Infant acute lymphoblastic leukaemia (ALL diagnosed under 1 year of age)
also called infant ALL · ALL in infancy · infant lymphoblastic leukaemia
Infant ALL is leukaemia of the blood-forming system diagnosed in a baby under one year old, and in about three quarters of these babies the cause is a broken KMT2A gene. It behaves like a different disease from the leukaemia of older children: the babies arrive sicker, most of them relapse while still on treatment, and only about half are alive six years later.
The same thing, for a scientist
Infant ALL (<1 year at diagnosis) is a biologically distinct entity dominated by KMT2A rearrangement (~70-80% of cases). Presentation is characteristically aggressive: very high leucocyte counts (median 145-213 x 10^9/L in the COG AALL0631 KMT2A-r cohort), frequent organomegaly, and CNS involvement in roughly half of KMT2A-rearranged cases by cytology. Interfant-06, the largest prospective series (n=651), reported 6-year EFS 46.1% (SE 2.1) and OS 58.2% (SE 2.0), unchanged from Interfant-99, with KMT2A rearrangement the strongest prognostic factor, followed by age, WBC and prednisone response. Two thirds of relapses occur within 2 years and usually on therapy. The first intervention in decades to move outcomes was the addition of one post-induction course of blinatumomab (2-year DFS 81.6% vs 49.4% historical control).
Why infant ALL is not just ALL in a small patient1 deeper
Three things separate it from the ALL of a 4-year-old, and all three follow from the biology rather than from the size of the patient.
- The lesion. ~70-80% carry a KMT2A rearrangement, compared with ~5% of ALL in older children 16. In the CCCG-ALL-2015 infant cohort 71 of 134 (53.0%) were KMT2A-rearranged, and outcome split sharply on that single variable: 5-year OS 35.6% (95% CI 25.7-49.4) for KMT2A-rearranged versus 69.8% (95% CI 59.3-82.1) for KMT2A-germline infants 4.
- The immunophenotype. The blast is arrested earlier in B-cell development, giving a CD19-positive, CD10-negative pro-B pattern with frequent aberrant myeloid antigen co-expression; over 90% of KMT2A-germline ALL is CD10-positive by contrast 6. See
concept-flow-cytometry-immunophenotype-kmt2a-r. - The clinical tempo. About two thirds of KMT2A-rearranged infants who relapse do so within 2 years of diagnosis, usually while still receiving treatment, and that relapse is generally refractory and fatal 5. There is no comfortable window in which to escalate therapy after a relapse; the first attempt has to work.
Where the boundary at 12 months comes from, and why it is soft
The under-1-year definition is an operational trial boundary, not a biological cliff. Within it, outcome grades continuously with age: in COG AALL0631 the high-risk group (KMT2A-rearranged and under 90 days) had 5-year EFS 17 +/- 7% against 40 +/- 5% for the 90-365 day intermediate-risk group 3. Interfant-06 uses 6 months rather than 3 as its clinical cut-point 1. Children over 1 year with an 11q23/KMT2A rearrangement are a separate and better-behaved population.
The numbers a family is actually quoted
| Cohort | n | Endpoint | Result |
|---|---|---|---|
| Interfant-06, all infants | 651 | 6-year EFS / OS | 46.1% (SE 2.1) / 58.2% (SE 2.0) 1 |
| Interfant-06, West European / North American groups | - | 6-year EFS / OS | 49.4% (SE 2.5) / 62.1% (SE 2.4) 1 |
| Interfant-06, high-risk group | - | 6-year EFS | 20.9% (SE 3.4) 1 |
| COG AALL0631, KMT2A-r IR+HR | 146 | 5-year EFS / OS | 34 +/- 4% / 41 +/- 4% 3 |
| CCCG-ALL-2015 infants | 134 | 5-year EFS / OS | 52.1% (95% CI 44.2-61.4) / 66.1% (95% CI 58.4-74.8) 4 |
| Interfant-06 + one blinatumomab course | 30 | 2-year DFS / OS | 81.6% (95% CI 60.8-92.0) / 93.3% (95% CI 75.9-98.3) 2 |
The last row is the only line in this table that improved on the one above it, and it did so with an immunotherapy rather than with more chemotherapy. Interfant-06 tested exactly the opposite hypothesis - that early intensification with myeloid-style courses would help - and found no difference (6-year DFS 39.3% for ADE+MAE versus 36.8% for lymphoid course IB, log-rank p = 0.47) 1.
