Late versus early response and depth of response are associated with improved outcomes in patients with newly diagnosed multiple myeloma enrolled in the TOURMALINE‐MM2 trial
Paul G. Richardson,
Thierry Facon,
Christopher P. Venner,
Nizar J. Bahlis,
Fritz Offner,
Darrell White,
Lionel Karlin,
Lotfi Benboubker,
Eric Voog,
Sung‐Soo Yoon,
Kenshi Suzuki,
Hirohiko Shibayama,
Xiaoquan Zhang,
Miguel Villarreal,
Philip Twumasi‐Ankrah,
Richard Labotka,
Robert M. Rifkin,
Sagar Lonial,
Shaji K. Kumar,
S. Vincent Rajkumar,
Philippe Moreau
Affiliations
Paul G. Richardson
Harvard Medical School Jerome Lipper Multiple Myeloma Center, Dana‐Farber Cancer Institute Boston Massachusetts USA
Thierry Facon
Centre Hospitalier Universitaire (CHU) Lille Service des Maladies du Sang, University of Lille LilleFrance
Christopher P. Venner
Cross Cancer Institute University of Alberta Edmonton Alberta Canada
Nizar J. Bahlis
Arnie Charbonneau Cancer Institute University of Calgary Calgary Alberta Canada
Fritz Offner
UZ Gent GentBelgium
Darrell White
QEII Health Sciences Center and Dalhousie University Halifax Nova Scotia Canada
Lionel Karlin
Hôpital Lyon Sud, Pierre‐Benite Lyon France
Lotfi Benboubker
CHRU TOURS ToursFrance
Eric Voog
Clinique Victor Hugo Le MansFrance
Sung‐Soo Yoon
Department of Internal Medicine Seoul National University Hospital SeoulRepublic of Korea
Kenshi Suzuki
Japan Red Cross Medical Center Shibuya‐ku Tokyo Japan
Hirohiko Shibayama
Osaka University Graduate School of Medicine Suita Osaka Japan
Xiaoquan Zhang
Takeda Development Center Americas, Inc. (TDCA) Lexington Massachusetts USA
Miguel Villarreal
Takeda Development Center Americas, Inc. (TDCA) Lexington Massachusetts USA
Philip Twumasi‐Ankrah
Takeda Development Center Americas, Inc. (TDCA) Lexington Massachusetts USA
Richard Labotka
Takeda Development Center Americas, Inc. (TDCA) Lexington Massachusetts USA
Robert M. Rifkin
US Oncology Research – Rocky Mountain Cancer Centers Denver Colorado USA
Sagar Lonial
Department of Hematology and Medical Oncology Winship Cancer Institute Emory University School of Medicine Atlanta Georgia USA
Shaji K. Kumar
Mayo Clinic Rochester Minnesota USA
S. Vincent Rajkumar
Mayo Clinic Rochester Minnesota USA
Philippe Moreau
Centre Hospitalier Universitaire de Nantes NantesFrance
Abstract Deeper responses are associated with longer survival in multiple myeloma (MM); however, limited data exist on the impact of response kinetics on outcomes. We investigated progression‐free survival (PFS) and duration of response (DOR) by response depth and in early (best confirmed response 0–4 months; n = 424) versus late responders (best confirmed response >4 months; n = 281). Newly diagnosed patients enrolled in TOURMALINE‐MM2 receiving ixazomib‐lenalidomide‐dexamethasone (IRd) (n = 351) or placebo‐Rd (n = 354) were evaluated post hoc. Deeper responses were associated with longer PFS (complete response [CR] not reached [NR], very good partial response [VGPR] 37.2 months, partial response [PR] 16.4 months) and DOR (CR NR, VGPR 42.6 months, PR 15.4 months). Among patients with a PFS (n = 511) or DOR (n = 484) of ≥6 months who achieved ≥PR, median PFS was prolonged among late versus early responders receiving IRd (59.7 vs. 17.9 months) or placebo‐Rd (56.6 vs. 12.4 months), as was median DOR (IRd, NR vs. 20.9 months; placebo‐Rd, 58.2 vs. 11.7 months). While the treatment paradigm for newly diagnosed MM is treatment to progression, our findings suggest slowness of response to a proteasome inhibitor‐immunomodulatory drug‐steroid combination is not a negative predictor of outcome.