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Annals of Oncology 2007 18(7):1127; doi:10.1093/annonc/mdm396
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© 2007 European Society for Medical Oncology

in this issue

In this issue


    Oral ibandronate versus intravenous zoledronic acid
 Top
 Oral ibandronate versus...
 FOLFOX, bevacizumab and...
 Phase I/II Study of...
 Effects of chemotherapy on...
 Quote
 
Bisphosphonates such as clodronate, ibandronate, pamidronate and zoledronic acid are the standard of care for patients with metastatic bone disease. Biochemical markers of bone resorption show potential in the initial evaluation of bone metastases, as surrogates of disease progression, as fracture predictors, and as prognostic factors of survival. In addition, serum levels of biochemical markers of bone cell activity are increasingly recognized as useful determinants for assessing the clinical response to antineoplastic and antiresorptive therapy in metastatic bone disease. In this issue Body et al. report the results of an open phase III study that aimed to compare directly the effect of treatment with oral ibandronate and intravenous zoledronic acid on markers of bone resorption and formation in breast cancer patients with bone metastases. These authors report that oral ibandronate was well tolerated and statistically non-inferior to zoledronic acid for the primary study endpoint, the percentage change in the bone resorption marker, S-CTX.


    FOLFOX, bevacizumab and erlotinib for metastastic colorectal cancer
 Top
 Oral ibandronate versus...
 FOLFOX, bevacizumab and...
 Phase I/II Study of...
 Effects of chemotherapy on...
 Quote
 
The epidermal growth factor receptor (EGFR) has emerged as an important therapeutic target in a variety of human cancers. In colorectal cancer, between 25-77% of tumors overexpress EGFR and this overexpression has been associated with poorer prognosis. While the oral inhibitors of the EGFR intracellular domain, such as erlotinib and gefitinib, do not appear to have measurable activity against metastatic colorectal cancer as single agents, they may enhance the activity of combination chemotherapy. In this issue, Meyerhardt et al. report the results of a multi-center phase II study that aimed to assess the efficacy and toxicity of a combination of infusional 5-fluorouracil (5-FU), leucovorin, oxaliplatin, bevacizumab and erlotinib for the first-line treatment of patients with metastatic colorectal cancer. These authors report that of the 35 patients enrolled all came off trial for reasons other than progression; 18 (51%) had protocol-defined adverse events requiring removal, 9 (26%) withdrew consent due to toxicity, 6 pursued surgery or localized therapies, and 2 requested a treatment holiday. The authors suggest that these findings raise concerns about the tolerability of adding more agents to already complex combination regimens for metastatic colorectal cancer.


    Phase I/II Study of galiximab with rituximab
 Top
 Oral ibandronate versus...
 FOLFOX, bevacizumab and...
 Phase I/II Study of...
 Effects of chemotherapy on...
 Quote
 
Treatment of follicular non-Hodgkin's lymphoma (NHL) is characteristically associated with a high rate of initial response, followed by relapse. Despite improvements in response rates with more aggressive combination regimens, the increased toxicity and/or logistics of administration with these regimens limit their use in a significant number of patients. Single-agent rituximab (anti-CD20 antibody) has demonstrated response rates of approximately 50% with a favorable safety profile in relapsed or refractory, low-grade or follicular B-cell NHL. Studies investigating maintenance/extended treatment with rituximab have shown prolonged progression-free survival and event-free survival in indolent NHL. Galiximab, a monoclonal antibody that targets CD80, has shown modest single-agent clinical activity and tolerability in a phase I study in relapsed or refractory, follicular NHL. In this issue, Leonard et al. report on a phase I/II study that aimed to evaluate galiximab in combination with a standard course of rituximab. These authors conclude that galiximab can be safely combined with a standard course of rituximab.


    Effects of chemotherapy on reactivation of tuberculosis
 Top
 Oral ibandronate versus...
 FOLFOX, bevacizumab and...
 Phase I/II Study of...
 Effects of chemotherapy on...
 Quote
 
Various malignancies and cytotoxic chemotherapy have been proposed to increase the risk of reactivation of tuberculosis, but the available literature on this topic is conflicting. In India tuberculosis continues to be a common infection in with reported prevalence of cases in Chengulpet in Tamil Nadu as high as 10.8/1000 person. In this issue, Nair et al. present a retrospective analysis of patients with high grade non- Hodgkin's lymphoma (NHL) with a past history of tuberculosis and who had had adequate antitubercular therapy. These patients were followed up during cytotoxic chemotherapy and later to assess the risk of reactivation of tuberculosis. These authors report that in cohort of 8 patients with past history of tuberculosis, selected from 141 patients of high grade NHL, all patients received cyclical cytotoxic chemotherapy. The median duration of follow up after completion of chemotherapy was 5 years (range- 10 months- 5 years), during which none of the patients developed reactivation of tuberculosis.


    Quote
 Top
 Oral ibandronate versus...
 FOLFOX, bevacizumab and...
 Phase I/II Study of...
 Effects of chemotherapy on...
 Quote
 
"Yet – when the dreadful steel was plunged into the breast – cutting through veins – arteries – flesh – nerves – I needed no injunctions not to restrain my cries. I began a scream that lasted unintermittingly during the whole of the incision - & I almost marvel that it rings not in my Ears still! so excruciating was the agony."

Fanny Burney recalls her mastectomy, 1811, from The Journal and Letters of Fanny Burney (Madame D'Arblay) 1791-1840.


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Related articles in Ann Oncol:

Oral ibandronate is as active as intravenous zoledronic acid for reducing bone turnover markers in women with breast cancer and bone metastases
J-J Body, M Lichinitser, S Tjulandin, P Garnero, and B Bergström
Ann Oncol 2007 18: 1165-1171. [Abstract] [Full Text]  

Phase II study of FOLFOX, bevacizumab and erlotinib as first-line therapy for patients with metastastic colorectal cancer
JA Meyerhardt, K Stuart, CS Fuchs, AX Zhu, CC Earle, P Bhargava, L Blaszkowsky, P Enzinger, RJ Mayer, S Battu, C Lawrence, and DP Ryan
Ann Oncol 2007 18: 1185-1189. [Abstract] [Full Text]  

A phase I/II study of galiximab (an anti-CD80 monoclonal antibody) in combination with rituximab for relapsed or refractory, follicular lymphoma
JP Leonard, JW Friedberg, A Younes, D Fisher, LI Gordon, J Moore, M Czuczman, T Miller, P Stiff, BD Cheson, A Forero-Torres, N Chieffo, B McKinney, D Finucane, and A Molina
Ann Oncol 2007 18: 1216-1223. [Abstract] [Full Text]  

The effect of short-term intensive chemotherapy on reactivation of tuberculosis
R Nair, K Prabhash, M Sengar, A Bakshi, S Gujral, S Gupta, and P Parikh
Ann Oncol 2007 18: 1243-1245. [Abstract] [Full Text]  




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