scholarly journals Maximal preservation of renal function in patients with bilateral Wilms’ tumor: therapeutic strategy of late kidney-sparing surgery and replacement of radiotherapy by high-dose melphalan and stem cell rescue

1998 ◽  
Vol 22 (1) ◽  
pp. 53-59 ◽  
Author(s):  
UM Saarinen-Pihkala ◽  
S Wikström ◽  
K Vettenranta
Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 5835-5835
Author(s):  
Zhen Wang ◽  
Noa Biran ◽  
Alan P Skarbnik ◽  
Andrew L. Pecora ◽  
Michele L. Donato ◽  
...  

Abstract Cryoglobulins (CGs) are immunoglobulins that precipitate at temperature below 37 C and re-dissolve after rewarming. Type I cryoglobulinemia is characterized by monoclonal immunoglobulins and is often driven by a lymphoproliferative disorder or plasma cell dyscrasia. Although CGs are often associated with hematologic malignancies which independently require therapy; this phenomenon can also be associated with more benign disorders. Monoclonal gammopathy of renal significance (MGRS) represents a group of disorders characterized by the presence of a paraprotein; although not fitting the diagnostic criteria for a symptomatic hematologic malignancy such as lymphoma or myeloma, can manifest by renal impairment through a variety of mechanisms. There exists no standard approach to manage these patients. As the driving force of these processes are characterized by the proliferation of malignant plasma cells (overproducing a nephrotoxic paraprotein) high-dose melphalan followed by autologous stem cell rescue represents an ideal approach to achieve organ function recovery and long term disease control Our patient is a 56-year-old man who was initially evaluated for fatigue, lower extremity swelling and leg ulcers in December of 2011. Workup revealed worsening renal function and proteinuria. A renal biopsy was performed showing abundant cryofibrinogen deposits and cryoglobulinemic glomerulonephritis with membranoproliferative pattern. Labs showed type I cryoglobulinemia composed of monoclonal IgG kappa proteins. He was treated by his rheumatologist with a short course of prednisone and cyclophosphamide with transient improvement in proteinuria and renal function. He was monitored without therapy until 2015 when the gradual worsening of his edema led him to be re-evaluated by a nephrologist who ultimately referred the patient for hematologic workup upon the discovery of a monoclonal protein. Bone marrow evaluation revealed 7% clonal plasma cells with FISH studies positive for gain of CKS1B, trisomy 9 and monosomy 13. Further evaluation did not confirm a diagnosis of symptomatic myeloma. At this time however, the creatinine had risen to over 2 with over 35 grams of proteinuria on a 24-hour urine specimen. Lab work confirmed the presence of a cryoglobulin. As the recurrent cryoglobulinemia was felt to be plasma cell driven and the etiology of the renal impairment; the decision was made to treat with Bortezomib, Cyclophosphamide and Dexamethasone (CyBorD). After 3 cycles of therapy the patient had normalization of his serum creatinine, marked improvement in edema, as well as significant improvement in proteinuria. Peripheral blood stem cells were mobilized following the administration of high-dose cyclophosphamide (2gm/m2) plus high dose filgrastim. He was subsequently conditioned for transplantation utilizing high-dose melphalan (HDM/200mg/m2) followed by autologous stem cell rescue. He tolerated the procedure well without any unexpected toxicities. Evaluations post transplant revealed no evidence of a circulating cryoglobulin and continued clinical improvement and reduction in proteinuria. (figure 1). Now, 5 months post transplant, the patient has no evidence of a detectable paraprotein and has returned to his premorbid condition. Type 1 Cryoglobulinemia associated renal disease represents a complicated disorder for which there is no standard of care. As this may be driven by clonal plasma cells; classical anti-myeloma therapy may provide an optimal strategy for management. Given the typical low plasma cell burden in these patients HDM has the potential to offer deep and durable remissions. Prospective studies are needed to validate this approach. Figure 1 Figure 1. Disclosures Biran: Amgen: Speakers Bureau; Takeda: Speakers Bureau; Celgene: Speakers Bureau; Novartis: Speakers Bureau. Skarbnik:Pharmacyclics: Consultancy; Gilead Sciences: Speakers Bureau; Genentech: Speakers Bureau; Seattle Genetics: Speakers Bureau; Abbvie: Consultancy. Siegel:Novartis: Honoraria, Speakers Bureau; Celgene: Honoraria, Speakers Bureau; BMS: Honoraria, Speakers Bureau; Takeda: Honoraria, Speakers Bureau; Amgen: Honoraria, Speakers Bureau; Merck: Honoraria. Vesole:Amgen: Speakers Bureau; Takeda: Speakers Bureau; Novartis: Speakers Bureau; Celgene: Speakers Bureau; Janssen: Speakers Bureau. Richter:Celgene: Consultancy, Speakers Bureau; Jannsen: Speakers Bureau; Amgen: Consultancy, Speakers Bureau; Takeda: Consultancy, Speakers Bureau.


