The impact of the graft-versus-leukemia effect on survival in acute lymphoblastic leukemia

Author:

Yeshurun Moshe12,Weisdorf Daniel3,Rowe Jacob M.4,Tallman Martin S.5,Zhang Mei-Jie67,Wang Hai-Lin6,Saber Wael6,de Lima Marcos8,Sandmaier Brenda M.9,Uy Geoffrey10,Kamble Rammurti T.11,Cairo Mitchell S.12,Cooper Brenda W.13,Cahn Jean-Yves14,Ganguly Siddhartha15,Camitta Bruce16,Verdonck Leo F.17,Dandoy Christopher18ORCID,Diaz Miguel Angel19,Savani Bipin N.20,George Biju21,Liesveld Jane22,McGuirk Joseph15,Byrne Michael20,Grunwald Michael R.23,Drobyski William R.24,Pulsipher Michael A.25,Abdel-Azim Hisham25,Prestidge Tim26,Wieduwilt Matthew J.27,Martino Rodrigo28,Norkin Maxim29,Beitinjaneh Amer30,Seo Sachiko31,Nishihori Taiga32ORCID,Wirk Baldeep33,Frangoul Haydar34,Bashey Asad35,Mori Shahram36,Marks David I.37,Bachanova Veronika38

Affiliation:

1. Institute of Haematology, Davidoff Cancer Centre, Rabin Medical Centre, Petah Tikva, Israel;

2. Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel;

3. Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota Medical Center, Minneapolis, MN;

4. Department of Hematology, Shaare Zedek Medical Center, Jerusalem, Israel;

5. Leukemia Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY;

6. Center for International Blood and Marrow Transplant Research, Department of Medicine, and

7. Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, WI;

8. Department of Medicine, Seidman Cancer Center, University Hospitals Case Medical Center, Cleveland, OH;

9. Division of Medical Oncology, University of Washington and Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;

10. Division of Oncology, Washington University School of Medicine, St. Louis, MO;

11. Division of Hematology and Oncology, Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX;

12. Division of Pediatric Hematology, Oncology and Stem Cell Transplantation, Department of Pediatrics, New York Medical College, Valhalla, NY;

13. Department of Medicine–Hematology and Oncology, University Hospitals Case Medical Center, Cleveland, OH;

14. Department of Hematology, Centre Hospitalier Universitaire Grenoble Alpes, Grenoble, France;

15. Division of Hematological Malignancy and Cellular Therapeutics, University of Kansas Health System, Kansas City, KS;

16. Midwest Center for Cancer and Blood Disorders, Medical College of Wisconsin and Children’s Hospital of Wisconsin, Milwaukee, WI;

17. Department of Hematology/Oncology, Isala Clinic, Zwolle, The Netherlands;

18. Division of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH;

19. Department of Hematology/Oncology, Hospital Infantil Universitario Nino Jesus, Madrid, Spain;

20. Division of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN;

21. Department of Clinical Hematology, Christian Medical College, Vellore, India;

22. Department of Medicine, University of Rochester Medical Center, Rochester, NY;

23. Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Atrium Health, Charlotte, NC;

24. Department of Medicine, Medical College of Wisconsin, Milwaukee, WI;

25. Division of Hematology, Oncology, and Blood and Marrow Transplantation, Children's Hospital Los Angeles, USC Keck School of Medicine, Los Angeles, CA;

26. Blood and Cancer Centre, Starship Children's Hospital, Auckland, New Zealand;

27. UCSD Moores Cancer Center, University of California San Diego Medical Center, La Jolla, CA;

28. Divison of Clinical Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain;

29. Division of Hematology/Oncology, University of Florida College of Medicine, Gainesville, FL;

30. Stem Cell Transplant and Cellular Therapy Program, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL;

31. Department of Hematology & Oncology, National Cancer Research Center East, Chiba, Japan;

32. Department of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL;

33. Division of Bone Marrow Transplant, Seattle Cancer Care Alliance, Seattle, WA;

34. The Children's Hospital at TriStar Centennial and Sarah Cannon Research Institute, Nashville, TN;

35. Blood and Marrow Transplant Program at Northside Hospital, Atlanta, GA;

36. Blood and Marrow Transplant Center, Florida Hospital Medical Group, Orlando, FL;

37. Adult Bone Marrow Transplant, University Hospitals Bristol NHS Trust, Bristol, United Kingdom; and

38. Bone and Marrow Transplant Program, University of Minnesota Medical Center, Minneapolis, MN

Abstract

Abstract Allogeneic hematopoietic cell transplant is a potential curative therapy for acute lymphoblastic leukemia (ALL). Delineating the graft-versus-leukemia (GVL) effect as a function of graft-versus-host disease (GVHD) offers the potential to improve survival. We examined 5215 transplant recipients with ALL reported to the Center for International Blood and Marrow Transplant Research registry. Overall survival (OS) was compared according to the presence and severity of GVHD and evaluated in 3 cohorts: 2593 adults in first or second complete remission (CR1/CR2), 1619 pediatric patients in CR1/CR2, and 1003 patients with advanced (CR ≥3 or active disease) ALL. For patients in CR1/CR2, development of acute GVHD (aGVHD) or chronic GVHD (cGVHD) was associated with lower risk of relapse than no GVHD (hazard ratio [HR], 0.49-0.69). Patients with advanced ALL developing grades III and IV aGVHD or cGVHD were also at lower risk of relapse (HRs varied from 0.52 to 0.67). Importantly, adult and children in CR1/CR2 with grades I and II aGVHD without cGVHD experienced the best OS compared with no GVHD (reduction of mortality with HR, 0.83-0.76). Increased nonrelapse mortality accompanied grades III and IV aGVHD (HRs varied from 2.69 to 3.91) in all 3 cohorts and abrogated any protection from relapse, resulting in inferior OS. Patients with advanced ALL had better OS (reduction in mortality; HR, 0.69-0.73) when they developed cGVHD with or without grades I and II aGVHD. In conclusion, GVHD was associated with an increased GVL effect in ALL. GVL exerted a net beneficial effect on OS only if associated with low-grade aGVHD in CR1/CR2 or with cGVHD in advanced ALL.

Publisher

American Society of Hematology

Subject

Hematology

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