Volume 164, Issue 1 pp. 113-123
Research Paper

Plerixafor on-demand combined with chemotherapy and granulocyte colony-stimulating factor: significant improvement in peripheral blood stem cells mobilization and harvest with no increase in costs

Giuseppe Milone

Corresponding Author

Giuseppe Milone

Programma di Trapianto Emopoietico, Azienda Ospedaliera Policlinico Vittorio Emanuele, Catania, Italy

Istituto Oncologico del Mediterraneo, Viagrande, Italy

Correspondence: Giuseppe Milone, Programma di Trapianto Emopoietico, Azienda Ospedaliera Universitaria, Policlinico Vittorio Emanuele, via Santa Sofia, 78 Catania, Italy.

E-mail: [email protected]

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Massimo Martino

Massimo Martino

Programma Trapianto di Midollo, Ospedali Melacrino-Morelli, Reggio Calabria, Italy

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Andrea Spadaro

Andrea Spadaro

Programma di Trapianto Emopoietico, Azienda Ospedaliera Policlinico Vittorio Emanuele, Catania, Italy

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Salvatore Leotta

Salvatore Leotta

Programma di Trapianto Emopoietico, Azienda Ospedaliera Policlinico Vittorio Emanuele, Catania, Italy

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Annalia Di Marco

Annalia Di Marco

Programma di Trapianto Emopoietico, Azienda Ospedaliera Policlinico Vittorio Emanuele, Catania, Italy

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Potito Scalzulli

Potito Scalzulli

Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy

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Alessandra Cupri

Alessandra Cupri

Programma di Trapianto Emopoietico, Azienda Ospedaliera Policlinico Vittorio Emanuele, Catania, Italy

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Valentina Di Martina

Valentina Di Martina

Programma di Trapianto Emopoietico, Azienda Ospedaliera Policlinico Vittorio Emanuele, Catania, Italy

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Elena Schinocca

Elena Schinocca

Programma di Trapianto Emopoietico, Azienda Ospedaliera Policlinico Vittorio Emanuele, Catania, Italy

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Eleonora Spina

Eleonora Spina

Programma di Trapianto Emopoietico, Azienda Ospedaliera Policlinico Vittorio Emanuele, Catania, Italy

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Giovanni Tripepi

Giovanni Tripepi

Clinical Epidemiology, IBIM-CNR, Reggio Calabria, Italy

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First published: 21 October 2013
Citations: 50

Summary

To date, no prospective study on Plerixafor ‘on-demand’ in combination with chemotherapy and granulocyte colony-stimulating factor (G-CSF) has been reported. We present an interim analysis of the first prospective study in which Plerixafor was administered on-demand in patients affected by multiple myeloma and lymphoma who received high dose cyclophosphamide or DHAP (dexamethasone, cytarabine, cisplatin) plus G-CSF to mobilize peripheral blood stem cells (PBSC). One hundred and two patients were evaluable for response. A cohort of 240 patients receiving the same mobilizing chemotherapy was retrospectively studied. Failure to mobilize CD34+ cells in peripheral blood was reduced by ‘on-demand’ strategy compared to conventional mobilization; from 13·0 to 3·0% (P = 0·004). Failure to harvest CD34+ cells 2 × 106/kg decreased from 20·9 to 4·0% (P = 0·0001). The on-demand Plerixafor strategy also resulted in a lower rate of mobilization failure (P = 0·03) and harvest failure (P = 0·0008) when compared to a ‘bias-adjusted set of controls’. Evaluation of economic costs of the two strategies showed that the overall cost of the two treatments were comparable when salvage mobilizations were taken into account. When in combination with cyclophosphamide or DHAP plus G-CSF, the ‘on-demand’ use of Plerixafor showed, in comparison to conventionally treated patients, a significant improvement in mobilization of PBSC with no increase in overall cost.

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