CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2021; 42(02): 199-203
DOI: 10.1055/s-0041-1731860
Brief Communication

Inotuzumab Ozogamicin Monotherapy as an Outpatient Salvage Treatment in Relapsed Refractory B-Cell Acute Lymphoblastic Leukemia: Compassionate Access

1   Clinical Hematology Oncology and Hematopoietic Cell Transplantation, Tata Medical Center, Kolkata, West Bengal, India
,
Ketan Modak
1   Clinical Hematology Oncology and Hematopoietic Cell Transplantation, Tata Medical Center, Kolkata, West Bengal, India
,
Saurabh J. Bhave
1   Clinical Hematology Oncology and Hematopoietic Cell Transplantation, Tata Medical Center, Kolkata, West Bengal, India
,
Jeevan Kumar
1   Clinical Hematology Oncology and Hematopoietic Cell Transplantation, Tata Medical Center, Kolkata, West Bengal, India
,
Mita Roychowdhury
1   Clinical Hematology Oncology and Hematopoietic Cell Transplantation, Tata Medical Center, Kolkata, West Bengal, India
,
Manik Ghosh
1   Clinical Hematology Oncology and Hematopoietic Cell Transplantation, Tata Medical Center, Kolkata, West Bengal, India
,
Mayur Parihar
2   Laboratory Hematology, Cytogenetics, and Molecular Pathology, Tata Medical Center, Kolkata, West Bengal, India
,
Neeraj Arora
2   Laboratory Hematology, Cytogenetics, and Molecular Pathology, Tata Medical Center, Kolkata, West Bengal, India
,
Deepak K. Mishra
2   Laboratory Hematology, Cytogenetics, and Molecular Pathology, Tata Medical Center, Kolkata, West Bengal, India
,
1   Clinical Hematology Oncology and Hematopoietic Cell Transplantation, Tata Medical Center, Kolkata, West Bengal, India
,
1   Clinical Hematology Oncology and Hematopoietic Cell Transplantation, Tata Medical Center, Kolkata, West Bengal, India
› Author Affiliations
Funding None.

Abstract

Relapsed and refractory (RR) acute lymphoblastic leukemia (ALL) poses unique and difficult challenges to a practicing clinician in India where access to novel immunotherapies is limited. Between 2017 and 2020, eight patients with B-cell ALL at our center received inotuzumab ozogamicin (IO) monotherapy on compassionate access, as salvage therapy after at least two lines of conventional therapy failure, and most often as outpatient infusion. Eight patients (21–60 years, three females) received IO. Three patients had morphologic relapse and five patients reported persistent measurable residual disease (MRD). The best response on IO therapy achieved was negative MRD in six of seven patients and complete response (CR) with persistent MRD in one. One patient died (intracranial hemorrhage) before completion of first cycle. All responding patients were transplant eligible and four patients (57%) underwent allogeneic hematopoietic cell transplantation (Allo-HCT). Median follow-up of this cohort is 9 months (4–29.6 months), four patients (57%) are alive as stable with negative MRD. No significant infusion reactions occurred during therapy. Three patients developed grades III and IV neutropenia, two patients showed grade III transaminitis, and two patients developed post-HCT severe sinusoidal obstruction syndrome (SOS). IO is a feasible outpatient based salvage therapy to improve the remission status in RR B-cell ALL.



Publication History

Article published online:
06 August 2021

© 2021. . Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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  • References

