An early post-transplant relapse prediction score in multiple myeloma: a large cohort study from the chronic malignancies working party of EBMT
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
37160942
DOI
10.1038/s41409-023-01999-1
PII: 10.1038/s41409-023-01999-1
Knihovny.cz E-zdroje
- MeSH
- autologní transplantace MeSH
- kohortové studie MeSH
- lidé MeSH
- lokální recidiva nádoru MeSH
- melfalan MeSH
- mnohočetný myelom * terapie MeSH
- příprava pacienta k transplantaci MeSH
- transplantace hematopoetických kmenových buněk * MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- melfalan MeSH
Early relapse (ER) following Autologous Hematopoietic Cell Transplantation (AHCT) confers a poor prognosis. We therefore developed a novel scoring system to predict ER. A total of 14,367 AHCT-1 patients were transplanted between 2014 and 2019, and were conditioned with Melphalan 200 mg/m2 (Mel200) (n = 7228; 2014-2017) (training cohort); Mel200 (n = 5616; 2018-2019) or Mel140 (n = 1523; 2018-2019) (validation cohorts). PFS-12 and the Cumulative Incidence of Relapse at 12 months were 84.1% and 14.7% (training Mel200), 87.2% and 11.6% (validation Mel200), and 80.3% and 16.9% (validation Mel140), respectively. The points in the risk score were: 0, 1,2 for ISS stages I, II, and III; Disease status: 0 (CR/VGPR); 1 (PR); 2 (SD/MR); 4 (Relapse/Progression); and 1 for Karnofsky ≤ 70. The distribution of scores: 0 (24%), 1 (33.9%), 2 (29.6 %), 3 (9.5%), and ≥4 (2.7%). The score separated PFS-12, with the lowest risk group (n = 1752) having a PFS-12 of 91.7% and the highest risk group (n = 195) 57.1%. This also applied in cytogenetically high-risk patients. If the pre-score baseline risks are 15% (standard risk) and 25% (high-risk), a score of ≥4 confers calculated risks of 38% and 54%, respectively. This novel EBMT ER score, therefore, allows for the identification of five discrete prognostic groups.
Ankara University Ankara Turkey
Asklepios Klinik St Georg Hamburg Germany
Centre Hospitalier Universitaire de Rennes Rennes France
Charles University Prague Czech Republic
CHU de Lille Univ Lille Infinite Lille France
CHU Lapeyronie Montpellier France
Clinica FOSCAL Floridablanca Santander Colombia
Department of Haematology School of Medicine Trinity College Dublin Dublin Ireland
Erasmus University Medical Center Daniel Den Hoed Rotterdam the Netherlands
European Society for Blood and Marrow Transplantation Leiden Study Unit Leiden the Netherlands
Institute Paoli Calmettes Marseille France
Queen's University Belfast Marseille France
Radboud University Nijmegen Medical Centre Nijmegen the Netherlands
Sheffield Teaching Hospitals NHS Trust Sheffield UK
Universidad Autónoma de Bucaramanga UNAB Bucaramanga Santander Colombia
University College London Hospitals NHS Foundation Trust London UK
University Hospital Brno Brno Czech Republic
University Hospital Duesseldorf Dusseldorf Germany
University Hospital of Bern Bern Switzerland
University Hospital Southampton NHS Foundation Trust Southampton UK
University Medical Center Freiburg Freiburg Germany
University of Heidelberg Heidelberg Germany
University of Rome Tor Vergata Rome Italy
Vilnius University Hospital Santariskiu Clinics Vilnius Lithuania
Zobrazit více v PubMed
Attal M, Lauwers-Cances V, Hulin C, Leleu X, Caillot D, Escoffre M, et al. Lenalidomide, bortezomib, and dexamethasone with transplantation for myeloma. N Engl J Med. 2017;376:1311–20. PubMed DOI PMC
Cavo M, Gay F, Beksac M, Pantani L, Petrucci MT, Dimopoulos MA, et al. Autologous haematopoietic stem-cell transplantation versus bortezomib–melphalan–prednisone, with or without bortezomib–lenalidomide–dexamethasone consolidation therapy, and lenalidomide maintenance for newly diagnosed multiple myeloma (EMN02/HO95): a multicentre, randomised, open-label, phase 3 study. Lancet Haematol. 2020;7:e456–68. PubMed DOI
Stadtmauer EA, Pasquini MC, Blackwell B, Hari P, Bashey A, Devine S, et al. Autologous transplantation, consolidation, and maintenance therapy in multiple myeloma: results of the BMT CTN 0702 Trial. J Clin Oncol. 2019;37:589–97. PubMed DOI PMC
