BEAM. Lymphoma group OxBMT SCHEDULE SUMMARY. Date:

Size: px
Start display at page:

Download "BEAM. Lymphoma group OxBMT SCHEDULE SUMMARY. Date:"

Transcription

1 xbt SCHEDULE SUARY Date: Day DRUG Admission Carmustine (BCNU) Etoposide Cytarabine (Ara-C) elphalan Stem cell infusion Pentamidine* To prevent a specific pneumonia called PCP Cyclizine (C) Dexamethasone (D) etoclopramide () ndansetron () Different anti-sickness D * Intravenous pentamidine for PCP prophylaxis should be considered for all patients during conditioning chemotherapy. Day +1 is the most logistically feasible time. If this falls at a weekend, defer to the next working day. D C 1 of 5

2 xbt INDICATIN Hodgkin and non-hodgkin lymphoma. TREATENT INTENT Curative/ Disease odification PRE-ASSESSENT 1. Ensure pre-transplant investigations are carried out as per protocol Ba 2. Ensure patient has double lumen central line inserted and working. 3. Ensure results of pre-transplant investigations are checked by a Haematology SpR and recorded in patient record. 4. Haematology SpR to complete electronic BT front sheet B.2.16g and to BT Administrator to distribute and file in patient record. 5. Treating Consultant to prescribe chemotherapy and stem cells at least 5 days before admission. 6. Supportive treatment to be prescribed by Haematology SPR at least 5 days before admission 7. Send Stem cells and Immunotherapies final report of donation and processing form v4.3.3 SCI at least 7 working days before the planned collection date and ensure a copy is placed in the medical notes 8. Ensure the patient receives irradiated blood products from the start of conditioning. See Guidelines for the use of blood components in adult haematology' for details and individual requirements / duration post-autograft. Ensure irradiation card is attached to the patient's notes and copy given to the patient. 9. Ensure pregnancy test is carried out on all women of child-bearing age unless they are postmenopausal, have been sterilised or have undergone a hysterectomy. 10. Consider NG Tube for feeding to be put in at Day Treatment should be agreed in the relevant DT. 2 of 5

3 xbt CHETHERAPY AND FLUIDS Encourage 3L oral fluids daily, give IV if oral intake insufficient. Day -6 Day -5 to -2 Day -5 to -2 Day -1 Day 0 CARUSTINE (BCNU) ETPSIDE CYTARABINE ELPHALAN Stem cell reinfusion (min 24 hrs post elphalan) 300 mg/m 2 IV D in 500 ml 5% glucose over 1 hour 200 mg/m 2 IV D in 1000 ml sodium chloride 0.9% over 2 hours 200 mg/m 2 IV BD in 100 ml sodium chloride 0.9% over 30 mins 06.00: 1000 ml sodium chloride 0.9% IV infusion over 4 hours 10.00: 140 mg/m 2 IV D in 100 ml sodium chloride 0.9% over 30 mins 10.30: 1000 ml sodium chloride 0.9% with 20 mmol potassium chloride IV infusion over 8 hours 06.00: 1000 ml sodium chloride 0.9% iv infusion over 6 hours Give hydrocortisone 100 mg IV, chlorphenamine 10 mg IV and cyclizine 50 mg IV 15 minutes before infusion. Day +1 Pentamidine 4 mg/kg IV in 100mL sodium chloride 0.9% over 1 hour, maximum 300 mg. Day +5 G-CSF SC Daily as per local policy until stable engraftment. NB: Document infusion details in medical notes, volume, number and ID of the bags given. NB: For obese patients refer to NSSG Guideline Guidelines on Dosing in bese Adult Patients undergoing Stem-cell / Bone arrow transplant. Administration of chemotherapy: Refer to nursing care plan N.3. Pentamidine: Refer to nursing care plan for administration N.73. Stem cell re-infusion: Refer to nursing care plan N.30. DSE DIFICATIN All dose modification to be discussed with consultant. ELPHALAN Renal Impairment Creatinine clearance ml/min elphalan dose > mg/m mg/m 2 <30 Clinical decision 3 of 5

4 xbt CARUSTINE Consider omitting BCNU if lung function tests < 75% predicted or heavy smoker. Renal Impairment limited data available, clinical decision Creatinine clearance ml/min Carmustine dose >45 - <60 80% % <30 Clinical decision ETPSIDE Renal impairment CrCl >50 ml/min CrCl ml/min CrCl <15 ml/min 100% dose 75% dose 50% dose Hepatic impairment - discuss with consultant Arguments for and against dose reduction. Bilirubin 26-51micromol/L or AST u/L -50% dose Bilirubin >51micromol/L or AST >180u/L -clinical decision INVESTIGATINS Daily FBC, U&E, urinalysis & weight on/wed/fri LFT, g 2+ and Ca 2+ (more frequently if clinically indicated) on/thurs Group and save & coagulation screen Chest X-ray on admission then as clinically indicated. CNCURRENT EDICATIN Norethisterone Fluconazole PPI 5-10 mg P TDS from day 0 until platelets >50 x 10 9 /L (menstruating women only). 50 mg P D from day 0 until neutrophils >1.0 x 10 9 /L (or longer if patient on steroids). Refer to Antifungal protocol. antifungal-therapy-guidelines.pdf meprazole 20mg D from start of conditioning until platelet count >50 x 10 9 /L. (or PPI as per local formulary) Aciclovir 200 mg P TDS (or 250 mg TDS IV) from day 0 until day +90. G-CSF SC Daily from Day +5 as per local policy until stable engraftment. Pentamidine 4mg/kg/day (max 300mg) iv on day+1 and day +30 (unless started on co-trimoxazole). 4 of 5