2021 ◽  
pp. 101-110
Author(s):  
Chandran K Nair

The treatment landscape in multiple myeloma has significantly changed since the introduction of high-dose melphalan with autologous stem cell rescue in the 1980s. Many randomised controlled trials have clearly demonstrated the superiority of autologous stem cell transplantation in improving survival compared to conventional chemotherapy. However, outcomes in myeloma are highly variable with median survival as short as 2 years and as long as 10 years or more. The main adverse factor predicting shorter survival is presence of high-risk cytogenetics. However, there are many other potential factors that can contribute to the treatment outcomes.  This review looks at the various pretransplant variables that are associated with  post-transplant outcomes in myeloma.


Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 3960-3960 ◽  
Author(s):  
Douglas W. Sborov ◽  
Misty Lamprecht ◽  
Don Benson ◽  
Karen Tackett ◽  
Yvonne A Efebera ◽  
...  

Abstract Introduction: Severe mucositis in the autologous transplant setting has been correlated with adverse outcomes; longer febrile neutropenia duration, doubling of infectious risk, 2.7 additional days of total parenteral nutrition, 2.6 additional days of IV narcotics, increased length of stay (LOS), 3.9-fold increase in 100-day mortality, and US$25,405 increase in hospital charges (Sonis, JCO, 2001 19(8)). In a 40 patient randomized trial investigating cryotherapy (6 hours versus none) following high dose melphalan, grade 3/4 mucositis occurred in only 14% of patients using cryotherapy compared to 74% of patients using saline rinses (Lilleby, BMT, 2006 37). Prolonged cryotherapy is a significant hardship for patients and has resulted in nausea, vomiting, headache, toothache, and chills. We performed a randomized study investigating 2 versus 6 hours of cryotherapy in multiple myeloma (MM) patients undergoing autologous stem cell transplant (ASCT) with melphalan conditioning. Hypothesis: We hypothesized that a 2-hour cryotherapy regimen would be non-inferior to 6-hours in severity of mucositis, LOS, and incidence of bacteremia. Methods: We conducted a non-inferiority investigation of 146 sequential MM patients undergoing high dose melphalan with autologous stem cell rescue. Patients were consented and randomized to either 2 (n = 73) or 6 hours (n = 73) of cryotherapy via block randomization based on hemoglobin (less or greater than 11 g/dL), fat free mass (30-50, 50-70, >70 kg), or measured 24hr creatinine clearance (<30, 30-60, >60 mL/min). The cryotherapy process consisted of patients’ melting shaved ice inside their mouth for the designated period of time; flavoring with snow cone syrup was permitted. Inpatient nurse practitioners graded mucositis via WHO criteria. Patients received antifungal (fluconazole) and antiviral (acyclovir or valacyclovir) prophylaxis. Subset analyses investigated the incidence of bacteremia in all patients. Results: Median age was 59 years (range 35 - 72) and 60 (range 38 – 71), and the median measured creatinine clearance was 90.6 mL/min (range 0.2 – 168.7) and 85.4 mL/min (range 21.5 – 196.5) for the 2 hour and 6 hour groups respectively. Length of hospitalization (mean of 15 days) did not differ significantly between the 2 cohorts (p = 0.54). Mucositis was graded daily after melphalan infusion. In the 2-hour cohort, 59% of the patients had mucositis (31 patients with grade 1, 10 with grade 2, and 2 patients with grade 3). In the 6-hour cohort, 64% had mucositis (35 patients with grade 1, 9 with grade 2, and 3 patients with grade 3). These results suggest that 2-hour cryotherapy was not inferior to 6-hour therapy in decreasing mucositis grade. In the entire 146 patient group, approximately 30% developed a positive blood culture after transplant, including 25 (34%) and 20 (27%) in the 6-hour and 2-hour groups respectively. The three most common infectious organisms included gram negatives (n = 12 patients), polymicrobial (n = 7), and non-group A streptococcus (n = 7). In the cohort treated with 2-hour cryotherapy, positive blood cultures did not correlate with grade of mucositis (r = 0.05, p = 0.65). Conclusions: In MM patients undergoing ASCT, 2-hour cryotherapy did not increase mucositis compared to 6-hours. The incidence of blood stream infection was not different between groups. In addition, having an infection did not correlate with grade of mucositis.These results suggest that a 2-hour cryotherapy regimen is not inferior to a 6-hour regimen, and may be considered a standard supportive care measure in patients receiving high dose melphalan. Disclosures Hofmeister: Celgene: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Millenium: Honoraria, Research Funding; ARNO Therapeutics: Research Funding; Onyx: Membership on an entity's Board of Directors or advisory committees.


2011 ◽  
Vol 29 (15_suppl) ◽  
pp. e18577-e18577
Author(s):  
M. V. Martino ◽  
R. Fedele ◽  
G. Console ◽  
E. Massara ◽  
L. Russo ◽  
...  

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