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1.
J Cancer Res Clin Oncol ; 132(2): 105-12, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16088404

ABSTRACT

PURPOSE: The purpose of this study was to compare the efficacy and toxicity of bendamustine, vincristine + prednisone (BOP) with a standard regimen of cyclophosphamide, vincristine + prednisone (COP) in patients with previously untreated advanced indolent non-Hodgkin's lymphoma (NHL) and mantle cell lymphoma. METHODS: A total of 164 patients with follicular lymphoma (grade 1/2), mantle cell lymphoma or lymphoplasmacytic lymphoma (immunocytoma) was randomised to treatment with vincristine 2 mg (day 1) and prednisone 100 mg/m2 (days 1-5) + bendamustine 60 mg/m2 (days 1-5) or + cyclophosphamide 400 mg/m2 (days 1-5) for a total of eight 21-day cycles. RESULTS: The rate of complete remission was 22% with BOP and 20% with COP. The projected 5-year survival rate was 61% with BOP and 46% with COP. The BOP-associated 5-year survival advantage almost reached significance in the subgroup of patients who responded to therapy (74% vs. 56%; P = 0.05), and did reach significance in responders who did not receive interferon maintenance therapy (70% vs. 47%; P = 0.03). Toxicity was acceptable in both treatment groups, although alopecia and leucopenia were more severe with COP. CONCLUSIONS: Bendamustine can efficaciously and safely replace cyclophosphamide, as used in standard COP therapy, for the treatment of patients with indolent NHL and mantle cell lymphoma. Long-term survival data suggest a clinically significant benefit for patients treated with BOP.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Leukemia, Lymphocytic, Chronic, B-Cell/drug therapy , Lymphoma, Follicular/drug therapy , Lymphoma, Mantle-Cell/drug therapy , Adult , Aged , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Bendamustine Hydrochloride , Cyclophosphamide/administration & dosage , Disease-Free Survival , Female , Humans , Leukemia, Lymphocytic, Chronic, B-Cell/mortality , Lymphoma, Follicular/mortality , Lymphoma, Mantle-Cell/mortality , Lymphoma, Non-Hodgkin/drug therapy , Male , Middle Aged , Nitrogen Mustard Compounds/administration & dosage , Prednisone/administration & dosage , Survival Analysis , Treatment Outcome , Vincristine/administration & dosage
2.
Eur J Cancer ; 32A(12): 2053-7, 1996 Nov.
Article in English | MEDLINE | ID: mdl-9014744

ABSTRACT

The relevance of quantitative determinations of urinary deoxypyridinolines (DPY) and pyridinolines (PY), and of serum type I collagen carboxyterminal cross-linked telopeptides (ICTP), has been evaluated for patient monitoring in multiple myeloma (MM). In 178 untreated MM patients, a clear correlation was found between ICTP concentrations, bone destructions and serum calcium levels. Furthermore, serum ICTP, urinary DPY and PY concentrations were estimated before and during treatment in a further 33 MM patients randomly allocated to four groups receiving intravenous melphalan/prednisone (MivP) chemotherapy alone, or MivP in combination with three different doses of i.v. clodronate. 1800 mg of i.v. clodronate combined monthly with MivP induced a rapid and sustained reduction in bone resorption parameters to the normal range, a result not obtained with either MivP alone, or with a lower clodronate dose. While confirming the relevance of determining pyridinium cross-links for estimating bone resorption in MM, our data indicate that measurements of these parameters could be useful for dose finding and monitoring of bisphosphonate therapy.


Subject(s)
Amino Acids/metabolism , Biomarkers, Tumor/metabolism , Bone Resorption/metabolism , Multiple Myeloma/complications , Paraneoplastic Syndromes/metabolism , Adult , Aged , Aged, 80 and over , Amino Acids/urine , Bone Resorption/drug therapy , Bone Resorption/etiology , Clodronic Acid/therapeutic use , Collagen/blood , Collagen Type I , Humans , Middle Aged , Multiple Myeloma/pathology , Neoplasm Staging , Paraneoplastic Syndromes/drug therapy , Paraneoplastic Syndromes/etiology , Peptides/blood , Pilot Projects
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