The present data provides an overview of the number of people dispensed at least one specified systemic anti-cancer therapy agent in Australia in any year from 2012 to 2016. The dataset consists of PBS and RPBS prescriptions prescribed from 1 January 2012 to 31 December 2016 (and processed on or before 31 July 2017). The data was extracted for selected drugs (Health Cancer Definition by ATC1) at the national level.
Unique patients are counted at the national level by calendar year. Patient postcode, patient gender and age are based on the first script supplied within each calendar year for each patient.
The postcode of the patient’s residential address at the time of the first dispensing of the relevant year was used to determine the relevant indices of remoteness and socioeconomic disadvantage. More information about the Index of Relative Socioeconomic Disadvantage used for this analysis can be found here: ABS - Socio-Economic Indexes for Areas (SEIFA), Australia, 2011.
Unit of analysis:
The number of people who were dispensed systemic anti-cancer related therapeutic items (as defined in Table 1 below) in a given individual year and for whom a reimbursement claim was processed under the Australian Government’s Pharmaceutical Benefits Scheme (PBS).
For brevity and ease of reading throughout the text, this unit of measure has been abbreviated to the term “people who used these therapies”.
To provide context of the use of these therapies within the Australian population, the number of people who accessed these therapies, were adjusted for the increase in population over the time period. Data are expressed as the number of people who accessed these therapies per 100,000 population for the relevant year (Estimated Resident Population data are sourced from the Australian Bureau of statistics). Crude rates were calculated by dividing the number of people accessing these therapies by the resident Australian population and multiplying by 100,000.
Scope:
Items related to systemic anti-cancer therapy treatment agents were selected as defined using the Anatomical Therapeutic Chemical (ATC) code information including anatomical main group, therapeutic and pharmacological subgroups and the actual chemical substance.
Relevant systemic anti-cancer therapy treatment subgroup items include selected: anti-neoplastic agents (including traditional chemotherapy drugs, and newer “targeted therapies” agents, category L01); endocrine (hormonal) therapy agents (L02); and immunomodulating agents that directly target the functioning of the immune system (including a small number of immunosuppressants and immunostimulants) from categories L03 and L04. Items are also included for a small number of supportive treatments (which treat the side-effects of the therapeutic agent). A list of the selected items is provided in Table 1.
A confirmatory check of the list of therapeutic drugs identified using the ATC code classification approach, was undertaken by comparing the selected list of drugs with those used in the current chemotherapy protocols indicated in the eviQ Cancer Treatments Online database2.
Data sources:
The data were obtained from the Pharmaceutical Benefits Scheme (PBS) and Repatriation Pharmaceutical Benefits Schedule (RPBS) prescriptions database, managed by the Australian Government Department of Health.
To estimate activity for this measure, data have been included only for the therapeutic agents prescribed and reimbursed from the PBS. To avoid duplication of counting of the number of people receiving systemic therapy, data does not include information regarding the procedures for delivery of these therapies (e.g. as included through the MBS or NHMD databases). For context, previously published data for admitted patients in 2014–15, showed 440,561 pharmacotherapy (systemic therapy) hospitalisations for delivery of these treatments (this does not include systemic therapy provided to non-admitted patients in public hospitals)3.
More information on the data sources can be found at: https://www.pbs.gov.au/info/browse/statistics.
Data caveats:
The PBS listing of therapeutic agents is updated monthly, with new items listed and other items delisted on an ongoing basis.
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The time-period for the data presented aligns with the introduction of The Revised Arrangements for the Efficient Funding of Chemotherapy Drugs3 (EFC) for injectable and infusible chemotherapy medicines used in the treatment of cancer was introduced in December 2011.
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As an individual may also be receiving systemic therapy in a year subsequent to their diagnosis, the data may count the same individual in subsequent years if still being prescribed relevant treatments. As such, the data outlining the number of people accessing these therapies may be ‘semi-cumulative’. In addition, the inclusions list (see below) includes drugs introduced onto the PBS after 2012 as well as drugs that have been delisted during the overall time period.
Data have been generated outlining the number of people to whom the therapeutic agent has been dispensed and reimbursement processed under the PBS and RPBS. Data for under co-payment prescriptions was unavailable prior to 1 April 2012.
The data are not able to measure:
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Current systemic therapy agents that have been approved by the Therapeutic Goods Administration (TGA) but are not yet listed on the PBS Schedules;
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PBS listed medicines that fall below the general beneficiary co-payment prior to April 2012;
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Data for under co-payment prescriptions was unavailable prior to 1 April 2012.
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Treatment received under clinical trials where the cost of the therapeutic agent is not reimbursed under the PBS Scheme.
Modes of delivery include infusion/ injection as well as oral delivery. Data captured is not able to measure whether or not therapies have been administered.
Inclusions:
Inclusions for the listing of therapeutic agents are provided in Table 1.
Exclusions:
The scope of the therapeutic agents is defined by the ATC Classification to be generally limited to cancer-related treatment items, but with the following exclusions applying:
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For a cancer-related treatment specified drug (as defined by ATC code), if there is also application for use of the drug for treatment of disease(s) other than cancer under the PBS Schedule (as indicated by a specific PBS item number descriptor), data for the individual non-cancer related PBS items are excluded from the total person count.
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Due to the limited application in cancer treatment of (i) low dose oral methotrexate and (ii) injectable methotrexate items not listed on the EFC schedule, data for these PBS item numbers have been excluded from the total person count.
