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- Siegel et al. Cancer statistics, 2015. CA 2015;65: 5
- Jamieson and Weissman. Stem-Cell Aging and Pathways to Precancer Evolution. NEJM 2023;389:1310
- Fröhling and Döhner. Chromosomal abnormalities in cancer. NEJM 2008;359:722
- Croce C. Oncogenes and cancer. NEJM 2008;358:502
- Uhlen et al. A pathology atlas of the human cancer transcriptome. Science 2017;357:eaan2507
- Dawson MA. The cancer epigenome: Concepts, challenges, and therapeutic opportunities. Science 2017;355:1147
- Huff et al. The paradox of response and survival in cancer therapeutics. Blood 2006;107:431(Cancer stem cells)
- Vogelstein et al. Cancer genome landscapes. Science 2013;339:1546
- Hahn and Weinberg. Rules for making human tumor cells. NEJM 2002;347:1593
- Kwok et al. DNA damage response defects in hematologic malignancies: mechanistic insights and therapeutic strategies. Blood 2024;143:2123
- Hotchkiss et al. Mechanisms of disease: cell death. NEJM 2009;1570
- Palucka and Coussens. The basis of oncoimmunology. Cell 2016;164:1233
- Boussiotis VA. Molecular and biochemical aspects of the PD-1 checkpoint pathway. NEJM 2016;375:1767
- Binnewies et al. Understanding the tumor immune microenvironment (TIME) for effective therapy. Nat Med 2018;24:541
- Tomasetti and Vogelstein. Variation in cancer risk among tissues can be explained by the number of stem cell divisions. Science 2015;347:78(Oncogenic mutations happen in proportion to the number of dividing stem cells in a tissue; with editorial)
- Popovic et al. Ubiquitination in disease pathogenesis and treatment. Nat Med 2014;20:1242
- Esteller M. Epigenetics in cancer. NEJM 2008;358:1148
- Aparicio and Caldas. The implications of clonal genome evolution for cancer medicine. NEJM 2013;368:842
- Yue and Rao.TET family dioxygenases and the TET activator vitamin C in immune responses and cancer. Blood 2020;136:1394
- Roodman GD. Mechanisms of bone metastasis. NEJM 2004;350:1655
- Chiang and Massagué. Molecular basis of metastasis. NEJM 2008;359:2814
- Leong and Karsan. Recent insights into the role of Notch signaling in tumorigenesis. Blood 2006;107:2223
- Platanias L. MAP kinase signalling pathways and hematologic malignancies. Blood 2003;101:4667
- Chen et al. Allosteric inhibition of SHP2 phosphatase inhibits cancers driven by receptor tyrosine kinases. Nature 2016;535:148
- Murtaza et al. Non-invasive analysis of acquired resistance to cancer therapy by sequencing of plasma DNA. Nature 2013;497:108
- Andor et al. Pan-cancer analysis of the extent and consequences of intratumor heterogeneity. Nat Med 2016;22:105
- Casey et al. The MYC oncogene is a global regulator of the immune response. Blood 2018;131:2007(“MYC may…prevent highly proliferative cells from eliciting an immune response. MYC-induced tumors may be particularly sensitive to immuno-oncology therapeutic interventions”)
- Xu et al. Cancer and platelet crosstalk: opportunities and challenges for aspirin and other antiplatelet agents. Blood 2018;131:1777
- Gordon-Alonso et al. Extracellular galectins as controllers of cytokines in hematological cancer. Blood 2018;132:484
- Reiter et al. Minimal functional driver gene heterogeneity among untreated metastases. Science 2018;361:6406(A single biopsy provides adequate information about driver genes in metastatic disease)
- Helmink et al. The microbiome, cancer, and cancer therapy. Nat Med 2019;25:377
- Duncan et al. Hematologic Cancer after Gene Therapy for Cerebral Adrenoleukodystrophy. NEJM 2024;391:1287
CHIP & CCUS
- Malcovati and Cazzola. How I manage patients with unexplained cytopenia. Blood 2025;145:1610
