Difference between revisions of "Mantle cell lymphoma"

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=BR=
 
=BR=
 
BR: '''<u>B</u>'''endamustine, '''<u>R</u>'''ituximab
 
BR: '''<u>B</u>'''endamustine, '''<u>R</u>'''ituximab
*Regimen is the same as [[#BR|BR in follicular lymphoma, Regimen #2, Rummel, et al. 2012 - StiL NH1]]
+
*Regimen is the same as [[Follicular_lymphoma#BR|BR in follicular lymphoma, Rummel, et al. 2012 - StiL NHL1]]
  
 
=CALGB 59909=
 
=CALGB 59909=
 
==Regimen==
 
==Regimen==
==Treatments 1-2, R-M-CHOP==
+
===Treatments 1-2, R-M-CHOP===
*[[Rituximab (Rituxan)]] 375 mg/m2 IV on day 1 (rituximab withheld if circulating mantle cells are >10,000 cells/uL)
+
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once on day 1 (rituximab withheld if circulating mantle cells are >10,000 cells/uL)
*[[Methotrexate (MTX)]] 300 mg/m2 IV over 4 hours on day 2
+
*[[Methotrexate (MTX)]] 300 mg/m2 IV over 4 hours once on day 2
 
*[[Folinic acid (Leucovorin)]] 50 mg/m2 IV every 6 hours x 3 doses, starting 24 hours after completion of methotrexate, then 10 mg/m2 IV/PO every 6 hours until serum methotrexate level <0.05 uM
 
*[[Folinic acid (Leucovorin)]] 50 mg/m2 IV every 6 hours x 3 doses, starting 24 hours after completion of methotrexate, then 10 mg/m2 IV/PO every 6 hours until serum methotrexate level <0.05 uM
*[[Cyclophosphamide (Cytoxan)]] 2000 mg/m2 IV over 2 hours on day 3
+
*[[Cyclophosphamide (Cytoxan)]] 2000 mg/m2 IV over 2 hours once on day 3
*[[Doxorubicin (Adriamycin)]] 50 mg/m2 IV on day 3
+
*[[Doxorubicin (Adriamycin)]] 50 mg/m2 IV once on day 3
*[[Vincristine (Oncovin)]] 1.4 mg/m2 (maximum dose of 2 mg for patients >40 years old) IV on day 3
+
*[[Vincristine (Oncovin)]] 1.4 mg/m2 (maximum dose of 2 mg for patients >40 years old) IV once on day 3
*[[Prednisone (Sterapred)]] 100 mg/m2 PO on days 3-7
+
*[[Prednisone (Sterapred)]] 100 mg/m2 PO once daily on days 3-7
  
 
'''Interval between treatment 1 & 2 based on count recovery.  Median days between treatment 1 & 2 was 23 days, with a range of 16-41 days observed.'''
 
'''Interval between treatment 1 & 2 based on count recovery.  Median days between treatment 1 & 2 was 23 days, with a range of 16-41 days observed.'''
  
 
Supportive medications:
 
Supportive medications:
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC daily starting on day 4, to continue until ANC >10000 once or >5000 twice  
+
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once daily starting on day 4, to continue until ANC >10000 once or >5000 twice  
*Levofloxacin (Levaquin) 500 mg PO daily, starting on day 6, to continue until ANC ≥1500
+
*Levofloxacin (Levaquin) 500 mg PO once daily, starting on day 6, to continue until ANC ≥1500
*Fluconazole (Diflucan) 200 mg PO daily, starting on day 6, to continue until ANC ≥1500
+
*Fluconazole (Diflucan) 200 mg PO once daily, starting on day 6, to continue until ANC ≥1500
  
 
Patients with ≤15% involvement by disease in bone marrow biopsy after treatment 2 proceed to treatment 3.  If bone marrow biopsy after treatment 2 has >15% involvement by disease, repeat treatment 2 (identified as "treatment 2.5").  Patients with >15% bone marrow involvement by disease after treatment 2.5 were removed from protocol.
 
Patients with ≤15% involvement by disease in bone marrow biopsy after treatment 2 proceed to treatment 3.  If bone marrow biopsy after treatment 2 has >15% involvement by disease, repeat treatment 2 (identified as "treatment 2.5").  Patients with >15% bone marrow involvement by disease after treatment 2.5 were removed from protocol.
  
==Treatment 3, "EAR"==
+
===Treatment 3, "EAR"===
 
EAR: '''<u>E</u>'''toposide, '''<u>A</u>'''ra-C, '''<u>R</u>'''ituximab ''
 
EAR: '''<u>E</u>'''toposide, '''<u>A</u>'''ra-C, '''<u>R</u>'''ituximab ''
 
<br>Treatment 3 begins 4 weeks after treatment 2, if ANC ≥1000, platelets ≥100,000/uL, Cr <2 mg/dL, total bilirubin <2x upper limit of normal, and AST <3x upper limit of normal.''
 
