Skip Navigation

Annals of Oncology 2007 18(10):1589; doi:10.1093/annonc/mdm473
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Related articles in Ann Oncol
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Search for Related Content
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2007 European Society for Medical Oncology

in this issue

in this issue


    Prognostic role of peritumoral vascular invasion in operable breast cancer
 Top
 Prognostic role of peritumoral...
 Gemcitabine plus platinum in...
 Disease progression in Hodgkin's...
 Immunotherapy versus DTIC in...
 Quote
 
For breast cancer patients with peritumoral vascular invasion (PVI), treatment choice follows an algorithm similar to that for node-positive disease. Nevertheless, controversies remain about the role of PVI in the risk assessment of patients with operable breast cancer, with several previous studies failing to confirm any prognostic role for vascular invasion. In this issue, Colleoni et al. [1632–1640] report the results of a study that aimed to prospectively analyze the prognostic role of PVI extent in terms of both disease-free and overall survival in a large group of patients with surgery, pathological evaluation and treatment recommendations performed by the same team of physicians. These authors found that in patients with node-negative disease a statistically significant difference in disease-free survival, risk of distant metastases and overall survival was observed at the multivariate analysis for extensive PVI versus no PVI.


    Gemcitabine plus platinum in pancreatic cancer
 Top
 Prognostic role of peritumoral...
 Gemcitabine plus platinum in...
 Disease progression in Hodgkin's...
 Immunotherapy versus DTIC in...
 Quote
 
Systemic chemotherapy with single-agent gemcitabine is regarded as a standard of care for treatment of locally advanced and metastatic pancreatic cancer. Several randomised trials are now available which consistently report the favourable impact of gemcitabine/platinum-analog combinations on the survival of patients with advanced pancreatic cancer, but none of these studies has had a sufficient statistical power to demonstrate a significant survival advantage. In this issue, Heinemann et al. [1652–1659] report a pooled analysis of the GERCOR/GISCAD intergroup study comparing gemcitabine plus oxaliplatin to gemcitabine and a German multicenter trial comparing gemcitabine plus cisplatin versus gemcitabine. These authors conclude that the combination of gemcitabine with a platinum analog such as oxaliplatin or cisplatin significantly improves progression-free and overall survival compared with single-agent gemcitabine in advanced pancreatic cancer.


    Disease progression in Hodgkin's lymphoma
 Top
 Prognostic role of peritumoral...
 Gemcitabine plus platinum in...
 Disease progression in Hodgkin's...
 Immunotherapy versus DTIC in...
 Quote
 
In the NCIC CTG/ECOG trial HD.6 patients with limited stage Hodgkin's lymphoma were randomized to receive treatment that included radiation or to chemotherapy, as a single modality, consisting of doxorubicin, bleomycin, vinblastine and dacarbazine (ABVD). With a median follow up of 4.2 years, this study showed progression-free survival (PFS) was superior in patients allocated to radiation therapy, but no difference in overall survival was seen. In this issue, Macdonald et al. [1680–1684] report on the patterns of progression and subsequent outcomes of patients with progression in the HD.6 trial. After a median of 4.2 years, 33 patients had progressed. Two radiation oncologists determined whether sites of progression were confined within radiation fields and compared freedom from second progression (FF2P) with freedom from second progression or death (FF2P/D). These authors conclude that treatment that includes radiation reduces the risk of progressive Hodgkin's lymphoma in sites receiving this therapy, but they were unable to detect differences in FF2P or FF2P/D.


    Immunotherapy versus DTIC in melanoma
 Top
 Prognostic role of peritumoral...
 Gemcitabine plus platinum in...
 Disease progression in Hodgkin's...
 Immunotherapy versus DTIC in...
 Quote
 
Currently, two agents are approved for use in stage IV melanoma patients; dacarbazine (DTIC) in Europe and the US, and high-dose intravenous interleukin-2 (IL-2) in the US. Single-agent interferon-alpha (IFN{alpha}) therapy, as well as single-agent IL-2 treatment, yields response rates of approximately 15% in metastatic melanoma with infrequent long-term responders and occasional long-term survivors. The combination of IFN{alpha} and IL-2 has been reported to increase response rates, but this has not been confirmed in a randomized phase III trial. Moreover, the use of histamine dihydrochloride (HDC) as a counter-suppressive agent in combination with IL-2 and/or IFN{alpha} has been under investigation in several clinical trials. In this issue, Middleton et al. [1691–1697] report on a study that aimed to evaluate the safety and efficacy of immunotherapy with HDC, IL-2 and IFN compared with DTIC in adults with stage IV melanoma. These authors report that while treatment with HDC/IL-2/IFN was safe on an outpatient basis, this regimen did not improve upon the response rate and overall survival seen with DTIC.


    Quote
 Top
 Prognostic role of peritumoral...
 Gemcitabine plus platinum in...
 Disease progression in Hodgkin's...
 Immunotherapy versus DTIC in...
 Quote
 
"I sat thinking, alone in the upstairs flat. I thought about Gloria taking the vitamin C and remembered her being sick the next day. She was only sick for a day! Vitamin C couldn't cause cancer, could it? I couldn't be to blame, could I? All because I kissed her when I had a cold."

Peter Turner considers the causes of Gloria Grahame's cancer in his memoir Film stars don't die in Liverpool.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?

Related articles in Ann Oncol:

Prognostic role of the extent of peritumoral vascular invasion in operable breast cancer
M. Colleoni, N. Rotmensz, P. Maisonneuve, A. Sonzogni, G. Pruneri, C. Casadio, A. Luini, P. Veronesi, M. Intra, V. Galimberti, R. Torrisi, S. Andrighetto, R. Ghisini, A. Goldhirsch, and G. Viale
Ann Oncol 2007 18: 1632-1640. [Abstract] [FREE Full Text]  

Increased survival using platinum analog combined with gemcitabine as compared to single-agent gemcitabine in advanced pancreatic cancer: pooled analysis of two randomized trials, the GERCOR/GISCAD intergroup study and a German multicenter study
V. Heinemann, R. Labianca, A. Hinke, and C. Louvet
Ann Oncol 2007 18: 1652-1659. [Abstract] [FREE Full Text]  

Patterns of disease progression and outcomes in a randomized trial testing ABVD alone for patients with limited-stage Hodgkin lymphoma
D. A. Macdonald, K. Ding, M. K. Gospodarowicz, W. A. Wells, R. G. Pearcey, J. M. Connors, J. N. Winter, S. J. Horning, M. S. Djurfeldt, L. E. Shepherd, and R. M. Meyer
Ann Oncol 2007 18: 1680-1684. [Abstract] [FREE Full Text]  

Results of a multicenter randomized study to evaluate the safety and efficacy of combined immunotherapy with interleukin-2, interferon-{alpha}2b and histamine dihydrochloride versus dacarbazine in patients with stage IV melanoma
M. Middleton, A. Hauschild, D. Thomson, R. Anderson, S. Burdette-Radoux, K. Gehlsen, K. Hellstrand, and P. Naredi
Ann Oncol 2007 18: 1691-1697. [Abstract] [FREE Full Text]  




This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Related articles in Ann Oncol
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Search for Related Content
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?