Blood Res.  2020 Sep;55(3):139-145. 10.5045/br.2020.2020130.

Use of generic imatinib as first-line treatment in patients with chronic myeloid leukemia (CML): the GIMS (Glivec to Imatinib Switch) study

Affiliations
  • 1Oncology Unit, San Gerardo Hospital, ASST-Monza, Italy
  • 2Hematology Division and Bone Marrow Unit, Ospedale San Gerardo, ASSTMonza, Monza, Italy
  • 3Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy
  • 4Hematology Division, Foundation IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan, Italy
  • 5Hematology and Bone Marrow Transplant Unit, ASST Papa Giovanni XXIII, Bergamo, Italy
  • 6Hematology Unit, Ospedale di Circolo, Varese, Italy
  • 7Division of Hematology, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy
  • 8Hematology and Transfusional Medicine Unit, ASST Fatebenefratelli Sacco, Milan, Italy
  • 9Department of Hematology, ASST Spedali Civili di Brescia, Brescia, Italy
  • 10Hematology and Bone Marrow Transplantation Unit, San Raffaele Scientific Institute, IRCCS Milano, Italy
  • 11Oncology Department, ASST Lecco, Lecco, Italy
  • 12Chair of Hematology, Unit of Blood Diseases and Stem Cell Transplantation, University of Brescia, ASST Spedali Civili di Brescia, Brescia, Italy
  • 13Department of Hematology, Cancer Center, IRCCS Humanitas Research Hospital/Humanitas University, Rozzano, Italy
  • 14Department of Medicine and Surgery, University of Milano-Bicocca, Italy
  • 15Center of Biostatistics for Clinical Epidemiology, Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy

Abstract

Background
Generic formulations of imatinib mesylate have been introduced in Western Europe since 2017 to treat patients with chronic myeloid leukemia (CML). However, results on the safety and efficacy of generic formulations are contrasting. The aim of this study was to investigate the safety and efficacy of generic imatinib in CML patients treated in 12 Italian institutes.
Methods
This is an observational, retro-prospective analysis of patients with CML for whom the treatment was switched from brand to generic imatinib. We analyzed and compared the variation in quantitative PCR values before and after the switch, and the proportion of patients who maintained molecular response after changing from brand to generic imatinib. Adverse events (AEs) were also evaluated.
Results
Two hundred patients were enrolled. The median PCR value after the switch was reduced by 0.25 compared to the values before the switch. A significant difference was found between median PCR values before and after the switch in favor of generic imatinib (P = 0 .0 0 3 ). Molecular responses remained stable in 69.0%, improved in 25.5%, and worsened in 5.5% of patients. AEs were similar in the pre- and post-switch periods; however, a significant difference was found in favor of generic imatinib for muscular cramps (P < 0.0001), periorbital edema (P =0.0028), edema of the limbs (P <0.0001), fatigue (P=0.0482), and diarrhea (P =0.0027).
Conclusion
Our data indicate that generic imatinib does not have deleterious effects on CML control and present an acceptable safety profile, similar or better than brand imatinib.

Keyword

Imatinib; Generic; Chronic myeloid leukemia; Generic imatinib; BCR/ABL; Adverse events

Figure

  • Fig. 1 Individual patient PCR values at each pre-defined time point: third, second and first PCR pre- and post-switch.

  • Fig. 2 Adverse events (AEs) with frequencies >1% and number and percentage of G3-G4 for each event pre- and post-switch.


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