<br>Treatment 3 begins 4 weeks after treatment 2, if ANC ≥1000, platelets ≥100,000/uL, Cr <2 mg/dL, total bilirubin <2x upper limit of normal, and AST <3x upper limit of normal.''
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*[[Etoposide (Vepesid)]] 10 mg/kg/day (40 mg/kg total dose) IV continuous infusion over 96 hours on days 1-4  
 
*[[Etoposide (Vepesid)]] 10 mg/kg/day (40 mg/kg total dose) IV continuous infusion over 96 hours on days 1-4  
 
*[[Cytarabine (Cytosar)]] 2000 mg/m2 IV over 2 hours BID on days 1-4 (8 total doses)
 
*[[Cytarabine (Cytosar)]] 2000 mg/m2 IV over 2 hours BID on days 1-4 (8 total doses)
*[[Rituximab (Rituxan)]] 375 mg/m2 IV on days 6 & 13
+
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once daily on days 6 & 13
 
*Daily leukapheresis to start when WBC ≥5000/uL
 
*Daily leukapheresis to start when WBC ≥5000/uL
  
 
Supportive medications:
 
Supportive medications:
*[[Filgrastim (Neupogen)]] 10 mcg/kg SC daily starting on day 14, to continue until peripheral blood stem cell collection is complete
+
*[[Filgrastim (Neupogen)]] 10 mcg/kg SC once daily starting on day 14, to continue until peripheral blood stem cell collection is complete
*Levofloxacin (Levaquin) 500 mg PO daily, starting on day 7, to continue until ANC ≥500
+
*Levofloxacin (Levaquin) 500 mg PO once daily, starting on day 7, to continue until ANC ≥500
*Fluconazole (Diflucan) 200 mg PO daily, starting on day 6, to continue until ANC ≥500
+
*Fluconazole (Diflucan) 200 mg PO once daily, starting on day 6, to continue until ANC ≥500
*Acyclovir (Zovirax) 200 mg PO TID, starting on day 6, to continue until 1 year after autologous stem cell transplant (ASCT)
+
*[[Acyclovir (Zovirax)]] 200 mg PO TID, starting on day 6, to continue until 1 year after autologous stem cell transplant (ASCT)
*Note: Text specified that Trimethoprim/Sulfamethoxazole (Bactrim DS) prophylaxis started during treatment 3 (see dose/schedule in treatment 4)--although table 1 did not list it--to continue until 3 months after ASCT.
+
*Note: Text specified that [[Trimethoprim/Sulfamethoxazole (Bactrim DS)]] prophylaxis started during treatment 3 (see dose/schedule in treatment 4)--although table 1 did not list it--to continue until 3 months after ASCT.
  
==Treatment 4, "CBV"==
+
===Treatment 4, "CBV"===
 
CBV: '''<u>C</u>'''yclophosphamide, '''<u>B</u>'''iCNU, '''<u>V</u>'''P-16  
 
CBV: '''<u>C</u>'''yclophosphamide, '''<u>B</u>'''iCNU, '''<u>V</u>'''P-16  
*[[Carmustine (BiCNU)]] 15 mg/kg (maximum dose of 550 mg/m2) IV over 1 hour on day -6
+
*[[Carmustine (BiCNU)]] 15 mg/kg (maximum dose of 550 mg/m2) IV over 1 hour once on day -6
*[[Etoposide (Vepesid)]] 60 mg/kg IV over 4 hours on day -4
+
*[[Etoposide (Vepesid)]] 60 mg/kg IV over 4 hours once on day -4
*[[Cyclophosphamide (Cytoxan)]] 100 mg/kg IV over 2 hours on day -2
+
*[[Cyclophosphamide (Cytoxan)]] 100 mg/kg IV over 2 hours once on day -2
 
*Autologous blood stem cells infused on day 0.
 
*Autologous blood stem cells infused on day 0.
  
 
Supportive medications:
 
Supportive medications:
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC daily starting on day +4, to continue until ANC >5000 once or >1500 twice
+
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once daily starting on day +4, to continue until ANC >5000 once or >1500 twice
*Levofloxacin (Levaquin) 500 mg PO daily, starting on day +2, to continue until ANC ≥500
+
*Levofloxacin (Levaquin) 500 mg PO once daily, starting on day +2, to continue until ANC ≥500
*Fluconazole (Diflucan) 200 mg PO daily, starting on day +1, to continue until ANC ≥500
+
*Fluconazole (Diflucan) 200 mg PO once daily, starting on day +1, to continue until ANC ≥500
*Acyclovir (Zovirax) 200 mg PO TID, starting on day -2, to continue until 1 year after ASCT
+
*[[Acyclovir (Zovirax)]] 200 mg PO TID, starting on day -2, to continue until 1 year after ASCT
 
