B-cell acute lymphoblastic leukemia
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Induction therapy
Hyper-CVAD (induction)
Hyper-CVAD: Hyperfractionated Cyclophosphamide, Vincristine, Adriamycin, Dexamethasone
Regimen
Part A (cycles 1, 3, 5, 7):
- Cyclophosphamide (Cytoxan) 300 mg/m2 IV over 2 hours Q12H on days 1-3 (6 total doses)
- Mesna (Mesnex) 600 mg/m2/day IV continuous infusion on days 1-3, starting 1 hour before cytoxan and completed 12 hours after the last dose of cytoxan
- Vincristine (Oncovin) 2 mg IV on days 4 & 11
- Doxorubicin (Adriamycin) 50 mg/m2 IV over 24 hours (over 48 hours in patients with ejection fractions (EF) <50%) on day 4
- Dexamethasone (Decadron) 40 mg PO/IV on days 1-4, 11-14
Next cycle to start as soon as absolute neutrophil count is > 1 x 10^9/L at least 24 hours off of G-CSF and platelet count > 60 x 10^9/L
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 1
- Cytarabine (Cytosar) 3000 mg/m2 (1000 mg/m2 for patients ≥60 years old) IV over 2 hours Q12H on days 2 & 3 (4 total doses)
- Folinic acid (Leucovorin) 50 mg IV x1 12 hours after methotrexate is complete, then 15 mg IV Q6H x 8 doses until serum methotrexate level <0.1 µM
Next cycle to start as soon as absolute neutrophil count is > 1 x 10^9/L at least 24 hours off of G-CSF and platelet count > 60 x 10^9/L
CNS prophylaxis:
- Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT on day 2
- Cytarabine (Cytosar) 100 mg IT on day 7 OR 8
Given each cycle for a total of 6 or 8 intrathecal treatments (i.e. 3 each of methotrexate and cytarabine or 4 each of methotrexate and cytarabine), depending on risk for CNS relapse based serum lactate dehydrogenase (LDH) >1400 IU/L and/or proliferative index percentage of S + G2M ≥14%
For known CNS disease:
- Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT alternating with Cytarabine (Cytosar) 100 mg IT, with both given every week until cell count in CSF normalizes and cytology is negative for malignancy
- Then Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT given weeks 1 & 3 and Cytarabine (Cytosar) 100 mg IT, given weeks 2 & 4
- Once those 4 weeks are complete, then intrathecal treatment is given similar to the prophylactic schedule, with each drug given once during every remaining cycle of induction therapy:
- Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT on day 2
- Cytarabine (Cytosar) 100 mg IT on day 7 OR 8
Supportive care:
- One of the following antibiotics:
- EITHER Ciprofloxacin (Cipro) 500 mg PO BID
- OR Levofloxacin (Levaquin) 500 mg PO daily
- OR Trimethoprim/Sulfamethoxazole (Bactrim DS) (160/800 mg) PO BID
- Fluconazole (Diflucan) 200 mg PO daily
- One of the following antivirals:
- EITHER Acyclovir (Zovirax) 200 mg PO BID
- OR Valacyclovir (Valtrex) 500 mg PO daily
- Filgrastim (Neupogen) 10 mcg/kg SC daily starting 24 hours after completion of intensive courses of chemotherapy (day 5 for part A, day 4 for part B), given until ANC >1 x 10^9/L
Certain patient populations (see Kantarjian, et al. 2004) received additional Hyper-CVAD maintenance therapy.
