IMPORTANCE Bevacizumab treatment beyond progression has been investigated in breast and metastatic colorectal cancers. Avastin in All Lines Lung (AvaALL) is the first randomized phase 3 study of bevacizumab across multiple lines of treatment beyond progression in non-small cell lung cancer (NSCLC).OBJECTIVE To assess the efficacy and safety of continuous bevacizumab treatment beyond first progression in NSCLC.DESIGN, SETTING, AND PARTICIPANTS AvaALL was a randomized, open-label, phase 3b trial, conducted from 2011 to 2015 in 123 centers worldwide. Patients with nonsquamous NSCLC previously treated with first-line bevacizumab plus platinum-doublet chemotherapy and at least 2 cycles of bevacizumab maintenance were randomized (1:1) at first progression to receive bevacizumab plus standard of care (SOC) or SOC alone.INTERVENTIONS Patients received bevacizumab (7.5 or 15 mg/kg intravenously every 21 days) and/or investigator's choice of SOC. For subsequent lines, patients treated with bevacizumab received SOC with or without bevacizumab; the SOC arm received SOC only.MAIN OUTCOMES AND MEASURES The primary outcome was overall survival (OS). Secondary outcomes included progression-free survival from first to second (PFS2) and third progression (PFS3), time to second (TTP2) and third progression (TTP3), and safety.RESULTS Between June 2011 and January 2015, 485 patients (median age, 63.0 years [range, 26-84 years]; 293 [60.4%] male) were randomized. Median OS was not significantly longer with bevacizumab plus SOC vs SOC alone: 11.9(90% CI, 10.2-13.7) vs 10.2(90% CI, 8.6-11.9) months (hazard ratio [HR], 0.84; 90% CI, 0.71-1.00; P=.104). Median PFS2 was numerically longer with bevacizumab plus SOC vs SOC alone: 5.5(90% CI, 4.2-5.7) vs 4.0(90% CI, 3.4-4.3) months(HR, 0.83; 90% CI, 0.70-0.98; P=.06). Median PFS3 appeared longer with bevacizumab plus SOC vs SOC alone: 4.0(90% CI, 2.9-4.5) vs 2.6(90% CI, 2.3-2.9) months(HR, 0.63; 90% CI, 0.49-0.83), as did TTP2 and TTP3. Grade 3/4 adverse events were more frequent with bevacizumab plus SOC (186 [76.5%]) vs SOC alone (140 [60.3%]). No new safety signals were observed.CONCLUSIONS AND RELEVANCE The primary end point was not met; however, OS was underpowered according to initial statistical assumptions. Continued therapy beyond first progression led to improved PFS3 (but not PFS2), TTP2, and TTP3. Although a result with P=.06 for PFS2 would conventionally be considered significant at a specified 2-sided a of .10, in the absence of adjustments for multiplicity, this result could be a chance finding. No new safety signals were identified with bevacizumab treatment beyond progression.

Safety and Efficacy of Bevacizumab Plus Standard-of-Care Treatment Beyond Disease Progression in Patients With Advanced Non-Small Cell Lung Cancer: The AvaALL Randomized Clinical Trial

Grossi, Francesco;
2018-01-01

Abstract

IMPORTANCE Bevacizumab treatment beyond progression has been investigated in breast and metastatic colorectal cancers. Avastin in All Lines Lung (AvaALL) is the first randomized phase 3 study of bevacizumab across multiple lines of treatment beyond progression in non-small cell lung cancer (NSCLC).OBJECTIVE To assess the efficacy and safety of continuous bevacizumab treatment beyond first progression in NSCLC.DESIGN, SETTING, AND PARTICIPANTS AvaALL was a randomized, open-label, phase 3b trial, conducted from 2011 to 2015 in 123 centers worldwide. Patients with nonsquamous NSCLC previously treated with first-line bevacizumab plus platinum-doublet chemotherapy and at least 2 cycles of bevacizumab maintenance were randomized (1:1) at first progression to receive bevacizumab plus standard of care (SOC) or SOC alone.INTERVENTIONS Patients received bevacizumab (7.5 or 15 mg/kg intravenously every 21 days) and/or investigator's choice of SOC. For subsequent lines, patients treated with bevacizumab received SOC with or without bevacizumab; the SOC arm received SOC only.MAIN OUTCOMES AND MEASURES The primary outcome was overall survival (OS). Secondary outcomes included progression-free survival from first to second (PFS2) and third progression (PFS3), time to second (TTP2) and third progression (TTP3), and safety.RESULTS Between June 2011 and January 2015, 485 patients (median age, 63.0 years [range, 26-84 years]; 293 [60.4%] male) were randomized. Median OS was not significantly longer with bevacizumab plus SOC vs SOC alone: 11.9(90% CI, 10.2-13.7) vs 10.2(90% CI, 8.6-11.9) months (hazard ratio [HR], 0.84; 90% CI, 0.71-1.00; P=.104). Median PFS2 was numerically longer with bevacizumab plus SOC vs SOC alone: 5.5(90% CI, 4.2-5.7) vs 4.0(90% CI, 3.4-4.3) months(HR, 0.83; 90% CI, 0.70-0.98; P=.06). Median PFS3 appeared longer with bevacizumab plus SOC vs SOC alone: 4.0(90% CI, 2.9-4.5) vs 2.6(90% CI, 2.3-2.9) months(HR, 0.63; 90% CI, 0.49-0.83), as did TTP2 and TTP3. Grade 3/4 adverse events were more frequent with bevacizumab plus SOC (186 [76.5%]) vs SOC alone (140 [60.3%]). No new safety signals were observed.CONCLUSIONS AND RELEVANCE The primary end point was not met; however, OS was underpowered according to initial statistical assumptions. Continued therapy beyond first progression led to improved PFS3 (but not PFS2), TTP2, and TTP3. Although a result with P=.06 for PFS2 would conventionally be considered significant at a specified 2-sided a of .10, in the absence of adjustments for multiplicity, this result could be a chance finding. No new safety signals were identified with bevacizumab treatment beyond progression.
2018
2018
Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Bevacizumab; Carcinoma, Non-Small-Cell Lung; Combined Modality Therapy; Disease Progression; Disease-Free Survival; Female; Humans; Lung Neoplasms; Male; Middle Aged; Survival Analysis; Treatment Outcome; Standard of Care
Gridelli, Cesare; de Castro Carpeno, Javier; Dingemans, Anne-Marie C; Griesinger, Frank; Grossi, Francesco; Langer, Corey; Ohe, Yuichiro; Syrigos, Konstantinos; Thatcher, Nick; Das-Gupta, Ashis; Truman, Matt; Donica, Margarita; Smoljanovic, Vlatka; Bennouna, Jaafar
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/2141976
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