*[[Trimethoprim/Sulfamethoxazole (Bactrim DS)]] 160/800 mg PO BID on Saturday and Sunday, to continue until 3 months after ASCT
 
*[[Trimethoprim/Sulfamethoxazole (Bactrim DS)]] 160/800 mg PO BID on Saturday and Sunday, to continue until 3 months after ASCT
  
==Treatment 5, Rituximab==
+
===Treatment 5, Rituximab===
*[[Rituximab (Rituxan)]] 375 mg/m2 IV weekly x 2 doses, 6 and 7 weeks after ASCT
+
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once per week x 2 doses, during the sixth and seventh weeks after ASCT
  
==Additional considerations==
+
===Additional considerations===
 
If cerebrospinal fluid (CSF) contained disease with CSF WBC ≤5 cells/uL:
 
If cerebrospinal fluid (CSF) contained disease with CSF WBC ≤5 cells/uL:
 
*[[Methotrexate (MTX)]] 12 mg intrathecal x 10 total doses during treatments 1-3; not given concurrently with intrathecal methotrexate or cytarabine
 
*[[Methotrexate (MTX)]] 12 mg intrathecal x 10 total doses during treatments 1-3; not given concurrently with intrathecal methotrexate or cytarabine
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=(R)-CHOP/R-DHAP -> autologous SCT=
 
=(R)-CHOP/R-DHAP -> autologous SCT=
 +
R-CHOP: '''<u>R</u>'''ituximab, '''<u>C</u>'''yclophosphamide, '''<u>H</u>'''ydroxydaunorubicin, '''<u>O</u>'''ncovin, '''<u>P</u>'''rednisone
 +
<br>R-DHAP: '''<u>R</u>'''ituximab, '''<u>D</u>'''examethasone, '''<u>H</u>'''igh-dose '''<u>A</u>'''ra-C (cytarabine), cis'''<u>P</u>'''latin
 +
 
[[Levels of Evidence]]:   
 
[[Levels of Evidence]]:   
 
<span  
 
<span  
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==Regimen==
 
==Regimen==
Part 1 (CHOP: cycles 1-2):
+
===Part 1 (CHOP: cycles 1-2)===
*[[Cyclophosphamide (Cytoxan)]] 750 mg/m2 IV on day 1
+
*[[Cyclophosphamide (Cytoxan)]] 750 mg/m2 IV once on day 1
*[[Doxorubicin (Adriamycin)]] 50 mg/m2 IV on day 1
+
*[[Doxorubicin (Adriamycin)]] 50 mg/m2 IV once on day 1
*[[Vincristine (Oncovin)]] 1.4 mg/m2 IV on day 1
+
*[[Vincristine (Oncovin)]] 1.4 mg/m2 IV once on day 1
*[[Prednisone (Sterapred)]] 40 mg/m2 PO on days 1-5
+
*[[Prednisone (Sterapred)]] 40 mg/m2 PO once daily on days 1-5
  
 
'''If progression, go to part 3, otherwise after 2 21-day cycles:'''
 
'''If progression, go to part 3, otherwise after 2 21-day cycles:'''
  
Part 2 (R-CHOP: cycle 3):
+
===Part 2 (R-CHOP: cycle 3)===
*[[Rituximab (Rituxan)]] 375 mg/m2 IV on day 1  
+
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once on day 1  
*[[Cyclophosphamide (Cytoxan)]] 750 mg/m2 IV on day 1
+
*[[Cyclophosphamide (Cytoxan)]] 750 mg/m2 IV once on day 1
*[[Doxorubicin (Adriamycin)]] 50 mg/m2 IV on day 1
+
*[[Doxorubicin (Adriamycin)]] 50 mg/m2 IV once on day 1
*[[Vincristine (Oncovin)]] 1.4 mg/m2 IV on day 1
+
*[[Vincristine (Oncovin)]] 1.4 mg/m2 IV once on day 1
*[[Prednisone (Sterapred)]] 40 mg/m2 on days 1-5
+
*[[Prednisone (Sterapred)]] 40 mg/m2 once daily on days 1-5
  
 
'''After one 21-day cycle:'''
 
'''After one 21-day cycle:'''
  
Part 3 (R-DHAP: cycles 4-6):
+
===Part 3 (R-DHAP: cycles 4-6)===
*[[Rituximab (Rituxan)]] 375 mg/m2 IV on day 1  
+
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once on day 1  
*[[Dexamethasone (Decadron)]] 40 mg days 1-4
+
*[[Dexamethasone (Decadron)]] 40 mg once daily on days 1-4
 