What this means for a menin-directed programme
Three design constraints fall directly out of the clinical picture. First, the therapeutic window is the first year of treatment, because that is when the relapses happen 5; an agent that only works in the relapsed setting arrives too late for most of these babies. Second, CNS penetration matters, because roughly half of KMT2A-rearranged infants have CNS involvement at diagnosis by cytology 3. Third, the bar is not survival alone: the babies who do survive carry the late effects of intensive chemotherapy delivered to an organism that is still developing, so a targeted agent's value includes what it lets you remove from the backbone.
| icd10 | C91.0 |
|---|---|
| age definition | diagnosis before 12 months of age |
| dominant lesion | fusion-kmt2a-aff1 and other KMT2A rearrangements |
| immunophenotype | CD19+ CD10-negative pro-B, frequent myeloid antigen co-expression |
| relapse timing | two thirds within 2 years of diagnosis, usually on therapy |
kmt2a rearranged fraction PCT
[ 70, 80 ]
presenting wbc median x10e9 per L — the numbers behind the chart
{
"cog_aall0631_intermediate_risk": 145,
"cog_aall0631_high_risk": 213,
"cccg_all_2015_all_infants": 62.7
}cns involvement at diagnosis PCT
{
"cog_aall0631_intermediate_risk_cns2_or_cns3": 48,
"cog_aall0631_high_risk_cns2_or_cns3": 83
}survival — the numbers behind the chart
[
{
"cohort": "Interfant-06 (n=651)",
"years": 6,
"efs_pct": 46.1,
"os_pct": 58.2,
"precision": "SE 2.1 / SE 2.0"
},
{
"cohort": "Interfant-06 high-risk group",
"years": 6,
"efs_pct": 20.9,
"precision": "SE 3.4"
},
{
"cohort": "COG AALL0631 KMT2A-r (n=146)",
"years": 5,
"efs_pct": 34,
"os_pct": 41,
"precision": "+/- 4%"
},
{
"cohort": "CCCG-ALL-2015 infants (n=134)",
"years": 5,
"efs_pct": 52.1,
"os_pct": 66.1,
"ci_efs": [
44.2,
61.4
],
"ci_os": [
58.4,
74.8
]
},
{
"cohort": "Interfant-06 + blinatumomab pilot (n=30)",
"years": 2,
"dfs_pct": 81.6,
"os_pct": 93.3,
"ci_dfs": [
60.8,
92
],
"ci_os": [
75.9,
98.3
]
}
]- Two thirds of relapses happen on treatment, so any new agent has to work in combination from the start; a sequential 'add at relapse' strategy will miss most patients.
- Roughly half of KMT2A-rearranged infants have CNS involvement at diagnosis, so a targeted agent with poor CNS penetration will leave a sanctuary site that reseeds the marrow.
- CD19-directed therapy is now part of the backbone, and lineage switch to a CD19-negative myeloid phenotype is a documented escape route in KMT2A-rearranged disease; it was rare (2% of Interfant-06 relapses) before immunotherapy was used routinely.
- The population is small and split across consortia with different risk definitions, so an underpowered trial can make an effective agent look inert.
- Interfant-06 showed that intensification does not help and the blinatumomab pilot suggests immunotherapy does; is the difference that chemotherapy cannot reach the KMT2A-rearranged clone's self-renewing compartment, or that it kills it only at a dose infants cannot survive?
- Why does outcome grade so steeply with age within the first year when the fusion is the same? Is the determinant the cell of origin, the residual fetal transcriptional programme, or the dose reduction that very young infants receive?
- In an era of blinatumomab and menin inhibition, is the 12-month trial boundary still the right way to define this population, or should it be defined by immunophenotype and MRD kinetics instead?
- E1established confidence 5 of 5: Multiple independent lines of evidence; treated as settled in the field.paper
Interfant-06 enrolled 651 infants with ALL and reported 6-year EFS 46.1% (SE 2.1) and OS 58.2% (SE 2.0); risk groups were low risk (KMT2A-germline), high risk (KMT2A-rearranged, older than 6 months with WBC >= 300 x 10^9/L or poor prednisone response) and medium risk (all other KMT2A-rearranged); myeloid-style consolidation was not superior to lymphoid course IB (6-year DFS 39.3% vs 36.8%, p = 0.47); high-risk 6-year EFS was 20.9% (SE 3.4); KMT2A rearrangement was the strongest prognostic factor, followed by age, WBC count and prednisone response.
Outcome of Infants Younger Than 1 Year With Acute Lymphoblastic Leukemia Treated With the Interfant-06 Protocol: Results From an International Phase III Randomized Study. · Pieters R, De Lorenzo P, Ancliffe P, et al. · Journal of Clinical Oncology 2019What this evidence cannot show
Survival is reported with standard errors rather than confidence intervals. The 18 participating groups differ in supportive care, and the paper itself notes a 10-12% survival gap between West European/North American groups and the rest, so the pooled figure is not transportable to any single health system. Only 46% of high-risk patients assigned to transplant actually received it because of early events, so the high-risk EFS conflates biology with failure to deliver the intended therapy.
