Yescarta (axicabtagene ciloleucel) — HCPCS Q2041

CareCost Estimate · CAR-T Billing Cheat Sheet
Kite Pharma (a Gilead company) Autologous anti-CD19 CAR-T (CD28 costim) · Single IV infusion FACT-accredited center only First 2L CAR-T (April 1, 2022, ZUMA-7) Reviewed: May 22, 2026 ASP: Q2 2026
GATE: FACT (or FACT-JACIE) accreditation + YESCARTA REMS certification (Kite) + prior therapy lines documented per indication + for 2L: explicit "primary refractory" or "≤12-mo relapse" timing. Missing any one = #1 cause of CAR-T claim denial.

The 5-stage Yescarta CAR-T workflow

  1. ApheresisCPT 38206 / 0540T
    FACT center
  2. Manufacture~14-17 days
    (fastest in class)
  3. LymphodepleteFlu J9185 30 mg/m^2 x3
    + Cy J9070 500 mg/m^2 x3
  4. CAR-T infusionQ2041 + 0537T-0541T
    MS-DRG 018
  5. CRS / ICANSTocilizumab J3262
    Monitor / readmit
HCPCS
Q2041
1 unit = 1 therapeutic dose
Route
Single IV
2 x 10^6 CAR+/kg, max 2 x 10^8
Inpatient DRG
018
CAR-T Immunotherapy
Admin CPTs
0537T-0541T
Cat III CAR-T set
Q2 2026 ASP+6%
$531,849.118
per single dose

Codes & NDC

HCPCSQ2041 — "Axicabtagene ciloleucel, up to 200M autologous anti-CD19 CAR+ viable T cells, incl leukapheresis + dose prep, per therapeutic dose"
NDC71287-119-XX Kite labeler 71287; patient-specific lot suffix from chain-of-identity label
ICD-10-PCSXW033C3 peripheral / XW043C3 central — drives MS-DRG 018
IndicationsR/R LBCL 3L+ (ZUMA-1), R/R FL 2L+ (ZUMA-5), R/R LBCL 2L (ZUMA-7)
BenefitMedical (hospital buy-and-bill); REMS-restricted

The 4-claim cadence

ClaimStageCodes
AApheresis38206 or 0540T + 6A550Z2 (inpt)
BLymphodepletionJ9185 + J9070 + 96413/96415
CCAR-T infusionQ2041 + 0537T-0541T + XW033C3
DCRS readmit (if)Principal manifestation DRG + D89.83x + G92.0x
Encounter spans 4-6 weeks across 3-4 distinct claims. Document chain of identity (apheresis date → ship → manufacture → return → infuse) on every claim file. Yescarta vein-to-vein is ~14-17 days (faster than Kymriah).

YESCARTA REMS & FACT — required

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

  • Facility on Kite Yescarta Treatment Center list (FACT or FACT-JACIE accredited + CRS/ICANS capability + tocilizumab on hand)
  • Prescriber completed YESCARTA REMS training + enrolled
  • Pharmacy / cell lab verifies prescriber + facility cert before accepting cellular product
Common error: apheresing at a FACT-accredited but non-Yescarta-certified center (e.g., Kymriah-only-certified). Each manufacturer's REMS is separately administered — Kite confirmation required before release.

CD19 CAR-T disambiguation

BrandHCPCSPrimary indication
Yescarta (axi-cel)Q2041R/R LBCL 2L+ / 3L+, R/R FL
Kymriah (tisa-cel)Q2042Peds ALL, R/R DLBCL/FL
Tecartus (brexu-cel)Q2053R/R MCL, adult B-ALL
Breyanzi (liso-cel)Q2054R/R LBCL, CLL, FL, MCL
Verify Q-code against the chain-of-identity label. Q2041/Q2042 (Yescarta/Kymriah) is the most common wrong-Q confusion pair. Kite labeler 71287 vs Novartis labeler 0078.

ICD-10 — by indication

CodeFor
C83.30-C83.39DLBCL (site-stratified)
C85.20-C85.29Primary mediastinal LBCL (PMBCL)
C82.0x-C82.2xFL grades 1-3a (ZUMA-5)
C83.3x + C82.xTransformed FL to DLBCL
D89.831-D89.835CRS by grade (G1-G5)
G92.0xICANS
Z94.81Bone marrow transplant 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 (primary)Inpatient FACT center (POS 21)MS-DRG 018 bundled
Stage 4 CAR-T (outpt)HOPD cellular therapy (22)OPPS APC 9248 + Q2041 line-item
Stage 5 CRS readmitInpatient (21)DRG by manifestation
MS-DRG 016 ≠ 018. 016 = autologous BMT; 018 = CAR-T Immunotherapy. Confirm XW033C3/XW043C3 PCS code drives 018 in current-FY grouper. Note: many payers default outpatient pathway to Kymriah/Breyanzi over Yescarta due to CRS profile.

Medicare & NTAP (FY 2026)

FieldValue
Q2041 ASP+6%$531,849.118 / single dose (Q2 2026)
MS-DRG 018Dedicated CAR-T Immunotherapy DRG (since FY 2021)
NTAPExpired for Yescarta after FY 2021; 2L ZUMA-7 approval did not trigger new NTAP
Outpatient APCAPC 9248 historically; verify current OPPS Addendum B
NCDNCD 110.24 (CAR-T) — CED sunset 2022, standard coverage incl. 2L

Top denials — Yescarta-specific

#Reason
1Non-FACT / non-Yescarta-REMS-certified center
22L timing not documented (ZUMA-7: "primary refractory" or "≤12-mo relapse")
3Prior therapy lines not satisfied (3L+ cases)
4REMS enrollment missing
5Apheresis-to-infusion timeline not documented
6Lymphodepletion missing or wrong agents
7CRS / ICANS not coded properly
8Wrong Q-code (Q2041 vs Q2042)
9Wrong DRG (016 vs 018)

Patient assistance — Kite Konnect

  • Kite Konnect — benefits, PA, appeal support, case-management; copay (commercial)
  • Gilead Advancing Access — free product for eligible uninsured / underinsured
  • Medicare foundations: PAN, HealthWell, CancerCare — verify open DLBCL/LBCL / FL funds quarterly
  • Travel grants available for patients >50-100 mi from FACT center
BOXED WARNING — CRS & ICANS: Yescarta has the highest CRS Grade 3+ rate (~13-25%) in the CD19 CAR-T class (CD28 costim drives faster, more potent expansion). ICANS 28-65% any-grade. Tocilizumab (J3262) on hand mandatory. ICU backup required at all FACT centers.
Sources: FDA Yescarta label (BLA 125643, original approval 10/18/2017; 2L approval 4/1/2022), CMS Q2 2026 ASP, FY 2026 IPPS Final Rule (MS-DRG 018 + NTAP), CY 2026 OPPS Final Rule, NCD 110.24, FACT standards, ZUMA-1 / ZUMA-5 / ZUMA-7 trials, Kite Konnect, Gilead Advancing Access. carecostestimate.com/drugs/yescarta