Bladder Cancer treatments
PDL1 IHC request form urothelial carcinoma (Word, 21 KB, 1 page)
5-Fluorouracil (5 day) and mitoMYcin Chemoradiation Therapy
Atezolizumab Monotherapy - 21 day
Indication
00544b
Treatment of adult patients with locally advanced or metastatic urothelial carcinoma (mUC) after prior platinum-containing chemotherapy
00544c
Atezolizumab as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (UC) who are considered cisplatin ineligible and whose tumours have a PD-L1 expression ≥5%
Atezolizumab 1680mg Monotherapy - 28 Day
Indication
00593b
Treatment of adult patients with locally advanced or metastatic
urothelial carcinoma (mUC) after prior platinum-containing
chemotherapy
00593c
Atezolizumab as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (UC) who are considered cisplatin ineligible and whose tumours have a PD-L1 expression ≥5%
Avelumab Monotherapy
Indication
00535b
First-line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma (UC) who are progression-free following platinum based chemotherapy
BCG Intravesical Induction and Maintenance Therapy
Indication
00807a
Non-Muscle Invasive Bladder Cancer – very high risk, high risk and intermediate risk groups
CISplatin 40mg/m2 Weekly with Radiotherapy (RT)
CISplatin, Methotrexate and vinBLAStine (CMV) Therapy
Indication
00337a
Neoadjuvant treatment of muscle invasive transitional cell carcinoma (TCC) of the urothelium.
Erdafitinib Monotherapy
Indication
00885a
As monotherapy for the treatment of adult patients with unresectable or metastatic urothelial carcinoma (UC), harbouring susceptible FGFR3 genetic alterations who have previously received at least one line of therapy containing a PD-1 or PD-L1 inhibitor in the unresectable or metastatic treatment setting.
Enfortumab vedotin Monotherapy
Indication
00846a
For the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (UC) who have previously received a platinum-containing chemotherapy and a programmed death receptor 1 (PD-1) or programmed death ligand 1 inhibitor (PD-L1).
Enfortumab Vedotin and Pembrolizumab Therapy
Indication
00945a
First-line treatment of adult patients with unresectable or metastatic urothelial cancer who are eligible for platinum-containing chemotherapy
Gemcitabine (100mg/m2) and Radiotherapy
Gemcitabine (1000mg/m2) and CARBOplatin (AUC5) Therapy-21 day
Indication
00310a
Treatment of patients with locally advanced or metastatic transitional cell carcinoma (TCC) of the urothelium where CISplatin is contraindicated*
Gemcitabine (1000mg/m2)and CISplatin (35mg/m2) Therapy-21 day
Indication
00622a
Treatment of patients with locally advanced or metastatic transitional cell carcinoma (TCC) of the urothelium in patients with impaired renal function
Gemcitabine (1000mg/m2)and CISplatin (70mg/m2)-21 day
Gemcitabine (1000mg/m2) and CISplatin (70mg/m2) Therapy-28 day
Indication
00282a
Treatment of patients with locally advanced or metastatic transitional cell carcinoma (TCC) of the urothelium
Gemcitabine and DOCEtaxel Intravesical Therapy
Indication
00894a
BCG-unresponsive high-risk non-muscle invasive bladder cancer (NMIBC)
00894b
Patients with high risk NMIBC who are intolerant of or ineligible for intravesical BCG
Methotrexate, vinBLAStine, DOXOrubicin, CISplatin (MVAC) Therapy-14 days
Indication
00333a
Locally advanced or metastatic transitional cell carcinoma (TCC) of the urothelium.
Methotrexate, vinBLAStine, DOXOrubicin, CISplatin (MVAC) Therapy-28 days
Indication
00338a
Neoadjuvant treatment of muscle invasive transitional cell carcinoma (TCC) of the urothelium.
00338b
Adjuvant treatment of muscle invasive TCC of the urothelium.
00338c
Locally advanced or metastatic TCC of the urothelium.
