April 2025 Content Release Copied
Clinical Profile Documentation
Additions
The Problems > Add Details area is updated with applicable documentation points for the following diagnoses.
Mismatch repair (MMR) status has been updated for Appendix Cancer, Carcinoma, Colon Cancer, Rectal Cancer, Small Intestine Cancer, and Solid Tumors (Parent) (excluding HL/NHL/including Solid Other) w/o CRC/SI/APP with the following documentation points:
- Deficient
- Proficient
- Unknown
Microsatellite instability (MSI) status has been updated for Appendix Cancer, Carcinoma, Colon Cancer, Rectal Cancer, Rectosigmoid Junction Cancer, Small Intestine Cancer, and Solid Tumors (Parent) (excluding HL/NHL/including Solid Other) w/o CRC/SI/APP with the following documentation points:
- High
- Stable
- Low
- Indeterminant
- Unknown
NTRK1/2/3 gene fusion status has been updated for Appendix Cancer, Carcinoma, Colon Cancer, Rectal Cancer, Small Intestine Cancer, and Solid Tumors (Parent) (excluding HL/NHL/including Solid Other) w/o CRC/SI/APP with the following documentation points:
- Positive
- Negative
- Unknown
- Other non-actionable finding
PIK3CA status is now available for documentation for Colon Cancer and Rectal Cancer with the following documentation points:
- Mutation
- Wild type
- Unknown
Lab Analytes & Panels
Additions
- Acetylcholine receptor binding ab
- Ambry DNA + RNA kit panel
- Ambry DNA only kit panel
- Androstenedione, ng/mL
- Antigen(s) to be tested
- burgdorferi ab, serum IA-aCnc
- burgdorferi ab, serum QL IA
- Desmoglein 1 antibody, RU/mL
- Desmoglein 3 antibody, RU/mL
- EBV nuclear Ag IgG, units/mL
- EBV VCA IgG, units/mL
- Factor II, DNA analysis reviewed by
- Factor VIII assay, % normal
- Fanconi’s anemia DNA mutation analysis
- Fanconi’s anemia DNA mutation analysis panel
- Hepatitis B surface antigen confirmation
- Invitae panel DNA + RNA kit panel
- Invitae panel DNA only kit panel
- Measles IgM, qual panel
- Measles IgM, serum
- Measles IgM, serum
- Metanephrines comment
- Metanephrines, urine 24 hr comment
- Mutated citrullinated vimentin (MCV) Ab, U/mL
- Neutrophil gelatinase associated lipocalin (NGAL)
- Neutrophil gelatinase associated lipocalin (NGAL) panel
- NorthStar liquid biopsy kit panel
- Oncodetect MRD, Exact Sciences
- Onkosight advanced NGS myeloid clinical trials 1
- Osmolality, stool, mOsm/kg
- Osmotic gap, stool, mOsm/kg
- Pap smear infection
- PAP smear, SurePath general categorization
- PAP smear, SurePath infection
- PNH Mono, %
- Pre cortisol, ug/dL
- Protein, total w/creat, random urine panel
- RBC band 3 protein reduction
- RBC band 3 protein reduction panel
- RPR interpretation
- SurePath imaging pap and HPV mRNA E6/E7 panel
- Tempus xG DNA + RNA kit panel
- Tempus xG DNA only kit panel
- Tempus xG plus CancerNext expanded + rnainsight panel
- Tempus xG plus CancerNext expanded amendment panel
- Tempus xT PD-L1 28-8 panel
- Tempus xT PD-L1 SP263 panel
- Ventana CLDN18 (43-14A) assay panel
- Ventana pathway HER2 (4B5) panel
- Vitamin K
Medications
Additions
- AU-007 invest IV
- BBO-11818 invest Oral
- CID-078 invest Oral
- HER3-DXd invest IV
- HLX22 invest IV
- HQP1351 invest Oral
- Magic Mouthwash NAHOA (Diphenhydramine/Dexamethasone/Lidocaine)
- Mezagitamab invest (TAK-079 invest Subcutaneous)
