1 / 33

Two CML- ogens : Radiation and Age

Epidemiology of Chronic Myeloid Leukemia Tom Radivoyevitch, PhD Assistant Professor Epidemiology and Biostatistics Case Western Reserve University . Two CML- ogens : Radiation and Age. Not exponential => use additive risk model. Sv = gamma ray dose ( Gy ) + 10 neutron dose ( Gy ).

ulema
Download Presentation

Two CML- ogens : Radiation and Age

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Epidemiology of Chronic Myeloid LeukemiaTom Radivoyevitch, PhDAssistant Professor Epidemiology and BiostatisticsCase Western Reserve University

  2. Two CML-ogens: Radiation and Age Not exponential => use additive risk model Sv = gamma ray dose (Gy) + 10 neutron dose (Gy)

  3. Radiation-induced CML is Multi-scale For a 500 keVincoming photon J = 6.2e18eV Gy = J/kg = 6.2e6eV/pL Figure by R.K. Sachs.

  4. Stochastic versus Deterministic Figure by R.K. Sachs.

  5. Why Study Radiation as the Input? • Best carcinogen exposure assessment: A-bomb survivors remember exactly where they were, so doses can be reconstructed • Compared to chemical carcinogen, cannot simply not use it: background, diagnostic, and therapeutic exposures are here to stay • Physics is understood, so results across x- & γ-rays, neutrons & protons, and α- andβparticles at different energies can be unified Other CML-ogen, aging, also cannot be avoided+exposure is known

  6. Why Study CML as the Output? • CML is homogeneous: all have BCR-ABL • CML is prevalent: introns large => per-cell target size for creating bcr-abl is large • leukemias have rapid onset kinetics: white blood cells go in and out of tissues naturally so they don’t need to learn to metastasize Chr9 = 136.3 Mb From 1KG browser Chr 22 49.2 Mb ~5 kb = introns between e12-e15 ~140 kb 139.6 Kb DNA Repair 10 (2011) 1131– 1137

  7. PML-RARA intron sizes 40%,55% Mediterr J Hematol Infect Dis. 2011;3(1) ~2kb Seer APL/CML 1234/10103 = 12%=1/8 40/700=1/18 ~20kb

  8. Dose Response N is the number of CML target cells in an individual P(ba|T) is the probability of BCR-ABL given a translocation w(t)=probability density that CML arrives at t given bcr-abl at t=0 Linear R = 0.0075/Gy. LQE posterior R = 0.0022/Gy

  9. CML Target Cell Numbers • A comparison of age responses for CML and total translocations suggests a CML target cell number of 4x108 • 1012 nucleated marrow cells per adult and one LTC-IC per 105 marrow cells suggests 107 CML target cells • P(ba|T) = 2TablTbcr/2 may not hold

  10. BCR-to-ABL 2D distances Kozubek et al. (1999) Chromosoma 108: 426-435

  11. Hi-C Data http://hic.umassmed.edu/heatmap/heatmap.php Lieberman-Aiden, et al. Science 9 October2009: 289-293. chr9 K562 = bcr-abl+ CML cells 133 chr22 23 Off by 2 Mb? GM06690 = EBV-transformed lymphoblasts 133 23

  12. Theory of Dual Radiation Action • P(ba|D)= probability of a BCR-ABL translocation per G0/G1 cell given a dose D • tD(r)dr = expected energy at r given an ionization event at the origin • = intra-track component + inter-track component • Sba(r) = the BCR-to-ABL distance probability density • g(r) = probability that two DSBs misrejoin if they are created r units apart • Y = 0.004 DSBs per Mb per Gy;  = mass density • TBCR = 5.8 kbp; TABL = 140 kbp

  13. Total Translocations → g(r) estimate din [.01, .025], dx in [.04, .05], d in [.05, .06] R = 3.7 m r0 = 0.24 m, p0 = 0.12 G=25 DSB/Gy 6.25 kev/m3 = 1 Gy

  14. Risk and Target Cell Numbers  Higher risk estimate is more biologically plausible Linear-to-quadratic transition dose changed from [0.011-0.022]/0.055= [0.2-0.4] Gy to 3.64/.45= 8.09 Gy Linear R = 0.0075/Gyfor D < 4Sv is higher here at 0.0094/Gy due to cell killing term