Evidence that argues against this (3)
- A trial cohort is not the disease population. Interfant-06 enrolled infants who were diagnosed at participating centres, survived to enrolment and consented, so early deaths and non-enrolled infants are missing from the denominator, and EFS on a protocol is not EFS in the world. Its own randomisation was informative in the negative direction: the trial did not show a benefit for the intensified myeloid-style arm it was designed to test. Journal of Clinical Oncology 2019
- These figures are also being superseded rather than merely qualified. Adding blinatumomab to the Interfant-06 backbone in infants with KMT2A-rearranged ALL produced substantially better outcomes than the historical protocol results quoted here, so a 6-year EFS of 46.1% describes the pre-immunotherapy era. Quoting it as the current prognosis for a newly diagnosed infant would be wrong. New England Journal of Medicine 2023
- The comparison across Interfant generations is not clean either. Interfant-99 reported 4-year EFS of 47.0% on 482 infants, which is close to Interfant-06's 6-year 46.1% at a different time point, so the apparent stability across protocols partly reflects different follow-up horizons rather than equivalent outcomes. The Lancet 2007
- E2established confidence 5 of 5: Multiple independent lines of evidence; treated as settled in the field.paper
Adding one post-induction course of blinatumomab to the Interfant-06 backbone in 30 newly diagnosed infants with KMT2A-rearranged ALL produced no toxic effect meeting the primary endpoint, 28 of 30 (93%) were MRD-negative or had MRD < 5 x 10^-4 after the infusion, and 2-year DFS was 81.6% (95% CI 60.8-92.0) versus 49.4% (95% CI 42.5-56.0) for Interfant-06 historical controls, with OS 93.3% (95% CI 75.9-98.3) versus 65.8% (95% CI 58.9-71.8).
Blinatumomab Added to Chemotherapy in Infant Lymphoblastic Leukemia · van der Sluis IM, de Lorenzo P, Kotecha RS, et al. · New England Journal of Medicine 2023What this evidence cannot show
Single-arm, n = 30, median follow-up 26.3 months, compared against historical rather than randomised controls. The confidence interval on 2-year DFS runs from 60.8% to 92.0%, so the true effect could be considerably smaller than the point estimate. Historical-control comparisons in infant ALL are vulnerable to improvements in supportive care over the same interval. **Regraded moderate -> established on 2026-09-20** under `concept-the-confidence-grading-rule`: this is the trial's own reported result, which is established as a fact about what the trial found.
Evidence that argues against this (1)
- The Interfant-06 randomised comparison shows that a plausible-looking intensification can produce no benefit at all, which is the base rate this single-arm result should be judged against. source 2019
- E3strong confidence 4 of 5: Replicated in peer-reviewed work by more than one group.paper
In COG AALL0631, 146 KMT2A-rearranged infants had 5-year EFS 34 +/- 4% and OS 41 +/- 4%; the high-risk group (KMT2A-r, age < 90 days, n = 35) had EFS 17 +/- 7% and OS 20 +/- 7% versus 40 +/- 5% and 48 +/- 5% for the intermediate-risk group (KMT2A-r, age 90-365 days, n = 111); median presenting WBC was 145 x 10^9/L (range 2-4335) in the intermediate-risk and 213 x 10^9/L (range 12-1800) in the high-risk group; CNS status was CNS1 in 50% of intermediate-risk and 17% of high-risk infants, CNS2 in 34% and 57%, and CNS3 in 14% and 26%.
FLT3 inhibitor lestaurtinib plus chemotherapy for newly diagnosed KMT2A-rearranged infant acute lymphoblastic leukemia: Children's Oncology Group trial AALL0631. · Brown PA, Kairalla JA, Hilden JM, et al. · Leukemia 2021What this evidence cannot show
The trial's own question (adding lestaurtinib) was negative, so these are the characteristics and outcomes of a cohort receiving an intensive COG backbone, not of a successful intervention. Survival is given as point estimate +/- standard error. CNS2 (low-level blasts in CSF without pleocytosis) is a less certain category than CNS3 and its reported frequency is sensitive to cytospin technique and to traumatic taps in a small infant.
Evidence that argues against this (1)
- The age-90-day boundary is a chosen cut-point on a continuous variable and the high-risk group it defines has 35 patients, so EFS 17 +/- 7% carries an interval from roughly 3% to 31%. The contrast with the intermediate group is real; its magnitude, and the position of the threshold that produced it, are not established by this analysis. Statistics in Medicine 2006
- E4strong confidence 4 of 5: Replicated in peer-reviewed work by more than one group.paper
In the CCCG-ALL-2015 infant cohort (n = 134, median age 254 days), median WBC was 62.7 x 10^9/L (range 1.3-777) with 11.2% having WBC >= 300 x 10^9/L; 71 (53.0%) were KMT2A-rearranged with partners AFF1 53.3%, MLLT3 25%, MLLT1 16.7% and MLLT10 5%; 5-year EFS was 52.1% (95% CI 44.2-61.4) and OS 66.1% (95% CI 58.4-74.8) overall, with 5-year OS 35.6% (95% CI 25.7-49.4) for KMT2A-rearranged versus 69.8% (95% CI 59.3-82.1) for KMT2A-germline infants.
Outcome of infants with acute lymphoblastic leukemia treated with the Chinese Children's Cancer Group Acute Lymphoblastic Leukemia 2015 study protocol · Leung AWK, Chan GCF, Li CK, et al. · Haematologica 2024What this evidence cannot show
A single-consortium cohort in China; the 53% KMT2A-rearranged fraction is lower than the 70-80% usually quoted, which may reflect ascertainment, referral pattern or detection method rather than a real population difference, and it makes the pooled EFS look better than KMT2A-r-only series. Median WBC of 62.7 x 10^9/L is also much lower than the COG KMT2A-r medians, consistent with the cohort containing many KMT2A-germline infants.