5 xbt ANTI-EETICS Days -6 to -1 Days -6 AND -1 Days -5 to -2 Day 0 5HT 3 antagonist (e.g. ndansetron 8mg IV/P BD) Dexamethasone 8 mg IV D etoclopramide mg IV/P TDS Cyclizine 50 mg IV/P TDS EDICATIN N DISCHARGE (TTS) Norethisterone Fluconazole Stop when platelets >50 x 10 9 /L (menstruating women only). Stop when neutrophils >1.0 x 10 9 /L (or longer if patient on steroids). Co-trimoxazole 480 mg daily on, Wed, Fri until day Start when neutrophils >1.0 x 10 9 /L. If allergic to co-trimoxazole, pentamidine 4 mg/kg IV (max 300 mg) monthly. Aciclovir 200 mg TDS P until day +90. PPI Stop when platelet count >50 x 10 9 /L unless clinically indicated. TREATENT RELATED RTALITY 3-5% REFERENCES 1. ills W, Chopra R, cillan A, Pearce R, Linch DC, Goldstone AH. chemotherapy and autologous bone marrow transplantation for patients with relapsed or refractory non-hodgkin's lymphoma. J Clin ncol ar;13(3): UCLH - Dosage Adjustment for Cytotoxics in Hepatic Impairment ( 3 - updated January 2009). 3. UCLH - Dosage Adjustment for Cytotoxics in Renal Impairment ( 3 - updated January 2009). 5 of 5

R-GDP: Rituximab, Gemcitabine, Dexamethasone &Cisplatin

R-GDP: Rituximab, Gemcitabine, Dexamethasone &Cisplatin : Rituximab, &Cisplatin INDICATION Relapsed or refractory Hodgkin and non-hodgkin lymphoma. Omit Rituximab for patients with Hodgkin Lymphoma. TREATMENT INTENT Palliative or curative depending on context.

More information

R-GDP: Rituximab, Gemcitabine, Dexamethasone &Cisplatin

R-GDP: Rituximab, Gemcitabine, Dexamethasone &Cisplatin : Rituximab, Gemcitabine, Dexamethasone &Cisplatin INDICATION Relapsed or refractory Hodgkin and non-hodgkin lymphoma. Omit Rituximab for patients with Hodgkin Lymphoma or high grade T cell non-hodgkin

More information

CD20-positive high-grade non-hodgkin Lymphoma in patients in which R-CHOP is not indicated

CD20-positive high-grade non-hodgkin Lymphoma in patients in which R-CHOP is not indicated INDICATION CD20-positive high-grade non-hodgkin Lymphoma in patients in which R-CHOP is not indicated TREATMENT INTENT Curative or Disease Modification. PRE-ASSESSMENT 1. Ensure histology is confirmed

More information

ALL Phase 2 Induction (25-60 years)

ALL Phase 2 Induction (25-60 years) ALL Phase 2 (25-60 years) INDICATION of remission in Adult Acute Lymphoblastic Leukaemia (ALL) patients This protocol is suitable for patients aged 25-60 years. It may sometimes be used in older patients

More information

Note: There are other bendamustine protocols, ensure this is the correct one for a given patient.

Note: There are other bendamustine protocols, ensure this is the correct one for a given patient. INDICATIONS 1 st line treatment for follicular lymphoma with FLIPI score 2 or higher: (NICE TA513- BLUETEQ required) Rituximab refractory follicular lymphoma (progression on R-chemo, R-maintenance or within

More information

This is a controlled document and therefore must not be changed or photocopied L.80 - R-CHOP-21 / CHOP-21

This is a controlled document and therefore must not be changed or photocopied L.80 - R-CHOP-21 / CHOP-21 R- / INDICATION Lymphoma Histiocytosis Omit rituximab if CD20-negative. TREATMENT INTENT Disease modification or curative depending on clinical circumstances PRE-ASSESSMENT 1. Ensure histology is confirmed

More information

DA-EPOCH-R (Etoposide/Inpatient)

DA-EPOCH-R (Etoposide/Inpatient) DA- (Etoposide/Inp) INDICATION High grade lymphoma. Omit rituximab if CD20 negative. PRE-ASSESSMENT 1. Ensure histology is confirmed prior to administration of chemotherapy and document in notes. 2. Record

More information

ALL MAINTENANCE (25-60 years)

ALL MAINTENANCE (25-60 years) ALL MAINTENANCE (25-60 years) INDICATION Adult Acute Lymphoblastic Leukaemia (ALL) in remission not eligible for allogeneic transplantation This protocol is suitable for patients aged 25-60 years. It may

More information

DERBY-BURTON LOCAL CANCER NETWORK FILENAME ESHAP.DOC CONTROLLED DOC NO: HCCPG B44. ESHAP Regimen

DERBY-BURTON LOCAL CANCER NETWORK FILENAME ESHAP.DOC CONTROLLED DOC NO: HCCPG B44. ESHAP Regimen ESHAP Regimen Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient Indication Relapsed/ refractory

More information

Gemcitabine, Dexamethasone and Cisplatin GDP Regimen

Gemcitabine, Dexamethasone and Cisplatin GDP Regimen Gemcitabine, Dexamethasone and Cisplatin GDP Regimen Available for Routine Use in Burton in-patient N/A Derby in-patient Burton day-case Derby day-case Burton outreach chemotherapy clinic N/A Derby outreach

More information

R-ICE Regimen- Rituximab, Etoposide, Ifosfamide (with MESNA), Carboplatin (+ Depocyte if CNS involvement)

R-ICE Regimen- Rituximab, Etoposide, Ifosfamide (with MESNA), Carboplatin (+ Depocyte if CNS involvement) R-ICE Regimen- Rituximab, Etoposide, Ifosfamide (with MESNA), Carboplatin (+ Depocyte if CNS involvement) Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case

More information

Rituximab, Gemcitabine, Dexamethasone and Cisplatin RGDP Regimen

Rituximab, Gemcitabine, Dexamethasone and Cisplatin RGDP Regimen Rituximab, Gemcitabine, Dexamethasone and Cisplatin RGDP Regimen Available for Routine Use in Burton in-patient N/A Derby in-patient Burton day-case Derby day-case Burton outreach chemotherapy clinic N/A

More information

Burkitt lymphoma, double hit lymphoma or high IPI diffuse large B-cell lymphoma.