References
- Cortes J, O'Brien SM, Pierce S, Keating MJ, Freireich EJ, Kantarjian HM. The value of high-dose systemic chemotherapy and intrathecal therapy for central nervous system prophylaxis in different risk groups of adult acute lymphoblastic leukemia. Blood. 1995 Sep 15;86(6):2091-7. link to original article PubMed
- Thomas DA, O'Brien S, Cortes J, Giles FJ, Faderl S, Verstovsek S, Ferrajoli A, Koller C, Beran M, Pierce S, Ha CS, Cabanillas F, Keating MJ, Kantarjian H. Outcome with the hyper-CVAD regimens in lymphoblastic lymphoma. Blood. 2004 Sep 15;104(6):1624-30. Epub 2004 Jun 3. link to original article contains verified protocol PubMed
- Kantarjian H, Thomas D, O'Brien S, Cortes J, Giles F, Jeha S, Bueso-Ramos CE, Pierce S, Shan J, Koller C, Beran M, Keating M, Freireich EJ. Long-term follow-up results of hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (Hyper-CVAD), a dose-intensive regimen, in adult acute lymphocytic leukemia. Cancer. 2004 Dec 15;101(12):2788-801. link to original article contains verified protocol PubMed
Hyper-CVAD & Dasatinib (Sprycel) (induction & maintenance)
Hyper-CVAD: Hyperfractionated Cyclophosphamide, Vincristine, Adriamycin, Dexamethasone
Regimen
For patients with Philadelphia chromosome (Ph+) disease
Part A (cycles 1, 3, 5, 7):
- Cyclophosphamide (Cytoxan) 300 mg/m2 IV over 2 hours Q12H on days 1-3 (6 total doses)
- Mesna (Mesnex) 600 mg/m2/day IV continuous infusion on days 1-3, starting 1 hour before cytoxan and completed 12 hours after the last dose of cytoxan
- Vincristine (Oncovin) 2 mg IV on days 4 & 11
- Doxorubicin (Adriamycin) 50 mg/m2 IV over 24 hours (over 48 hours in patients with ejection fractions (EF) <50%) on day 4
- Dexamethasone (Decadron) 40 mg PO/IV on days 1-4, 11-14
- Dasatinib (Sprycel) 50 mg PO BID (or, alternatively, 100 mg PO daily) on days 1-14
Next cycle to start after count recovery. No definite criteria listed by the reference, but other Hyper-CVAD regimens used absolute neutrophil count > 1 x 10^9/L at least 24 hours off of G-CSF and platelet count > 60 x 10^9/L
Supportive medications:
- One of the following antibiotics:
- EITHER Ciprofloxacin (Cipro) 500 mg PO BID
- OR Levofloxacin (Levaquin) 500 mg PO daily
- OR Trimethoprim/Sulfamethoxazole (Bactrim DS) (160/800 mg) PO BID
- Fluconazole (Diflucan) 200 mg PO daily
- One of the following antivirals:
- EITHER Acyclovir (Zovirax) 200 mg PO BID
- OR Valacyclovir (Valtrex) 500 mg PO daily
- Filgrastim (Neupogen) 10 mcg/kg SC daily starting 24 hours after completion of intensive courses of chemotherapy (day 5 for part A, day 4 for part B), given until ANC >1 x 10^9/L
- Cycle 1 also involved:
- Hydration options included D5 water or 1/2 NS with 75-100 mEq sodium acetate per liter at 50-100 mL/H
- Allopurinol to decrease likelihood of tumor lysis syndrome; rasburicase could be used instead for patients with high white blood cell counts at initial presentation
- Oral sodium bicarbonate (no dosage or frequency listed) on days 1-3
Part B (cycles 2, 4, 6, 8):
- Methotrexate (MTX) 1000 mg/m2 IV over 24 hours on day 1
- Cytarabine (Cytosar) 3000 mg/m2 (1000 mg/m2 for patients at least 60 years old) IV over 2 hours Q12H on days 2 & 3 (4 total doses)
- Folinic acid (Leucovorin) 50 mg IV x1 12 hours after methotrexate is complete, then 15 mg IV Q6H x 8 doses until serum methotrexate level <0.1 µM
- Leucovorin rescue with Folinic acid (Leucovorin) 50 mg IV Q6H if methotrexate blood levels were greater than 20 uM at 0 hours after completion of MTX; >1 uM at 24 hours; >0.1 uM at 48 hours
- Dasatinib (Sprycel) 50 mg PO BID (or, alternatively, 100 mg PO daily) on days 1-14