Nivolumab Monotherapy - 14 day
Indication
00483h
As monotherapy for the adjuvant treatment of adults with muscle invasive urothelial carcinoma (MIUC) with tumour cell PD-L1 expression ≥1%, who are at high risk of recurrence after undergoing radical resection of MIUC, providing patients are unsuitable for adjuvant treatment with platinum based chemotherapy.
Nivolumab Monotherapy - 28 day
Indication
00484h
As monotherapy for the adjuvant treatment of adults with muscle invasive urothelial carcinoma (MIUC) with tumour cell PD-L1 expression ≥1%, who are at high risk of recurrence after undergoing radical resection of MIUC, providing patients are unsuitable for adjuvant treatment with platinum-based chemotherapy.
PACLitaxel Monotherapy 80mg/m2 Day 1, 8, 15 and 22 – 28 Day
PACLitaxel 80mg/m2 Day 1, 8, 15 Monotherapy-28 Day
Pembrolizumab 200mg Monotherapy
Indication
00455e
As monotherapy for the treatment of locally advanced or metastatic urothelialcarcinoma in adults who have received prior platinum-containing chemotherapy
Pembrolizumab 200mg Monotherapy
Indication
00455f
As monotherapy is indicated for the treatment of locally advanced or metastaticurothelial carcinoma in adults who are not eligible for cisplatin-containingchemotherapy whose tumours express PD-L1 with a combined positive score (CPS)≥10
Pembrolizumab 400mg Monotherapy
Indication
00558e
As monotherapy for the treatment of locally advanced or metastatic urothelialcarcinoma in adults who have received prior platinum-containing chemotherapy
00558f
As monotherapy is indicated for the treatment of locally advanced or metastaticurothelial carcinoma in adults who are not eligible for cisplatin-containing chemotherapy whose tumours express PD-L1 with a combined positive score (CPS)≥10
Germ Cell treatments
Bleomycin, Etoposide and CISplatin (BEP) Therapy
Indication
00300a
Adjuvant treatment of high risk (vascular invasion carcinoma) stage 1 nonseminoma germ cell tumour.
00300b
Metastatic germ cell tumours of the testis.
00300c
Advanced stage or metastatic germ cell tumours (dysgermimoma) of the ovaries.
00300d
Extra-gonadal germ cell tumours.
CARBOplatin (AUC7) and Etoposide- Autologous Conditioning Germ Cell Tumour Regimen
Etoposide and CISplatin 20mg/m2 (EP) 5 Day Therapy
Indication
00301a
Treatment of good prognosis (IGCCCG criteria) metastatic germ cell tumours (both non-seminoma and seminoma).
PACLitaxel, Ifosfamide, and CISplatin (TIP) Therapy
Prostate treatments
* Unlicensed indication. See Regimen for more details.
Abiraterone and prednisoLONE Therapy (mCRPC)
Indication
00103a
Abiraterone is indicated in combination with predniSONE or prednisoLONE for the treatment of metastatic castration resistant prostate cancer (mCRPC) in adult men whose disease has progressed on or after a docetaxel-based chemotherapy regimen.
00103b
Treatment of metastatic castration resistant prostate cancer in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated
Abiraterone and prednisoLONE Therapy (mHSPC)
Indication
00577a
Abiraterone is indicated with predniSONE or prednisoLONE for:
the treatment of newly diagnosed high risk metastatic hormone sensitive
prostate cancer (mHSPC) in adult men in combination with androgen deprivation therapy (ADT)
Apalutamide Therapy
Indication
00574a
Apalutamide is indicated for the treatment of adult men with nonmetastaticcastration resistant prostate cancer (nmCRPC) who are at high risk of developing metastatic disease.
00574b
For the treatment of patients with metastatic hormone sensitive prostate cancer (mHSPC) in combination with androgen deprivation therapy.
Bicalutamide Therapy
Indication
00482a
Treatment of advanced prostate cancer in combination with luteinizing-hormone releasing hormone (LHRH) analogue therapy or surgical castration
Cabazitaxel and prednisoLONE
Indication
00101a
Cabazitaxel is indicated in combination with predniSONE or prednisoLONE for the treatment of patients with hormone refractory metastatic prostate cancer previously treated with a docetaxel-containing regimen
Darolutamide Therapy
Indication
00693a
Treatment of adult men with non-metastatic castration-resistant prostate cancer (nmCRPC) who are at high risk of developing metastatic disease.