Dimopoulos MA, Moreau P, Terpos E, Mateos MV, Zweegman S, Cook G, et al. Multiple myeloma: EHA-ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2021;32:309–22. PubMed DOI
Dhakal B, Shah N, Kansagra A, Kumar A, Lonial S, Garfall A, et al. ASTCT clinical practice recommendations for transplantation and cellular therapies in multiple myeloma. Transpl Cell Ther. 2022;28:284–93. DOI
Kumar S, Mahmood ST, Lacy MQ, Diapenzieri A, Hayman SR, Buadi FK, et al. Impact of early relapse after auto-SCT for multiple myeloma. Bone Marrow Transpl. 2008;42:413–20. DOI
Kastritis E, Roussou M, Eleutherakis-Papaiakovou E, Gavriatopoulou M, Migkou M, Gika D, et al. Early relapse after autologous transplant is associated with very poor survival and identifies an ultra-high-risk group of patients with myeloma. Clin Lymphoma Myeloma Leuk. 2020;20:445–52. PubMed DOI
Corre J, Montes L, Martin E, Perrot A, Caillot D, Leleu X, et al. Early relapse after autologous transplant for myeloma is associated with poor survival regardless of cytogenetic risk. Haematologica 2020;105:e480–3. PubMed DOI PMC
Bygrave C, Pawlyn C, Davies F, Craig Z, Cairns D, Hockaday A, et al. Early relapse after high‐dose melphalan autologous stem cell transplant predicts inferior survival and is associated with high disease burden and genetically high‐risk disease in multiple myeloma. Br J Haematol. 2020;193:551–5. PubMed DOI
Lahuerta JJ, Paiva B, Vidriales MB, Cordon L, Cedena MT, Puig N, et al. Depth of response in multiple myeloma: a pooled analysis of three PETHEMA/GEM clinical trials. J Clin Oncol. 2017;35:2900–10. PubMed DOI
Chakraborty R, Muchtar E, Kumar SK, Jevremovic D, Buadi FK, Dingli D, et al. Impact of post-transplant response and minimal residual disease on survival in myeloma with high-risk cytogenetics. Biol Blood Marrow Transpl. 2017;23:598–605. DOI
Dhakal B, D’Souza A, Callander N, Chhabra S, Fraser R, Davila O, et al. Novel prognostic scoring system for autologous hematopoietic cell transplantation in multiple myeloma. Br J Haematol. 2020;191:442–52. PubMed DOI PMC
Zaccaria GM, Bertamini L, Petrucci MT, Offidani M, Corradini P, Capra A, et al. Development and validation of a simplified score to predict early relapse in newly diagnosed multiple myeloma in a pooled dataset of 2190 patients. Clin Cancer Res Off J Am Assoc Cancer Res. 2021;27:3695–703. DOI
Harrell, FE (ed) Regression modeling strategies: with applications to linear models, logistic regression, and survival analysis. 2nd ed. Springer-Verlag, New York, 2001.
Heagerty PJ, Lumley T, Pepe MS. Time-dependent ROC curves for censored survival data and a diagnostic marker. Biometrics 2000;56:337–44. PubMed DOI
Auner HW, Iacobelli S, Sbianchi G, Knol-Bout C, Blaise D, Russell NH, et al. Melphalan 140 mg/m PubMed DOI
Cerchione C, Usmani SZ, Stewart AK, Kaiser M, Rasche L, Kortüm M, et al. Gene expression profiling in multiple myeloma: redefining the paradigm of risk-adapted treatment. Front Oncol 2022;12:820768. PubMed DOI PMC
Jethava Y, Mitchell A, Zangari M, Waheed S, Schinke C, Thanendrarajan S, et al. Dose-dense and less dose-intense Total Therapy 5 for gene expression profiling-defined high-risk multiple myeloma. Blood Cancer J. 2016;6:e453–e453. PubMed DOI PMC
Karam D, Kumar S. Post-transplant maintenance treatment options in multiple myeloma. Oncol Ther. 2021;9:69–88. PubMed DOI PMC
Moreau P, Attal M, Hulin C, Arnulf B, Belhadj K, Benboubker L, et al. Bortezomib, thalidomide, and dexamethasone with or without daratumumab before and after autologous stem-cell transplantation for newly diagnosed multiple myeloma (CASSIOPEIA): a randomized, open-label, phase 3 study. Lancet 2019;394:29–38. PubMed DOI
Van de Donk NWCJ, Agha M, Cohen A, Cohen YC, Anguille S, Kerre T, et al. Biological correlative analyses and updated clinical data of ciltacabtagene autoleucel (cilta-cel), a BCMA-directed CAR-T cell therapy, in patients with multiple myeloma (MM) and early relapse after initial therapy: CARTITUDE-2, cohort B. J Clin Oncol. 2022;40:8029. DOI