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Experimental treatment consists of an induction phase followed by a consolidation or intensified phase according to tumor response.

* dd -2 to 1: Methylprednisolone
* dd 0-1, Cyclophosphamide, associated on day 0 with Vincristine
* dd 2, Rituximab
* dd 7, Methotrexate
* dd 14, Rituximab
* dd 15, Etoposide
* dd 21, Methotrexate
* dd 29, Rituximab and Doxorubicin
* dd 36, Rituximab and VCR

At the end of this induction phase, subsequent treatment will be performed according to the objective response:

1. pts in CR: consolidation phase followed by bulky site irradiation
2. pts in PR: consolidation phase followed by BEAM conditioning regimen supported by ASCT and bulky irradiation
3. pts with SD after induction or PD during or after induction: intensification phase followed by BEAM conditioning regimen supported by ASCT and bulky irradiation

Induction Phase

* dd 1-2: cytarabine twice a day
* dd 3 and 11: rituximab
* dd 11-13: leukapheresis for PBPC collection.

Consolidation Phase (on day +50)

1. One or two courses of R-IVAC or R-ICE chemoimmunotherapy regimen, every three weeks as debulking.
2. CTX (dd 1) associated with rituximab on dd 3 and 10, followed by PBPC collection (dd 11-13);
3. AraC every 12 hours for four days (dd -5 to -2) supported by reinfusion of CD34+ cells (dd 0), rituximab infusion (dd -1 and +11) and second in-vivo purged PBPC collection (if needed).

Intensification phase

BCNU on dd 1; VP-16 every 12 hours on dd 2-5 and araC every 12 hours on dd 2-5; melphalan on dd 6, followed by the reinfusion of CD34+ cells

BEAM conditioning

At the end of the whole program, patients will be evaluated for involved-field irradiation with 6-10 MeV photons and a dose of 36 Gy (2 Gy/d, five fractions a week). Three subgroups of patients will be considered for radiotherapy

Consolidation radiotherapy

Andrés JM Ferreri, MD

This is a multicenter,open-label trial to evaluate activity and safety of the investigational intensive in HIV+ patients with Burkitt's lymphoma.

Experimental treatment consists of an induction phase followed by a consolidation or intensified phase according to tumor response.

Until recently, the immuno-compromised state of patients with concomitant HIV/AIDS and BL was thought to limit the ability to administer intensive chemotherapeutic regimens due to infection rate. However, the advent of highly active antiretroviral therapy (HAART) and evidence in diffuse large B-cell lymphomas that HIV-positive patients can tolerate standard chemotherapeutic regimens with improved outcomes have led investigators to treat HIV-positive patients with the same intensive chemotherapy regimens used to treat immuno-competent patients. Data suggest that these current approaches, along with supportive care, may result in improved patient outcomes, similar to those in the immuno-competent patient population.

The activity of feasibility of the proposed program will be assessed in HIV+ patients with Burkitt lymphoma with the aim to improve tolerability, minimize source consuming and supporting treatment and redu ce late sequels. Available combinations in this setting are really source demanding and toxic combinations showing high rates of septic complication and a treatment-related mortality of near 20%.

Short Term Intensified Chemo-immunotherapy in HIV-positive Patients With Burkitt Lymphoma

Phase II Study on Safety and Activity of a Short Term Intensified Chemo-immunotherapy Combination in HIV-positive Patients Affected by Burkitt Lymphoma

Objective lymphoma response achieved after the induction phase of the experimental treatment.

Assessment of incidence of grade 4 AE during experimental treatment (induction, consolidation and intensification phases as well as conditioning and autologous stem cell transplantation (if indicated)

Participants who will not achieve a complete or partial response after induction and consolidation phases will be referred to intensification phase, which will be followed by BEAM + ASCT. These patients will be assess for tolerabbility and AE during these therapeutic phases.

Participants will be assessed by conventional exams to define complete remission rate after the whole experiemntal program; that is after consolidation phase for patients who achieved complete remission after induction phase, after BEAM + ASCt for patients who achieved partial response after induction phase, and after intensification phase for patients who did not achieve an objective response after induction phase.

Andres J. M. Ferreri

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization	Link
Short Term Intensified Chemo-immunotherapy in HIV-positive Patients With Burkitt Lymphoma	NCT01516593	HIV Burkitt's Lymph...	Induction Phase Consolidation P... Intensification... BEAM conditioni... Consolidation r...	18 Years - 60 Years	IRCCS San Raffaele
Short Term Intensified Chemo-immunotherapy in HIV-positive Patients With Burkitt Lymphoma	NCT01516593	HIV Burkitt's Lymph...	Induction Phase Consolidation P... Intensification... BEAM conditioni... Consolidation r...	18 Years - 60 Years	IRCCS San Raffaele

Spots Global Cancer Trial Database for intensive

Every month we try and update this database with for intensive cancer trials from around the world to help patients and their families find trials that might be right for them.
We offer this 100% free of charge and do not endorse any of the trials listed here, we hope it helps you or a loved one.

Spots Global Cancer Trial Database for intensive

Every month we try and update this database with for intensive cancer trials from around the world to help patients and their families find trials that might be right for them. We offer this 100% free of charge and do not endorse any of the trials listed here, we hope it helps you or a loved one.

Every month we try and update this database with for intensive cancer trials from around the world to help patients and their families find trials that might be right for them.
We offer this 100% free of charge and do not endorse any of the trials listed here, we hope it helps you or a loved one.