Degarelix Therapy
Indication
00481a
Treatment of adult male patients with advanced hormone-dependent prostate cancer
DOCEtaxel 75 mg/m2 - prednisoLONE Combination Therapy
Indication
00546a
In combination with predniSONE or prednisoLONE is indicated for the treatment of patients with hormone refractory metastatic prostate cancer
Docetaxel Monotherapy 50mg/m2 – 14 day cycle
Indication
00313a
In combination with prednisone or prednisolone is indicated for the treatment of patients with hormone refractory metastatic prostate cancer.
DOCEtaxel Monotherapy 75mg/m2 - 21 day cycle
Indication
00203b
First line in high risk non metastic castration sensitive prostate cancer.
00203c
First line in metastatic castration sensitive prostate cancer.
Enzalutamide Monotherapy
Indication
00233a
Treatment of adult men with metastatic castration-resistant prostate cancer whose disease has progressed on or after docetaxel therapy.
00233b
Treatment of adult men with metastatic castration-resistant prostate cancer who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated.
00233c
The treatment of adult men with high-risk non-metastatic castration-resistant prostate cancer (nmCRPC)
Goserelin 10.8mg Therapy -12week
Indication
00477a
Treatment of locally advanced or metastatic hormone sensitive prostate cancer
Goserelin 3.6mg Therapy -28 day
Indication
00478a
Treatment of locally advanced or metastatic hormone sensitive prostate cancer
Leuprorelin 11.25mg Therapy-12 week
Indication
00492a
Management of prostatic carcinoma for which a suppression of testosterone is indicated
Leuprorelin 22.5mg Therapy-12 week
Indication
00479a
Treatment of hormone dependent advanced prostate cancer
00479b
Treatment of high-risk localized and locally advanced hormone dependent prostate cancer in combination with radiotherapy
Leuprorelin 3.75mg Therapy-28 day
Indication
00494a
Management of prostatic carcinoma for which a suppression of testosterone is indicated
Leuprorelin 30mg-24 week
Indication
00493a
Treatment of locally advanced or metastatic hormone dependent advanced prostate cancer
Leuprorelin 45mg Therapy-24 week
Indication
00491a
Treatment of hormone dependent advanced prostate cancer
00491b
Treatment of high-risk localized and locally advanced hormone dependent prostate cancer in combination with radiotherapy
Leuprorelin 7.5mg Therapy-28 day
Indication
00490a
Treatment of hormone dependent advanced prostate cancer
00490b
Treatment of high-risk localized and locally advanced hormone dependent prostate cancer in combination with radiotherapy
Niraparib and Abiraterone acetate (Akeega®) and prednisoLONE Therapy
Indication
00848a
Niraparib in combination with abiraterone acetate (Akeega®) and predniSONE/prednisoLONE for the treatment of adults with metastatic castration resistant prostate cancer (mCRPC) and BRCA1/2 mutations (germline and/or somatic) in whom chemotherapy is not clinically indicated
Olaparib (Tablet) Monotherapy
Indication
00588g
As monotherapy for the treatment of adult patients with metastatic castration-resistant prostate cancer and BRCA1/2-mutations (germline and/or somatic) who have progressed following prior therapy that included a new hormonal agent.
Radium 223 Therapy
Indication
00257a
As monotherapy or in combination with LHRH analogues for the treatment of adults with progressive castration-resistant metastatic prostate cancer (mCRPC, symptomatic bone metastases and no extensive visceral metastases after at least two prior lines of systemic therapy for mCRPC (other than LHRH analogues), or ineligible for any available licensed systemic mCRPC treatment
Relugolix Therapy
Indication
00830a
Treatment of adult patients with advanced hormone-sensitive prostate cancer (HSPC).