Next cycle to start after count recovery. No definite criteria listed by the reference, but other Hyper-CVAD regimens used absolute neutrophil count > 1 x 10^9/L at least 24 hours off of G-CSF and platelet count > 60 x 10^9/L
Supportive medications:
- One of the following antibiotics:
- EITHER Ciprofloxacin (Cipro) 500 mg PO BID
- OR Levofloxacin (Levaquin) 500 mg PO daily
- OR Trimethoprim/Sulfamethoxazole (Bactrim DS) (160/800 mg) PO BID
- Fluconazole (Diflucan) 200 mg PO daily
- One of the following antivirals:
- EITHER Acyclovir (Zovirax) 200 mg PO BID
- OR Valacyclovir (Valtrex) 500 mg PO daily
- D5W or 1/2 NS with 75-100 mEq sodium acetate per liter at 100-125 mL/H
- Filgrastim (Neupogen) 10 mcg/kg SC daily starting 24 hours after completion of intensive courses of chemotherapy (day 5 for part A, day 4 for part B), given until ANC >1 x 10^9/L
- Acetazolamide (Diamox) (no dosage/schedule listed) used if urine pH <7 to promote excretion
CNS prophylaxis:
- Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT on day 2
- Cytarabine (Cytosar) 100 mg IT on day 7
Given each cycle for a total of 6 or 8 intrathecal treatments (i.e. 3 each of methotrexate and cytarabine or 4 each of methotrexate and cytarabine), depending on risk for CNS relapse based serum lactate dehydrogenase (LDH) >1400 IU/L and/or proliferative index percentage of S + G2M of at least 14%
For known CNS disease:
- Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT alternating with Cytarabine (Cytosar) 100 mg IT, with both given every week until cell count in CSF normalizes and cytology is negative for malignancy
- Then Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT given weeks 1 & 3 and Cytarabine (Cytosar) 100 mg IT, given weeks 2 & 4
- Once those 4 weeks are complete, then intrathecal treatment is given similar to the prophylactic schedule, with each drug given once during every remaining cycle of induction therapy:
- Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT on day 2
- Cytarabine (Cytosar) 100 mg IT on day 7
- Therapeutic external radiation is given to patients with CNS disease at presentation
Maintenance therapy for 2 years after completing 8 cycles of the intensive Part A and Part B chemotherapy:
- Dasatinib (Sprycel) 50 mg PO BID (or, alternatively, 100 mg PO daily) on days 1-28
- Vincristine (Oncovin) 2 mg IV on day 1
- Prednisone (Sterapred) 200 mg PO daily on days 1-5
28-day cycles x 2 years; maintenance therapy could be interrupted by provider's choice--typically only given to people with at least minimal residual disease (MRD) or more--in month 6 and 13 to give Hyper-CVAD Part A x 1 cycle
Then, after 2 years of maintenance therapy:
- Dasatinib (Sprycel) 50 mg PO BID (or, alternatively, 100 mg PO daily), continued indefinitely
References
- Ravandi F, O'Brien S, Thomas D, Faderl S, Jones D, Garris R, Dara S, Jorgensen J, Kebriaei P, Champlin R, Borthakur G, Burger J, Ferrajoli A, Garcia-Manero G, Wierda W, Cortes J, Kantarjian H. First report of phase 2 study of dasatinib with hyper-CVAD for the frontline treatment of patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia. Blood. 2010 Sep 23;116(12):2070-7. Epub 2010 May 13. link to original article contains verified protocol--parts of the protocol were not explicitly listed in this reference, which instead referred to Thomas, et al. 2004 and Kantarjian, et al. 2004 PubMed
Hyper-CVAD & Imatinib (Gleevec) (induction & maintenance)
Hyper-CVAD: Hyperfractionated Cyclophosphamide, Vincristine, Adriamycin, Dexamethasone
Regimen
For patients with Philadelphia chromosome (Ph+) disease
Part A (cycles 1, 3, 5, 7):
- Cyclophosphamide (Cytoxan) 300 mg/m2 IV over 2 hours Q12H on days 1-3 (6 total doses)
- Mesna (Mesnex) 600 mg/m2/day IV continuous infusion on days 1-3, starting 1 hour before cytoxan and completed 12 hours after the last dose of cytoxan