Evidence that argues against this (1)
- CCCG-ALL-2015's better survival is not evidence of better treatment. Only 53% of its 134 infants are KMT2A-rearranged against 100% of the AALL0631 cohort, and a KMT2A-germline infant has a substantially better outcome, so most of the difference between 52.1% and 34% EFS is cohort composition. The partner distribution is also detection-limited by whatever assay the trial used. Leukemia 2021
- E5strong confidence 4 of 5: Replicated in peer-reviewed work by more than one group.review
About 75% of infant ALL is driven by KMT2A rearrangement; roughly two thirds of KMT2A-rearranged infants who relapse do so within 2 years of diagnosis while still on active treatment, usually with refractory and fatal disease; lineage switch accounted for only 2% (5 of 231) of first relapses in Interfant-06; and 80% of KMT2A-rearranged infants still have detectable MRD at the end of induction, half of them at high levels.
KMT2A-rearranged acute lymphoblastic leukemia in infants: current progress and challenges · Stutterheim J, van der Sluis IM, Pieters R, et al. · Haematologica 2025What this evidence cannot show
A narrative review by the Interfant investigators, so it is a map of their own trial programme rather than an independent synthesis; percentages are summary statements whose primary sources must be read for the exact denominators. The 2% lineage-switch figure predates widespread CD19-directed therapy and the same review cautions it may rise.
Evidence that argues against this (1)
- A review aggregating four quantities from four different sources gives each the same apparent standing. The lineage-switch figure is the one most likely to be an underestimate: 5 of 231 first relapses in Interfant-06 predates routine CD19-directed therapy, and this graph's own entries record lineage switch as a recognised failure mode of blinatumomab and CD19 CAR-T in KMT2A-rearranged infants. A historical rate cannot be carried into the immunotherapy era. Leukemia 2021
- E6moderate confidence 3 of 5: One strong study, or several smaller consistent ones.review
KMT2A rearrangement is present in up to 80% of infant ALL, with partner frequencies AFF1 48%, MLLT1 24%, MLLT3 16%, MLLT10 6% and other 6%; the blasts are CD19-positive and CD10-negative with frequent myeloid antigen co-expression, whereas over 90% of KMT2A-germline ALL is CD10-positive.
Infant Acute Lymphoblastic Leukemia-New Therapeutic Opportunities · Kulczycka M, Derlatka K, Tasior J, et al. · International Journal of Molecular Sciences 2024What this evidence cannot show
A review; the partner frequencies are re-quoted from the Meyer/Marschalek recurrent-rearrangement series and differ by a few percentage points between publications and between referral cohorts. The 'up to 80%' upper bound is the top of a range, not a central estimate.
Evidence that argues against this (1)
- The CCCG-ALL-2015 infant cohort found only 53.0% KMT2A-rearranged, well below the quoted 70-80%, which shows the fraction is cohort-dependent. source 2024
low HDAC7 in t(4;11) infant pro-B-ALL, associated with poor therapeutic response
NCT02553460 gave vorinostat with bortezomib to 50 newly diagnosed infants, 35 KMT2A-rearranged; tolerability endpoint only
identified by unbiased screening of primary MLL-rearranged infant ALL lines; preclinical only, never given to an infant
prognostic claim is specific to infant t(4;11) B-ALL
- ← analogous toTerm structure of risk — a steeply falling hazard curve is a statement about heterogeneity, not about time
reads the front-loaded relapse hazard as a seasoning credit pool
- ← related toEach partner prefers a different KMT2A exon: partner-specific break position in 3,401 patients
Counter-evidence to breakpoint-position prognostics: Interfant-06, 651 infants across 18 groups, found KMT2A rearrangement, age, white cell count and prednisone response to be the prognostic factors. Breakpoint position has never been entered into such a model (Pieters 2019, PMID 31283407).
- ← related toWhich partner, in which patient: KMT2A partner frequencies across six age-lineage strata
Counter-evidence lowering the clinical stake in partner frequencies: in 175 infants typed by karyotype, FISH and RNA-seq, survival did not differ by KMT2A partner gene (KMT2A::AFF1 2-year EFS 36% vs 37% for all others, p = 0.9), and 17.7% had no KMT2A rearrangement at all (Ilyasova 2025, PMID 40000924).
