small-cell lung cancer

Articolo
Data di Pubblicazione:
2022
Abstract:
Background: Several strategies have been investigated to improve the 4% survival advantage of adjuvant chemotherapy in early-stage non-small-cell lung cancer (NSCLC). In this investigator-initiated study we aimed to evaluate the predictive utility of the messenger RNA (mRNA) expression levels of excision repair cross complementation group 1 (ERCC1) and thymidylate synthase (TS) as assessed in resected tumor. Patients and methods: Seven hundred and seventy-three completely resected stage II-III NSCLC patients were enrolled and randomly assigned in each of the four genomic subgroups to investigator's choice of platinum-based chemotherapy (C, n = 389) or tailored chemotherapy (T, n = 384). All anticancer drugs were administered according to standard doses and schedules. Stratification factors included stage and smoking status. The primary endpoint of the study was overall survival (OS). Results: Six hundred and ninety patients were included in the primary analysis. At a median follow-up of 45.9 months, 85 (24.6%) and 70 (20.3%) patients died in arms C and T, respectively. Five-year survival for patients in arms C and T was of 65.4% (95% CI (confidence interval): 58.5% to 71.4%) and 72.9% (95% CI: 66.5% to 78.3%), respectively. The estimated hazard ratio (HR) was 0.77 (95% CI: 0.56-1.06, P value: 0.109) for arm T versus arm C. HR for recurrence-free survival was 0.89 (95% CI: 0.69-1.14, P value: 0.341) for arm T versus arm C. Grade 3-5 toxicities were more frequently reported in arm C than in arm T. Conclusion: In completely resected stage II-III NSCLC tailoring adjuvant chemotherapy conferred a non-statistically significant trend for OS favoring the T arm. In terms of safety, the T arm was associated with better efficacy/toxicity ratio related to the different therapeutic choices in the experimental arm.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
adjuvant chemotherapy; excision repair cross-complementation 1; messenger RNA; non-small-cell lung cancer; pharmacogenomics; thymidylate synthase; Antineoplastic Combined Chemotherapy Protocols; Chemotherapy, Adjuvant; Humans; Neoplasm Staging; Pharmacogenetics; Antineoplastic Agents; Carcinoma, Non-Small-Cell Lung; Lung Neoplasms
Elenco autori:
Novello, S.; Torri, V.; Grohe, C.; Kurz, S.; Serke, M.; Wehler, T.; Meyer, A.; Ladage, D.; Geissler, M.; Colantonio, I.; Cauchi, C.; Stoelben, E.; Ceribelli, A.; Kropf-Sanchen, C.; Valmadre, G.; Borra, G.; Schena, M.; Morabito, A.; Santo, A.; Gregorc, V.; Chiari, R.; Reck, M.; Schmid-Bindert, G.; Folprecht, G.; Griesinger, F.; Follador, A.; Pedrazzoli, P.; Bearz, A.; Caffo, O.; Dickgreber, N. J.; Irtelli, L.; Wiest, G.; Monica, V.; Porcu, L.; Manegold, C.; Scagliotti, G. V.
Autori di Ateneo:
PEDRAZZOLI PAOLO
Link alla scheda completa:
https://iris.unipv.it/handle/11571/1453166
Pubblicato in:
ANNALS OF ONCOLOGY
Journal
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