Burkitt lymphoma, double hit lymphoma or high IPI diffuse large B-cell lymphoma. INDICATION Burkitt lymphoma, double hit lymphoma or high IPI diffuse large B-cell lymphoma. TREATMENT INTENT Curative. PRE-ASSESSMENT 1. Ensure histology is confirmed prior to administration of chemotherapy

More information

R-GemOx. Lymphoma group INDICATION. Relapsed or Refractory Lymphoma, for patients unsuitable for R-GDP regimen. Omit rituximab if CD20- negative

R-GemOx. Lymphoma group INDICATION. Relapsed or Refractory Lymphoma, for patients unsuitable for R-GDP regimen. Omit rituximab if CD20- negative R-GemOx INDICATION Relapsed or Refractory Lymphoma, for patients unsuitable for R-GDP regimen. Omit rituximab if CD20- negative TREATMENT INTENT Disease modification PRE-ASSESSMENT 1. Ensure histology

More information

ALL CONSOLIDATION- Cycle 3 (25-60 years)

ALL CONSOLIDATION- Cycle 3 (25-60 years) ALL CONSOLIDATION- (25-60 years) INDICATION Adult Acute Lymphoblastic Leukaemia (ALL) in remission not eligible for allogeneic transplantation This protocol is suitable for patients aged 25-60 years. It

More information

NB. This version combines both previous inpatient and ambulatory protocols. See DRUG REGIMEN section for details.

NB. This version combines both previous inpatient and ambulatory protocols. See DRUG REGIMEN section for details. DA- INDICATION High grade lymphoma. Omit rituximab if CD20 negative. NB. This version combines both previous inpatient and ambulatory protocols. See DRUG REGIMEN section for details. TREATMENT INTENT Curative

More information

(primary CNS lymphoma)

(primary CNS lymphoma) (primary CNS lymphoma) INDICATION CNS Lymphoma TREATMENT INTENT Curative PRE-ASSESSMENT 1. Ensure histology is confirmed and documented in the notes. Although it is sometimes difficult to obtain tissue

More information

SMILE (Etoposide, Ifosfamide, Methotrexate and Dexamethasone)

SMILE (Etoposide, Ifosfamide, Methotrexate and Dexamethasone) SMILE (Etoposide, Ifosfamide, Methotrexate and Dexamethasone) INDICATION Natural Killer/T-cell lymphoma TREATMENT INTENT Curative SPECIAL PRECAUTIONS This protocol causes marked myelosuppression despite

More information

High Dose Cytarabine plus high dose Methotrexate for CNS Lymphoma

High Dose Cytarabine plus high dose Methotrexate for CNS Lymphoma High Dose Cytarabine plus high dose Methotrexate for CNS Lymphoma Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton

More information

Definition of high risk disease for diffuse large B-cell lymphoma is score 4 or 5 based on the following risk factors:

Definition of high risk disease for diffuse large B-cell lymphoma is score 4 or 5 based on the following risk factors: INDICATION High grade lymphoma with high risk of CNS involvement Definition of high risk disease for diffuse large B-cell lymphoma is score 4 or 5 based on the following risk factors: Age > 60 Raised serum

More information

PVACE-BOP (Hodgkin s Lymphoma)

PVACE-BOP (Hodgkin s Lymphoma) DRUG ADMINISTRATION SCHEDULE Day Drug Dose Route Diluent Rate 1 Ondansetron 8mg IV / Oral vinblastine 6mg/m 2 (Max: 10mg) IV Infusion Etoposide 100mg/m 2 IV infusion Patients over 65 years by 15 min infusion

More information

Burkitt s Lymphoma or DLBCL with adverse features PATIENTS WITH GOOD PERFORMANCE STATUS

Burkitt s Lymphoma or DLBCL with adverse features PATIENTS WITH GOOD PERFORMANCE STATUS Regimen R-CODOX M Indication Burkitt s Lymphoma or DLBCL with adverse features Therapeutic Intent Radical/Curative PATIENTS WITH GOOD PERFORMANCE STATUS Day Medication Dose Route Administration Details

More information

(High dose METHOTREXATE, high dose CYTARABINE, RITUXIMAB and THIOTEPA)

(High dose METHOTREXATE, high dose CYTARABINE, RITUXIMAB and THIOTEPA) MATRix (High dose METHOTREXATE, high dose CYTARABINE, RITUXIMAB and THIOTEPA) INDICATION CNS Lymphoma. TREATMENT INTENT Curative. PRE-ASSESSMENT 1. Ensure histology is confirmed and documented in the notes.

More information

R-IDARAM. Dexamethasone is administered as an IV infusion in 100mL sodium chloride 0.9% over 30 minutes.

R-IDARAM. Dexamethasone is administered as an IV infusion in 100mL sodium chloride 0.9% over 30 minutes. R-IDARAM Indication Secondary CNS lymphoma ICD-10 codes Codes with a prefix C85 Regimen details Day Drug Dose Route 1 Rituximab 375mg/m 2 IV infusion 1 Methotrexate 12.5mg Intrathecal 1 Cytarabine 70mg

More information

NCCP Chemotherapy Regimen. LEAM Autologous Transplant Conditioning Protocol

NCCP Chemotherapy Regimen. LEAM Autologous Transplant Conditioning Protocol INDICATIONS FOR USE: LEAM Autologous Transplant Conditioning Protocol Regimen *Reimbursement INDICATION ICD10 Code Status Autologous conditioning in non-hodgkins Lymphoma (NHL) C85 00468a Hospital Autologous

More information

R-BAC-500 (Rituximab, Bendamustine, Cytarabine) for Mantle Cell Lymphoma

R-BAC-500 (Rituximab, Bendamustine, Cytarabine) for Mantle Cell Lymphoma R-BAC-500 (Rituximab, Bendamustine, Cytarabine) for Mantle Cell Lymphoma Not routinely commissioned, each case requires prior documented approval before offering & commencing therapy from NHS England Cancer

