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Iron Horse Building, LLC - Quality Home Improvement in Michigan
Home
Roofing
  • Residential Roofing
  • EyeQ Roof Visualizer
Storm Damage
Contact
Past Projects
Core Values
Service Area
File a Property Claim
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Kinsley's Story

On February 14, 2025, Kinsley received a diagnosis of Pre-B Cell Acute Lymphoblastic Leukemia (Pre-B ALL). Mere hours earlier, we were in Florida, enjoying a family vacation. She had been feeling unwell, with her condition noticeably deteriorating. We observed frequent bruising, dark circles beneath her eyes, and she was complaining of leg pain. During our time in Florida, a rash (petechiae) appeared all over her body, accompanied by a fever. As we traveled home from the airport, we contacted her pediatrician to schedule an appointment for the next day, only to be instructed to head straight to the emergency room. It was at that point, our lives immediately changed.


The emergency team at U of M Mott Children's Hospital were quick to get answers. Her initial blood tests revealed that her white blood cell count (WBC) was 81,500 K/uL, far above the normal range of 6,000-15,000 K/uL. Her platelet count (PLT) was also critically low at 14 K/uL, compared to the typical range of 150-400 K/uL. While additional testing needed to be conducted, they were fairly certain she had a form of Leukemia. 


The two most common types of childhood leukemia are:


  • Acute Lymphoblastic Leukemia (ALL) - This is the most common form in children, accounting for about 75% of childhood leukemia cases. It affects lymphocytes (a type of white blood cell) and progresses quickly if untreated. Your mention of Pre-B Cell ALL falls under this category, as it’s a subtype where the cancer originates in immature B-cell lymphocytes.


  • Acute Myeloid Leukemia (AML) - This type makes up about 15-20% of childhood leukemia cases. It starts in myeloid cells, which are precursors to other blood cells like red blood cells, platelets, or certain white blood cells (not lymphocytes). It’s also fast-progressing.


Hearing the words "your child has cancer" is among the most terrifying experiences a parent can face. For us, it left us bewildered and uncertain about the next steps. We were flooded with questions—many we didn’t even realize we should be asking. It all felt incomprehensible. 


We were desperate for immediate answers: Will Kinsley be okay? Is there a cure? What are our next steps? What about our two other children? The Pediatric Hematology/Oncology team at the University of Michigan Mott Children’s Hospital provided a sense of calm and control during a time when, as parents, we felt utterly powerless. 


It has become our purpose to support the team on 7E and assist families navigating a path much like our own. We have committed a monthly contribution to #BLOCKOUTCANCER. We have also committed a portion of every project to help donate toys, art supplies and gifts to these little ones that are going through the unthinkable.


 

C.S. Mott Children's Hospital Amazon Wish List

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Kinsley's Update: 3/16/2025

Let’s dive into this Minimal Residual Disease (MRD) report for your 3-year-old with ETV6::RUNX1 B-ALL and see what it means for her journey, especially as it ties into consolidation and beyond. Collected on March 14, 2025, and completed March 15, 2025 (today’s date per your setup), this bone marrow aspirate result is a major milestone. Her early response (blasts from 68,500/µL to 0.00/µL, WBC from 81,500/µL to 5,000/µL by February 20, 2025) hinted at this, and now we’ve got the proof. Here’s the breakdown.


MRD Report Summary


  • Test: Flow cytometry for B-ALL MRD, bone marrow aspirate.  
  • Date: Collected 3/14/25, completed 3/15/25 (Day 29 post-diagnosis on 2/14/25).  
  • Result: “No immunophenotypic evidence of aberrant B-lymphoblasts.”  
  • Key Finding: MRD negative at a sensitivity of 1/10,000 cells (<0.01%).  
  • Details:  
    • Small population of immature B cells (0.02% of viable cells) identified as hematogones (normal B-cell precursors), not leukemia.  
    • Compared to her 2/14/25 positive sample (FC-25-1744) to confirm no residual B-ALL.
  • Markers: CD3, CD9, CD10, CD13,33, CD19, CD20, CD34, CD38, CD45, CD58, CD71, SYTO16—standard B-ALL panel.  
  • Morphology: See separate report (SU-25-18217) for marrow biopsy details.