- Vincristine (Oncovin) 2 mg IV on days 4 & 11
- Doxorubicin (Adriamycin) 50 mg/m2 IV over 24 hours (over 48 hours in patients with ejection fractions (EF) <50%) on day 4
- Dexamethasone (Decadron) 40 mg PO/IV on days 1-4, 11-14
- Imatinib (Gleevec) 400 mg PO daily on days 1-14
Next cycle to start after count recovery. No definite criteria listed by the reference, but other Hyper-CVAD regimens used absolute neutrophil count > 1 x 10^9/L at least 24 hours off of G-CSF and platelet count > 60 x 10^9/L
Supportive medications:
- One of the following antibiotics:
- EITHER Ciprofloxacin (Cipro) 500 mg PO BID
- OR Levofloxacin (Levaquin) 500 mg PO daily
- OR Trimethoprim/Sulfamethoxazole (Bactrim DS) (160/800 mg) PO BID
- Fluconazole (Diflucan) 200 mg PO daily
- One of the following antivirals:
- EITHER Acyclovir (Zovirax) 200 mg PO BID
- OR Valacyclovir (Valtrex) 500 mg PO daily
- Filgrastim (Neupogen) 10 mcg/kg SC daily starting 24 hours after completion of intensive courses of chemotherapy (day 5 for part A, day 4 for part B), given until ANC >1 x 10^9/L
- Cycle 1 also involved:
- Hydration options included D5 water or 1/2 NS with 75-100 mEq sodium acetate per liter at 50-100 mL/H
- Allopurinol to decrease likelihood of tumor lysis syndrome; rasburicase could be used instead for patients with high white blood cell counts at initial presentation
- Oral sodium bicarbonate (no dosage or frequency listed) on days 1-3
Part B (cycles 2, 4, 6, 8):
- Methotrexate (MTX) 1000 mg/m2 IV over 24 hours on day 1
- Cytarabine (Cytosar) 3000 mg/m2 (1000 mg/m2 for patients at least 60 years old) IV over 2 hours Q12H on days 2 & 3 (4 total doses)
- Folinic acid (Leucovorin) 50 mg IV x1 12 hours after methotrexate is complete, then 15 mg IV Q6H x 8 doses until serum methotrexate level <0.1 µM
- Leucovorin rescue with Folinic acid (Leucovorin) 50 mg IV Q6H if methotrexate blood levels were greater than 20 uM at 0 hours after completion of MTX; >1 uM at 24 hours; >0.1 uM at 48 hours
- Imatinib (Gleevec) 400 mg PO daily on days 1-14
Next cycle to start after count recovery. No definite criteria listed by the reference, but other Hyper-CVAD regimens used absolute neutrophil count > 1 x 10^9/L at least 24 hours off of G-CSF and platelet count > 60 x 10^9/L
Supportive medications:
- One of the following antibiotics:
- EITHER Ciprofloxacin (Cipro) 500 mg PO BID
- OR Levofloxacin (Levaquin) 500 mg PO daily
- OR Trimethoprim/Sulfamethoxazole (Bactrim DS) (160/800 mg) PO BID
- Fluconazole (Diflucan) 200 mg PO daily
- One of the following antivirals:
- EITHER Acyclovir (Zovirax) 200 mg PO BID
- OR Valacyclovir (Valtrex) 500 mg PO daily
- D5W or 1/2 NS with 75-100 mEq sodium acetate per liter at 100-125 mL/H
- Filgrastim (Neupogen) 10 mcg/kg SC daily starting 24 hours after completion of intensive courses of chemotherapy (day 5 for part A, day 4 for part B), given until ANC >1 x 10^9/L
- Acetazolamide (Diamox) (no dosage/schedule listed) used if urine pH <7 to promote excretion
CNS prophylaxis:
- Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT on day 2
- Cytarabine (Cytosar) 100 mg IT on day 7 OR 8
Given each cycle for a total of 6 or 8 intrathecal treatments (i.e. 3 each of methotrexate and cytarabine or 4 each of methotrexate and cytarabine), depending on risk for CNS relapse based serum lactate dehydrogenase (LDH) >1400 IU/L and/or proliferative index percentage of S + G2M of at least 14%
For known CNS disease:
- Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT alternating with Cytarabine (Cytosar) 100 mg IT, with both given every week until cell count in CSF normalizes and cytology is negative for malignancy
