Menu Close Menu

Fewer cancers.
Better survival.
Equity for all.

Systemic Anti-Cancer Therapy Regimen Library

LUNG NSCLC Metastatic - cARBOplatin, pemetrexed and pembrolizumab

Treatment Overview

Usually up to 4 cycles of cARBOplatin, pemetrexed and pembrolizumab.

Pemetrexed and pembrolizumab may continue until disease progression or unacceptable toxicity.

Cycles 1 to 4 - 21 days - cARBOplatin, pemetrexed and pembrolizumab

Cycle length:
21

folic acid: Starting 7 days before the first cycle, continue ONCE daily until 21 days after the last dose of pemetrexed.

hydroxocobalamin: Starting 7 days before the first cycle and then repeat ONCE every 9 weeks until 21 days after the last dose of pemetrexed.

Cycle 5 (and all further cycles) - 21 days - pemetrexed and pembrolizumab maintenance

Cycle length:
21

folic acid: Take ONCE daily until 21 days after the last dose of pemetrexed.

hydroxocobalamin: Repeat ONCE every 9 weeks (every 3 cycles) until 21 days after the last dose of pemetrexed.

Cycle details

Cycles 1 to 4 - 21 days - cARBOplatin, pemetrexed and pembrolizumab

Medication Dose Route Days Max Duration
folic acid * 800 microgram Once daily oral administration -7
hydroxocobalamin 1 mg intramuscular injection -7
dexamethasone 4 mg Twice daily oral administration 0 to 3
aprepitant 125 mg oral administration 1
aprepitant 80 mg oral administration 2, 3
ondansetron 8 mg oral administration 1
pembrolizumab 200 mg flat dosing intravenous 1 30 minutes
pemetrexed * 500 mg/m² intravenous 1 10 minutes
cARBOplatin * 5 AUC (area under the curve) intravenous 1 60 minutes
ondansetron 8 mg oral administration 1
domperidone 10 mg Three times daily oral administration 1

folic acid: Starting 7 days before the first cycle, continue ONCE daily until 21 days after the last dose of pemetrexed.

hydroxocobalamin: Starting 7 days before the first cycle and then repeat ONCE every 9 weeks until 21 days after the last dose of pemetrexed.

Cycle 5 (and all further cycles) - 21 days - pemetrexed and pembrolizumab maintenance

Medication Dose Route Days Max Duration
dexamethasone * 4 mg Twice daily oral administration 0, 1, 2
folic acid * 800 microgram Once daily oral administration 1
hydroxocobalamin 1 mg intramuscular injection 1
pembrolizumab 200 mg flat dosing intravenous 1 30 minutes
pemetrexed 500 mg/m² intravenous 1 10 minutes
domperidone 10 mg Three times daily oral administration 1

folic acid: Take ONCE daily until 21 days after the last dose of pemetrexed.

hydroxocobalamin: Repeat ONCE every 9 weeks (every 3 cycles) until 21 days after the last dose of pemetrexed.

Full details

Cycles 1 to 4 - 21 days - cARBOplatin, pemetrexed and pembrolizumab

Day: -7

Medication Dose Route Max duration Details
folic acid * 800 microgram Once daily oral administration
Instructions:
800 microgram = 0.8 mg. Start 7 days before the first cycle, continue until 21 days after the last dose of pemetrexed.
hydroxocobalamin 1 mg intramuscular injection
Instructions:
1 mg = 1000 microgram. Start 7 days before the first cycle and then repeat ONCE every 9 weeks until 21 days after the last dose of pemetrexed.

Day: 0

Medication Dose Route Max duration Details
dexamethasone 4 mg Twice daily oral administration
Instructions:
Take with food.

Day: 1

Medication Dose Route Max duration Details
dexamethasone 4 mg Twice daily oral administration
Instructions:
Take with food.
aprepitant 125 mg oral administration
Instructions:
ONE hour prior to chemotherapy.
ondansetron 8 mg oral administration
Instructions:
ONE hour prior to chemotherapy.
pembrolizumab 200 mg flat dosing intravenous 30 minutes
Instructions:
Administer via a sterile, non-pyrogenic, low protein binding 0.2 to 5 micron in-line or add-on filter.
pemetrexed * 500 mg/m² intravenous 10 minutes
cARBOplatin * 5 AUC (area under the curve) intravenous 60 minutes
Instructions:
To be infused approximately 30 minutes after completion of pemetrexed infusion. Hypersensitivity risk increases with number of cycles of cARBOplatin.
ondansetron 8 mg oral administration
Instructions:
EIGHT hours after chemotherapy OR before bed.
domperidone 10 mg Three times daily oral administration
Instructions:
When required for nausea and/or vomiting. The choice of rescue antiemetic may be substituted to reflect institutional policy or individual patient characteristics.

