Medicare Benefits Schedule - Note PN.7.19

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Category 6 - PATHOLOGY SERVICES

PN.7.19

Practice note for item 73307

PBS restrictions for PARP inhibitors for a patient with homologous recombination deficiency (HRD) may include:

HRD positivity is considered to be a score of 42 or greater using the Myriad MyChoice HRD assay or a validated equivalent.

Related Items: 73307


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Category 6 - PATHOLOGY SERVICES

73307

73307 - Additional Information

Item Start Date:
01-Jan-2024
Description Updated:
01-Jan-2024
Schedule Fee Updated:
01-Jan-2024

A test of tumour tissue from a patient with advanced (FIGO III-IV), high-grade serous or other high-grade ovarian, fallopian tube or primary peritoneal carcinoma, requested by a specialist or consultant physician, if the test is:

(a)    to determine eligibility with respect to homologous recombination deficiency (HRD) status, including BRCA1 or BRCA2 status, to provide access to poly (adenosine diphosphate [ADP]-ribose) polymerase (PARP) inhibitor therapy under the Pharmaceutical Benefits Scheme; and

(b)    including a service described in item 73301

Applicable once per primary tumour diagnosis

Fee: $3,000.00 Benefit: 75% = $2,250.00 85% = $2,895.50

(See para PN.7.19 of explanatory notes to this Category)


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  • Assist - Addition/Deletion of (Assist.)
  • Amend - Amended Description
  • Anaes - Anaesthetic Values Amended
  • Emsn - EMSN Change
  • Fee - Fee Amended
  • Renum - Item Number Change (renumbered)
  • New - New Item
  • NewMin - New Item (previous Ministerial Determination)
  • Qfe - QFE Change