- Then Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT given weeks 1 & 3 and Cytarabine (Cytosar) 100 mg IT, given weeks 2 & 4
- Once those 4 weeks are complete, then intrathecal treatment is given similar to the prophylactic schedule, with each drug given once during every remaining cycle of induction therapy:
- Methotrexate (MTX) 12 mg (6 mg if given via Ommaya reservoir) IT on day 2
- Cytarabine (Cytosar) 100 mg IT on day 7 OR 8
- Therapeutic external radiation is given to patients with CNS disease at presentation
Maintenance therapy after completing 8 cycles of the intensive Part A and Part B chemotherapy:
- Imatinib (Gleevec) 600 mg PO daily on days 1-28
- Vincristine (Oncovin) 2 mg IV on day 1
- Prednisone (Sterapred) 200 mg PO daily on days 1-5
28-day cycles x 5 cycles; then, in month 6, Hyper-CVAD Part A x 1 cycle as described above; then resume maintenance therapy, 28-day cycles x 6 cycles; then, in month 13, Hyper-CVAD Part A x 1 cycle as described above
References
- Thomas DA, Faderl S, Cortes J, O'Brien S, Giles FJ, Kornblau SM, Garcia-Manero G, Keating MJ, Andreeff M, Jeha S, Beran M, Verstovsek S, Pierce S, Letvak L, Salvado A, Champlin R, Talpaz M, Kantarjian H. Treatment of Philadelphia chromosome-positive acute lymphocytic leukemia with hyper-CVAD and imatinib mesylate. Blood. 2004 Jun 15;103(12):4396-407. Epub 2003 Oct 9. link to original article contains verified protocol PubMed
Larson/CALGB 8811 regimen (induction)
Regimen
Course I (induction):
For patients <60 years old:
- Cyclophosphamide (Cytoxan) 1200 mg/m2 IV on day 1
- Daunorubicin (Cerubidine) 45 mg/m2 IV on days 1-3
- Vincristine (Oncovin) 2 mg IV on days 1, 8, 15, 22
- Prednisone (Sterapred) 60 mg/m2 PO on days 1-21
- Asparaginase (Elspar) 6000 units/m2 SC on days 5, 8, 11, 15, 18, 22
For patients ≥60 years old:
- Cyclophosphamide (Cytoxan) 800 mg/m2 IV on day 1
- Daunorubicin (Cerubidine) 30 mg/m2 IV on days 1-3
- Vincristine (Oncovin) 2 mg IV on days 1, 8, 15, 22
- Prednisone (Sterapred) 60 mg/m2 PO on days 1-7
- Asparaginase (Elspar) 6000 units/m2 SC on days 5, 8, 11, 15, 18, 22
To be followed by Larson/CALGB 8811 regimen courses II-IV (maintenance).
References
- Larson RA, Dodge RK, Burns CP, Lee EJ, Stone RM, Schulman P, Duggan D, Davey FR, Sobol RE, Frankel SR, et al. A five-drug remission induction regimen with intensive consolidation for adults with acute lymphoblastic leukemia: cancer and leukemia group B study 8811. Blood. 1995 Apr 15;85(8):2025-37. link to original article contains verified protocol PubMed
Linker regimen (induction)
Regimen
- Daunorubicin (Cerubidine) 50 mg/m2 IV on days 1-3
- Vincristine (Oncovin) 2 mg IV on days 1, 8, 15, 22
- Prednisone (Sterapred) 60 mg/m2 PO on days 1-28
- Asparaginase (Elspar) 6000 units/m2 IM on days 17-28
If bone marrow on day 14 has residual leukemia:
- Daunorubicin (Cerubidine) 50 mg/m2 IV on day 15
If bone marrow on day 28 has residual leukemia:
- Daunorubicin (Cerubidine) 50 mg/m2 IV on days 29 & 30
- Vincristine (Oncovin) 2 mg IV on days 29 & 36
- Prednisone (Sterapred) 60 mg/m2 PO on days 29-42
- Asparaginase (Elspar) 6000 units/m2 IM on days 29-35
Central nervous system (CNS) prophylaxis for patients without CNS involvement at diagnosis is started within 1 week of achieving complete remission:
- Cranial radiation, 18 Gy total given in 10 fractions over 12-14 days
- Methotrexate (MTX) 12 mg IT weekly x 6 doses concurrent with radiation
Central nervous system (CNS) treatment for patients with CNS involvement at diagnosis:
- Cranial radiation, 28 Gy total given
- Methotrexate (MTX) 12 mg IT weekly x 10 doses that starts while they are receiving induction therapy, then given monthly during the first year of therapy
To be followed by Linker regimen consolidation therapy.