prophase agent and prognostic instrument
intrathecal CNS-directed steroid
infant blasts 1.9-3.3 fold MORE sensitive than older children's
induction and reinduction glucocorticoid
in the protocol; in-vitro sensitivity indistinguishable from older children's
induction anthracycline
experimental-arm consolidation and, in a current study, front-line induction
systemic consolidation, maintenance and CNS-directed therapy
induction enzyme therapy against a 12-fold resistant blast
consolidation and reinduction enzyme therapy, fixed dose, no activity monitoring
consolidation alkylator
maintenance backbone for up to two years
reinduction thiopurine, 42 days total
about 26 KMT2A-rearranged infant leukaemias per million infant-years, roughly 1 in 38,000
MLL-rearranged infant ALL is the named exception in paediatric ALL xenografts where venetoclax alone recapitulates navitoclax, i.e. BCL-2-dependent without BCL-XL co-dependence
identified in diagnostic marrow and blood of infants with MLL-rearranged ALL by two single-cell platforms; abundance predicted relapse better than in vivo prednisone response
KMT2A-rearranged infant B-ALL is uniquely dominated by an ELP state against a developing marrow reference, unlike NUTM1-rearranged infant ALL and most childhood B-ALL
fully murine immunocompetent KMT2A-AFF1 mixed-lineage infant leukaemia model; CNS- versus BM-derived leukaemia-propagating cells
the standing explanation for measurable residual disease and late relapse
proposed explanation for aggressiveness despite few cooperating mutations
- ← related toThe neonatal window — the state in which an MLL fusion can transform, bounded at both ends
the clinical counterpart of a neonatal permissive window
- ← related toFLT3 is the second largest KMT2A-selective dependency and it is HEAVIER in B-lineage than in myeloid cells
FLT3 inhibition is cytotoxic in primary MLL-rearranged infant ALL samples
- ← related toBig liver, big spleen: the organomegaly numbers measured in infants, not pooled from children
infant-specific organomegaly frequency replaces the age 0-18 pooled figure
- ← related toThe white cell count at diagnosis in infants, and why the reported medians disagree by fivefold
presenting white cell count distribution in infants
bounded absence in the presenting-feature description of infant ALL
how presenting features are ascertained in the first year of life
presenting skin signs in the first year of life
- ← related toCNS disease at diagnosis in infants: a real excess, measured by a procedure that partly creates it
CNS disease at diagnosis in infant ALL
presenting emergency of infant leukaemia
- ← part ofLeukaemia diagnosed in the first month of life: a different presentation and a different prognosis
the first-month-of-life stratum of infant ALL
induction mortality and infection in infant ALL
how infants are sorted into risk groups
preclinical triple combination matched VXL induction in infant KMT2A-r PDX
119-infant cohort with a full presenting-feature table
- ← related toNine survivors in ten carry a long-term complication, and it is worse the younger they were
89.6% of >=5-year survivors carry a long-term complication
the setting in which the class assumption is asserted to fail
- ← related toWhen infant leukaemia comes back, it comes back early and while treatment is still running
relapse incidence, timing and post-relapse prognosis
principal preclinical laboratory for this disease
evidence audit for the infant clinical presentation beat
Selection correction (Lehmann 2011, PMID 21502956): 29% of unselected APL patients die within 30 days, 41% haemorrhagic, a third never receiving ATRA. The 100% CR that anchors this analogy is conditional on surviving to randomisation.
Counter-evidence on inferring stage from mutation pattern (Andersson 2015, PMID 25730765): infant KMT2A-r ALL carries a mean of 1.3 non-silent mutations, with RAS-pathway lesions in 47% that are often subclonal and lost at relapse, against 6.5 in older children. A cross-sectional ordering cannot separate developmental stage from clonal turnover.
- ← co-occurs withKRAS - the commonest co-mutation in a disease that has almost none, and it is usually in a minority of the cells
recurrent in 4/22 WGS cases; subclonal in two thirds
- ← co-occurs withNRAS - the other RAS, the one whose 0.3% clone came back, and a UniProt record that lists HRAS1 as its own synonym
recurrent in 2/22 WGS cases; resistant subclones at 0.06-0.34% expand at relapse
- ← co-occurs withNF1 - the only tumour-suppressor loss in this disease, and it is a deletion, so a mutation panel cannot see it
one homozygous deletion in 22 WGS cases; under-ascertained wherever copy number was not assayed
- ← co-occurs withPAX5 - the most frequently hit non-KMT2A gene in infant KMT2A-rearranged ALL, and it is a deletion in one allele, not a mutation
focal loss in 5/22 (23%) infant KMT2A-r ALL; the most frequently hit non-KMT2A gene
deleted in 4/47 (8.5%), against 28% of infant ALL without a KMT2A rearrangement
the load-bearing negative: genotype-selected combination logic has no substrate here
PIK3CA plus PIK3R1 in 11% of infant MLL-R cases; an inter-SH2 ITD in two of them
Counter-evidence (Wolfl 2018, PMID 29898879): KMT2A-rearranged infant ALL underwent a blinatumomab-induced ALL-to-AML lineage switch and then spontaneously reverted -- the truncal fusion is stable while the phenotype is not, so fusion stability cannot carry an MRD or antigen-selection argument
initiating event occurs in fetal haematopoiesis, before birth
- ← related toTwin concordance: near-total for infant KMT2A-rearranged leukaemia, about 5% for childhood ALL overall
concordance and latency in infant KMT2A-r pairs differ sharply from childhood ALL overall
candidate primary prevention route, assessed and rejected
- ← related toH3K79me2 builds up as B cells mature - so in B-ALL the drug's target is what the rescued compartment runs on
the B-lineage compartment a DOT1L agent must spare in infant ALL
in vivo efficacy in MLL-rearranged ALL xenografts; the only ALL trial was terminated for lack of efficacy
the RNF20/RNF40/WAC axis is implicated in maintenance of MLL-rearranged ALL
the one immune-evasion route measured in the index fusion, lineage and age group
- ← refutesThe counter-argument: the menin field is an adult field, and the infant studies were withdrawn
Counter-evidence (NCT05848687 TINI 2, read 2026-09-18): a frontline total-therapy protocol for infants under one year lists ZIFTOMENIB among its interventions with KURA ONCOLOGY as a named collaborator, 90 infants planned, recruiting since 2023-11-03. A menin inhibitor is already being given frontline to infants with its manufacturer participating, which is the precedent this node says does not exist.