Table 1: Therapeutic agent inclusions
Therapeutic agent & ATC code – Antineoplastic (L01)
|
Arsenic (trioxide)
|
L01XX27
|
Epirubicin
|
L01DB03
|
Ofatumumab
|
L01XC10
|
Axitinib
|
L01XE17
|
Eribulin
|
L01XX41
|
Oxaliplatin
|
L01XA03
|
Azacitidine
|
L01BC07
|
Erlotinib
|
L01XE03
|
Paclitaxel
|
L01CD01
|
Bendamustine
|
L01AA09
|
Etoposide
|
L01CB01
|
Paclitaxel Nanoparticle Albumin Bound
|
L01CD01
|
Bevacizumab
|
L01XC07
|
Everolimus
|
L01XE10
|
Panitumumab
|
L01XC08
|
Bleomycin Sulfate
|
L01DC01
|
Fludarabine
|
L01BB05
|
Pazopanib
|
L01XE11
|
Bortezomib
|
L01XX32
|
Fluorouracil
|
L01BC02
|
Pembrolizumab
|
L01XC18
|
Brentuximab Vedotin
|
L01XC12
|
Fotemustine
|
L01AD05
|
Pemetrexed
|
L01BA03
|
Busulfan
|
L01AB01
|
Gefitinib
|
L01XE02
|
Pertuzumab
|
L01XC13
|
Cabazitaxel
|
L01CD04
|
Gemcitabine
|
L01BC05
|
Ponatinib
|
L01XE24
|
Capecitabine
|
L01BC06
|
Hydroxyurea
|
L01XX05
|
Raltitrexed
|
L01XC02
|
Carboplatin
|
L01XA02
|
Idarubicin
|
L01DB06
|
Rituximab
|
L01XE05
|
Carmustine
|
L01AD01
|
Ifosfamide
|
L01AA06
|
Ruxolitinib
|
L01XE18
|
Cetuximab
|
L01XC06
|
Imatinib
|
L01XE01
|
Sorafenib
|
L01XE05
|
Chlorambucil
|
L01AA02
|
Ipilimumab
|
L01XC11
|
Sunitinib
|
L01XE04
|
Cisplatin
|
L01XA01
|
Irinotecan
|
L01XX19
|
Temozolomide
|
L01AX03
|
Cladribine
|
L01BB04
|
Lapatinib
|
L01XE07
|
Thioguanine
|
LO1XXX
|
Crizotinib
|
L01XE16
|
Lenvatinib
|
L01XE29
|
Thiotepa
|
L01XX17
|
Cyclophosphamide
|
L01AA01
|
Melphalan
|
L01AA03
|
Topotecan
|
L01XX17
|
Cytarabine
|
L01BC01
|
Mercaptopurine
|
L01BB02
|
Trametinib
|
L01XE25
|
Dabrafenib
|
L01XE23
|
Methotrexate
|
L01BA01
|
Trastuzumab
|
L01XC03
|
Dasatinib
|
L01XE06
|
Mitozantrone
|
L01DB07
|
Trastuzumab Emtansine
|
L01XC14
|
Docetaxel
|
L01CD02
|
Nilotinib
|
L01XE08
|
Vinblastine
|
L01CA01
|
Doxorubicin
|
L01DB01
|
Nivolumab
|
L01XC17
|
Vincristine
|
L01CA02
|
Doxorubicin Hydrochloride-Pegylated Liposomal
|
L01DB01
|
Obinutuzumab
|
L01XC15
|
Vinorelbine
|
L01CA04
|
Table 1 continued: Therapeutic Agent Inclusions
Therapeutic agent & ATC code
|
Endocrine therapies (ATC Category - L02)
|
Abiraterone
|
L02BX03
|
Letrozole
|
L02BG04
|
Anastrozole
|
L02BG03
|
Leuprorelin
|
L02AE02
|
Bicalutamide
|
L02BB03
|
Medroxyprogesterone
|
L02AB02
|
Degarelix
|
L02BX02
|
Megestrol
|
L02AB01
|
Enzalutamide
|
L02BB04
|
Nilutamide
|
L02BB02
|
Exemestane
|
L02BG06
|
Tamoxifen
|
L02BA01
|
Flutamide
|
L02BB01
|
Toremifene
|
L02BA02
|
Goserelin
|
L02AE03
|
Triptorelin
|
L02AE04
|
Goserelin (&) Bicalutamide
|
L02AE03/ L02BB03
|
Immunostimulants (ATC Category - L03)/ Immunosuppressants (ATC Category - L04) /
Sex hormones & modulators of the genital system (ATC Category – G03)
|
Bacillus Calmette and Guerin-Connaught strain
|
L03AX03
|
Lenalidomide
|
L04AX04
|
Bacillus Calmette and Guerin-Tice strain
|
L03AX03
|
Thalidomide
|
L04AX02
|
Interferon Alfa-2A
|
L03AB04
|
Pomalidomide
|
L04AX06
|
Interferon Alfa-2B
|
L03AB05
|
Cyproterone
|
G03HA01
|
Treatment of bone related malignancies and/ or myeloma - including anti-osteoporotics
|
- Hypercalcaemia of malignancy – Clodronate and Pamidronate Disodium;
- Giant cell tumour of bone and bone metastases - Denosumab
- Multiple Myeloma and bone metastases - Zoledronic acid
|
Supportive therapeutic agents
|
Chemotherapy-induced neutropenia and/ or mobilisation of (haematopoietic) stem cells: Lenograstim; Lipegfilgrastim; Pegfilgrastim; Filgrastim and Plerixafor.
|