References
- Linker CA, Levitt LJ, O'Donnell M, Ries CA, Link MP, Forman SJ, Farbstein MJ. Improved results of treatment of adult acute lymphoblastic leukemia. Blood. 1987 Apr;69(4):1242-8. link to original article contains verified protocol PubMed
- Linker CA, Levitt LJ, O'Donnell M, Forman SJ, Ries CA. Treatment of adult acute lymphoblastic leukemia with intensive cyclical chemotherapy: a follow-up report. Blood. 1991 Dec 1;78(11):2814-22. link to original article contains verified protocol PubMed
Consolidation therapy
Larson/CALGB 8811 regimen (consolidation)
Preceded by Larson/CALGB 8811 regimen course I (induction).
Regimen
Course II (early intensification):
- Methotrexate (MTX) 15 mg IT on day 1
- Cyclophosphamide (Cytoxan) 1000 mg/m2 IV on day 1
- Mercaptopurine (Purinethol) 60 mg/m2 PO on days 1-14
- Cytarabine (Cytosar) 75 mg/m2 SC on days 1-4, 8-11
- Vincristine (Oncovin) 2 mg IV on days 15 & 22
- Asparaginase (Elspar) 6000 units/m2 SC on days 15, 18, 22, 25
28-day cycles x 2 cycles
Course III (CNS prophylaxis and interim maintenance):
- Cranial radiation, 24 Gy total given in 10 fractions from days 1-12
- Methotrexate (MTX) 15 mg IT on days 1, 8, 15, 22, 29
- Mercaptopurine (Purinethol) 60 mg/m2 PO on days 1-70
- Methotrexate (MTX) 20 mg/m2 PO on days 36, 43, 50, 57, 64
12-week course
Course IV (late intensification):
- Doxorubicin (Adriamycin) 30 mg/m2 IV on days 1, 8, 15
- Vincristine (Oncovin) 2 mg IV on days 1, 8, 15
- Dexamethasone (Decadron) 10 mg/m2 PO on days 1-14
- Cyclophosphamide (Cytoxan) 1000 mg/m2 IV on day 29
- Thioguanine (Tabloid) 60 mg/m2 PO on days 29-42
- Cytarabine (Cytosar) 75 mg/m2 SC on days 29-32, 36-39
8-week course
To be followed by Larson/CALGB 8811 regimen course V (maintenance).
References
- Larson RA, Dodge RK, Burns CP, Lee EJ, Stone RM, Schulman P, Duggan D, Davey FR, Sobol RE, Frankel SR, et al. A five-drug remission induction regimen with intensive consolidation for adults with acute lymphoblastic leukemia: cancer and leukemia group B study 8811. Blood. 1995 Apr 15;85(8):2025-37. link to original article contains verified protocol PubMed
Linker regimen (consolidation)
Preceded by Linker regimen induction therapy.
Regimen
Treatment A (cycles 1, 3, 5, 7):
- Daunorubicin (Cerubidine) 50 mg/m2 IV on days 1 & 2
- Vincristine (Oncovin) 2 mg IV on days 1 & 8
- Prednisone (Sterapred) 60 mg/m2 PO on days 1-14
- Asparaginase (Elspar) 12000 units/m2 IM on days 2, 4, 7, 9, 11, 14
Treatment B (cycles 2, 4, 6, 8):
- Teniposide (Vumon) 165 mg/m2 IV on days 1, 4, 8, 11
- Cytarabine (Cytosar) 300 mg/m2 IV on days 1, 4, 8, 11
Treatment C (cycle 9):
- Methotrexate (MTX) 690 mg/m2 IV over 42 hours on day 1
- Folinic acid (Leucovorin) 15 mg/m2 IV every 6 hours x 12 doses, starting after methotrexate is complete (at 42 hours)
- Prednisone (Sterapred) 60 mg/m2 PO on days 1-14
- Asparaginase (Elspar) 12000 units/m2 IM on days 2, 4, 7, 9, 11, 14
Central nervous system (CNS) prophylaxis for patients without CNS involvement at diagnosis is started within 1 week of achieving complete remission:
- Cranial radiation, 18 Gy total given in 10 fractions over 12-14 days
- Methotrexate (MTX) 12 mg IT weekly x 6 doses concurrent with radiation
To be followed by Linker regimen maintenance therapy.