  • 1 Terwilliger T, Abdul-Hay M. Acute lymphoblastic leukemia: a comprehensive review and 2017 update. Blood Cancer J 2017; 7 (06) e577
  • 2 Kantarjian H, Thomas D, O’Brien S. et al. Long-term follow-up results of hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (Hyper-CVAD), a dose-intensive regimen, in adult acute lymphocytic leukemia. Cancer 2004; 101 (12) 2788-2801
  • 3 Thomas X, Boiron JM, Huguet F. et al. Outcome of treatment in adults with acute lymphoblastic leukemia: analysis of the LALA-94 trial. J Clin Oncol 2004; 22 (20) 4075-4086
  • 4 Gökbuget N, Stanze D, Beck J. et al. German Multicenter Study Group for Adult Acute Lymphoblastic Leukemia. Outcome of relapsed adult lymphoblastic leukemia depends on response to salvage chemotherapy, prognostic factors, and performance of stem cell transplantation. Blood 2012; 120 (10) 2032-2041
  • 5 Thomas DA, Kantarjian H, Smith TL. et al. Primary refractory and relapsed adult acute lymphoblastic leukemia: characteristics, treatment results, and prognosis with salvage therapy. Cancer 1999; 86 (07) 1216-1230
  • 6 Tavernier E, Boiron JM, Huguet F. et al. GET-LALA Group, Swiss Group for Clinical Cancer Research SAKK, Australasian Leukaemia and Lymphoma Group. Outcome of treatment after first relapse in adults with acute lymphoblastic leukemia initially treated by the LALA-94 trial. Leukemia 2007; 21 (09) 1907-1914
  • 7 Samra B, Jabbour E, Ravandi F, Kantarjian H, Short NJ. Evolving therapy of adult acute lymphoblastic leukemia: state-of-the-art treatment and future directions. J Hematol Oncol 2020; 13 (01) 70
  • 8 Kantarjian HM, DeAngelo DJ, Stelljes M. et al. Inotuzumab ozogamicin versus standard therapy for acute lymphoblastic leukemia. N Engl J Med 2016; 375 (08) 740-753
  • 9 Raponi S, De Propris MS, Intoppa S. et al. Flow cytometric study of potential target antigens (CD19, CD20, CD22, CD33) for antibody-based immunotherapy in acute lymphoblastic leukemia: analysis of 552 cases. Leuk Lymphoma 2011; 52 (06) 1098-1107
  • 10 Marks DI, Kebriaei P, Stelljes M. et al. Outcomes of allogeneic stem cell transplantation after inotuzumab ozogamicin treatment for relapsed or refractory acute lymphoblastic leukemia. Biol Blood Marrow Transplant 2019; 25 (09) 1720-1729
  • 11 Lamb YN. Inotuzumab ozogamicin: first global approval. Drugs 2017; 77 (14) 1603-1610
  • 12 Kebriaei P, Cutler C, de Lima M. et al. Management of important adverse events associated with inotuzumab ozogamicin: expert panel review. Bone Marrow Transplant 2018; 53 (04) 449-456
  • 13 Pawar RN, Banerjee S, Bramha S. et al. Mixed-phenotypic acute leukemia series from tertiary care center. Indian J Pathol Microbiol 2017; 60 (01) 43-49
  • 14 U.S. Department of Health and Human Services, National Institutes of Health; National Cancer Institute. Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0. Available at: https://ctep.cancer.gov/protocolDevelopment/electronic_applications/docs/CTCAE_v5_Quick_Reference_8.5x11.pdf. Accessed June 8, 2021
  • 15 Selvaraj S, Farooqui HH, Karan A. Quantifying the financial burden of households’ out-of-pocket payments on medicines in India: a repeated cross-sectional analysis of National Sample Survey data, 1994-2014. BMJ Open 2018; 8 (05) e018020
  • 16 Kantarjian HM, DeAngelo DJ, Stelljes M. et al. Inotuzumab ozogamicin versus standard of care in relapsed or refractory acute lymphoblastic leukemia: Final report and long-term survival follow-up from the randomized, phase 3 INO-VATE study. Cancer 2019; 125 (14) 2474-2487
  • 17 Kantarjian H, Ravandi F, Short NJ. et al. Inotuzumab ozogamicin in combination with low-intensity chemotherapy for older patients with Philadelphia chromosome-negative acute lymphoblastic leukaemia: a single-arm, phase 2 study. Lancet Oncol 2018; 19 (02) 240-248
  • 18 Guerra VA, Jabbour EJ, Ravandi F, Kantarjian H, Short NJ. Novel monoclonal antibody-based treatment strategies in adults with acute lymphoblastic leukemia. Ther Adv Hematol 2019; 10 2040620719849496
  • 19 McNeer JL, Rau RE, Gupta S, Maude SL, O’Brien MM. Cutting to the front of the line: immunotherapy for childhood acute lymphoblastic leukemia. Am Soc Clin Oncol Educ Book 2020; 40: 1-12