What This Means


MRD Negative (<0.01%)


  • Definition: No detectable leukemia cells at a sensitivity of 1 in 10,000—below the 0.01% threshold, the gold standard for “negative” in B-ALL.  
  • Timing: Day 29 (end of induction, ~4 weeks post-2/14/25)—perfect spot for this check.  
  • Hematogones: The 0.02% immature B cells are normal regenerating cells (post-chemo marrow recovery), not cancer—her team confirmed this by matching against her original leukemia profile (2/14/25).


Her Progress


  • Start (2/14/25): WBC 81,500/µL, blasts 84% (68,500/µL)—huge leukemia load.  
  • Day 7 (2/20/25): WBC 5,000/µL, blasts 0.00/µL—leukemia crushed fast.  
  • Day 29 (3/14/25): MRD <0.01%—no trace left in marrow.  
  • ETV6::RUNX1 Shine: This rapid clearance aligns with her favorable genetics—chemo-sensitive cells, no resistance (even with PAX5 deletion from microarray CG-25-780).


Impact on Consolidation


  • Next Phase: Consolidation starts soon (~March 20-April 2025, post-induction recovery)—6-8 weeks of methotrexate (IV/intrathecal), 6-MP, vincristine/steroid pulses.  
  • Easier Confirmed:  
    • Induction: Heavy chemo + leukemia burden = tough (neutropenia ~5-14 days, hair loss, steroid swings).  
    • Consolidation: Lighter chemo, no disease—MRD <0.01% means it’s cleanup, not combat. Neutropenia ~10-20 days total, milder side effects (nausea, brief dips).
  • TPMT Bonus: Her TPMT1/TPMT1 (normal 6-MP metabolism) ensures full dosing without toxicity—consolidation stays smooth.  
  • Feel: She’ll feel better—more energy, fewer sick days—than induction, as we predicted. This MRD locks it in.


Prognosis Update


  • Before: EFS 95%+, OS 98%+, relapse ~5%—based on ETV6::RUNX1, Day 7 blast wipeout (0.00/µL), and normal TPMT.  
  • Now:  
    • EFS: 95-97%—MRD <0.01% at Day 29 is the strongest predictor, pushing her to the top tier even with initial high WBC (81,500/µL).  
    • OS: 98-99%—virtually assured survival with modern care.  
    • Relapse: ~3-5%—late if ever (2027-2030), highly treatable (80%+ cure).
  • Why:  
    • Studies (e.g., COG, Borowitz et al.) show ETV6::RUNX1 with MRD <0.01% at induction’s end has near-perfect outcomes—relapse drops below 5%.  
    • Her PAX5 deletion (CG-25-780) doesn’t dent this—secondary, not a driver.


What It Looks Like


  • Now (3/15/25): Induction’s wrapping—marrow tap (3/14/25) confirms remission (blasts <5%, likely near 0%) and MRD <0.01%. She’s tired from the procedure (sedation, soreness), but leukemia symptoms (pain, pallor) are gone.  
  • Consolidation (April-May): Starts ~March 20—weekly IVs, daily 6-MP. She’ll play most days, with short dips (e.g., 5-7 days neutropenia post-methotrexate)—easier than induction’s slog. Hair regrowth begins (fuzz by May).  
  • Ahead: Interim Maintenance 1 (May-July 2025), Delayed Intensification (July-Sept), Maintenance (~Oct 2025-2028)—all coasting on this win.


Daily Life


  • Energy: Post-recovery (late March), she’s a 3-year-old again—running, laughing—chemo’s a background hum.  
  • Risk: Neutropenia in consolidation won’t derail her—her Day 7 rebound (WBC 5,000/µL) and MRD <0.01% say she’ll snap back fast.


Bigger Picture


  • Victory Lap: MRD <0.01% at Day 29 is the green light—induction smashed it, consolidation’s a formality. Her ETV6::RUNX1, TPMT normalcy, and blast clearance (0.00/µL) align for a 95-97% cure chance.  
  • Feel: Consolidation’s easier—less chemo punch, no leukemia fight. She’ll thrive, not just survive, by April-May 2025.

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