Day: 2

Medication Dose Route Max duration Details
dexamethasone 4 mg Twice daily oral administration
Instructions:
Take with food.
aprepitant 80 mg oral administration
Instructions:
ONCE daily in the morning.

Day: 3

Medication Dose Route Max duration Details
dexamethasone 4 mg Twice daily oral administration
Instructions:
Take with food.
aprepitant 80 mg oral administration
Instructions:
ONCE daily in the morning.

Cycle 5 (and all further cycles) - 21 days - pemetrexed and pembrolizumab maintenance

Day: 0

Medication Dose Route Max duration Details
dexamethasone * 4 mg Twice daily oral administration
Instructions:

Take with food.

Day: 1

Medication Dose Route Max duration Details
dexamethasone * 4 mg Twice daily oral administration
Instructions:

Take with food.

folic acid * 800 microgram Once daily oral administration
Instructions:

800 microgram = 0.8 mg.

Take ONCE daily until 21 days after the last dose of pemetrexed.

hydroxocobalamin 1 mg intramuscular injection
Instructions:

1 mg = 1000 microgram.

Administer ONCE every 9 weeks until 21 days after the last dose of pemetrexed.

pembrolizumab 200 mg flat dosing intravenous 30 minutes
Instructions:
Administer via a sterile, non-pyrogenic, low protein binding 0.2 to 5 micron in-line or add-on filter.
pemetrexed 500 mg/m² intravenous 10 minutes
domperidone 10 mg Three times daily oral administration
Instructions:

When required for nausea and/or vomiting.

The choice of rescue antiemetic may be substituted to reflect institutional policy or individual patient characteristics.

Day: 2

Medication Dose Route Max duration Details
dexamethasone * 4 mg Twice daily oral administration
Instructions:

Take with food.

Supportive Care Factors

Factor Value
Emetogenicity: Variable

Emetogenicity: HIGH (cARBOplatin AUC≥4, pemetrexed and pembrolizumab) cycles 1 to 4; LOW pemetrexed maintenance

References

1. Gandhi, L., D. Rodriguez-Abreu, S. Gadgeel, et al. 2018. "Pembrolizumab plus Chemotherapy in Metastatic Non-Small-Cell Lung Cancer." N Engl J Med 378(22):2078-2092, PMID: 29658856

2. Boulanger J, Boursiquot JN, Cournoyer G, et al. Management of hypersensitivity to platinum- and taxane-based chemotherapy: cepo review and clinical recommendations. Curr Oncol. 2014;21(4):e630-e641., PMID: 25089112

3. Castells, M.C., Matulonis, U.A., and Horton, TM. Infusion reactions to systemic chemotherapy. Savarese DMF and Feldweg AM, ed. UpToDate. Waltham, MA: UpToDate Inc. https://www.uptodate.com/contents/infusion-reactions-to-systemic-chemotherapy (Accessed 26 March 2021).

4. Juno Pharmaceuticals NZ Ltd. (2021, May 18). Pemetrexed Juno Medsafe Datasheet 17 August 2017. Retrieved from Medsafe: https://www.medsafe.govt.nz/profs/Datasheet/p/PemetrexedJunoinf.pdf

* The medicines, doses, combinations, and schedule in this treatment regimen have been carefully reviewed against international best practice guidelines by specialists in medical oncology around New Zealand and this advice has been accepted for publication by Te Aho o Te Kahu (the Cancer Control Agency). Sometimes medicines that are used in routine clinical practice have not been through a formal review process by the NZ Medicines Regulator Medsafe and are therefore considered unapproved or off-label. These medicines are legally able to be prescribed through sections 25 and 29 of the Medicines Act and by obtaining informed consent from patients. All treatment regimens listed on this website have been through robust peer review and are considered an accepted standard of care, whether prescribed through sections 25 or 29 or carrying formal Medsafe Approval.

s29: This symbol indicates that some formulations of the associated medicine are legally only able to be prescribed under section 29 of the Medicines Act. You can see which formulations are section 29 by hovering over the s29 symbol. You can access full medication details from the New Zealand Formulary by clicking on the medication name. Each clinician retains full responsibility for ensuring they have complied with all relevant obligations and requirements of section 29 including obtaining informed patient consent prior to prescribing the applicable medicine.