More information

DERBY-BURTON LOCAL CANCER NETWORK FILENAME R-IVE.DOC CONTROLLED DOC NO: HCCPG B53 CSIS Regimen Name: R-IVE. R-IVE Regimen

DERBY-BURTON LOCAL CANCER NETWORK FILENAME R-IVE.DOC CONTROLLED DOC NO: HCCPG B53 CSIS Regimen Name: R-IVE. R-IVE Regimen R-IVE Regimen Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient Indication Relapsed/ refractory

More information

BEACOPP-14/ BEACOPP- Escalated

BEACOPP-14/ BEACOPP- Escalated BEACOPP-14/ BEACOPP- Escalated INDICATION Early Stage Classical Hodgkin Lymphoma with positive interim PET-CT (Deauville 3 or more) Advanced Classical Hodgkin lymphoma This protocol should normally be

More information

O-CVP with maintenance Obinutuzumab

O-CVP with maintenance Obinutuzumab with maintenance Obinutuzumab INDICATION Follicular Lymphoma: 1 st line treatment in advanced symptomatic patients (NICE TA513 for FLIPI score 2 or higher - BLUETEQ required) TREATMENT INTENT Disease modification.

More information

Obinutuzumab+Bendamustine followed by Obinutuzumab Maintenance Burton in-patient Derby in-patient Burton day-case Derby day-case

Obinutuzumab+Bendamustine followed by Obinutuzumab Maintenance Burton in-patient Derby in-patient Burton day-case Derby day-case Obinutuzumab+Bendamustine followed by Obinutuzumab Maintenance Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient Available

More information

E 90 C followed by Weekly Paclitaxel

E 90 C followed by Weekly Paclitaxel E 90 C followed by Weekly Paclitaxel Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient

More information

Fludarabine-Cyclophosphamide plus Rituximab (FC-R) for Chronic Lymphocytic Leukaemia

Fludarabine-Cyclophosphamide plus Rituximab (FC-R) for Chronic Lymphocytic Leukaemia DRUG ADMINISTRATION SCHEDULE First Cycle Only: Day Drug Dose Route Diluent Rate 1 Paracetamol 1gram Oral 1 Hydrocortisone 100mg IV bolus 1 Chlorphenamine 10mg IV bolus 1 Rituximab 375mg/m 2 IV infusion

More information

FLAG-Ida + Gemtuzumab Ozogamicin Regimen (Also known as FLAG-Ida + GO3x2) (AML19 Trial Course 1)

FLAG-Ida + Gemtuzumab Ozogamicin Regimen (Also known as FLAG-Ida + GO3x2) (AML19 Trial Course 1) FLAG-Ida + Gemtuzumab Ozogamicin Regimen (Also known as FLAG-Ida + GO3x2) (AML19 Trial Course 1) AML19 Adults with Acute Myeloid Leukaemia or High-Risk Myelodysplastic Syndrome ***Refer to trial protocol

More information

X M/ (R) Dose adjusted (DA)-EPOCH-R

X M/ (R) Dose adjusted (DA)-EPOCH-R X M/ (R) adjusted (DA)-EPOCH-R Indication High-risk CD20+ diffuse large B cell lymphoma especially C-MYC and BCL-2 activated (i.e. double hit lymphoma) and mediastinal sclerosing (thymic) large B cell

More information

DERBY-BURTON LOCAL CANCER NETWORK FILENAME R-GCVP.DOC CONTROLLED DOC NO: HCCPG B12 CSIS Regimen Name: R-GCVP. R-GCVP Regimen

DERBY-BURTON LOCAL CANCER NETWORK FILENAME R-GCVP.DOC CONTROLLED DOC NO: HCCPG B12 CSIS Regimen Name: R-GCVP. R-GCVP Regimen R-GCVP Regimen Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient Indication CD 20 positive

More information

Carboplatin / Gemcitabine Gynaecological Cancer

Carboplatin / Gemcitabine Gynaecological Cancer Systemic Anti Cancer Treatment Protocol Carboplatin / Gemcitabine Gynaecological Cancer PROCTOCOL REF: MPHAGYNCAG (Version No: 1.0) Approved for use in: Recurrent/metastatic endometrial carcinoma Previously

More information

Fludarabine + Cyclophosphamide + Rituximab (FCR) - FLAIR Study

Fludarabine + Cyclophosphamide + Rituximab (FCR) - FLAIR Study Fludarabine + Cyclophosphamide + Rituximab (FCR) - FLAIR Study Front-Line therapy in CLL: Assessment of Ibrutinib-containing Regimes. ***See protocol for further details*** Available for Routine Use in

More information

ALL Phase 1 Induction (25-60 years)

ALL Phase 1 Induction (25-60 years) ALL Phase 1 (25-60 years) INDICATION of remission in Adult Acute Lymphoblastic Leukaemia (ALL) patients This protocol is suitable for patients aged 25-60 years. It may sometimes be used in older patients

More information

MATRIX (Methotrexate, Cytarabine, Thiotepa and Rituximab)

MATRIX (Methotrexate, Cytarabine, Thiotepa and Rituximab) MATRIX (Methotrexate, Cytarabine, Thiotepa and Rituximab) Indication First line treatment of primary CNS lymphoma. ICD-10 codes Codes with a prefix C85 Regimen details Day Drug Dose Route 1 and 6 Rituximab

More information

DERBY-BURTON LOCAL CANCER NETWORK FILENAME R-CODOX-M.DOC CONTROLLED DOC NO: HCCPG B115 CSIS Regimen Name: R-CODOXM. Rituximab + CODOX-M

DERBY-BURTON LOCAL CANCER NETWORK FILENAME R-CODOX-M.DOC CONTROLLED DOC NO: HCCPG B115 CSIS Regimen Name: R-CODOXM. Rituximab + CODOX-M Rituximab + CODOX-M Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient Indication Burkitt

More information

Gemcitabine + Cisplatin Regimen

Gemcitabine + Cisplatin Regimen Gemcitabine + Cisplatin Regimen Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient Indication