*[[Cytarabine (Cytosar)]] 2000 mg/m2 IV Q12H on day 2 (2 total doses)
 
*[[Cytarabine (Cytosar)]] 2000 mg/m2 IV Q12H on day 2 (2 total doses)
 
*[[Cisplatin (Platinol)]] 100 mg/m2 IV continuous infusion over 24 hours on day 1
 
*[[Cisplatin (Platinol)]] 100 mg/m2 IV continuous infusion over 24 hours on day 1
Line 110: Line 113:
 
'''After three 21-day cycles:'''
 
'''After three 21-day cycles:'''
  
Part 4 (Stem cell collection and intensified therapy):
+
===Part 4 (Stem cell collection and intensified therapy)===
 
+
*[[Transplant conditioning regimens#TAM6 | TAM6]] or [[Transplant conditioning regimens#BEAM | BEAM]] regimen (see [[Transplant conditioning regimens]])
*TAM6 or BEAM regimen (see [[Transplant conditioning regimens]])
 
  
 
==References==
 
==References==
Line 118: Line 120:
  
 
=R-Hyper-CVAD/R-MTX-Ara-C=
 
=R-Hyper-CVAD/R-MTX-Ara-C=
CVAD: '''<u>C</u>'''yclophosphamide, '''<u>V</u>'''incristine, '''<u>A</u>'''driamycin, '''<u>D</u>'''examethasone
+
R-Hyper-CVAD: '''<u>R</u>'''ituximab, '''<u>Hyper</u>'''fractionated '''<u>C</u>'''yclophosphamide, '''<u>V</u>'''incristine, '''<u>A</u>'''driamycin, '''<u>D</u>'''examethasone
 +
<br>R-MTX-Ara-C: '''<u>R</u>'''ituximab, '''<u>MTX</u>''' (Methotrexate), '''<u>A</u>'''ra-'''<u>C</u>''' (Cytarabine)
  
 
[[Levels of Evidence]]:   
 
[[Levels of Evidence]]:   
Line 129: Line 132:
  
 
==Regimen==
 
==Regimen==
Part A (cycles 1, 3, 5, 7):
+
===Part A (cycles 1, 3, 5, 7)===
 
*[[Cyclophosphamide (Cytoxan)]] 300 mg/m2 IV over 3 hours Q12H on days 2-4 (6 total doses)
 
*[[Cyclophosphamide (Cytoxan)]] 300 mg/m2 IV over 3 hours Q12H on days 2-4 (6 total doses)
*[[Mesna (Mesnex)]] 600 mg/m2/day IV continuous infusion on days 2-4, starting 1 hour before cytoxan and completed 12 hours after the last dose of cytoxan
+
*[[Mesna (Mesnex)]] 600 mg/m2/day IV continuous infusion on days 2-4, starting 1 hour before cyclophosphamide and completed 12 hours after the last dose of cyclophosphamide
*[[Vincristine (Oncovin)]] 1.4 mg/m2 (maximum dose of 2 mg per cycle) IV piggyback on day 5, 12 hours after the last dose of cyclophosphamide, and on day 12
+
*[[Vincristine (Oncovin)]] 1.4 mg/m2 (maximum dose of 2 mg per cycle) IV piggyback once daily on days 5 & 12; day 5 dose is given 12 hours after the last dose of cyclophosphamide
*[[Doxorubicin (Adriamycin)]] 16.6-16.7 (note: reference had slightly different dosages in the text vs. table 1) mg/m2/day IV continuous infusion over 72 hours on days 5-7  
+
*[[Doxorubicin (Adriamycin)]] 16.6-16.7 (note: reference had slightly different dosages in the text vs. table 1) mg/m2/day (total dose per cycle: 49.8-50.1 mg/m2) IV continuous infusion over 72 hours on days 5-7  
*[[Dexamethasone (Decadron)]] 40 mg PO/IV on days 2-5, 12-15
+
*[[Dexamethasone (Decadron)]] 40 mg PO/IV once daily on days 2-5, 12-15
*[[Rituximab (Rituxan)]] 375 mg/m2 IV on day 1
+
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once on day 1
 
**Patients with peripheral blood involvement could have the cycle 1 dose of rituximab delayed or omitted by clinician discretion
 
**Patients with peripheral blood involvement could have the cycle 1 dose of rituximab delayed or omitted by clinician discretion
  
 
'''21-day cycles, alternating every 21 days with Part B, for a total of 4 cycles of Part A and 4 cycles of Part B'''
 
'''21-day cycles, alternating every 21 days with Part B, for a total of 4 cycles of Part A and 4 cycles of Part B'''
  