worldwide annual case estimate for this disease
cost of frontline care for this disease
the kind of disease the voucher programme exists for
derived from a 9-day-old infant with KMT2A-rearranged B-ALL
- ← related toPER-494 (CVCL_A8JU) — infant t(4;11;7) line, and the one whose AFF1 was never demonstrated
derived from an 11-month-old infant at diagnosis
derived at 66 days of age from a child who survived
- ← related toALL-PO (CVCL_1069) — an infant KMT2A::AFF1 line that is already in DepMap and has never been screened
derived from a 4-month-old infant
infant-derived KMT2A::AFF1 B-precursor line
infant-derived KMT2A::AFF1 B-precursor line
all four donors under one year of age
- ← related toThe 'infant ALL' PDX panel with four KMT2A::AFF1 models — one of which the full text calls adult
patient-derived xenograft panel of infant ALL
inventory of material for the index disease
- ← expressed inFLT3 / CD135 — the strongest non-tether co-dependency, and a target the field may have written off on a badly executed trial
near-universal overexpression of the wild-type receptor
genome-wide CRISPR hit in a KMT2A-rearranged B-ALL line; DepMap selectivity -0.211
the patient arm the prompt asked for would attach documented cases to this disease entry
- ← part ofFever and infection: the reason most of these babies see a doctor, and the reason some of them die
the reason most of these babies reach a doctor
step 1 of the diagnostic path
a late effect that sets the bar any new therapy must beat
- ← treated byInterfant-06 — 651 infants, and the definitive answer that myeloid-style consolidation does not help
651 infants; settled the myeloid-versus-lymphoid consolidation question
- ← treated byBlinatumomab in infant KMT2A-rearranged ALL — the largest single outcome gain in thirty years
the largest single improvement in this disease in thirty years
transplant, and what it actually buys in this population
which trials a child could actually enter right now
presenting sign: organ infiltration, often the finding that prompts the blood count
presenting sign: cutaneous infiltration, disproportionately common in infant KMT2A-r disease
presenting feature: CNS disease at diagnosis
presenting emergency: hyperleukocytosis
first diagnostic step in the infant leukaemia workup
a silencing class described specifically in t(4;11) infant disease
the initiating and usually near-sole driver lesion
approved in relapsed or refractory KMT2A-rearranged acute leukemia from 1 year of age
- ← related toWhat the treated brain looks like later: neurocognitive late effects after CNS-directed therapy in infancy
what survivors live with, which sets the bar for any new therapy
- ← related toHow many children this affects
how many children, and the denominator trap
MLL3 compound heterozygosity in every infant AML and 50% of infant ALL in the MLL-rearrangement-NEGATIVE COG cohort
Counter-evidence (NCT05521087 WhyStopped = 'Business Decision', MinimumAge = 30 days): J&J registered and then withdrew a genuinely infant-inclusive bleximenib study for commercial reasons, not for a paediatric safety finding
- ← related toKura Oncology — ziftomenib (KO-539): an adults-only sponsor that quietly supplies infant trials
TINI 2 (NCT05848687) is a RECRUITING frontline infant total-therapy protocol with ziftomenib dose-finding as a secondary objective -- but infants also receive blinatumomab, confounding any menin correlative analysis
- ← related toOpen ground: the questions in this graph that nobody in the landscape appears to be working on
Counter-evidence (Andersson 2015, PMID 25730765): open-ground area 6 is blocked by power, not access -- 47 infant MLL-r whole genomes at a mean 1.3 non-silent mutations per clone cannot support a regulatory-variant recurrence analysis
Counter-evidence (NCT00005603 COG-P9906 MinimumAge = 1 Year; NCT00075725 AALL0232 likewise): TARGET-ALL's B-ALL cohorts came from COG frontline high-risk protocols that exclude infants, so TARGET holds essentially no infant KMT2A-r cases
Counter-evidence (Andersson 2015, PMID 25730765): the infant KMT2A-r subset is ~47 sequenced cases at a mean 1.3 non-silent mutations per clone -- the binding constraint on this resource is statistical power, not the data-access agreement
frames infant t(4;11) B-ALL as a developmental, prenatal-origin, near-silent-genome disease
in-utero origin framework; explicitly notes infant KMT2A-r as the exception to his two-step causal model
the only global infant-ALL trial network; defines the treatment backbone and risk stratification
predicts that the lymphoid phenotype of infant KMT2A-rearranged disease is partly environmental
excluded infants by protocol (minimum age 3 years), so the population generating the rationale was not studied
the untested population; registry absence is an upper bound because condition strings rarely carry fusion genotypes
Counter-evidence: COG AALL15P1 (PMID 38867582) achieved on-target demethylation in 87% of infants with KMT2A-r ALL and produced no survival benefit, and bulk methylome differences are confounded by blast/leukocyte composition (Houseman 2012, PMID 22568884).