Triptorelin 11.25mg Therapy-12 week
Indication
00480a
Treatment of locally advanced or metastatic hormone dependent advanced prostate cancer
Triptorelin 22.6mg Therapy-24 week
Indication
00488a
Treatment of locally advanced or metastatic hormone dependent advanced prostate cancer
Triptorelin 3mg Therapy-28 day
Indication
00489a
Treatment of locally advanced or metastatic hormone dependent advanced prostate cancer
Renal chemotherapy regimens
* Unlicensed indication. See Regimen for more details.
Axitinib Therapy
Indication
00104a
Treatment of adult patients with advanced RCC after failure, on a previous line of therapy, i.e. treatment with SUNItinib, or a cytokine.
Atezolizumab 840mg Monotherapy – 14 day
Indication
00592a
Treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) after prior chemotherapy.
00592b
Treatment of adult patients with locally advanced or metastatic urothelial carcinoma (mUC) after prior platinum-containing chemotherapy.
00592c
Treatment of adult patients with locally advanced or metastatic
urothelial carcinoma (UC) who are considered cisplatin ineligible and
whose tumours have a PD-L1 expression ≥5%.
Bevacizumab 10 mg/kg -14 days
Indication
00212d
In combination with interferon alfa-2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer.
Cabozantinib Therapy
Indication
00518a
Treatment of advanced renal cell carcinoma (RCC) in adults following prior VEGF targeted therapy
Everolimus Therapy
Indication
00320a
Treatment of patients with advanced renal cell carcinoma, whose disease has progressed on or after treatment with VEGF-targeted therapy.
Olaparib (Tablet) Monotherapy
Indication
00588c
Maintenance treatment of adult patients with advanced (FIGO stages III and IV) BRCA1/2‐mutated (germline and/or somatic) primary peritoneal carcinoma who are in response (complete or partial) following completion of first‐line platinum based chemotherapy
00588f
Maintenance treatment of adult patients with platinum -sensitive relapsed BRCA-mutated (germline and/or somatic) primary peritoneal cancer who are in response (complete response or partial response) to platinum-based chemotherapy.
Nivolumab Monotherapy - 14 day
Indication
00483b
As monotherapy for the treatment of advanced renal cell carcinoma (RCC) after prior therapy in adults.
Nivolumab Monotherapy - 28 day
Indication
00484b
As monotherapy for the treatment of advanced renal cell carcinoma (RCC) after prior therapy in adults.
Nivolumab 3mg/kg with Ipilimumab 1mg/kg Therapy
Indication
00551a
Nivolumab in combination with ipilimumab for the first-line treatment of adult patients with intermediate/poor-risk advanced renal cell carcinoma (RCC).
PAZOPanib Therapy
Indication
00445a
First line treatment of advanced Renal Cell Carcinoma (RCC) in adults and for patients who have received prior cytokine therapy for advanced disease.
Pembrolizumab 200mg Monotherapy
Indication
00455m
For the adjuvant treatment of adult patients with renal cell carcinoma (RCC) at increased risk of recurrence following nephrectomy, or following nephrectomy and resection of metastatic lesions.
Pembrolizumab 400mg Monotherapy
Indication
00558m
For the adjuvant treatment of adult patients with renal cell carcinoma (RCC) at increased risk of recurrence following nephrectomy, or following nephrectomy and resection of metastatic lesions.
Pembrolizumab 200mg and Axitinib Therapy
Indication
00583a
Pembrolizumab in combination with axitinib for the first-line treatment ofadvanced renal cell carcinoma (RCC) in adults.
SORAfenib Therapy
Indication
00294b
Treatment of patients with advanced renal cell carcinoma (RCC) who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy.
SUNitinib 50mg Therapy - 42 days
SUNitinib 50mg Therapy (21 days)
Temsirolimus Monotherapy
Indication
00326a
First-line treatment of adult patients with advanced renal cell carcinoma (RCC) who have at least three of six prognostic risk factors.
Tivozanib Therapy
Indication
00564a
Tivozanib for the first line treatment of adult patients with advanced renal cell carcinoma (RCC) and for adult patients who are VEGFR and mTOR pathway inhibitor-naïve following disease progression after one prior treatment with cytokine therapy for advanced RCC