Part B (cycles 2, 4, 6, 8):
+
===Part B (cycles 2, 4, 6, 8)===
*[[Methotrexate (MTX)]] 200 mg/m2 IV over 2 hours, then 800 mg/m2 IV over 22 hours on day 2
+
*[[Methotrexate (MTX)]] 200 mg/m2 IV over 2 hours, then 800 mg/m2 IV over 22 hours once on day 2
 
**Patients with a Cr >1.5 mg/dL received a 50% reduced dose of methotrexate  
 
**Patients with a Cr >1.5 mg/dL received a 50% reduced dose of methotrexate  
 
*[[Cytarabine (Cytosar)]] 3000 mg/m2 (1000 mg/m2 for patients >60 years old or with Cr >1.5) IV over 2 hours Q12H on days 3 & 4 (4 total doses)
 
*[[Cytarabine (Cytosar)]] 3000 mg/m2 (1000 mg/m2 for patients >60 years old or with Cr >1.5) IV over 2 hours Q12H on days 3 & 4 (4 total doses)
 
*[[Folinic acid (Leucovorin)]] 50 mg PO x1 12 hours after methotrexate is complete, then 15 mg PO Q6H x 8 doses.  If serum methotrexate level at 24 hours is >1 umol/L or at 48 hours is >0.1 umol/L, dose of folinic acid is increased to 100 mg IV Q3H.
 
*[[Folinic acid (Leucovorin)]] 50 mg PO x1 12 hours after methotrexate is complete, then 15 mg PO Q6H x 8 doses.  If serum methotrexate level at 24 hours is >1 umol/L or at 48 hours is >0.1 umol/L, dose of folinic acid is increased to 100 mg IV Q3H.
*[[Rituximab (Rituxan)]] 375 mg/m2 IV on day 1
+
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once on day 1
 
*Urine alkalinized to pH of 6.8 or more prior to the start of methotrexate and kept within that range until methotrexate is cleared
 
*Urine alkalinized to pH of 6.8 or more prior to the start of methotrexate and kept within that range until methotrexate is cleared
*Prednisolone 1% ophthalmic solution 2 drops in each eye 4 times per day on days 3-9was started on the day of the start of cytarabine infusion and was continued for 7 days to prevent chemical conjunctivitis.
+
*[[Prednisolone (Millipred) | Prednisolone]] 1% ophthalmic solution 2 drops in each eye 4 times per day on days 3-9 was started on the day of the start of cytarabine infusion and was continued for 7 days to prevent chemical conjunctivitis.
  
 
'''21-day cycles, alternating every 21 days with Part A, for a total of 4 cycles of Part A and 4 cycles of Part B'''
 
'''21-day cycles, alternating every 21 days with Part A, for a total of 4 cycles of Part A and 4 cycles of Part B'''
Line 153: Line 156:
 
Supportive medications (for both Part A and Part B):
 
Supportive medications (for both Part A and Part B):
 
<br>''All medications given for 10 days, starting 24-36 hours after doxorubicin infusion is complete''
 
<br>''All medications given for 10 days, starting 24-36 hours after doxorubicin infusion is complete''
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC daily  
+
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once daily  
*Valacyclovir (Valtrex) 500 mg PO daily
+
*[[Valacyclovir (Valtrex)]] 500 mg PO once daily
*Fluconazole (Diflucan) 100 mg PO daily
+
*Fluconazole (Diflucan) 100 mg PO once daily
*Levofloxacin (Levaquin) 500 mg PO daily or Ciprofloxacin (Cipro) (reference did not specify dose/frequency)
+
*Levofloxacin (Levaquin) 500 mg PO once daily or Ciprofloxacin (Cipro) (reference did not specify dose/frequency)
 
*"Erythropoietin was permitted throughout therapy"
 
*"Erythropoietin was permitted throughout therapy"
  
Line 179: Line 182:
 
''Protocol originally started rituximab during cycle 4, but the protocol was amended to start it on cycle 2.''
 
''Protocol originally started rituximab during cycle 4, but the protocol was amended to start it on cycle 2.''
 
<br>''Cycle 1 uses maxi-CHOP, cycle 2 uses HiDAC, cycle 3 uses maxi-CHOP, etc.''
 
<br>''Cycle 1 uses maxi-CHOP, cycle 2 uses HiDAC, cycle 3 uses maxi-CHOP, etc.''
*[[Rituximab (Rituxan)]] 375 mg/m2 IV on day 1 of cycles 2-5, and 375 mg/m2 IV on days 1 & 9 of cycle 6
+
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once on day 1 of cycles 2-5, and 375 mg/m2 IV once daily on days 1 & 9 of cycle 6
  