- ← related toWhich step is rate-limiting, and what compensates when you block it — the bite-back map for the causal chain
Scope counter (Adriaanse 2024, PMID 38892207): the differentiation-blockage framing is an AML observation; KMT2A-r ALL dies rapidly under menin inhibition rather than differentiating.
- ← related toPlain-English: chromatin and epigenetics — the sticky notes on the DNA, and which ones matter here
Counter-evidence (COG AALL15P1, PMID 38867582): azacitidine priming demethylated 87% of infant KMT2A-r ALL samples and did not change event-free survival.
Standing limitation, now with the specific gap named: the eleven-line KMT2A-r DepMap panel has no infant-derived line (Cellosaurus ages 1Y-65Y), while KOPN-8 (CVCL_1866, 3-month-old infant, KMT2A-r B-ALL) has a DepMap id ACH-001106 and is not in the panel.
- ← related toDataset: TARGET via the GDC - open expression and mutations, but the fusion calls themselves are controlled
Hard counter-evidence from the trial registry: TARGET-ALL Phase II accrued through COG AALL03B1 (NCT00482352, minimum age 1 Year), so infants are excluded by design; infant ALL went to COG AALL0631 (NCT00557193, maximum age 1 Year).
Counter-evidence: menin-inhibitor response is lineage-dependent (ALL dies, AML differentiates; PMID 38892207), and the trial labels available differ in disease, drug, age and analysis set - so a pooled response label leaks study identity (PMID 37720327).
Counter-evidence (Jin 2015, PMID 25884180): SIRT1 is higher in primary ALL cells than in healthy PBMC, and the SIRT1/2 INHIBITOR tenovin-6 activates p53, kills primary cells from 41 children with ALL, eliminates CD133+CD19- ALL stem/progenitor cells and sensitises to etoposide and cytarabine - the opposite direction from this entry's agonism thesis.
high MCL-1 associated with poor in vivo prednisone response in MLL-rearranged infant ALL
retained from the conserved fetal HSPC programme that persists in infant ALL blasts
predicts adult t(4;11) B-ALL will not share the infant metabolic phenotype
- ← co-occurs withWho the 460 KMT2A::MLLT1 patients actually are: 88% lymphoblastic, 53% infants, and only 47 cases of AML in the whole series
242 of 460 KMT2A::MLLT1 cases are infants, 234 of them ALL
157 infant ALL cases, the partner's largest single cell
derived from a 13-month-old with B-ALL
- ← related toMRD by genomic breakpoint: the only assay in this disease that is fusion-specific by construction
the MRD assay of record in infant KMT2A-rearranged ALL
- ← related toMRD by fusion transcript: fast, standardised, partner-limited - and structurally blind to KMT2A*
used as the molecular MRD target in the MLL-Baby infant protocol
Ig/TCR targets are fewer, more oligoclonal and less stable in infants
applied to this population exactly once, as a case report
the standard backbone for infant ALL
three infant MLL-rearranged PDX models
zero records for infant plus NF-kB in KMT2A-rearranged leukaemia
infection is a leading cause of treatment-related mortality in the index population
- ← related toNUP98::HOXD13, t(2;11)(q31;p15) — the myelodysplasia fusion, and a warning against targeting p53
first report linking NUP98 rearrangement to infant leukaemia (infant AMML, not ALL)
universal molecular partner genotyping; no significant EFS difference between the three major partners
- ← related toInfant BCP-ALL (n=175): KMT2A::AFF1 2-year EFS 36% versus 37% for every other partner (P=0.9)
AFF1 2-year EFS 36% versus 37% for other partners, P=0.9, n=175
bounded absence of partner-stratified outcome in the two global infant protocols
38-point EFS split from age, CNS status and MRD with no partner term
the index disease the proxies stand in for
22 of 55 recombinome patients are infants with ALL, the modal presentation of this fusion
pro-B, CD10-negative infant ALL at 6 months
- ← part ofSkin first, blood later: a three-day-old referred for purple spots, with KMT2A::MLLT3 neonatal ALL
neonatal ALL diagnosed in the first week of life
treated on the Interfant-06 high-risk arm as infant leukaemia
pro-B ALL diagnosed at 5 months of age
- ← part ofThree pairs of twins who both got leukaemia: the patients who proved the fusion happens before birth
concordant infant leukaemia; approximately 75% of infant acute leukaemias carry an 11q23 translocation
arm 4 is runnable today on existing infant cohort whole-genome sequencing
no paediatric formulation, dose or exposure data exists; the case rests on one xenograft
KMT2A-WILD-TYPE infant B-ALL: NUTM1-r is 21.7% of evaluated KMT2A-wildtype Interfant infants, and BRD9 is 26% of the infant NUTM1-r partners
the largest named genetic group inside the KMT2A-WILD-TYPE arm of infant ALL: 35 of 161 evaluated KMT2A-wildtype Interfant infants (21.7%), and 9 of 33 (27%) in an independent 175-infant series
necessary for initiation of KMT2A::AFF1 infant ALL in human fetal cells in the absence of co-operating mutations
an initiation experiment for the disease's defining in-utero origin
the epidemiology being explained: in-utero initiation, postnatal presentation, short latency, no cooperating mutations