More information

DERBY-BURTON LOCAL CANCER NETWORK FILENAME SMILE.DOC CONTROLLED DOC NO: HCCPG B57 CSIS Regimen Name: SMILE. SMILE chemotherapy

DERBY-BURTON LOCAL CANCER NETWORK FILENAME SMILE.DOC CONTROLLED DOC NO: HCCPG B57 CSIS Regimen Name: SMILE. SMILE chemotherapy SMILE chemotherapy Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient Indication Extranodal

More information

Rituximab-CHOP Regimen - ENRICH Study

Rituximab-CHOP Regimen - ENRICH Study Rituximab-CHOP Regimen - Study Randomised, open label study of Rituximab/Ibrutinib vs Rituximab/Chemotherapy in older patients with untreated mantle cell lymphoma ***See protocol for further details***

More information

Nordic Protocol (MaxiCHOP/R-MaxiCHOP plus R-HDAraC)

Nordic Protocol (MaxiCHOP/R-MaxiCHOP plus R-HDAraC) Nordic Protocol (MaxiCHOP/R-MaxiCHOP plus R-HDAraC) Available for Routine Use in Burton in-patient Derby in-patient (First cycle if bulky disease & risk of tumour lysis syndrome) Burton day-case Derby

More information

Cisplatin / Paclitaxel Gynaecological Cancer

Cisplatin / Paclitaxel Gynaecological Cancer Systemic Anti Cancer Treatment Protocol Cisplatin / Paclitaxel Gynaecological Cancer PROCTOCOL REF: MPHAGYNCIP (Version No: 1.0) Approved for use in: First line treatment for stage Ib-IV with minimal residual

More information

(R) CHOEP. May be used for stage IA - IV Diffuse Large B Cell non-hodgkin lymphoma in combination with rituximab.

(R) CHOEP. May be used for stage IA - IV Diffuse Large B Cell non-hodgkin lymphoma in combination with rituximab. (R) CHOEP Indication Treatment of stage IA - IV T cell non-hodgkin lymphoma as an alternative to CHOP in younger, fitter patients with normal LDH level. May be used for stage IA - IV Diffuse Large B Cell

More information

Lung Pathway Group Cisplatin & IV Vinorelbine in Non- Small Cell Lung Cancer (NSCLC)

Lung Pathway Group Cisplatin & IV Vinorelbine in Non- Small Cell Lung Cancer (NSCLC) Lung Pathway Group Cisplatin & IV Vinorelbine in Non- Small Cell Lung Cancer (NSCLC) Indication: First line in radical/induction treatment in locally advanced NSCLC First line palliative treatment in advanced/metastatic

More information

SUBCUTANEOUS Bortezomib + Thalidomide +Dexamethasone Available for Routine Use in

SUBCUTANEOUS Bortezomib + Thalidomide +Dexamethasone Available for Routine Use in SUBCUTANEOUS Bortezomib + Thalidomide +Dexamethasone Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby

More information

ECN Protocol Book. Generic Chemotherapy Protocol Guidelines. ECN_Protocol_Book_generic chemotherapy protocol guidelines guidelines_1

ECN Protocol Book. Generic Chemotherapy Protocol Guidelines. ECN_Protocol_Book_generic chemotherapy protocol guidelines guidelines_1 ECN Protocol Book Generic Chemotherapy Protocol Guidelines Name of person presenting document: Reason for document development: Names of development team: Specify groups of staff to whom the document relates:

More information

Cisplatin Doxorubicin Sarcoma

Cisplatin Doxorubicin Sarcoma Systemic Anti Cancer Treatment Protocol Cisplatin Doxorubicin Sarcoma PROCEDURE REF: MPHACISDOX (Version No. _1.0) Approved for use in: Osteosarcoma Palliative / advanced disease Not suitable for PAM schedule

More information

StRs and CT doctors in haematology. September Folinic acid dose modified.

StRs and CT doctors in haematology. September Folinic acid dose modified. High dose Methotrexate and folinic acid rescue Full Title of Guideline: Author (include email and role): Division & Speciality: Clinical Guideline Review Date September 2018 GUIDELINE FOR THE USE OF HIGH

More information

NCCP Chemotherapy Regimen. CARBOplatin (AUC7) and Etoposide- Autologous Conditioning Germ Cell Tumour Regimen

NCCP Chemotherapy Regimen. CARBOplatin (AUC7) and Etoposide- Autologous Conditioning Germ Cell Tumour Regimen CARBOplatin (AUC7) and Etoposide- Autologous Conditioning Germ Cell INDICATIONS FOR USE: Regimen INDICATION ICD10 Code Treatment of metastatic relapsed/refractory germ cell tumours C62 00453a *Reimbursement

More information

THE CLATTERBRIDGE CANCER CENTRE NHS FOUNDATION TRUST. Systemic Anti Cancer Treatment Protocol. EDP + mitotane

THE CLATTERBRIDGE CANCER CENTRE NHS FOUNDATION TRUST. Systemic Anti Cancer Treatment Protocol. EDP + mitotane Systemic Anti Cancer Treatment Protocol EDP + mitotane PROCEDURE REF: MPHAHANEDP (Version No: 1.0) Approved for use in: Symptomatic treatment for advanced (unresectable, metastatic or relapsed) adrenocortical

More information

DTPACE. Myeloma group INDICATION

DTPACE. Myeloma group INDICATION INDICATION Relapsed or refractory myeloma patients suitable for intensive salvage chemotherapy. Plasma cell leukaemia or presentation with extra-medullary disease. TREATMENT INTENT Disease Modification

More information

Skin Pathway Group Alemtuzumab in Cutaneous Lymphoma

Skin Pathway Group Alemtuzumab in Cutaneous Lymphoma Skin Pathway Group Alemtuzumab in Cutaneous Lymphoma Indication: Treatment of patients with Cutaneous Lymphoma (Unlicensed use) Disease control prior to Reduced Intensity Conditioning Stem Cell Transplant

More information

DERBY-BURTON CANCER NETWORK CONTROLLED DOC NO:

DERBY-BURTON CANCER NETWORK CONTROLLED DOC NO: OBINUTUZUMAB+CHLORAMBUCIL Regimen RDH; Day 1 and 2 Dose to be given on Ward Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community

More information

DERBY-BURTON LOCAL CANCER NETWORK FILENAME CEOP.DOC CONTROLLED DOC NO: HCCPG B21 CSIS Regimen Name: CEOP. CEOP Regimen

DERBY-BURTON LOCAL CANCER NETWORK FILENAME CEOP.DOC CONTROLLED DOC NO: HCCPG B21 CSIS Regimen Name: CEOP. CEOP Regimen CEOP Regimen Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient Indication T-cell non-hodgkin

More information

Cisplatin and Gemcitabine Bladder Cancer: Full and split dose

Cisplatin and Gemcitabine Bladder Cancer: Full and split dose Systemic Anti Cancer Treatment Protocol Cisplatin and Gemcitabine Bladder Cancer: Full and split dose PROCTOCOL REF: MPHAUROCIG (Version No: 1.0) Approved for use in: Neoadjuvant and palliative indications

More information

This is a controlled document and therefore must not be changed

This is a controlled document and therefore must not be changed AZACITIDINE NICE TA218 Treatment of adults not eligible for haematopoietic stem cell transplantation who have: Intermediate-2 and high-risk MDS according to the International Prognostic Scoring System

More information

Carfilzomib and Dexamethasone (CarDex)

Carfilzomib and Dexamethasone (CarDex) Carfilzomib and Dexamethasone (CarDex) Indication Relapsed multiple myeloma for patients who have had only one previous line of therapy (that did not include bortezomib). (NICE TA457) ICD-10 codes Codes

More information

Carboplatin and Gemcitabine

Carboplatin and Gemcitabine Systemic Anti Cancer Treatment Protocol Carboplatin and Gemcitabine PROTOCOL REF: MPHACAGELU (Version No: 1.0) Approved for use in: Advanced non-small cell lung cancer Performance status: 0 to 2 Re-challenge

More information

4.05 Protocol name: Alemtuzumab (MabCampath ), intravenous

4.05 Protocol name: Alemtuzumab (MabCampath ), intravenous 4.05 Protocol name: (MabCampath ), intravenous Indication Treatment of CLL refractory to fludarabine (either primary i.e. 17p deletion, or secondary i.e. following previous fludarabine treatment), without

More information

Bortezomib, Thalidomide & Dexamethasone

Bortezomib, Thalidomide & Dexamethasone DRUG ADMINISTRATION SCHEDULE Cumbria, Northumberland, Tyne & Wear Area Team Day Drug Dose Route Diluent Rate 1, 4, 8, & 11 2 Bortezomib 1.3mg/m IV bolus/ SC injection* None Fast bolus: 3 to 5 seconds 1

More information

Breast Pathway Group EC x 4 Docetaxel x 4: Epirubicin & Cyclophosphamide followed by Docetaxel in Early Breast Cancer

Breast Pathway Group EC x 4 Docetaxel x 4: Epirubicin & Cyclophosphamide followed by Docetaxel in Early Breast Cancer Breast Pathway Group EC x 4 Docetaxel x 4: Epirubicin & Cyclophosphamide followed by Docetaxel in Early Breast Indication: Neoadjuvant therapy for high risk and fit breast cancer patients suitable for

More information

Docetaxel + Nintedanib

Docetaxel + Nintedanib Docetaxel + Nintedanib Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient Indication Second

More information

Cisplatin + Etoposide + Thoracic Radiotherapy (TRT) INDICATIONS FOR USE:

Cisplatin + Etoposide + Thoracic Radiotherapy (TRT) INDICATIONS FOR USE: Cisplatin + Etoposide + Thoracic Radiotherapy (TRT) INDICATIONS FOR USE: Protocol INDICATION ICD10 Code Small cell lung cancer (SCLC) limited disease C34 00279a ELIGIBILTY: Indications as above ECOG 0-2

More information

Cisplatin + Etoposide IV / Oral therapy followed by Chemo-radiotherapy in Small Cell Carcinoma of the Cervix

Cisplatin + Etoposide IV / Oral therapy followed by Chemo-radiotherapy in Small Cell Carcinoma of the Cervix Cisplatin + Etoposide IV / Oral therapy followed by Chemo-radiotherapy in Small Cell Carcinoma of the Cervix Indication: Neoadjuvant chemotherapy followed by Chemo-radiotherapy in Small Cell Carcinoma

More information

Bevacizumab + Paclitaxel & Carboplatin

Bevacizumab + Paclitaxel & Carboplatin Bevacizumab + Paclitaxel & Carboplatin Available for Routine Use in Not routinely commissioned, each case requires prior documented approval before offering & commencing therapy from NHS England Cancer

More information

(R) CODOX M / (R) IVAC

(R) CODOX M / (R) IVAC (R) CODOX M / (R) IVAC Indication Burkitt's or Burkitt's-like lymphoma, especially those with 1 or more of the following poor risk criteria: - Raised LDH level - WHO performance status 2-4 - Ann Arbor

More information

Breast Pathway Group TC (Docetaxel / Cyclophosphamide) in Early Breast Cancer

Breast Pathway Group TC (Docetaxel / Cyclophosphamide) in Early Breast Cancer Breast Pathway Group TC (Docetaxel / Cyclophosphamide) in Early Breast Cancer Indication: Neoadjuvant or adjuvant treatment for patients in whom anthracyclines are contraindicated or inappropriate Regimen

More information

TCHP Docetaxel, Carboplatin, Trastuzumab, Pertuzumab Neoadjuvant Protocol

TCHP Docetaxel, Carboplatin, Trastuzumab, Pertuzumab Neoadjuvant Protocol Systemic Anti Cancer Treatment Protocol TCHP Docetaxel, Carboplatin, Trastuzumab, Pertuzumab Neoadjuvant Protocol PROTOCOL REF: MPHATCHP (Version No: 1.0) Approved for use in: Neoadjuvant breast: The neoadjuvant