 
==maxi-CHOP==
 
==maxi-CHOP==
*[[Cyclophosphamide (Cytoxan)]] 1200 mg/m2 IV on day 1
+
*[[Cyclophosphamide (Cytoxan)]] 1200 mg/m2 IV once on day 1
*[[Doxorubicin (Adriamycin)]] 75 mg/m2 IV on day 1
+
*[[Doxorubicin (Adriamycin)]] 75 mg/m2 IV once on day 1
*[[Vincristine (Oncovin)]] 2 mg IV on day 1
+
*[[Vincristine (Oncovin)]] 2 mg IV once on day 1
*[[Prednisone (Sterapred)]] 100 mg PO on days 1-5
+
*[[Prednisone (Sterapred)]] 100 mg PO once daily on days 1-5
  
 
'''21-day cycles, alternating with high-dose cytarabine, for a total of 3 cycles of maxi-CHOP and 3 cycles of high-dose cytarabine'''  
 
'''21-day cycles, alternating with high-dose cytarabine, for a total of 3 cycles of maxi-CHOP and 3 cycles of high-dose cytarabine'''  

Revision as of 06:16, 2 March 2013

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BR

BR: Bendamustine, Rituximab

CALGB 59909

Regimen

Treatments 1-2, R-M-CHOP

Interval between treatment 1 & 2 based on count recovery. Median days between treatment 1 & 2 was 23 days, with a range of 16-41 days observed.

Supportive medications:

  • Filgrastim (Neupogen) 5 mcg/kg SC once daily starting on day 4, to continue until ANC >10000 once or >5000 twice
  • Levofloxacin (Levaquin) 500 mg PO once daily, starting on day 6, to continue until ANC ≥1500
  • Fluconazole (Diflucan) 200 mg PO once daily, starting on day 6, to continue until ANC ≥1500

Patients with ≤15% involvement by disease in bone marrow biopsy after treatment 2 proceed to treatment 3. If bone marrow biopsy after treatment 2 has >15% involvement by disease, repeat treatment 2 (identified as "treatment 2.5"). Patients with >15% bone marrow involvement by disease after treatment 2.5 were removed from protocol.

Treatment 3, "EAR"

EAR: Etoposide, Ara-C, Rituximab
Treatment 3 begins 4 weeks after treatment 2, if ANC ≥1000, platelets ≥100,000/uL, Cr <2 mg/dL, total bilirubin <2x upper limit of normal, and AST <3x upper limit of normal.

  • Etoposide (Vepesid) 10 mg/kg/day (40 mg/kg total dose) IV continuous infusion over 96 hours on days 1-4
  • Cytarabine (Cytosar) 2000 mg/m2 IV over 2 hours BID on days 1-4 (8 total doses)
  • Rituximab (Rituxan) 375 mg/m2 IV once daily on days 6 & 13
  • Daily leukapheresis to start when WBC ≥5000/uL

Supportive medications:

  • Filgrastim (Neupogen) 10 mcg/kg SC once daily starting on day 14, to continue until peripheral blood stem cell collection is complete
  • Levofloxacin (Levaquin) 500 mg PO once daily, starting on day 7, to continue until ANC ≥500
  • Fluconazole (Diflucan) 200 mg PO once daily, starting on day 6, to continue until ANC ≥500
  • Acyclovir (Zovirax) 200 mg PO TID, starting on day 6, to continue until 1 year after autologous stem cell transplant (ASCT)
  • Note: Text specified that Trimethoprim/Sulfamethoxazole (Bactrim DS) prophylaxis started during treatment 3 (see dose/schedule in treatment 4)--although table 1 did not list it--to continue until 3 months after ASCT.

Treatment 4, "CBV"

CBV: Cyclophosphamide, BiCNU, VP-16

Supportive medications:

  • Filgrastim (Neupogen) 5 mcg/kg SC once daily starting on day +4, to continue until ANC >5000 once or >1500 twice
  • Levofloxacin (Levaquin) 500 mg PO once daily, starting on day +2, to continue until ANC ≥500
  • Fluconazole (Diflucan) 200 mg PO once daily, starting on day +1, to continue until ANC ≥500
  • Acyclovir (Zovirax) 200 mg PO TID, starting on day -2, to continue until 1 year after ASCT
  • Trimethoprim/Sulfamethoxazole (Bactrim DS) 160/800 mg PO BID on Saturday and Sunday, to continue until 3 months after ASCT

Treatment 5, Rituximab

  • Rituximab (Rituxan) 375 mg/m2 IV once per week x 2 doses, during the sixth and seventh weeks after ASCT

Additional considerations

If cerebrospinal fluid (CSF) contained disease with CSF WBC ≤5 cells/uL:

  • Methotrexate (MTX) 12 mg intrathecal x 10 total doses during treatments 1-3; not given concurrently with intrathecal methotrexate or cytarabine

If CSF contained >5 cells/uL:

  • In addition to intrathecal chemotherapy above, patient also received 2 Gy x 12 fractions (total dose 24 Gy) cranial radiation

