7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Chemotherapy or allogeneic transplantation in high-risk Philadelphia chromosome–negative adult lymphoblastic leukemia

      1 , 1 , 2 , 3 , 4 , 1 , 5 , 1 , 6 , 7 , 8 , 1 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 , 30 , 2 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 40 , 2 , 1 , 1 , 41 , 1 , 2
      Blood
      American Society of Hematology

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The need for allogeneic hematopoietic stem cell transplantation (allo-HSCT) in adults with Philadelphia chromosome–negative (Ph−) acute lymphoblastic leukemia (ALL) with high-risk (HR) features and adequate measurable residual disease (MRD) clearance remains unclear. The aim of the ALL-HR-11 trial was to evaluate the outcomes of HR Ph− adult ALL patients following chemotherapy or allo-HSCT administered based on end-induction and consolidation MRD levels. Patients aged 15 to 60 years with HR-ALL in complete response (CR) and MRD levels (centrally assessed by 8-color flow cytometry) <0.1% after induction and <0.01% after early consolidation were assigned to receive delayed consolidation and maintenance therapy up to 2 years in CR. The remaining patients were allocated to allo-HSCT. CR was attained in 315/348 patients (91%), with MRD <0.1% after induction in 220/289 patients (76%). By intention-to-treat, 218 patients were assigned to chemotherapy and 106 to allo-HSCT. The 5-year (±95% confidence interval) cumulative incidence of relapse (CIR), overall survival (OS), and event-free survival probabilities for the whole series were 43% ± 7%, 49% ± 7%, and 40% ± 6%, respectively, with CIR and OS rates of 45% ± 8% and 59% ± 9% for patients assigned to chemotherapy and of 40% ± 12% and 38% ± 11% for those assigned to allo-HSCT, respectively. Our results show that avoiding allo-HSCT does not hamper the outcomes of HR Ph− adult ALL patients up to 60 years with adequate MRD response after induction and consolidation. Better postremission alternative therapies are especially needed for patients with poor MRD clearance. This trial was registered at www.clinicaltrials.gov as # NCT01540812.

          Related collections

          Most cited references43

          • Record: found
          • Abstract: found
          • Article: found

          Blinatumomab versus Chemotherapy for Advanced Acute Lymphoblastic Leukemia

          Background Blinatumomab, a bispecific monoclonal antibody construct that enables CD3-positive T cells to recognize and eliminate CD19-positive acute lymphoblastic leukemia (ALL) blasts, was approved for use in patients with relapsed or refractory B-cell precursor ALL on the basis of single-group trials that showed efficacy and manageable toxic effects. Methods In this multi-institutional phase 3 trial, we randomly assigned adults with heavily pretreated B-cell precursor ALL, in a 2:1 ratio, to receive either blinatumomab or standard-of-care chemotherapy. The primary end point was overall survival. Results Of the 405 patients who were randomly assigned to receive blinatumomab (271 patients) or chemotherapy (134 patients), 376 patients received at least one dose. Overall survival was significantly longer in the blinatumomab group than in the chemotherapy group. The median overall survival was 7.7 months in the blinatumomab group and 4.0 months in the chemotherapy group (hazard ratio for death with blinatumomab vs. chemotherapy, 0.71; 95% confidence interval [CI], 0.55 to 0.93; P=0.01). Remission rates within 12 weeks after treatment initiation were significantly higher in the blinatumomab group than in the chemotherapy group, both with respect to complete remission with full hematologic recovery (34% vs. 16%, P<0.001) and with respect to complete remission with full, partial, or incomplete hematologic recovery (44% vs. 25%, P<0.001). Treatment with blinatumomab resulted in a higher rate of event-free survival than that with chemotherapy (6-month estimates, 31% vs. 12%; hazard ratio for an event of relapse after achieving a complete remission with full, partial, or incomplete hematologic recovery, or death, 0.55; 95% CI, 0.43 to 0.71; P<0.001), as well as a longer median duration of remission (7.3 vs. 4.6 months). A total of 24% of the patients in each treatment group underwent allogeneic stem-cell transplantation. Adverse events of grade 3 or higher were reported in 87% of the patients in the blinatumomab group and in 92% of the patients in the chemotherapy group. Conclusions Treatment with blinatumomab resulted in significantly longer overall survival than chemotherapy among adult patients with relapsed or refractory B-cell precursor ALL. (Funded by Amgen; TOWER ClinicalTrials.gov number, NCT02013167 .).
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Inotuzumab Ozogamicin versus Standard Therapy for Acute Lymphoblastic Leukemia

            The prognosis for adults with relapsed acute lymphoblastic leukemia is poor. We sought to determine whether inotuzumab ozogamicin, an anti-CD22 antibody conjugated to calicheamicin, results in better outcomes in patients with relapsed or refractory acute lymphoblastic leukemia than does standard therapy.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Blinatumomab for minimal residual disease in adults with B-cell precursor acute lymphoblastic leukemia.