More information

NCCP Chemotherapy Regimen. Dose Dense DOXOrubicin, Cyclophosphamide (AC 60/600) 14 day followed by PACLItaxel (175) 14 day Therapy (DD AC-T)

NCCP Chemotherapy Regimen. Dose Dense DOXOrubicin, Cyclophosphamide (AC 60/600) 14 day followed by PACLItaxel (175) 14 day Therapy (DD AC-T) Dose Dense DOXOrubicin, Cyclophosphamide (AC 60/600) 14 day followed by PACLItaxel (175) 14 day Therapy (DD AC-T) Note: There is an option for DOXOrubicin, cyclophosphamide followed by weekly PACLItaxel

More information

Gemcitabine & Cisplatin

Gemcitabine & Cisplatin Gemcitabine & Cisplatin Available for Routine Use in Burton in-patient Derby in-patient Burton day-case Derby day-case Burton community Derby community Burton out-patient Derby out-patient Indication Advanced

More information

Bevacizumab + Paclitaxel + Cisplatin

Bevacizumab + Paclitaxel + Cisplatin Bevacizumab + Paclitaxel + Cisplatin Available for Routine Use in Not routinely commissioned, each case requires prior documented approval before offering & commencing therapy from the Cancer Drugs Fund

More information

CISPLATIN Chemo-radiation regimen Gynaecological Cancer

CISPLATIN Chemo-radiation regimen Gynaecological Cancer Systemic Anti Cancer Treatment Protocol CISPLATIN Chemo-radiation regimen Gynaecological Cancer PROCTOCOL REF: MPHAGYNCIX (Version No: 1.0) Approved for use in: Locally advanced cervical cancer (adjuvant/curative)

More information

NCCP Chemotherapy Regimen. TICE - Autologous Conditioning Germ Cell Tumour Regimen

NCCP Chemotherapy Regimen. TICE - Autologous Conditioning Germ Cell Tumour Regimen TICE - Autologous INDICATIONS FOR USE: Regimen INDICATION ICD10 Code Treatment of metastatic relapsed/refractory germ cell tumours C62 00437a *Reimbursement Indicator If a reimbursement indicator (e.g.

More information

Breast Pathway Group Docetaxel in Advanced Breast Cancer

Breast Pathway Group Docetaxel in Advanced Breast Cancer Breast Pathway Group Docetaxel in Advanced Breast Cancer Indication: First-line palliative treatment, with or without trastuzumab, for advanced breast cancer in patients for whom an anthracycline is not

More information

Lung Pathway Group Cisplatin & PO Vinorelbine in Non- Small Cell Lung Cancer (NSCLC)

Lung Pathway Group Cisplatin & PO Vinorelbine in Non- Small Cell Lung Cancer (NSCLC) Lung Pathway Group Cisplatin & PO Vinorelbine in Non- Small Cell Lung Cancer (NSCLC) Indication: First line in radical/induction treatment in locally advanced NSCLC First line palliative treatment in advanced/metastatic

More information

Paclitaxel Gynaecological Cancer

Paclitaxel Gynaecological Cancer Systemic Anti Cancer Treatment Protocol Paclitaxel Gynaecological Cancer PROTOCOL REF: MPHAGYNPAC (Version No: 1.0) Approved for use in: Second/ third line option for advanced ovarian cancers (3 weekly

More information

Lung Pathway Group Docetaxel & Carboplatin in Non- Small Cell Lung Cancer (NSCLC)

Lung Pathway Group Docetaxel & Carboplatin in Non- Small Cell Lung Cancer (NSCLC) Lung Pathway Group Docetaxel & Carboplatin in Non- Small Cell Lung Cancer (NSCLC) Indication: First line palliative therapy for previously untreated Stage IIIB or IV NSCLC patients Regimen details: Docetaxel

More information

TIP Paclitaxel, Ifosfamide and Cisplatin

TIP Paclitaxel, Ifosfamide and Cisplatin Systemic Anti Cancer Treatment Protocol TIP Paclitaxel, Ifosfamide and Cisplatin PROTOCOL REF: MPHATIPGC (Version No: 1.0) Approved for use in: Second line treatment of germ cell tumours Dosage: Drug Dosage

More information

1 Acute Lymphoblastic Leukaemia

1 Acute Lymphoblastic Leukaemia 1 Acute Lymphoblastic Leukaemia 1.05 Intensification - Philadelphia Negative Patients Indication ALL Philadelphia negative patients Pre-treatment Evaluation The intensification module begins two weeks

More information

NCCP Chemotherapy Regimen. Dose Dense DOXOrubicin, Cyclophosphamide (AC 60/600) 14 day followed by PACLitaxel (80) 7 day Therapy (DD AC-T)

NCCP Chemotherapy Regimen. Dose Dense DOXOrubicin, Cyclophosphamide (AC 60/600) 14 day followed by PACLitaxel (80) 7 day Therapy (DD AC-T) Dose Dense DOXOrubicin, Cyclophosphamide (AC 60/600) 14 day followed by PACLitaxel (80) 7 day Therapy (DD AC-T) INDICATIONS FOR USE: INDICATION Adjuvant Treatment of High Risk Node Negative or Node Positive

More information

LD-ARA-C and Clofarabine

LD-ARA-C and Clofarabine LD-ARA-C and Clofarabine INDICATION Induction plus consolidation chemotherapy for patients with acute myeloid leukaemia (AML). Its use is particularly for patients over 60 years of age but it can be applied

More information

NCCP Chemotherapy Protocol. CHOEP Therapy 21 days. Treatment of T-cell Non-Hodgkins Lymphoma C a

NCCP Chemotherapy Protocol. CHOEP Therapy 21 days. Treatment of T-cell Non-Hodgkins Lymphoma C a CHOEP Therapy 21 days INDICATIONS FOR USE: INDICATION ICD10 Protocol Code Treatment of T-cell Non-Hodgkins Lymphoma C85 00396a ELIGIBILTY: Indication as above Age < 60 years Adequate haematological, renal