References
- Linker CA, Levitt LJ, O'Donnell M, Ries CA, Link MP, Forman SJ, Farbstein MJ. Improved results of treatment of adult acute lymphoblastic leukemia. Blood. 1987 Apr;69(4):1242-8. link to original article contains verified protocol PubMed content property of HemOnc.org
- Linker CA, Levitt LJ, O'Donnell M, Forman SJ, Ries CA. Treatment of adult acute lymphoblastic leukemia with intensive cyclical chemotherapy: a follow-up report. Blood. 1991 Dec 1;78(11):2814-22. link to original article contains verified protocol PubMed
Maintenance therapy
Hyper-CVAD (maintenance) - POMP
Preceded by Hyper-CVAD (induction).
POMP: 6-MP, Oncovin, Methotrexate, Prednisone
Regimen
Kantarjian, et al. 2004 said how many days each drug is given per month, but did not specifically say, for example, that certain drugs are taken on days 1-5 of the cycle.
- Mercaptopurine (Purinethol) 1000 mg/m2 IV over 1 hour once daily x 5 days
- Methotrexate (MTX) 10 mg/m2 IV over 1 hour once daily x 5 days
- Vincristine (Oncovin) 2 mg IV once per month
- Prednisone (Sterapred) 200 mg PO once daily x 5 days, given with vincristine
1-month cycles
Supportive medications:
- Trimethoprim/Sulfamethoxazole (dosage not listed) PO BID on Saturday and Sunday for the first 6 months
- One of the following antivirals:
- EITHER Acyclovir (Zovirax) 200 mg PO once daily or 3 times per week for the first 6 months
- OR Valacyclovir (Valtrex) 500 mg PO once daily or 3 times per week for the first 6 months
References
- Kantarjian H, Thomas D, O'Brien S, Cortes J, Giles F, Jeha S, Bueso-Ramos CE, Pierce S, Shan J, Koller C, Beran M, Keating M, Freireich EJ. Long-term follow-up results of hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (Hyper-CVAD), a dose-intensive regimen, in adult acute lymphocytic leukemia. Cancer. 2004 Dec 15;101(12):2788-801. link to original article contains verified protocol PubMed
Larson/CALGB 8811 regimen (maintenance)
Preceded by Larson/CALGB 8811 regimen courses II-IV (consolidation).
Regimen
Course V (prolonged maintenance):
- Vincristine (Oncovin) 2 mg IV on day 1
- Prednisone (Sterapred) 60 mg/m2 PO on days 1-5
- Methotrexate (MTX) 20 mg/m2 PO on days 1, 8, 15, 22
- Mercaptopurine (Purinethol) 60 mg/m2 PO on days 1-28
28-day cycles, continue until 24 months from diagnosis
References
- Larson RA, Dodge RK, Burns CP, Lee EJ, Stone RM, Schulman P, Duggan D, Davey FR, Sobol RE, Frankel SR, et al. A five-drug remission induction regimen with intensive consolidation for adults with acute lymphoblastic leukemia: cancer and leukemia group B study 8811. Blood. 1995 Apr 15;85(8):2025-37. link to original article contains verified protocol PubMed
Linker regimen (maintenance)
Preceded by Linker regimen consolidation therapy.
Regimen
- Methotrexate (MTX) 20 mg/m2 PO weekly x 30 months
- Mercaptopurine (Purinethol) 75 mg/m2 PO daily x 30 months
References
- Linker CA, Levitt LJ, O'Donnell M, Ries CA, Link MP, Forman SJ, Farbstein MJ. Improved results of treatment of adult acute lymphoblastic leukemia. Blood. 1987 Apr;69(4):1242-8. link to original article contains verified protocol PubMed
- Linker CA, Levitt LJ, O'Donnell M, Forman SJ, Ries CA. Treatment of adult acute lymphoblastic leukemia with intensive cyclical chemotherapy: a follow-up report. Blood. 1991 Dec 1;78(11):2814-22. link to original article contains verified protocol PubMed
Relapsed/refractory
Clofarabine (Clolar)
Currently, no positive prospective trials using clofarabine have been published in adults. The retrospective series below reports a variety of regimens used in off-label fashion, based on pediatric regimens.