- Olverembatinib invest (HQP1351 invest Oral)
- TAK-079 invest Subcutaneous
- VT3989 invest Oral
- WTX-124 invest IV
Updates
| Medications | Updates |
| ABBV-383 invest IV | New Alias available: Etentamig invest |
| ABBV-400 invest IV | New Alias available: Telisotuzumab Adizutecan invest
New Form available:
New Quick Sig Pick available:
New Instructions available: “See Pharmacy Manual for preparation, handling, and administration, observation guidance.” |
| ACE2016 invest IV | New Dose Unit available: mL |
| AK117 invest IV | New Form available: 500 mg/10 mL (50 mg/mL) solution |
| Aldesleukin Subcutaneous | New Quick Sig Pick available:
|
| Capecitabine invest Oral | New Forms available:
New Quick Sig Pick available: 1,000 mg/m2 orally 2 times per day |
| Mirdametinib Oral | New Maximum Single Dose available:
New Sig Options available:
|
| PCS6422 invest Oral | New Form available: 20 mg capsule |
| Rituximab IV | New Instructions available:
“Dilute with NS to a final concentration of 1-4 mg/mL. First Infusion: Administer at an initial rate of 50 mg/hr. If no infusion-related events occur, increase rate by 50 mg/hr increments every 30 minutes to a maximum rate of 400 mg/hr. Subsequent Infusions: Administer at an initial rate of 100 mg/hr. If no infusion-related events occur, increase rate by 100 mg/hr increments every 30 minutes to a maximum rate of 400 mg/hr. If patient tolerates at least one dose at standard infusion rate and meets criteria, may consider rapid infusion in accordance with the Rituximab Rapid Infusion Protocol and/or local standards. NOTE: This is Rituxan.” |
| Rituximab-abbs IV | New Instructions available:
“Dilute with NS to a final concentration of 1-4 mg/mL. First Infusion: Administer at an initial rate of 50 mg/hr. If no infusion-related events occur, increase rate by 50 mg/hr increments every 30 minutes to a maximum rate of 400 mg/hr. Subsequent Infusions: Administer at an initial rate of 100 mg/hr. If no infusion-related events occur, increase rate by 100 mg/hr increments every 30 minutes to a maximum rate of 400 mg/hr. If patient tolerates at least one dose at standard infusion rate and meets criteria, may consider rapid infusion in accordance with the Rituximab Rapid Infusion Protocol and/or local standards. NOTE: This is Truxima.” |
| Rituximab-arrx IV | Updated Instructions:
“Dilute with NS to a final concentration of 1-4 mg/mL. First Infusion: Administer at an initial rate of 50 mg/hr. If no infusion-related events occur, increase rate by 50 mg/hr increments every 30 minutes to a maximum rate of 400 mg/hr. Subsequent Infusions: Administer at an initial rate of 100 mg/hr. If no infusion-related events occur, increase rate by 100 mg/hr increments every 30 minutes to a maximum rate of 400 mg/hr. If patient tolerates at least one dose at standard infusion rate and meets criteria, may consider rapid infusion in accordance with the Rituximab Rapid Infusion Protocol and/or local standards. NOTE: This is Riabni.” |
| Rituximab-pvvr IV | Updated Instructions:
“Dilute with NS to a final concentration of 1-4 mg/mL. First Infusion: Administer at an initial rate of 50 mg/hr. If no infusion-related events occur, increase rate by 50 mg/hr increments every 30 minutes to a maximum rate of 400 mg/hr. Subsequent Infusions: Administer at an initial rate of 100 mg/hr. If no infusion-related events occur, increase rate by 100 mg/hr increments every 30 minutes to a maximum rate of 400 mg/hr. If patient tolerates at least one dose at standard infusion rate and meets criteria, may consider rapid infusion in accordance with the Rituximab Rapid Infusion Protocol and/or local standards. NOTE: This is Ruxience.” |
| RO7198457 invest IV | New Form available:
New Instructions available:
|
| Vimseltinib Dose Pack 14 mg | New Max Single Dose available: 14 mg
New default SIG available:
|
| Vimseltinib Dose Pack 20 mg | New Max Single Dose available: 20 mg
New default SIG available:
|
| Vimseltinib Dose Pack 30 mg | New Max Single Dose available: 30 mg
New default SIG available: 30 mg orally 2 times per week New Quick Sig Pick available: 30 mg orally As Directed |
| Vimseltinib Oral | New Max Single Dose available: 30 mg
New default SIG available: 30 mg orally 2 times per week New Quick Sig Pick available:
|
| ZN-c3 invest Oral | New Alias available: Azenosertib invest
New Form available: 50 mg tablet New Quick Sig Pick available:
|
Regimen Library
Additions
| Regimen Name | Diagnosis |
| Capecitabine D1-14 + Cisplatin + Nivolumab SQ Q21D | Esophageal Cancer (Parent) |
| Capecitabine D1-14 + Oxaliplatin (XELOX/CAPOX) + Nivolumab SQ Q21D | Esophageal Cancer (Parent); Gastric Cancer |
| Gemcitabine + Darcarbazine Q14D | Sarcoma, Soft Tissue (Parent) |
| Intrathecal Topotecan D1,4,8,11 | Brain Tumor (Parent) |
| Intrathecal Topotecan D1,8 (Consolidation) | Brain Tumor (Parent) |
| Isatuximab-irfc IV + Lenalidomide + Bortezomib + Dexamethasone (RVD) Q42D (Induction, non-transplant candidates) | Multiple Myeloma (MM) |
| Mirdametinib D1-21 Q28D | Brain Tumor (Parent) |
| Momelotinib + Darbepoetin alfa Q7D (Myelofibrosis) | Myelofibrosis; Myeloproliferative Disorder |
| Momelotinib + Epoetin alfa Q7D (Myelofibrosis) | Myelofibrosis; Myeloproliferative Disorder |
| Momelotinib + Luspatercept-aamt Q21D (Myelofibrosis) | Myelofibrosis; Myeloproliferative Disorder |
| Nivolumab SQ + Gemcitabine D1,8 + Carboplatin Q21D (Neoadjuvant NSCLC) | Lung Cancer, Non-small Cell (NSCLC) |
| Nivolumab SQ + Gemcitabine D1,8 + Cisplatin Q21D (Neoadjuvant NSCLC) | Lung Cancer, Non-small Cell (NSCLC) |
| Nivolumab SQ + Paclitaxel + Cisplatin Q21D (Neoadjuvant NSCLC) | Lung Cancer, Non-small Cell (NSCLC) |
| Nivolumab SQ D1,15 + Fluorouracil CIV D1-5 + Cisplatin Q28D | Esophageal Cancer (Parent) |
| Nivolumab SQ Q14D (Adjuvant Melanoma, Esophageal, Bladder) | Bladder Cancer; Esophageal Cancer (Parent); Melanoma, Skin; Renal Pelvis and Ureter Cancer; Urethral Cancer |
| Nivolumab SQ Q28D (Perioperative Esophageal, Gastric) | Esophageal Cancer (Parent); Gastric Cancer |
| Obinutuzumab D1 fb Glofitamab-gxbm (Columvi) D8,15 fb D1 Q21D (MCL) | Lymphoma, Non-Hodgkin (NHL) (Parent) |
| Pentamidine IV Q28D Supportive Care | All Malignancies |
| Retifanlimab-dlwr + Paclitaxel D1,8,15 + Carboplatin Q28D fb Retifanlimab-dlwr Q28D | Anal Cancer (Parent) |
Updates
Regimens for the following diagnoses have been updated based on the Collaborative Care Committee voting. Changes include but are not limited to reference update, drug infusion instruction updates, renaming of regimens, premedication template updates and number of cycles.