More information

Cisplatin and Vinorelbine and radiotherapy (NSCLC)

Cisplatin and Vinorelbine and radiotherapy (NSCLC) Cisplatin and Vinorelbine and radiotherapy (NSCLC) Indication First-line chemotherapy for use with concomitant radical radiotherapy for early or locally advanced non-small cell carcinoma (NSCLC) ICD-10

More information

Cisplatin and Vinorelbine and radiotherapy (NSCLC)

Cisplatin and Vinorelbine and radiotherapy (NSCLC) Cisplatin and Vinorelbine and radiotherapy (NSCLC) Indication First-line chemotherapy for use with concomitant radical radiotherapy for early or locally advanced non-small cell carcinoma (NSCLC) ICD-10

More information

Gemcitabine + Capecitabine (ESPAC-4 Trial)

Gemcitabine + Capecitabine (ESPAC-4 Trial) Gemcitabine + Capecitabine (ESPAC-4 Trial) European Study Group For Pancreatic Cancer - Trial 4. Combination versus single agent chemotherapy in resectable pancreatic ductal and ampullary cancers. ***

More information

Carboplatin and Fluorouracil

Carboplatin and Fluorouracil Carboplatin and Fluorouracil Indication Palliative chemotherapy for recurrent or metastatic head and neck squamous cell cancer for patients where cisplatin and / or cetuximab are not appropriate. Performance

More information

ULYRICE. Protocol Code. Lymphoma. Tumour Group. Dr. Laurie Sehn. Contact Physician

ULYRICE. Protocol Code. Lymphoma. Tumour Group. Dr. Laurie Sehn. Contact Physician BCCA Protocol Summary for the Treatment of Relapsed or Refractory Advanced Stage Aggressive B-Cell Non-Hodgkin s Lymphoma with Ifosfamide, CARBOplatin, Etoposide and rituximab Protocol Code Tumour Group

More information

NCCP Chemotherapy Regimen

NCCP Chemotherapy Regimen Dose Dense DOXOrubicin, Cyclophosphamide (AC 60/600) 14 day followed by PACLitaxel (175) 14 day and Trastuzumab Therapy (DD AC-TH) Note: There is an option for Dose Dense DOXOrubicin, cyclophosphamide

More information

Paclitaxel Gastric Cancer

Paclitaxel Gastric Cancer Systemic Anti Cancer Treatment Handbook Paclitaxel Gastric Cancer PROTOCOL REF: MPHAUGIPAC (Version No: 1.0) Approved for use in: Second line treatment of locally advanced and metastatic gastric / gastro-oesophageal

More information

Breast Pathway Group EC x 4 Paclitaxel x 4 (3-weekly): Epirubicin & Cyclophosphamide x 4 followed by Paclitaxel x 4 (3-weekly) in Early Breast Cancer

Breast Pathway Group EC x 4 Paclitaxel x 4 (3-weekly): Epirubicin & Cyclophosphamide x 4 followed by Paclitaxel x 4 (3-weekly) in Early Breast Cancer Breast Pathway Group EC x 4 Paclitaxel x 4 (3-weekly): Epirubicin & Cyclophosphamide x 4 followed by Paclitaxel x Indication: Neoadjuvant or adjuvant therapy for moderate to high risk node positive breast

More information

Ixazomib with Lenalidomide and Dexamethasone (IRd)

Ixazomib with Lenalidomide and Dexamethasone (IRd) Indication Ixazomib, with lenalidomide and dexamethasone, is recommended for use within the Cancer Drugs Fund as an option for treating multiple myeloma for patients who have already had 2 or 3 lines of

More information

IBRUTINIB + Rituximab, Treatment Period - ENRICH Study

IBRUTINIB + Rituximab, Treatment Period - ENRICH Study IBRUTINIB + Rituximab, Treatment Period - Study Randomised, open label study of Rituximab/Ibrutinib vs Rituximab/Chemotherapy in older patients with untreated mantle cell lymphoma ***See protocol for further

More information

Lung Pathway Group Carboplatin & PO Vinorelbine in Non-Small Cell Lung Cancer (NSCLC)

Lung Pathway Group Carboplatin & PO Vinorelbine in Non-Small Cell Lung Cancer (NSCLC) Lung Pathway Group Carboplatin & PO Vinorelbine in Non-Small Cell Lung Cancer (NSCLC) Indication: First line in radical/induction treatment in locally advanced NSCLC First line palliative treatment in

More information

TIP: Paclitaxel / Ifosfamide / Cisplatin in Relapsed Germ Cell Tumour

TIP: Paclitaxel / Ifosfamide / Cisplatin in Relapsed Germ Cell Tumour TIP: Paclitaxel / Ifosfamide / Cisplatin in Relapsed Germ Cell Tumour Indication: Second line therapy in Relapsed Germ Cell Tumours Regimen details: Paclitaxel 175mg/m 2 IV Cisplatin 20mg/m 2 IV - D5 Ifosfamide

More information

Breast Pathway Group Gemcitabine & Paclitaxel in Advanced Breast Cancer

Breast Pathway Group Gemcitabine & Paclitaxel in Advanced Breast Cancer Breast Pathway Group Gemcitabine & Paclitaxel in Advanced Breast Cancer Indication: Alternative palliative treatment for advanced breast cancer in patients where docetaxel monotherapy or docetaxel/capecitabine

More information

FEC-T plus trastuzumab & pertuzumab

FEC-T plus trastuzumab & pertuzumab Page 1 of 5 Indication Treatment Intent Frequency and number of cycles Monitoring parameters pre-treatment The neoadjuvant treatment of locally advanced, inflammatory or early HER2 positive breast cancer

More information

Nivolumab and Ipilimumab

Nivolumab and Ipilimumab Nivolumab and Ipilimumab Indication Advanced (unresectable or metastatic) melanoma. (NICE TA400) ICD-10 codes Codes prefixed with C43 Regimen details Cycles 1-4 Nivolumab and Ipilimumab every 3 weeks Day

More information