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Hevylite® to Monitor Response to Therapy in Multiple Myeloma

Xavier Leleu, MD
Hopital Claude Huriez
CHRU Lille
Lille, France

01.06.15

Program: Oral and Poster Abstracts
Session: 651. Myeloma: Biology and Pathophysiology, excluding Therapy: Poster I

 

Guillemette Fouquet, MD1*, Susanna Schraen, MD2*, Jean-Luc Faucompré, MD2*, Lionel Karlin3*, Margaret Macro, MD4*, Cyrille Hulin, MD5*, Brigitte Onraed, MD2*, Laurent Garderet, MD6, Murielle Roussel, MD7*, Bertrand Arnulf8*, Brigitte Pegourie, MD9*, Brigitte Kolb10*, Anne-Marie Stoppa, MD11, Sabine Brechignac, MD12*, Mauricette Michallet, MD, PhD13, Gerald Marit14*, Claire Mathiot, MD15*, Anne Banos, MD16*, Mourad Tiab, MD17*, Mamoun Dib18*, Jean-Gabriel Fuzibet, MD19*, Marie-Odile Petillon, MD1*, Philippe Rodon, MD20, Marc Wetterwald, MD, PhD21*, Bruno Royer, MD22*, Laurence Legros, MD19*, Lofti Benboubker, MD23*, Olivier Decaux24*, Denis Caillot, MD25*, Martine Escoffre-Barbe, MD24*, Jean-Paul Fermand, MD26, Philippe Moreau, MD27*, Michel Attal7, Hervé Avet-Loiseau28, Thierry Facon, MD29 and Xavier Leleu, MD1

1Service des Maladies du Sang, Hopital Claude Huriez, CHRU Lille, Lille, France
2Service de biochimie proteine, Hôpital Huriez, CHRU Lille, LILLE, France
3Centre Hospitalier Lyon-Sud, Pierre-Benite, France
4Hematology, Hôpital Côte de Nacre, CHU, Caen, France
5Service d’Hématologie, CHU Nancy – Brabois, Vandoeuvre, France
6Hematology, Centre Hospitalier Universitaire Hopital St-Antoine, Paris, France
7Hématologie Clinique, CHU Purpan, Toulouse, France
8Hôpital Saint-Louis, Paris, France
9Hôpital A.Michallon, CHU Grenoble, Grenoble, France
10Hôpital Robert Debré, CHU, REIMS, France
11Hematology, Institut Paoli Calmettes, Marseille, France
12Hematologie Clinique, Hopital Avicenne APHP Université Paris 13, Bobigny, France
13Hematology, Edouard Herriot Hospital, Lyon, France
14Service d'Hématologie et de Thérapie Cellulaire, University Hospital of Bordeaux, Pessac, France
15Institut Curie, APHP, paris, France
16Centre Hospitalier de la Côte Basque, Bayonne, France
17Departemental Medecine Interne Les Oudairies, Centre Hospitalier, La Roche sur Yon, France
18CHRU Hopital du bocage, Dijon, France
19CH de l'Archet, Nice, France
20Hematology, Centre Hospitalier, Perigueux, France
21CHD Dunkerque, Dunkerque, France
22Département d'hématologie clinique, Centre hospitalier universitaire, Amiens, France
23University Hospital Tours, Tours, France
24Hematology, CHU Rennes, Rennes, France
25Hematology Department, CHU de Dijon - Hospital `Le Bocage`,, Dijon, France
26Service d'Immuno-Hematologie, Hôpital Saint-Louis, Paris, France
27University Hospital of Nantes, Nantes, France
28Hematology, CHU RANGUEIL, Toulouse, France
29Hopital Claude Huriez, CHRU Lille, Lille, France