- Fabre and Vassiliou. The lifelong natural history of clonal hematopoiesis and its links to myeloid neoplasia. Blood 2024;143:573
- Weeks and Ebert. Causes and consequences of clonal hematopoiesis. Blood 2023;142:2235
- Weeks et al. Prediction of Risk for Myeloid Malignancy in Clonal Hematopoiesis. NEJM Evid 2023 (Epub) (A risk score to predict likelihood of myeloid neoplasm in CH)
- Xie et al. Risk prediction for clonal cytopenia: multicenter real-world evidence. Blood 2024;144:2033 (3-parameter risk score including presence of splicing mutation, plts < 100K and 2 or more mutations predict progression)
- Boettcher and Ebert. Clonal hematopoiesis of indeterminate potential. J Clin Oncol 2019;37:419
- Challen and Goodell. Clonal hematopoiesis: mechanisms driving dominance of stem cell clones. Blood 2020;136:1590
- Warren and Link. Clonal hematopoiesis and risk for hematologic malignancy. Blood 2020;136:1599
- Jaiswal S. Clonal hematopoiesis and nonhematologic disorders. Blood 2020;136:1606
- Shlush LI. Age-related clonal hematopoiesis. Blood 2018;131:496
- Jaiswal et al. Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes. NEJM 2014:371:2488(>10 fold increased risk of heme malignancy in pts with somatic mutations in peripheral blood cells)
- Xie et al.Age-related mutations associated with clonal hematopoietic expansion and malignancies. Nat Med 2014;20:1472(“The blood cells of more than 2% of individuals [5–6% of people older than 70 years] contain mutations that may represent premalignant events)
- Rossi et al. Clinical relevance of clonal hematopoiesis in persons aged ≥80 years. Blood 2021;138:2093 (Specific mutational patterns predict risk of evolution to myeloid neoplasia)
- Watson et al. The evolutionary dynamics and fitness landscape of clonal hematopoiesis. Science 2020;367:6485
- Genovese et al. Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence. NEJM 2014;371:2477(Results similar to above article)
- Steensma et al. Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes. Blood 2015;126:9
- Steensma D. Predicting therapy-related myeloid neoplasms – and preventing them? Lancet Oncol 2017;18:11(Overt malignancy develops at a rate of 0.5-1% per year in people with CHIP)
- Jaiswal et al. Clonal Hematopoiesis and Risk of Atherosclerotic Cardiovascular Disease. NEJM 2017;377:111(CHIP associated with 2x higher risk of CAD in humans and accelerated atherosclerosis in mouse model)
- Libby abd Ebert. CHIP (Clonal Hematopoiesis of Indeterminate Potential). Potent and Newly Recognized Contributor to Cardiovascular Risk. Circulation 2018;138:666
- Arends et al. Associations of clonal hematopoiesis with recurrent vascular events and death in patients with incident ischemic stroke. Blood 2023;141:787
- Miller et al. Association of clonal hematopoiesis with chronic obstructive pulmonary disease. Blood 2022;139:357
- Agrawal et al. TET2-mutant clonal hematopoiesis and risk of gout. Blood 2022;140:1094
- Zink et al. Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly. Blood 2017;130:742 (Evidence of clonal hematopoiesis found in less than 1% of those under 35 and over 50% in those over 85)
- Buscarlet et al. DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions. Blood 2017;130:753(TET2 mutations age-dependent, associated with mild neutropenia, showed some familial clustering)
- Malcovati et al. Clinical significance of somatic mutation in unexplained blood cytopenia. Blood 2017;129:3371(Presence of somatic mutation increased likelihood of developing a myeloid neoplasm by about 14-fold)
- van Zeventer et al. Mutational spectrum and dynamics of clonal hematopoiesis in anemia of older individuals. Blood 2020;135:1161
