The Mantle Cell Lymphoma International Prognostic Index (MIPI) is superior to the International Prognostic Index (IPI) in predicting survival following intensive first-line immunochemotherapy and autologous stem cell transplantation (ASCT)

Author:

Geisler Christian H.1,Kolstad Arne2,Laurell Anna3,Räty Riikka4,Jerkeman Mats5,Eriksson Mikael5,Nordström Marie6,Kimby Eva6,Boesen Anne Marie7,Nilsson-Ehle Herman8,Kuittinen Outi9,Lauritzsen Grete F.2,Ralfkiær Elisabeth1,Ehinger Mats5,Sundström Christer3,Delabie Jan2,Karjalainen-Lindsberg Marja-Liisa4,Brown Peter1,Elonen Erkki4,

Affiliation:

1. Rigshospitalet, Copenhagen, Denmark;

2. Norwegian Radium Hospital, Oslo, Norway;

3. Uppsala University Hospital, Uppsala, Sweden;

4. Helsinki University Central Hospital, Helsinki, Finland;

5. Lund University Hospital, Lund, Sweden;

6. Karolinska Institutet, Stockholm, Sweden;

7. Aarhus University Hospital, Aarhus, Denmark;

8. Sahlgrenska Hospital, Gothenburg, Sweden; and

9. Oulu University Hospital, Oulu, Finland

Abstract

Abstract Mantle cell lymphoma (MCL) has a heterogeneous clinical course. The recently proposed Mantle Cell Lymphoma International Prognostic Index (MIPI) predicted the survival of MCL better than the International Prognostic Index in MCL patients treated with conventional chemotherapy, but its validity in MCL treated with more intensive immunochemotherapy has been questioned. Applied here to 158 patients of the Nordic MCL2 trial of first-line intensive immunochemotherapy followed by high-dose chemotherapy and autologous stem cell transplantation, the MIPI and the simplified MIPI (s-MIPI) predicted survival significantly better (P < .001) than the International Prognostic Index (P > .004). Both the MIPI and the s-MIPI mainly identified 2 risk groups, low and intermediate versus high risk, with the more easily applied s-MIPI being just as powerful as the MIPI. The MIPIB (biological), incorporating Ki-67 expression, identified almost half of the patients as high risk. We suggest that also a simplified MIPIB is feasible. This trial was registered at www.isrctn.org as #ISRCTN 87866680.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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