If any patient appeared to be experiencing carmustine-induced pneumonitis:

References

  1. Damon LE, Johnson JL, Niedzwiecki D, Cheson BD, Hurd DD, Bartlett NL, Lacasce AS, Blum KA, Byrd JC, Kelly M, Stock W, Linker CA, Canellos GP. Immunochemotherapy and autologous stem-cell transplantation for untreated patients with mantle-cell lymphoma: CALGB 59909. J Clin Oncol. 2009 Dec 20;27(36):6101-8. Epub 2009 Nov 16. link to original article contains protocol PubMed

(R)-CHOP/R-DHAP -> autologous SCT

R-CHOP: Rituximab, Cyclophosphamide, Hydroxydaunorubicin, Oncovin, Prednisone
R-DHAP: Rituximab, Dexamethasone, High-dose Ara-C (cytarabine), cisPlatin

Levels of Evidence: Phase II

Regimen

Part 1 (CHOP: cycles 1-2)

If progression, go to part 3, otherwise after 2 21-day cycles:

Part 2 (R-CHOP: cycle 3)

After one 21-day cycle:

Part 3 (R-DHAP: cycles 4-6)

After three 21-day cycles:

Part 4 (Stem cell collection and intensified therapy)

References

  1. Delarue R, Haioun C, Ribrag V, Brice P, Delmer A, Tilly H, Salles G, Van Hoof A, Casasnovas O, Brousse N, Lefrere F, Hermine O; for the Groupe d'Etude des Lymphomes de l'Adulte (GELA). CHOP and DHAP plus rituximab followed by autologous stem cell transplantation in mantle cell lymphoma: a phase 2 study from the Groupe d'Etude des Lymphomes de l'Adulte. Blood. 2013 Jan 3;121(1):48-53. Epub 2012 Jun 20. link to original article contains protocol PubMed

R-Hyper-CVAD/R-MTX-Ara-C

R-Hyper-CVAD: Rituximab, Hyperfractionated Cyclophosphamide, Vincristine, Adriamycin, Dexamethasone
R-MTX-Ara-C: Rituximab, MTX (Methotrexate), Ara-C (Cytarabine)

Levels of Evidence: Phase II

Regimen

Part A (cycles 1, 3, 5, 7)

  • Cyclophosphamide (Cytoxan) 300 mg/m2 IV over 3 hours Q12H on days 2-4 (6 total doses)
  • Mesna (Mesnex) 600 mg/m2/day IV continuous infusion on days 2-4, starting 1 hour before cyclophosphamide and completed 12 hours after the last dose of cyclophosphamide
  • Vincristine (Oncovin) 1.4 mg/m2 (maximum dose of 2 mg per cycle) IV piggyback once daily on days 5 & 12; day 5 dose is given 12 hours after the last dose of cyclophosphamide
  • Doxorubicin (Adriamycin) 16.6-16.7 (note: reference had slightly different dosages in the text vs. table 1) mg/m2/day (total dose per cycle: 49.8-50.1 mg/m2) IV continuous infusion over 72 hours on days 5-7
  • Dexamethasone (Decadron) 40 mg PO/IV once daily on days 2-5, 12-15
  • Rituximab (Rituxan) 375 mg/m2 IV once on day 1
    • Patients with peripheral blood involvement could have the cycle 1 dose of rituximab delayed or omitted by clinician discretion

21-day cycles, alternating every 21 days with Part B, for a total of 4 cycles of Part A and 4 cycles of Part B

Part B (cycles 2, 4, 6, 8)

  • Methotrexate (MTX) 200 mg/m2 IV over 2 hours, then 800 mg/m2 IV over 22 hours once on day 2
    • Patients with a Cr >1.5 mg/dL received a 50% reduced dose of methotrexate
  • Cytarabine (Cytosar) 3000 mg/m2 (1000 mg/m2 for patients >60 years old or with Cr >1.5) IV over 2 hours Q12H on days 3 & 4 (4 total doses)
  • Folinic acid (Leucovorin) 50 mg PO x1 12 hours after methotrexate is complete, then 15 mg PO Q6H x 8 doses. If serum methotrexate level at 24 hours is >1 umol/L or at 48 hours is >0.1 umol/L, dose of folinic acid is increased to 100 mg IV Q3H.
  • Rituximab (Rituxan) 375 mg/m2 IV once on day 1
  • Urine alkalinized to pH of 6.8 or more prior to the start of methotrexate and kept within that range until methotrexate is cleared
  • Prednisolone 1% ophthalmic solution 2 drops in each eye 4 times per day on days 3-9 was started on the day of the start of cytarabine infusion and was continued for 7 days to prevent chemical conjunctivitis.