- Cooper and Young. Clonality in context: hematopoietic clones in their marrow environment. Blood 2017;130:2363
- Nagase et al. Expression of mutant Asxl1 perturbs hematopoiesis and promotes susceptibility to leukemic transformation. J Exp Med 2018;215:1729(Mouse model of CHIP; see this discussion in NEJM)
- Meisel et al. Microbial signals drive pre-leukaemic myeloproliferation in a Tet2-deficient host. Nature 2018;557:580
- Desai et al. Somatic mutations precede acute myeloid leukemia years before diagnosis. Nat Med 2018;24:1015(IDH1, IDH2, TP53, DNMT3A, TET2 and spliceosome gene mutations predict progression to AML; with editorial)
- Loh et al. Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations. Nature 2018;559:350(Identifies several genetic loci that substantially increase risk to develop CHIP)
- Hansen et al. Clonal hematopoiesis in elderly twins: concordance, discordance, and mortality. Blood 2020;135:261(No evidence that there is a genetic predisposition to CHIP or that it increases mortality)
- Fabre et al. Concordance for clonal hematopoiesis is limited in elderly twins. Blood 2020;135:269
- Bick et al Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature 2020;586:763
- DeBoy et al. Familial Clonal Hematopoiesis in a Long Telomere Syndrome. NEJM 2023;388:2422
- Tsaknakis et al. Incidence and prognosis of clonal hematopoiesis in patients with chronic idiopathic neutropenia. Blood 2021;138:1249 (Prevalence <3%, 31-fold higher risk of transformation to myeloid neoplasm)
- Galli et al. Relationship between clone metrics and clinical outcome in clonal cytopenia. Blood 2021;138:965 (30% of patients with idiopathic cytopenia have CCUS)
- Vlasschaert et al. Clonal hematopoiesis of indeterminate potential is associated with acute kidney injury. Nat Med 2024;30:810
- Pich et al. Tumor-Infiltrating Clonal Hematopoiesis. NEJM 2025;392:1594 (CH cells remodel tumor microenvironment, increase recurrence risk; with editorial)
VEXAS syndrome & related conditions
- Beck et al. Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease. NEJM 2021;383:2628 (“VEXAS” syndrome, X-linked condition – somatic hematopoietic stem cell mutations impair ubiquitination and protein degradation in phagocytes, activate autoimmune pathways; with editorial)
- Koster et al. VEXAS syndrome: Clinical, hematologic features and a practical approach to diagnosis and management. Am J Hematol 2024;99:284
- Sirenko et al. Molecular and clinical presentation of UBA1-mutated myelodysplastic syndromes. Blood 2024;144:1221 (Found in 1% of MDS patients, all male. 83% had inflammatory presentation)
- Arlet et al. Mutant UBA1 and Severe Adult-Onset Autoinflammatory Disease. NEJM 2021;384:2163(VEXAS syndrome in 2 women with acquired monosomy X)
- Grayson et al. VEXAS syndrome. Blood 2021;137:3591
- Bourbon et al. Therapeutic options in VEXAS syndrome: insights from a retrospective series. Blood 2021;137:3682
- Gurnari et al. Vacuolization of hematopoietic precursors: an enigma with multiple etiologies. Blood 2021;137:3685
- Ferrada et al. Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis Blood 2022;140:1496
- De Langhe et al. TET2-Driver and NLRC4-Passenger Variants in Adult-Onset Autoinflammation. NEJM 2023;388:1626 (VEXAS-like syndrome with TET2-driven myeloid clone bearing an NLRC4 variant causing inflammation)
- Gutierrez-Rodrigues et al. Spectrum of clonal hematopoiesis in VEXAS syndrome. Blood 2023;142:244
- Gurnari et al. Diagnostic capabilities, clinical features, and longitudinal UBA1 clonal dynamics of a nationwide VEXAS cohort. Am J Hematol 2024;99:254
- Kusne et al. Venous and arterial thrombosis in patients with VEXAS syndrome. Blood 2024;143:2190 (40% incidence of VTE)