 
Background. Protein electrophoresis and immunofixation in the serum (SPEP - SIF) and urine (UPEP – UIF) have been routinely used for decades for characterizing and quantifying the M protein in Multiple Myeloma (MM). However, these techniques are notoriously tarnished with inaccuracy, despite improvements in recent years. The most important breakthrough in the field in recent years was the discovery of the Serum Free Light Chain Assay (sFLC), a routine quantitative and automated assay that measures kappa and lambda sFLC, however this was added to / rather than replaced traditional tests in the diagnostic armamentarium of MM. Recently, a new test quantifying paired clonal and non-clonal immunoglobulins (heavy/light chains HLC  i.e. IgGκ/IgGλ) in serum was developed. Here we aim to assess the new HLC assays as tools to replace SPEP / IFE during MM patient monitoring

 

Materials and methods. 110 Myeloma treated with pomalidomide and dexamethasone in two IFM studies (IFM 2009-02 in end stage RRMM and IFM 2010-02 in del17p and t(4;14) RRMM ) were included. The criteria for selection were that patients had measurable intact immunoglobulin myeloma according to IMWG criteria (M spike ≥10g/L), using serum and/or urine protein electrophoresis, with exclusion of patients solely measurable on UPEP and sFLC. All sera were collected centrally before initiation of treatment and sequentially every cycle until progression. Hevylite® (HLC) was measured in the biology laboratory of CHRU of Lille, France and results compared to traditional measurements. Along with SPEP, SIF, UPEP, UIF, and sFLC, we have also measured IgA HLC (IgA k and IgA l) and IgG (IgG k and IgG l) and the corresponding difference (clonal - non clonal) and ratio (clonal/non clonal).

 

Results. Overall, 80% were measurable on SPEP with a median serum level of 31g/L (CI95% 19;42), and the remaining also had UPEP measurable myeloma with a median serum level of 0.66g/24h (CI95% 0.4;1.3). The median involved HLC level was 29.7g/L (CI95% 17.6;43.3), the median involved HLC difference clonal - non clonal was 28.8g/L (CI95% 15.6;42.7), the median involved HLC ratio clonal / non clonal was 51.9 (CI95% 18.3;203.9).

 

Since all patients had a measurable intact immunoglobulin-based disease according to IMWG criteria, we have first confirmed that patients had also a measurable disease by HLC. All patients had an abnormal HLC ratio but one patient, who was measurable with an abnormal IgG L involved HLC test. Approximately 32% of patients had an M-spike below 20g/L and/or an electrophoretic migration in beta region meaning in the range of lack of sensitivity of the techniques used, all of whom had a measurable disease using involved HLC level and/or a measurable HLC ratio.

 

We then sought to study the response rate according to HLC, and for that purpose we applied the exact same criteria as to the sFLC-based response criteria recommended by IMWG (e.g. normal ratio is CR and if abnormal ratio, then <50% reduction in the difference clonal – non clonal is SD, ≥50% - <90% reduction is PR, >90% reduction is VGPR). The ORR in the 2 studies as a whole using traditional measurements was 32%, including 29% PR rate, absence of CR, and 44% had SD (SD and MR). Using HLC, the ORR was 36%, including 26% PR rate and 4.0% CR, and 33% had SD (r² 0.823, p<.0001). Interestingly, 7 patients classified as SD with regular techniques, were progressive disease using HLC, anticipating a progression of Myeloma. Similarly, 5 patients classified as SD with regular techniques, were ≥PR using HLC.

 

Conclusion. HLC is a new routine quantitative and automated assay that measures Immunoglobulin heavy chain/light chain pairs immunoassay, allowing diagnosis, prognosis and precise assessment of the response to treatment and disease progression in all cases with Myeloma treated with pomalidomide and dexamethasone in 2 different clinical trials. Our study indicates that HLC may be used as a replacement for traditional tests and may offer greater sensitivity in some instances. Furthermore, obviating the need for interpretation may standardize assessments of patients during trials. Future studies might confirm this data analysis in larger trials.


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  • Imaging
  • Relapse and New Drugs

Social Media Team
ASH 2014 Social Media Team
Tune in as the IMF brings myeloma support group leaders and patients to San Francisco for the 56th annual meeting of the American Society of Hematology (ASH), an exciting convergence of 20,000 health care professionals from around the world. Start following the IMF ASH team members now on social media as they ramp up to share the latest clinical updates in myeloma research, therapies, and practice strategies via Twitter (#IMFASH2014), Facebook, blogs and videos.