Tecartus (brexucabtagene autoleucel) — HCPCS Q2053

CareCost Estimate · CAR-T Billing Cheat Sheet
Kite Pharma (a Gilead company) Autologous anti-CD19 CAR-T (CD28 costim) + T-cell enrichment · Single IV infusion FACT-accredited center only First CAR-T in MCL (July 24, 2020, ZUMA-2) Reviewed: May 22, 2026 ASP: Q2 2026
GATE: FACT (or FACT-JACIE) accreditation + TECARTUS REMS certification (Kite, separate from Yescarta REMS) + indication gate: MCL = documented BTKi failure; adult B-ALL = age ≥18 + CD19+ B-precursor pathology. Missing any one = #1 cause of CAR-T claim denial.

The 5-stage Tecartus CAR-T workflow

  1. ApheresisCPT 38206 / 0540T
    FACT center
  2. Manufacture~16-19 days
    T-cell enrichment
  3. LymphodepleteMCL: Flu 30 + Cy 500 (d -5 to -3)
    ALL: Flu 25 + Cy 900 (d -4 to -2)
  4. CAR-T infusionQ2053 + 0537T-0541T
    MS-DRG 018
  5. CRS / ICANSTocilizumab J3262
    Monitor / readmit
HCPCS
Q2053
1 unit = 1 therapeutic dose
Route
Single IV
MCL 2 x 10^6/kg; ALL 1 x 10^6/kg
Inpatient DRG
018
CAR-T Immunotherapy
Admin CPTs
0537T-0541T
Cat III CAR-T set
Q2 2026 ASP+6%
$489,290.601
per single dose

Codes & NDC

HCPCSQ2053 — "Brexucabtagene autoleucel, up to 200M autologous anti-CD19 CAR+ viable T cells, incl leukapheresis + dose prep, per therapeutic dose"
NDC71287-129-XX Kite labeler 71287 + product suffix 129; patient-specific lot suffix from chain-of-identity label
ICD-10-PCSXW033C3 peripheral / XW043C3 central (common in B-ALL) — drives MS-DRG 018
IndicationsR/R MCL post-BTKi (ZUMA-2); Adult R/R B-precursor ALL (ZUMA-3, age ≥18)
BenefitMedical (hospital buy-and-bill); REMS-restricted

The 4-claim cadence

ClaimStageCodes
AApheresis38206 or 0540T + 6A550Z2 (inpt)
BLymphodepletionJ9185 + J9070 + 96413/96415 (dose differs by indication)
CCAR-T infusionQ2053 + 0537T-0541T + XW033C3/XW043C3
DCRS readmit (if)Principal manifestation DRG + D89.83x + G92.0x
Encounter spans 4-6 weeks across 3-4 distinct claims. Vein-to-vein ~16-19 days (longer than Yescarta due to T-cell enrichment step). Document chain of identity on every claim file.

TECARTUS REMS & FACT — required

Closed distribution. All three layers must be in place before any apheresis:

  • Facility on Kite Tecartus Treatment Center list (FACT or FACT-JACIE + CRS/ICANS capability + tocilizumab on hand)
  • Prescriber completed TECARTUS REMS training + enrolled
  • Pharmacy / cell lab verifies prescriber + facility cert before accepting cellular product
Common error: Yescarta certification does NOT auto-extend to Tecartus. Each Kite product has a separate REMS certification cycle. Verify Tecartus-specific Kite cert before scheduling Stage 1.

CD19 CAR-T disambiguation

BrandHCPCSPrimary indication
Tecartus (brexu-cel)Q2053R/R MCL post-BTKi, adult R/R B-ALL
Yescarta (axi-cel)Q2041R/R LBCL 2L+/3L+, R/R FL
Kymriah (tisa-cel)Q2042Peds/young adult ALL (≤25), R/R DLBCL/FL
Breyanzi (liso-cel)Q2054R/R LBCL, CLL, FL, MCL
Q2053 vs Q2041 is the highest-frequency Kite confusion pair — both labeler 71287. Disambiguate by carton suffix: Tecartus 71287-129-XX vs Yescarta 71287-119-XX. Verify against chain-of-identity label.