- All Problems
- Arthritis, Rheumatoid
- Breast Cancer
- Head and Neck Cancer (Parent)
- Hemolytic Uremic Syndrome
- Leukemia, Acute Myeloid (AML)
- Leukemia, Chronic Myelomonocytic (CMML)
- Myasthenia Gravis
- Myelodysplastic Syndrome (MDS)
- Myelofibrosis
- Paroxysmal Nocturnal Hemoglobinuria
Removals
| Regimen Name | Diagnosis |
| Nivolumab + Ipilimumab + Pemetrexed + Cisplatin Q21D | Lung Cancer, Non-small Cell (NSCLC) |
Billing & HCPCS Codes
Updates
| Medication | HCPCS Codes |
| Aminocaproic Acid IV | J0281 per 1000 mg |
| Buprenorphine Subcutaneous ER Solution (Sublocade) | Q9991 per 100 mg |
| Buprenorphine Subcutaneous ER Solution (Sublocade) | Q9992 per 100 mg |
| COVID vaccine (Novavax)-adjuv-matrix (PF) IM (12 yrs & older) (EUA) | 91304 per 0.5 mL |
| Fitusiran Subcutaneous | J3490 per 20 mg |
| Fitusiran Subcutaneous Pen Injector | J3490 per 50 mg |
| Hepatitis B Virus Vaccine (PF) IM | 90740 per 1 mL |
| Hepatitis B Virus Vaccine (PF) Subcutaneous | 90747 per 1 mL |
| Ifosfamide IV | J9208 per 1000 mg |
| Magnesium Sulfate IM | J3475 per 0.5 g |
| Magnesium Sulfate IV | J3475 per 0.5g |
| Proteinase Inhibitor (Human) IV (Glassia) | J0256 per 10 mg |
| Proteinase Inhibitor (Human) IV (Glassia) | J0257 per 10 mg |
| Revakinagene taroretcel-lwey Intravitreal | J3590 per 1 implant |
| Sulfamethoxazole 5 mg and trimethoprim 1 mg | J2865 per 6 mg |
| Ustekinumab-aekn IV | Q9998 per 1 mg |
NDC – HCPCS Crosswalk
Additions
| Medication (Brand) | HCPCS Codes | NDC |
| Hepatitis B Virus Vaccine (PF) IM (Engerix-B) | 90740 | 58160-0821-01 58160-0821-11 58160-0821-43 58160-0821-52 |
| Hepatitis B Virus Vaccine (PF) Subcutaneous (Engerix-B) | 90740 | 58160-0821-01 58160-0821-11 58160-0821-43 58160-0821-52 |
| Hepatitis B Virus Vaccine (PF) IM (Engerix-B) | 90746 | 58160-0821-01 58160-0821-11 58160-0821-43 58160-0821-52 |
| Hepatitis B Virus Vaccine (PF) Subcutaneous (Engerix-B) | 90746 | 58160-0821-01 58160-0821-11 58160-0821-43 58160-0821-52 |
| Hepatitis B Virus Vaccine (PF) IM (Engerix-B) | 90747 | 58160-0821-01 58160-0821-11 58160-0821-43 58160-0821-52 |
| Hepatitis B Virus Vaccine (PF) Subcutaneous (Engerix-B) | 90747 | 58160-0821-01 58160-0821-11 58160-0821-43 58160-0821-52 |
| Hepatitis B Virus Vaccine (PF) IM (Recombivax HB) | 90743 | 00006-4094-01 00006-4094-02 00006-4995-00 00006-4995-01 00006-4995-41 |
| Hepatitis B Virus Vaccine (PF) Subcutaneous (Recombivax HB) | 90743 | 00006-4094-01 00006-4094-02 00006-4995-00 00006-4995-01 00006-4995-41 |
| Hepatitis B Virus Vaccine (PF) IM (Recombivax HB) | 90746 | 00006-4995-00 00006-4995-01 00006-4995-41 |
| Hepatitis B Virus Vaccine (PF) Subcutaneous (Recombivax HB) | 90746 | 00006-4995-00 00006-4995-01 00006-4995-41 |
| Hepatitis B Virus Vaccine (PF) IM (Recombivax HB) | 90740 | 00006-4992-00 00006-4992-01 |
| Hepatitis B Virus Vaccine (PF) Subcutaneous (Recombivax HB) | 90747 | 00006-4992-00 00006-4992-01 |
| Hepatitis B Virus (PF) IM (Recombivax HB) | 90747 | 00006-4992-01 |
| Hepatitis B Virus Vaccine (PF) Subcutaneous (Recombivax HB) |
90747 | 00006-4992-00 00006-4992-01 |
