Formulary Chapter 8: Malignant disease and immunosuppression - Full Chapter
|
Notes: |
Unless explicitly stated, any brand names included in brackets next to a drug's generic name are there solely to aid searching and identification, and should not be considered to limit use to that specific brand. |
|
Chapter Links... |
Haematology and Oncology Protocols and Guidelines |
DSU: Medicines with teratogenic potential: what is effective contraception and how often is pregnancy testing needed? (March 2019) |
Details... |
08.01.05 |
Other antineoplastic drugs |
|
|
|
08.01.05 |
Amsacrine |
|
|
08.01.05 |
Arsenic trioxide |
|
|
08.01.05 |
Bevacizumab |
|
|
08.01.05 |
Bexarotene |
|
|
08.01.05 |
Bortezomib |
|
|
08.01.05 |
Cetuximab |
|
|
08.01.05 |
Crisantaspase |
|
|
08.01.05 |
Dacarbazine and Temozolomide |
|
|
08.01.05 |
Hydroxycarbamide |
|
|
08.01.05 |
Ipilimumab |
|
|
08.01.05 |
Mitotane |
|
|
08.01.05 |
Panitumumab |
|
|
08.01.05 |
Pentostatin |
|
|
08.01.05 |
Platinum compounds |
|
|
08.01.05 |
Porfimer sodium and temoporfin |
|
|
08.01.05 |
Procarbazine |
|
|
08.01.05 |
Protein kinase inhibitors |
|
|
Abemaciclib tablets (Verzenios® )
|
Restricted
|
- Abemaciclib tablets (Verzenios®)
Consultant Oncologist use only.
Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
NICE TA563: Abemaciclib with an aromatase inhibitor for previously untreated, hormone receptor-positive, HER2-negative, locally advanced or metastatic breast cancer (February 2019)
NICE TA579: Abemaciclib with fulvestrant for treating hormone receptor-positive, HER2-negative advanced breast cancer after endocrine therapy (May 2019)
NICE TA579: Abemaciclib with fulvestrant for treating hormone receptor-positive, HER2-negative advanced breast cancer after endocrine therapy (May 2019)
|
Afatinib (Giotrif®)
|
Restricted
|
- Afatinib Tablets (Giotrif®)
|
NICE TA310: Afatinib for treating epidermal growth factor receptor mutation-positive locally advanced or metastatic non-small-cell lung cancer (April 2014)
|
Alectinib capsules (Alecensa®)
|
Restricted
|
- Alectinib Capsules (Alecensa®)
Consultant Medical Oncologist use only. Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
NICE TA536: Alectinib for untreated ALK-positive advanced non-small-cell lung cancer (August 2018)
|
Bosutinib (Bosulif®)
|
Restricted

|
- Bosutinib Tablets
Consultant Haematologist use only.
Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
MHRA Drug Safety Update: BCR-ABL tyrosine kinase inhibitors: risk of hepatitis B reactivation(May 2016)
NICE TA401: Bosutinib for previously treated chronic myeloid leukaemia (August 2016)
|
Brigatinib tablets (Alunbrig®)
|
Restricted
|
- Brigatinib tablets (Alunbrig®)
Consultant Medical Oncologist use only. Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
NICE TA571:Brigatinib for treating ALK-positive advanced non-small-cell lung cancer after crizotinib (March 2019)
|
Ceritinib capsules (Zykadia®)
|
Restricted
|
- Ceritinib Capsules (Zykadia®)
Consultant Medical Oncologist use only. Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
NICE TA395: Ceritinib for previously treated anaplastic lymphoma kinase positive non-small-cell lung cancer (June 2016)
NICE TA500: Ceritinib for untreated ALK-positive non-small-cell lung cancer (January 2018)
|
Dacomitinib (Vizimpro®)
|
Restricted
|
Consultant Oncology use only
Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
NICE TA595: Dacomitinib for untreated EGFR mutation-positive non-small-cell lung cancer (August 2019)
|
Erlotinib
|
Restricted
|
|
NICE TA227: Erlotinib monotherapy for maintenance treatment of non-small-cell lung cancer [Not recommended] (June 2011)
NICE TA258: Erlotinib for the first-line treatment of locally advanced or metastatic EGFR-TK mutation-positive non-small-cell lung cancer (June 2012)
NICE TA374: Erlotinib and gefitinib for treating non-small-cell lung cancer that has progressed after prior chemotherapy (December 2015)
|
Everolimus (Afinitor®)
|
Restricted
|
- Everolimus Tablets (Afinitor®)
Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
NICE TA 449: Everolimus and sunitinib for treating unresectable or metastatic neuroendocrine tumours in people with progressive disease (June 2017) [Specialist Centre Only]
NICE TA219: Everolimus for the second-line treatment of advanced renal cell carcinoma (April 2011) NOT RECOMMENDED [Specialist Centre Only]
NICE TA348: Everolimus for preventing organ rejection in liver transplantation (July 2015)
NICE TA421: Everolimus with exemestane for treating advanced breast cancer after endocrine therapy (December 2016)
NICE TA432: Everolimus for advanced renal cell carcinoma after previous treatment (Feb 2017) [Specialist Centre Only]
NICE TA498: Lenvatinib with everolimus for previously treated advanced renal cell carcinoma (January 2018) [Specialist Centre Only]
|
Gefitinib
|
Restricted
|
|
NICE TA192: Gefitinib for the first-line treatment of locally advanced or metastatic non-small-cell lung cancer (July 2010)
NICE TA374: Erlotinib and gefitinib for treating non-small-cell lung cancer that has progressed after prior chemotherapy (December 2015)
|
Idelalisib (Zydelig®)
|
Restricted
|
|
EMA recommends new safety measures for Zydelig (March 2016)
MHRA Drug Safety Update: Idelalisib (Zydelig): updated indications and advice on minimising the risk of infection (September 2016)
NICE TA359 Idelalisib for treating chronic lymphocytic leukaemia (October 2015)
NICE TA604: Idelalisib for treating refractory follicular lymphoma (October 2019)
|
Imatinib
|
Restricted
|
|
MHRA Drug Safety Update: BCR-ABL tyrosine kinase inhibitors: risk of hepatitis B reactivation (May 2016)
NICE TA209: Imatinib for the treatment of unresectable and/or metastatic gastrointestinal stromal tumours (November 2010)
NICE TA425: Dasatinib, nilotinib and high-dose imatinib for treating imatinib-resistant or intolerant chronic myeloid leukaemia (December 2016)
NICE TA426: Dasatinib, nilotinib and imatinib for untreated chronic myeloid leukaemia (December 2016)
NICE TA70: Guidance on the use of imatinib for chronic myeloid leukaemia (January 2016)
NICE TA86: Imatinib for the treatment of unresectable and/or metastatic gastro-intestinal stromal tumours (November 2010)
|
Larotrectinib 20mg/mL oral solution (Vitrakvi®)
|
Restricted