21-day cycles, alternating every 21 days with Part A, for a total of 4 cycles of Part A and 4 cycles of Part B

Supportive medications (for both Part A and Part B):
All medications given for 10 days, starting 24-36 hours after doxorubicin infusion is complete

  • Filgrastim (Neupogen) 5 mcg/kg SC once daily
  • Valacyclovir (Valtrex) 500 mg PO once daily
  • Fluconazole (Diflucan) 100 mg PO once daily
  • Levofloxacin (Levaquin) 500 mg PO once daily or Ciprofloxacin (Cipro) (reference did not specify dose/frequency)
  • "Erythropoietin was permitted throughout therapy"

References

  1. Romaguera JE, Fayad L, Rodriguez MA, Broglio KR, Hagemeister FB, Pro B, McLaughlin P, Younes A, Samaniego F, Goy A, Sarris AH, Dang NH, Wang M, Beasley V, Medeiros LJ, Katz RL, Gagneja H, Samuels BI, Smith TL, Cabanillas FF. High rate of durable remissions after treatment of newly diagnosed aggressive mantle-cell lymphoma with rituximab plus hyper-CVAD alternating with rituximab plus high-dose methotrexate and cytarabine. J Clin Oncol. 2005 Oct 1;23(28):7013-23. Epub 2005 Sep 6. link to original article contains protocol PubMed
  2. Wang M, Fayad L, Cabanillas F, Hagemeister F, McLaughlin P, Rodriguez MA, Kwak LW, Zhou Y, Kantarjian H, Romaguera J. Phase 2 trial of rituximab plus hyper-CVAD alternating with rituximab plus methotrexate-cytarabine for relapsed or refractory aggressive mantle cell lymphoma. Cancer. 2008 Nov 15;113(10):2734-41. doi: 10.1002/cncr.23880. link to original article contains protocol PubMed
  3. Romaguera JE, Fayad LE, Feng L, Hartig K, Weaver P, Rodriguez MA, Hagemeister FB, Pro B, McLaughlin P, Younes A, Samaniego F, Goy A, Cabanillas F, Kantarjian H, Kwak L, Wang M. Ten-year follow-up after intense chemoimmunotherapy with Rituximab-HyperCVAD alternating with Rituximab-high dose methotrexate/cytarabine (R-MA) and without stem cell transplantation in patients with untreated aggressive mantle cell lymphoma. Br J Haematol. 2010 Jul;150(2):200-8. doi: 10.1111/j.1365-2141.2010.08228.x. Epub 2010 May 26. Review. Erratum in: Br J Haematol.n 2010 Oct;151(1):111. link to original article contains protocol PubMed

Nordic regimen, maxi-CHOP, HiDAC, Rituximab (Rituxan)

CHOP: Cyclophosphamide, Hydroxydaunorubicin, Oncovin, Prednisone
HiDAC: High Dose Ara-C

Levels of Evidence: Phase II

Regimen

Protocol originally started rituximab during cycle 4, but the protocol was amended to start it on cycle 2.
Cycle 1 uses maxi-CHOP, cycle 2 uses HiDAC, cycle 3 uses maxi-CHOP, etc.

  • Rituximab (Rituxan) 375 mg/m2 IV once on day 1 of cycles 2-5, and 375 mg/m2 IV once daily on days 1 & 9 of cycle 6

maxi-CHOP

21-day cycles, alternating with high-dose cytarabine, for a total of 3 cycles of maxi-CHOP and 3 cycles of high-dose cytarabine

HiDAC/HDAC, high-dose Cytarabine (Cytosar)

21-day cycles, alternating with maxi-CHOP, for a total of 3 cycles of maxi-CHOP and 3 cycles of high-dose cytarabine

Supportive medications:

  • Filgrastim (Neupogen) given during cycle 6 as part of stem cell mobilization, with at least 2 million CD34+ cells/kg harvested

High-dose chemotherapy with BEAM or BEAC started 1-2 weeks after completion of cycle 6, followed by stem cell transplant. If transplant was delayed, an additional 1-2 cycles of chemotherapy with maxi-CHOP or HiDAC could be given.

References

  1. Geisler CH, Kolstad A, Laurell A, Andersen NS, Pedersen LB, Jerkeman M, Eriksson M, Nordström M, Kimby E, Boesen AM, Kuittinen O, Lauritzsen GF, Nilsson-Ehle H, Ralfkiaer E, Akerman M, Ehinger M, Sundström C, Langholm R, Delabie J, Karjalainen-Lindsberg ML, Brown P, Elonen E; Nordic Lymphoma Group. Long-term progression-free survival of mantle cell lymphoma after intensive front-line immunochemotherapy with in vivo-purged stem cell rescue: a nonrandomized phase 2 multicenter study by the Nordic Lymphoma Group. Blood. 2008 Oct 1;112(7):2687-93. Epub 2008 Jul 14. link to original article PubMed