              Approximately 30% to 50% of adults with acute lymphoblastic leukemia (ALL) in hematologic complete remission after multiagent therapy exhibit minimal residual disease (MRD) by reverse transcriptase-polymerase chain reaction or flow cytometry. MRD is the strongest predictor of relapse in ALL. In this open-label, single-arm study, adults with B-cell precursor ALL in hematologic complete remission with MRD (≥10-3) received blinatumomab 15 µg/m2 per day by continuous IV infusion for up to 4 cycles. Patients could undergo allogeneic hematopoietic stem-cell transplantation any time after cycle 1. The primary end point was complete MRD response status after 1 cycle of blinatumomab. One hundred sixteen patients received blinatumomab. Eighty-eight (78%) of 113 evaluable patients achieved a complete MRD response. In the subgroup of 110 patients with Ph-negative ALL in hematologic remission, the Kaplan-Meier estimate of relapse-free survival (RFS) at 18 months was 54%. Median overall survival (OS) was 36.5 months. In landmark analyses, complete MRD responders had longer RFS (23.6 vs 5.7 months; P = .002) and OS (38.9 vs 12.5 months; P = .002) compared with MRD nonresponders. Adverse events were consistent with previous studies of blinatumomab. Twelve (10%) and 3 patients (3%) had grade 3 or 4 neurologic events, respectively. Four patients (3%) had cytokine release syndrome grade 1, n = 2; grade 3, n = 2), all during cycle 1. After treatment with blinatumomab in a population of patients with MRD-positive B-cell precursor ALL, a majority achieved a complete MRD response, which was associated with significantly longer RFS and OS compared with MRD nonresponders. This study is registered at www.clinicaltrials.gov as #NCT01207388.
                Bookmark

                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Blood
                American Society of Hematology
                0006-4971
                1528-0020
                April 8 2021
                April 8 2021
                : 137
                : 14
                : 1879-1894
                Affiliations
                [1 ]Institut Català d’Oncologia-Hospital Germans Trias i Pujol, Josep Carreras Research Institute, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain;
                [2 ]Instituto de Investigación Biomédica de Salamanca (IBSAL), Instituto de Biología Molecular y Celular del Cáncer (IBMCC), Centro de Investigación del Cáncer, Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Universidad de Salamanca–Centro Superior de Investigaciones Científicas (CSIC), Hospital Universitario, Salamanca, Spain;
                [3 ]Department of Hematology, Hospital Universitario La Fe, Valencia, Spain;
                [4 ]Department of Hematology, Hospital Clínic, Institut D'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain;
                [5 ]Department of Hematology, Hospital Vall d’Hebron, Barcelona, Spain;
                [6 ]Department of Hematology, Hospital de Sant Pau, Barcelona, Spain;
                [7 ]Department of Hematology, Hospital Virgen de la Victoria, Málaga, Spain;
                [8 ]Department of Hematology, Hospital Central de Asturias, Oviedo, Spain;
                [9 ]Department of Hematology, Hospital Doce de Octubre, Madrid, Spain;
                [10 ]Department of Hematology, Hospital Gregorio Marañón, Madrid, Spain;
                [11 ]Department of Hematology, Hospital General, Alicante, Spain;
                [12 ]Department of Hematology, Hospital Clínico, Instituto de Investigación INCLIVA, Valencia, Spain;
                [13 ]Department of Hematology, Hospital Universitario, Donostia, Spain;
                [14 ]Institut Català d’Oncologia-Hospital Joan XXIII, Tarragona, Spain;
                [15 ]Department of Hematology, Hospital Universitario Virgen del Rocío, Sevilla, Spain;
                [16 ]Department of Hematology, Hospital Doctor Negrín, Las Palmas de Gran Canaria, Spain;
                [17 ]Department of Hematology, Hospital Marqués de Valdecilla, Santander, Spain;
                [18 ]Department of Hematology, Hospital Son Espases, Palma de Mallorca, Spain;
                [19 ]Department of Hematology, Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain;
                [20 ]Institut Català d’Oncologia-Hospital Josep Trueta, Girona, Spain;
                [21 ]Department of Hematology, Hospital Morales Meseguer, Murcia, Spain;
                [22 ]Department of Hematology, Hospital Arnau de Vilanova, Valencia, Spain;
                [23 ]Department of Hematology, Hospital Universitario Insular, Las Palmas de Gran Canaria, Spain;
                [24 ]Department of Hematology, Hospital Reina Sofía, Córdoba, Spain;
                [25 ]Institut Català d’Oncologia-Hospital Duran i Reynals, L’Hospitalet de Llobregat, Spain;
                [26 ]Department of Hematology, Hospital Son Llàtzer, Palma de Mallorca, Spain;
                [27 ]Department of Hematology, Hospital Italiano, Buenos Aires, Argentina;
                [28 ]Department of Hematology, Hospital Clínico, Valladolid, Spain;
                [29 ]Department of Hematology, Hospital del Mar, Barcelona, Spain;
                [30 ]Department of Hematology, Hospital Universitari Mútua, Terrassa, Spain;
                [31 ]Department of Hematology, Hospital Arnau de Vilanova, Lleida, Spain;
                [32 ]Department of Hematology, Hospital San Pedro de Alcántara, Cáceres, Spain;
                [33 ]Department of Hematology, Hospital Miguel Servet, Zaragoza, Spain;
                [34 ]Department of Hematology, Hospital Lucus Augusti, Lugo, Spain;
                [35 ]Department of Hematology, Hospital HM Sanchinarro, Madrid, Spain;
                [36 ]Department of Hematology, Hospital Ramón y Cajal, Madrid, Spain;
                [37 ]Department of Hematology, Hospital Clínico, Santiago de Compostela, Spain;
                [38 ]Department of Hematology, Complejo Hospitalario, Ourense, Spain;
                [39 ]Department of Hematology, Hospital General, Castellón, Spain;
                [40 ]Department of Hematology, Hospital Universitario, Galdakao, Spain; and
                [41 ]Université de Paris, Institut Necker-Enfants Malades, Institut National de Recherche Médicale U1151, Laboratory of Onco-Hematology, Assistance Publique-Hôpitaux de Paris, Hôpital Necker Enfants-Malades, Paris, France
                Article
                10.1182/blood.2020007311
                33150388
                ca940690-e232-4486-913c-43e0465dd6cf
                © 2021
                History

                Comments

                Comment on this article