|
|
NICE TA630: Larotrectinib for treating NTRK fusion-positive solid tumours (May 2020)
|
Lorlatinib (Lorviqua®)
|
Restricted

|
- Lorlatinib Tablets (Lorviqua®)
Consultant Medical Oncologist use only.
Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
NICE TA628: Lorlatinib for previously treated ALK-positive advanced non-small-cell lung cancer (May 2020)
|
Nilotinib (Tasigna®)
|
Restricted
|
- Nilotinib Tablets
Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
MHRA Drug Safety Update: BCR-ABL tyrosine kinase inhibitors: risk of hepatitis B reactivation (May 2016)
NICE TA241: Dasatinib, high-dose imatinib and nilotinib for use in patients who are resistant or intolerant to imatinib (January 2012)
NICE TA425: Dasatinib, nilotinib and high-dose imatinib for treating imatinib-resistant or intolerant chronic myeloid leukaemia (December 2016)
NICE TA426: Dasatinib, nilotinib and imatinib for untreated chronic myeloid leukaemia (December 2016)
|
Nintedanib capsules (Vargatef®)
|
Restricted
|
- Nintedanib Capsules (Vargatef®)
|
NICE TA347: Nintedanib for previously treated locally advanced, metastatic, or locally recurrent non‑small‑cell lung cancer (July 2015)
NICE TA379: Nintedanib for treating idiopathic pulmonary fibrosis (January 2016)
|
Osimertinib mesylate ( Tagrisso®)
|
Restricted

|
Consultant Medical Oncologist use only.
Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
NICE TA416: Osimertinib for treating locally advanced or metastatic EGFR T790M mutation-positive non-small-cell lung cancer (October 2016)
|
Palbociclib (Ibrance®)
|
Restricted
|
- Palbociclib capsules
- Palbociclib capsules with fulvestrant injection
Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
NICE TA495: Palbociclib with an aromatase inhibitor for previously untreated, hormone receptor-positive, HER2-negative, locally advanced or metastatic breast cancer (December 2017)
NICE TA619: Palbociclib with fulvestrant for treating hormone receptor-positive, HER2-negative, advanced breast cancer (January 2020)
|
Ribociclib (Kiskali®)
|
Restricted
|
- Ribociclib Tablets
Blueteq® registration and approval for use is required for this product before it may be dispensed.
|
NICE TA496: Ribociclib with an aromatase inhibitor for previously untreated, hormone receptor-positive, HER2-negative, locally advanced or metastatic breast cancer (December 2017)
TA593: Ribociclib with fulvestrant for treating hormone receptor-positive, HER2-negative, advanced breast cancer (August 2019)
|
Ruxolitinib (Jakavi®)
|
Restricted
|
|
NICE TA386: Ruxolitinib for treating disease-related splenomegaly or symptoms in adults with myelofibrosis (March 2016)
|
08.01.05 |
Taxanes |
|
|
08.01.05 |
Topoisomerase I inhibitors |
|
|
08.01.05 |
Trabectedin |
|
|
08.01.05 |
Trastuzumab |
|
|
08.01.05 |
Tretinoin |
|
|
.... |
Key |
|
|
Cytotoxic Drug
|
|
Controlled Drug
|
|
High Cost Medicine
|
|
Cancer Drugs Fund
|
|
NHS England |
|
Homecare |
|
CCG |
|
Traffic Light Status Information
Status |
Description |

|
Green - Drugs suitable for generalised use in accordance with position summary.
Inform primary care of need to prescribe using a TTO chart if in patient or Treatment Advice Note (TAN) if Outpatient.
|

|
Amber - these drugs require specialist initiation or recommendation |

|
Amber Share Care - Drugs suitable for generalist use, in accordance with position summary, normally following specialist initiation and stabilisation. Ongoing division of responsibility for drug and disease monitoring between specialist and GP by a Shared Care Guideline (SCG). If no SCG in place status reverts to red. |

|
Red - Drugs for specialist use only, in accordance with position summary. GP’s should not be asked to prescribe these products. |

|
Red ULM - Unlicensed medicines for specialist use only, in accordance with position summary. GP’s should not be asked to prescribe these products. |

|
Grey drugs - No formal commissioning position. Check appropriate CCG /NHSE commissioning list or contact CCG/NHSE Medicines Management team for advice. Fill in individual funding request for appropriate CCG/NHSE. This will need to be signed by the Chief Pharmacist and a copy of the relevant DTC submission attached. |

|
Black - Drugs not routinely commissioned so should not usually be prescribed |
|
|
|