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Docetaxel 75 / Cisplatin 75, Non-Small Cell Lung Carcinoma

Protocol-ID: 144 V1.1 (Short), DOCE75/CISP75, NSCLC

Indication(s)

  • Lung Carcinoma, Non-Small Cell; ICD-10 C34.-

Protocol classification

  • Classification: current standard
  • Intensity: Standard dose
  • Therapy mode: First line
  • Therapy intention: palliative

Cycles

Cycle length 21 days, recommended cycles: 6

Risks

  • Emetogenicity (MASCC/ESMO): high (>90%)
  • Neutropenia: very high (>41%)
  • Febrile Neutropenia: intermediate (10-20%)
  • Thrombocytopenia below 50 000/µl: low (<10%)
  • Anemia Hb below 8g/dl: moderate (6-15%)
  • Cardiotoxicity: low (<10%)

Therapy

AP
Allergy prophylaxis: Docetaxel allergy prophylaxis, Dexamethasone
Access: - none -
Docetaxel SmPC
DaySubstanceDosageSolutionAppl.Inf. timeProcedure
-1 Dexamethasone 8 mg  p.o. 1-0-1-0 
From day before therapy with Docetaxel, antihistamine therapy not provided for in summary of product characteristics.
HYD
Hydration: Hydration to Cisplatin (from 50 mg/m²)
Access: peripheral venous
Modified from Crona DJ et al 2017 and Hamroun A et al 2019.
DaySubstanceDosageSolutionAppl.Inf. timeProcedure
Balanced Crystalloid Solution 3000 ml   i.v.6 h60 min before Docetaxel (d1) 
Parallel to cisplatin and beyond. 20 mmol KCl and 4 mmol (10 ml) MgSO4 added to 1000 ml balanced crystalloid solution
Potassium chloride 60 mmol none  i.v.6 h60 min before Docetaxel (d1) 
Magnesium sulfate 12 mmol none  i.v.6 h60 min before Docetaxel (d1) 
AE
Antiemesis: Emetogenicity high, FOSAP, GRAN i.v., DEXA i.v.
Access: peripheral venous
DGHO 2016, DKG 2016, MASCC/ESMO 2016
DaySubstanceDosageSolutionAppl.Inf. timeProcedure
Fosaprepitant 150 mg NaCl 0.9% 150 ml i.v.20 min30 min before Docetaxel (d1) 
Dexamethasone 12 mg NaCl 0.9% 50 ml i.v.5 min30 min before Docetaxel (d1) 
Granisetron 1 mg NaCl 0.9% 50 ml i.v.5 min15 min before Docetaxel (d1) 
or other 5-HT3 receptor antagonist
2-4 Dexamethasone 8 mg  p.o. 1-0-0-0 
alternatively 4 mg 1-0-1
CTX
Medical tumor therapy: CISP75/DOCE75
Access: peripheral venous
Palliative therapy in advanced NSCLC
DaySubstanceDosageSolutionAppl.Inf. timeProcedure
Docetaxel 75 mg/m² BSA NaCl 0.9% 250 ml i.v.60 minSequence 
Give docetaxel concurrently with hydration before cisplatin.
Cisplatin 75 mg/m² BSA NaCl 0.9% 500 ml i.v.60 minSequence 
HW
Hematopoietic growth factors: FN risk 10-20%, G-CSF long-acting, pegylated
Access: - none -
Risk of febrile neutropenia (FN) 10-20% and 1 risk factor: age > 65 y, laboratory parameters (anemia, lymphocytopenia < 700/µl, hypalbuminemia, hyperbilirubinemia) previous chemotherapy, comorbidities, low performance status, advanced symptomatic tumor disease (DKG 2016)
DaySubstanceDosageSolutionAppl.Inf. timeProcedure
Pegfilgrastim 6 mg   subcBolus24 h after Cisplatin (d1) 
Use at risk: FN 10-20% and 1 risk factor, other long-acting G-CSF possible.
SUP
Supportive therapy: Magnesium p.o.
Access: - none -
For magnesium substitution in cisplatin therapies from 50mg/m².
DaySubstanceDosageSolutionAppl.Inf. timeProcedure
1-3 Magnesium 150 mg  p.o. 1-0-1-0 
For Cisplatin-containing therapies, 150 mg Magnesium corresponds to about 6.2 mmol.

Concomitant therapy supplements

Dexamethasone of allergy prophylaxis is covered by dexamethasone of antiemesis on days 1 and 2.

References

  • Schiller JH, Comparison of four chemotherapy regimens for advanced non-small-cell lung cancer., N Engl J Med 2002 Jan 10;346(2):92-8 [PMID]
  • Millward MJ, Phase I trial of docetaxel and cisplatin in previously untreated patients with advanced non-small-cell lung cancer., J Clin Oncol. 1997 Feb;15(2):750-8 [PMID]
  • Fossella F, Randomized, multinational, phase III study of docetaxel plus platinum combinations versus vinorelbine plus cisplatin for advanced non-small-cell lung cancer: the TAX 326 Study Group, J Clin Oncol. 2003 Aug 15;21(16):3016-24. Epub 2003 Jul 1. [PMID]
  • Novello S, Metastatic non-small-cell lung cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up., Ann Oncol 2016 Sep;27(suppl 5):v1-v27 [PMID]

Recommendations

The publishers and authors assume no liability for the accuracy of the contents. The application is at the own responsibility of the treating physician. ©Onkopti.

Valid since: 22.02.2023