Regimen
- Clofarabine (Clolar) at a total dose per cycle of 200 to 250 mg/m2
References
- Retrospective: Barba P, Sampol A, Calbacho M, Gonzalez J, Serrano J, Martínez-Sánchez P, Fernández P, García-Boyero R, Bueno J, Ribera JM. Clofarabine-based chemotherapy for relapsed/refractory adult acute lymphoblastic leukemia and lymphoblastic lymphoma. The Spanish experience. Am J Hematol. 2012 Jun;87(6):631-4. doi:10.1002/ajh.23167. Epub 2012 Mar 19. link to original article PubMed
Ponatinib (Iclusig)
Regimen
- Ponatinib (Iclusig) 45 mg PO daily; may be taken either with or without food
given until progression of disease or unacceptable toxicity
References
- Cortes JE, Kantarjian H, Shah NP, Bixby D, Mauro MJ, Flinn I, O'Hare T, Hu S, Narasimhan NI, Rivera VM, Clackson T, Turner CD, Haluska FG, Druker BJ, Deininger MW, Talpaz M. Ponatinib in refractory Philadelphia chromosome-positive leukemias. N Engl J Med. 2012 Nov 29;367(22):2075-88. doi: 10.1056/NEJMoa1205127. link to original article contains verified protocol PubMed
- Jorge E. Cortes, MD, Dong-Wook Kim, MD, Javier Pinilla-Ibarz, MD, PhD, Philipp le Coutre, MD, Ron Paquette, MD, PhD, Charles Chuah, MD6, Franck E Nicolini, MD, PhD, Jane Apperley, H. Jean Khoury, Moshe Talpaz, MD, John F. DiPersio, MD, PhD, Daniel J. DeAngelo, MD, PhD, Elisabetta Abruzzese, Delphine Rea, MD, PhD, Michele Baccarani, MD, Martin C Muller, Carlo Gambacorti-Passerini, MD, Stephane Wong, PhD, Stephanie Lustgarten, Victor M. Rivera, PhD, Tim Clackson, PhD, Christopher D. Turner, MD, FAAP, Frank G Haluska, MD, PhD, Francois Guilhot, MD, Michael W. Deininger, MD, PhD, Andreas Hochhaus, MD, Timothy Hughes, John M Goldman, MD, Neil Shah, MD, PhD, Hagop M Kantarjian, M.D. and The PACE Study Group. A Pivotal Phase 2 Trial of Ponatinib in Patients with Chronic Myeloid Leukemia (CML) and Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia (Ph+ALL) Resistant or Intolerant to Dasatinib or Nilotinib, or with the T315I BCR-ABL Mutation: 12-Month Follow-up of the PACE Trial. 2012 ASH Annual Meeting abstract 163. link to abstract
- Ponatinib (Iclusig) package insert
Vincristine liposomal (Marqibo)
Regimen
- Vincristine liposomal (Marqibo) 2.25 mg/m2 IV over 1 hour on day 1
7-day cycles
References
- Jeffrey A. Silverman, Walter Aulitzky, John Lister, Lori Maness, Gary Schiller, Karen Seiter, Scott E. Smith, Wendy Stock, Dina Ben Yehuda, Steven R. Deitcher. Marqibo® (vincristine sulfate liposomes injection; VSLI) Optimizes the Dosing, Delivery, and Pharmacokinetic (PK) Profile of Vincristine Sulfate (VCR) in Adults with Relapsed and Refractory Acute Lymphoblastic Leukemia (ALL). ASH 2010 abstract 2142. link to abstract
- Vincristine liposomal (Marqibo) package insert
- Marqibo completed trials summary at Talon Therapeutics
- FDA drug approval announcement for vincristine sulfate liposome injection (Marqibo) on 8/9/2012