  15. Bcr-Abl to CML Waiting Times M/F=1.6 tf-tm=10 yrs M/F=1.42 tf-tm=6.3y

  16. Age at Exposure Dependence

  17. Nagasaki HSC Reserve Loss? 6 Nagasaki CML vs 53 in Hiroshima Hiroshima PY=1558995 Nagasaki PY= 690084 (i.e. 2.26 lower), 53/2.26 = ~23 cases expectedin Nagasaki HSC reserve permanently depleted to 25%? Human T-cell leukemia virus (HTLV): 22 adult T-cell leukemias (ATLs) in Nagasaki compared to 1 in Hiroshima (2.26 more PY => expect ~50)

  18. Dead-Band Control of HSC levels • Transplant doses of 10, 100, and 1000 CRU => CRU levels 1-20% or 15-60% normal Blood (1996) 88: 2852-2858 • Broad variation in human HSC levels Stem Cells (1995) 13: 512-516 • Low levels of HSCs in BMT patients Blood (1998) 91: 1959-1965

  19. HSC Reserve Loss Trend? Ave last 7 ratios 0.70 0.49 0.80 0.54 1995 data yielded k= 0.041 [RadiatEnviron Biophys (1999) 38:201–206]. 0.031 in 2006 is consistent withtlcnsleading CML by 10 yrs

  20. All Cancer Incidence Conclusion: Cancer therapy is not the cause of the HSC reserve depletion Other Guesses? Does obesity increase bone marrow fat and thus squeeze out HSC? 1. Mississippi (34.4%) 51. Colorado (19.8%) 0.1*x+1(1-x)=0.5 => .5=.9x => x=.555 Prevalence of cause must be greater than 55% Cancer Epidemiol Biomarkers Prev2009;18:1501-1506 => obesity causes CML Easier travel=> greater loads on immune system?

  21. Or is it CMML Misclassification? CML=ICD9 205.1 includes 20% CMML CML = ICDO-2 9863 does not include CMML. Maybe all were called CML <1985, 50% in 1985-1995, and 0 after

  22. CMML rises at older ages ICDO-2 9945 = CMML Counts of CMML per year. None before 1985 1984 1986 1987 1988 1989 1990 1991 1992 1993 1994 1995 1996 1997 1998 1999 2000 2001 2002 1 40 41 43 50 53 70 61 68 66 65 79 93 65 85 78 82 87 2003 2004 2005 2006 2007 2008 2009 93 127 84 91 104 80 123

  23. AML More APL or better diagnostics?

  24. Retinoic Acid and Imatinib Cures found for cancers that are molecularly homogeneous: simpler cancers are being solved first

  25. AML and CLL More typically progress is slower

  26. Acknowledgements • Department of Epidemiology & Biostatistics • Rainer Sachs (UC Berkeley) • YogenSaunthararajah (Cleveland Clinic) • Thank you for listening!

  27. SEER Underreporting Possibility Most conservative claims-based algorithm vs. SEER. B. M. Craig et al. Cancer Epidemiol Biomarkers Prev; 21(3) March 2012

  28. Radiation Doses Rising

  29. AML Assuming all CML-ogens are also AML-ogens, this implies CML decreases are NOT due to decreases in exposures to bcr-abl forming agents. No AML trend is consistent with target cells being lineage committed and thus more tightly regulated than HSCs.

  30. Others

  31. All Cancer Incidence

  32. All Cancer Incidence

  33. Nagasaki HSC Reserve Loss? Hiroshima 6 Nagasaki CML vs 53 in Hiroshima Hiroshima PY=1558995 Nagasaki PY= 690084 (i.e. 2.26 lower), 53/2.26 = ~23 cases expectedin Nagasaki HSC reserve permanently depleted to 25%? Human T-cell leukemia virus (HTLV): 22 adult T-cell leukemias (ATLs) in Nagasaki compared to 1 in Hiroshima (2.26 more PY => expect ~40) Nagasaki

More Related