the self-limiting-target problem: target falls with age, lethality concentrates at relapse
the disease in which a fusion-directed immunotherapy would be needed and is least likely to be available
target selection for the population this disease occurs in
NG2 associates with CNS disease and lower event-free survival in MLL-rearranged infant B-ALL
infant basal ganglia are developing and CNS-directed therapy is routine in this disease
18 of the 25 profiled patients were infants; the <6-month subgroup carries the most plasticity
SEM is infant-derived and is the index fusion's own disease context
p279 and p454 are infant B-ALL; p318 is the lineage-switched AML of p279
the HOXA-negative infant subgroup, seen as occupancy
infant B-ALL at diagnosis (sample 148752)
primary infant B-ALL
infant B-ALL and infant pre-B-ALL samples from four institutions
- ← related toIRX1 — Iroquois homeobox 1, the gene that names the HOXA-negative half of infant t(4;11) ALL
names the iALL-IRX1 subgroup, worse prognosis
seven infant/pediatric KMT2A::AFF1 patients
one of two states of infant KMT2A::AFF1 ALL, the adverse one
- ← part ofiALL-HOXA9 — the HOXA-high state of infant KMT2A::AFF1 ALL, and the one everything is modelled on
the canonical, better-prognosis state
- ← arises inp279 and p318: one infant, two diseases, and an oncoprotein target map that does not carry over
the first disease is infant B-ALL
COG P9407, 97 infant ALL patients
97 infant ALL patients, COG P9407
IRX2 is one of three genes predictive of event-free survival in COG P9407 infant ALL
97 infant ALL patients on COG trial P9407
- ← expressed inPOU2AF1 (OCA-B / OBF-1 / BOB-1) - the B-cell-restricted OCT coactivator, in the Q152 AFF1-only core
B-cell-restricted OCT coactivator; the index disease is infant B-ALL
the seductive lineage argument: a B-cell kinase in a B-ALL lesion, joined across an osteosarcoma row
the population at risk is infants, in whom an imprinting or neurodevelopmental effect would be detected latest
the validating line SEM and the co-screened ALL-PO are infant KMT2A::AFF1 B-ALL lines
the population the liability is about - children on curative protocols containing etoposide or an anthracycline
CXCR4 antagonism reverses stromal protection in primary infant MLL-rearranged ALL
no infant with leukaemia has received a CXCR4 antagonist in a registered trial; both paediatric protocols set a floor of 2-3 years
the index disease whose niche literature this census bounds
MLL-rearranged but not MLL-wild-type lines are selectively sensitive, and single-agent decitabine prolongs survival in infant KMT2A-r ALL xenografts. No trial in infants.
Safe (6.5% DLT) and pharmacodynamically active (87% of WGBS samples demethylated) in infants with newly diagnosed KMT2A-rearranged ALL, with NO effect on survival.
Where the therapeutic index actually bites: marrow and gut, across four courses, in a patient with a normal life expectancy of eighty years if cured.
the population the drug class is being taken into has no chromatin dataset under the drug
correlative sampling is scarcest in the population the class is being taken into
- ← analogous toKMT2A-rearranged soft tissue sarcoma - the same gene as infant B-ALL, in a young adult's leg, as a solid tumour
same gene rearranged, opposite lineage and four decades later; the sarcoma fusions lack KMT2A exon 1
- ← analogous to0.2% of profiled sarcomas, median age 38, and every number here has a denominator that is not the population
the same gene rearranged four decades earlier in life, with a registry-based incidence this entity has no counterpart for
Present in t(4;11) infant B-ALL, the commonest KMT2A rearrangement in that disease.
- ← expressed inInfants whose leukaemia expresses the reciprocal fusion survive far better - 62.4% versus 11.7% event-free at four years
Measured in 124 Interfant 99/06 infants, 43 of them t(4;11).
Proposed initiating event for t(4;11) infant ALL; demonstrated in mouse, not in human cells.
CDK6 arm of the axis is documented in MLL-rearranged infant ALL; CCND3 itself is inferred from the D-cyclin/CDK6 biochemistry
- ← treated byCDK4/6 inhibition in KMT2A-rearranged leukemia — the class was already tried, and the trial never reported
CDK6 arm documented in MLL-rearranged infant ALL; no infant trial exists
no CLEC12A safety or expression data exist in infants; infection is already the leading non-relapse cause of death on infant protocols
lestaurtinib + chemotherapy; 3-year EFS 36% vs 39%, p=0.67
azacitidine before each of four post-induction courses; safe, DLT 6.5%, no survival impact
randomised in KMT2A-rearranged infants on NCT06317662
conditioning agent for high-risk infants proceeding to allogeneic HSCT in first remission
defines which infants are offered transplant and records that the benefit is contested
four organ systems maturing at once in the population the whole protocol treats as one age category
t(4;11) is about 57% of KMT2A-rearranged pro-B ALL and the reciprocal transcript is present in about 45% of those infants.