Fee
| Component | Value |
|---|---|
| Provider fee | $262.40 |
Schedule and sources
- Fee edition
- October 1, 2026
- Record effective
- 2025-04-01
- Schedule edition
- July 22, 2026; effective July 1, 2026
- Official files
- Fee masterSchedule PDFOntario source page
Supervision of chemotherapy for induction phase of acute leukemia or myeloablative therapy prior to bone marrow transplantation (maximum of 1 per induction phase or myeloablative therapy); and/or supervision of biologic agent(s) such as Chimeric Antigen Receptor T-Cell Therapy (CAR-T) infusion (maximum of 1 per infusion); and/or supervision of bispecific antibody infusion, during initial dosing phase, where there is a high risk of cytokine release
Passages mentioning G390
Chemotherapy and patient assessment provided by a physician includes all patient
assessments by any physician for a 24 hour period following treatment administration.
Note:
1.G381, G345 and G359 are only eligible for payment with respect to the following classes of
biologic agents:
a.monoclonal antibodies; and
b.cytokines.
2.G381, G345, G359, G075 and G390 include venipuncture, establishment of any vascular
access line and administration of agent(s).
[Commentary:
Examples that are not considered biologic agents for payment purposes are blood products,
insulin, and immunizing agents.]
+ G381 Standard chemotherapy - agents with minor toxicity that
require physician monitoring, including any additional
standard chemotherapy other than the initial agent ........... 54.50
[Commentary:
Examples of standard chemotherapy agents include cyclophosphamide, methotrexate,
fluorouracil, leucovorin, and zoledronic acid.]
G345 Complex single agent or multi-agent therapy – chemotherapy
and/or biologic agent(s) that can cause vesicant damage,
infusion reactions, cardiac, neurologic, marrow or renal
toxicities that may require immediate intervention by the
physician ............................................................................ 75.00
[Commentary:
Examples of complex single agents include rituxamib, bevacizumab, trastuzumab,
anthracyclines, bortezomib, taxanes, cisplatin, and etoposide fludarabine.]
G359 Special single agent or multi-agent therapy – chemotherapy
and/or biologic agent(s) with major toxicity that require
frequent monitoring and prolonged administration periods
and may require immediate intervention by the physician . 105.15
[Commentary:
Examples of special agent therapy include high-dose methotrexate with folinic acid rescue,
methotrexate given in a dose of greater than 1 g/m2, high dose cisplatin greater than 75 mg/m2
given concurrently with hydration and osmotic diuresis, high dose cystosine, arabinoside
(greater than 2 g/m2), high dose cyclophosphamide (greater than 1 g/m2), ifosfamide with
MESNA protection, combination of biologic agents with complex chemotherapy, bispecific
antibody.]G390 Supervision of chemotherapy for induction phase of acute
leukemia or myeloablative therapy prior to bone marrow
transplantation (maximum of 1 per induction phase or
myeloablative therapy); and/or supervision of biologic
agent(s) such as Chimeric Antigen Receptor T-Cell Therapy
(CAR-T) infusion (maximum of 1 per infusion); and/or
supervision of bispecific antibody infusion, during initial
dosing phase, where there is a high risk of cytokine release
syndrome (maximum of 3 per initial dosing phase)............ 262.40Fee master record
Master, record 2101. Record Layout PDF, page 1.
G39020250401999999990000262400000000000000000000000000000000000000000000000
Auxiliary master fields are preserved as raw scaled values. The linked layout calls them zero-filled, but this edition contains non-zero values. They are not presented as final dollar fees or PDF units.
| Field | Raw / scale 10,000 |
|---|---|
| provider | 00002624000 / 262.4 |
| assistant | 00000000000 / 0 |
| specialist | 00000000000 / 0 |
| anaesthetist | 00000000000 / 0 |
| non anaesthetist | 00000000000 / 0 |
Explanation
AI-generated. Unreviewed.
This is physician supervision of certain high-risk treatments, including induction chemotherapy for acute leukemia or myeloablative therapy before bone marrow transplantation, CAR-T cell infusion, and bispecific antibody infusion during initial dosing where there is a high risk of cytokine release.
Watch out for
Maximum of 1 per induction phase or myeloablative therapy, 1 per CAR-T infusion, and 1 per bispecific antibody infusion, as the source states.
Report an issue
Something off?
Report an issue with G390. Do not include patient names, health details or other personal information.