ICD-10 — by indication

CodeFor
C83.10-C83.19Mantle cell lymphoma (site-stratified)
C91.00B-cell ALL, not in remission
C91.02B-cell ALL, in relapse
Chart narrativeBTKi exposure (MCL) / age ≥18 + CD19+ flow (ALL)
D89.831-D89.835CRS by grade (G1-G5)
G92.0xICANS
Z94.81BMT status (post-HSCT cases)

Site of care & payment

StageSetting / POSPayment
Stage 1 ApheresisHOPD (22) or office (11) at FACT centerOPPS APC or MPFS
Stage 3 LymphoHOPD (22) or office (11)APC + J-codes
Stage 4 CAR-T (MCL)Inpatient (21) or outpt (22)MS-DRG 018 or APC 9248
Stage 4 CAR-T (B-ALL)Inpatient (21) — near-universalMS-DRG 018 bundled
Stage 5 CRS readmitInpatient (21)DRG by manifestation
MS-DRG 016 ≠ 018. 016 = autologous BMT; 018 = CAR-T Immunotherapy. Confirm XW033C3/XW043C3 in current-FY grouper. B-ALL: inpatient by default regardless of payer outpatient policy (high CRS Grade 3+ ~26% in ZUMA-3).

Medicare & NTAP (FY 2026)

FieldValue
Q2053 ASP+6%$489,290.601 / single dose (Q2 2026)
MS-DRG 018Dedicated CAR-T Immunotherapy DRG (since FY 2021)
NTAPExpired for Tecartus after FY 2023; 2021 B-ALL approval did not trigger new NTAP
Outpatient APCAPC 9248 historically; verify current OPPS Addendum B
NCDNCD 110.24 (CAR-T) — covers both MCL + adult B-ALL

Top denials — Tecartus-specific

#Reason
1Non-FACT / non-Tecartus-REMS-certified center (Yescarta cert does not extend)
2BTKi failure not documented (MCL ZUMA-2 gate)
3Age + CD19+ not documented (adult B-ALL ZUMA-3 gate)
4Prior therapy lines not satisfied
5Wrong REMS letter (Yescarta REMS on a Tecartus claim)
6Lymphodepletion regimen wrong for indication (MCL dose on ALL or vice versa)
7CRS / ICANS not coded properly (especially in high-CRS B-ALL)
8Wrong Q-code (Q2053 vs Q2041 — both Kite labeler 71287)
9Wrong DRG (016 vs 018)
10Outpatient pathway rejected for B-ALL

Patient assistance — Kite Konnect

  • Kite Konnect — benefits, PA, appeal, case mgmt; copay (commercial). Same hub as Yescarta.
  • Gilead Advancing Access — free product for eligible uninsured / underinsured
  • Foundations: PAN, HealthWell, LLS Co-Pay (open MCL + ALL funds quarterly)
  • Travel grants available for patients >50-100 mi from FACT center; LLS travel grants for ALL
BOXED WARNING — CRS & ICANS: Tecartus shares Yescarta's CD28 high-CRS profile. MCL (ZUMA-2): ~91% any-grade, ~15% Grade 3+. B-ALL (ZUMA-3): ~89% any-grade, ~26% Grade 3+ — highest in CD19 class, driven by high circulating tumor burden. Tocilizumab (J3262) on hand mandatory; ICU backup required.
Sources: FDA Tecartus label (BLA 125703, MCL 7/24/2020; B-ALL 10/1/2021), CMS Q2 2026 ASP, FY 2026 IPPS Final Rule (MS-DRG 018 + NTAP), CY 2026 OPPS Final Rule, NCD 110.24, FACT standards, ZUMA-2 (Wang NEJM 2020) / ZUMA-3 (Shah Lancet 2021), Kite Konnect, Gilead Advancing Access. carecostestimate.com/drugs/tecartus