Long term outcome of Ph+ CML patients achieving complete cytogenetic remission with interferon based therapy moving from interferon to imatinib era. Issue 2 (February 2014)
- Record Type:
- Journal Article
- Title:
- Long term outcome of Ph+ CML patients achieving complete cytogenetic remission with interferon based therapy moving from interferon to imatinib era. Issue 2 (February 2014)
- Main Title:
- Long term outcome of Ph+ CML patients achieving complete cytogenetic remission with interferon based therapy moving from interferon to imatinib era
- Authors:
- Malagola, Michele
Breccia, Massimo
Skert, Cristina
Cancelli, Valeria
Soverini, Simona
Iacobucci, Ilaria
Cattina, Federica
Liberati, Anna Maria
Tiribelli, Mario
Annunziata, Mario
Trabacchi, Elena
De, Antonio
Castagnetti, Fausto
Martinelli, Giovanni
Fogli, Miriam
Stagno, Fabio
Pica, Gianmatteo
Iurlo, Alessandra
Pregno, Patrizia
Abruzzese, Elisabetta
Pardini, Simonetta
Bocchia, Monica
Russo, Sabina
Pierri, Ivana
Lunghi, Monia
Barulli, Sara
Merante, Serena
Mandelli, Franco
Alimena, Giuliana
Rosti, Gianatonio
Baccarani, Michele
Russo, Domenico
… (more) - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Interferon α (IFNα) prolongs survival of CML patients achieving CCyR and potentially synergizes with TKIs. We report on the molecular status and long term outcome of 121 patients who were treated in Italy between 1986 and 2000 with IFNα based therapy and who obtained CCyR. After a median follow up of 16.5 years, 74 (61%) patients were switched to standard imatinib: 48 (65%) lost the CCyR on IFNα, and 36 (75%) are alive and in CCyR; 26 (35%) were switched to imatinib when they were still in CCyR on IFNα, and all 26 are alive and in CCyR. Forty‐seven patients (39%) were never switched to imatinib: 24 (51%) continued and 23 (49%) discontinued IFNα, respectively, and 39/47 (83%) are alive and in CCyR. At last follow‐up, the BCR‐ABL transcripts level was available in 96/101 living patients (95%) The BCR‐ABL:ABL ratio was between 0.1 and 0.01% (MR<sup>3.0</sup>) in 17%, and less than 0.01% (MR<sup>4.0</sup>) in 81% of patients. No patient was completely molecular negative (MR<sup>4.5</sup> or MR<sup>5.0</sup>). The OS at 10 and 20 years is 92 and 84%, respectively. This study confirms that CCyR achieved with IFNα and maintained with or without imatinib or any other therapy significantly correlates with long term survival in CML patients who mostly have MR<sup>4.0</sup>. Complete molecular response (MR<sup>4.5</sup> or MR<sup>5.0</sup>) seems to be unnecessary for such a long survival. This<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Interferon α (IFNα) prolongs survival of CML patients achieving CCyR and potentially synergizes with TKIs. We report on the molecular status and long term outcome of 121 patients who were treated in Italy between 1986 and 2000 with IFNα based therapy and who obtained CCyR. After a median follow up of 16.5 years, 74 (61%) patients were switched to standard imatinib: 48 (65%) lost the CCyR on IFNα, and 36 (75%) are alive and in CCyR; 26 (35%) were switched to imatinib when they were still in CCyR on IFNα, and all 26 are alive and in CCyR. Forty‐seven patients (39%) were never switched to imatinib: 24 (51%) continued and 23 (49%) discontinued IFNα, respectively, and 39/47 (83%) are alive and in CCyR. At last follow‐up, the BCR‐ABL transcripts level was available in 96/101 living patients (95%) The BCR‐ABL:ABL ratio was between 0.1 and 0.01% (MR<sup>3.0</sup>) in 17%, and less than 0.01% (MR<sup>4.0</sup>) in 81% of patients. No patient was completely molecular negative (MR<sup>4.5</sup> or MR<sup>5.0</sup>). The OS at 10 and 20 years is 92 and 84%, respectively. This study confirms that CCyR achieved with IFNα and maintained with or without imatinib or any other therapy significantly correlates with long term survival in CML patients who mostly have MR<sup>4.0</sup>. Complete molecular response (MR<sup>4.5</sup> or MR<sup>5.0</sup>) seems to be unnecessary for such a long survival. This study further supports development of studies testing the clinical effect of the combinations of TKIs with IFNα. Am. J. Hematol. 89:119–124, 2014. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- American journal of hematology. Volume 89:Issue 2(2014:Feb.)
- Journal:
- American journal of hematology
- Issue:
- Volume 89:Issue 2(2014:Feb.)
- Issue Display:
- Volume 89, Issue 2 (2014)
- Year:
- 2014
- Volume:
- 89
- Issue:
- 2
- Issue Sort Value:
- 2014-0089-0002-0000
- Page Start:
- 119
- Page End:
- 124
- Publication Date:
- 2014-02
- Subjects:
- Hematology -- Periodicals
616.15 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1096-8652 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ajh.23593 ↗
- Languages:
- English
- ISSNs:
- 0361-8609
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0824.800000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3050.xml