Your browser doesn't support javascript.
loading
Osimertinib beyond disease progression in T790M EGFR-positive NSCLC patients: a multicenter study of clinicians' attitudes.
Cortellini, A; Leonetti, A; Catino, A; Pizzutillo, P; Ricciuti, B; De Giglio, A; Chiari, R; Bordi, P; Santini, D; Giusti, R; De Tursi, M; Brocco, D; Zoratto, F; Rastelli, F; Citarella, F; Russano, M; Filetti, M; Marchetti, P; Berardi, R; Torniai, M; Cortinovis, D; Sala, E; Maggioni, C; Follador, A; Macerelli, M; Nigro, O; Tuzi, A; Iacono, D; Migliorino, M R; Banna, G; Porzio, G; Cannita, K; Ferrara, M G; Bria, E; Galetta, D; Ficorella, C; Tiseo, M.
Afiliação
  • Cortellini A; Medical Oncology Unit, St. Salvatore Hospital, Via Vetoio, 67100, L'Aquila, Italy. alessiocortellini@gmail.com.
  • Leonetti A; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy. alessiocortellini@gmail.com.
  • Catino A; Medical Oncology, University Hospital of Parma, Parma, Italy.
  • Pizzutillo P; Thoracic Oncology Unit, Clinical Cancer Centre "Giovanni Paolo II", Bari, Italy.
  • Ricciuti B; Thoracic Oncology Unit, Clinical Cancer Centre "Giovanni Paolo II", Bari, Italy.
  • De Giglio A; Department of Surgical and Biomedical Sciences, University of Perugia, Perugia, Italy.
  • Chiari R; Department of Surgical and Biomedical Sciences, University of Perugia, Perugia, Italy.
  • Bordi P; Medical Oncology, Ospedali Riuniti Padova Sud "Madre Teresa Di Calcutta", Monselice, Italy.
  • Santini D; Medical Oncology, University Hospital of Parma, Parma, Italy.
  • Giusti R; Medical Oncology, Campus Bio-Medico University, Rome, Italy.
  • De Tursi M; Medical Oncology, Sant'Andrea Hospital, Rome, Italy.
  • Brocco D; Department of Medical, Oral and Biotechnological Sciences, University G. D'Annunzio, Chieti-Pescara, Italy.
  • Zoratto F; Clinical Oncology Unit, S.S. Annunziata Hospital, Chieti, Italy.
  • Rastelli F; Medical Oncology, Santa Maria Goretti Hospital, Latina, Italy.
  • Citarella F; Medical Oncology, Fermo Area Vasta 4, Fermo, Italy.
  • Russano M; Medical Oncology, Campus Bio-Medico University, Rome, Italy.
  • Filetti M; Medical Oncology, Campus Bio-Medico University, Rome, Italy.
  • Marchetti P; Medical Oncology, Sant'Andrea Hospital, Rome, Italy.
  • Berardi R; Medical Oncology, Sant'Andrea Hospital, Rome, Italy.
  • Torniai M; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
  • Cortinovis D; Oncology Clinic, Università Politecnica Delle Marche, Ospedali Riuniti Di Ancona, Ancona, Italy.
  • Sala E; Oncology Clinic, Università Politecnica Delle Marche, Ospedali Riuniti Di Ancona, Ancona, Italy.
  • Maggioni C; Medical Oncology, Ospedale San Gerardo, Monza, Italy.
  • Follador A; Medical Oncology, Ospedale San Gerardo, Monza, Italy.
  • Macerelli M; Medical Oncology, Ospedale San Gerardo, Monza, Italy.
  • Nigro O; Department of Oncology, University Hospital Santa Maria Della Misericordia, Udine, Italy.
  • Tuzi A; Department of Oncology, University Hospital Santa Maria Della Misericordia, Udine, Italy.
  • Iacono D; Medical Oncology, ASST-Sette Laghi, Varese, Italy.
  • Migliorino MR; Medical Oncology, ASST-Sette Laghi, Varese, Italy.
  • Banna G; Pulmonary Oncology Unit, St. Camillo-Forlanini Hospital, Rome, Italy.
  • Porzio G; Pulmonary Oncology Unit, St. Camillo-Forlanini Hospital, Rome, Italy.
  • Cannita K; Medical Oncology Unit, Cannizzaro Hospital, Catania, Italy.
  • Ferrara MG; Medical Oncology Unit, St. Salvatore Hospital, Via Vetoio, 67100, L'Aquila, Italy.
  • Bria E; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
  • Galetta D; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
  • Ficorella C; Comprehensive Cancer Center, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.
  • Tiseo M; Medical Oncology, Università Cattolica del Sacro Cuore, Rome, Italy.
Clin Transl Oncol ; 22(6): 844-851, 2020 Jun.
Article em En | MEDLINE | ID: mdl-31392645
ABSTRACT

BACKGROUND:

In most cases, T790M EGFR-positive NSCLC patients receiving osimertinib developed "non-drugable" progression, as the patients with common EGFR-sensitizing mutations were treated with first-line osimertinib. In both settings, chemotherapy represents the standard treatment and local ablative treatments (LATs) are potential useful options in the case of oligo-progression.

METHODS:

We conducted a study on "post-progression" (pp) outcomes of T790M EGFR-positive NSCLC patients treated with osimertinib, according to the therapeutic strategy applied osimertinib beyond progression (± LATs), "switched therapies" or best supportive care only (BSC).

RESULTS:

144 consecutive patients were evaluated 53 (36.8%) did not received post-progression treatments (BSC), while 91 (63.2%) patients received at least 1 subsequent treatment; 50 patients (54.9%) received osimertinib beyond disease progression [19 (20.9%) of them with adjunctive LATs] and 41 (45.1%) a switched therapy. Median ppPFS (progression-free survival) and median ppOS (overall survival) of patients who received osimertinib beyond progression vs. switched therapies were 6.4 months vs. 4.7 months, respectively [HR 0.57 (95% CI 0.35-0.92), p = 0.0239] and 11.3 months vs 7.8 months, respectively [HR 0.57 (95% CI 0.33-0.98), p = 0.0446]. Among patients who received osimertinib beyond progression with and without LATs median ppPFS was 6.4 months and 5.7 months, respectively [HR 0.90 (95% CI 0.68-1.18), p = 0.4560], while median ppOS was 20.2 months and 9.9 months, respectively [HR 0.73 (95% CI 0.52-1.03), p = 0.0748]. At the univariate analysis, the only factor significantly related to the ppPFS was the therapeutic strategy in favor of osimertinib beyond progression (± LATs). Moreover, the only variable which was significantly related to ppOS at the multivariate analysis was osimertinib beyond progression (± LATs).

CONCLUSION:

Our study confirmed that in clinical practice, in case of "non-druggable" disease progression, maintaining osimertinib beyond progression (with adjunctive LATs) is an effective option.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Acrilamidas / Carcinoma Pulmonar de Células não Pequenas / Receptores ErbB / Compostos de Anilina / Neoplasias Pulmonares / Antineoplásicos Tipo de estudo: Clinical_trials Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Clin Transl Oncol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Acrilamidas / Carcinoma Pulmonar de Células não Pequenas / Receptores ErbB / Compostos de Anilina / Neoplasias Pulmonares / Antineoplásicos Tipo de estudo: Clinical_trials Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Clin Transl Oncol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália