P2.113. Post operative radiation with and without concurrent chemotherapy in node positive oral cancer

2009 ◽  
Vol 3 (1) ◽  
pp. 197
Author(s):  
A. Jamshed ◽  
R. Hussain ◽  
H. Iqbal ◽  
K. Rehman
Health Care ◽  
2013 ◽  
Vol 1 (3) ◽  
pp. 89
Author(s):  
Mohamed Mahmoud ◽  
Tarek Souman ◽  
Mohamed Amin ◽  
Mona Aboelenin

2008 ◽  
Vol 20 (3) ◽  
pp. 499-511 ◽  
Author(s):  
Dimitrios Nikolarakos ◽  
R. Bryan Bell
Keyword(s):  

2017 ◽  
Vol 35 (4) ◽  
pp. 349-358 ◽  
Author(s):  
Jinju Oh ◽  
Ki Ho Seol ◽  
Hyun Joo Lee ◽  
Youn Seok Choi ◽  
Ji Y. Park ◽  
...  

2013 ◽  
Vol 04 (11) ◽  
pp. 1-9
Author(s):  
Mohamed Mahmoud ◽  
Tarek Shouman ◽  
Hesham Elhosseny ◽  
Mona Aboelenin ◽  
Mohamed Amin

1991 ◽  
Vol 9 (9) ◽  
pp. 1662-1667 ◽  
Author(s):  
A Recht ◽  
S E Come ◽  
R S Gelman ◽  
M Goldstein ◽  
S Tishler ◽  
...  

The optimal means of combining breast-conserving surgery, radiation therapy, and chemotherapy for the treatment of patients with early-stage, node-positive breast cancer is not known. We reviewed the results in 295 patients treated at the Joint Center for Radiation Therapy and affiliated institutions from 1976 to 1985. All patients had positive axillary nodes on dissection, had no gross residual disease in the breast or axilla after surgery, and received breast irradiation (with or without nodal irradiation) and three or more cycles of a cyclophosphamide, methotrexate, and fluorouracil (CMF)-based or doxorubicin-containing regimen. Median follow-up in patients without any failure was 78 months. Breast failure rates were assessed in relation to the sequencing of radiotherapy and chemotherapy. The different sequences were not randomly assigned, and the characteristics of the sequence groups differed. The actuarial 5-year breast failure rate was 4% in 99 patients receiving radiotherapy before chemotherapy; 8% in 54 patients sequentially receiving some chemotherapy, then radiotherapy without concurrent chemotherapy, then further chemotherapy; and 6% in 116 patients receiving concurrent chemotherapy and radiotherapy. However, the failure rate was 41% in 26 patients who received all chemotherapy before radiotherapy. The crude incidences of local failure within 4 years of treatment in these groups were 3%, 2%, 4%, and 15%, respectively (P = .065 for all four groups not being the same). The actuarial 5-year local failure rate was 5% for 252 patients irradiated within 16 weeks after surgery compared with 35% for 34 patients irradiated more than 16 weeks after surgery. The 4-year crude incidences were 4% and 12% for the two groups, respectively (P = .06). These results suggest that delaying the initiation of radiotherapy may result in an increased likelihood of local failure. Formal randomized controlled trials will be needed to confirm these results and to improve the integration of these treatment modalities.


2003 ◽  
Vol 21 (8) ◽  
pp. 1431-1439 ◽  
Author(s):  
Marc L. Citron ◽  
Donald A. Berry ◽  
Constance Cirrincione ◽  
Clifford Hudis ◽  
Eric P. Winer ◽  
...  

Purpose: Using a 2 × 2 factorial design, we studied the adjuvant chemotherapy of women with axillary node–positive breast cancer to compare sequential doxorubicin (A), paclitaxel (T), and cyclophosphamide (C) with concurrent doxorubicin and cyclophosphamide (AC) followed by paclitaxel (T) for disease-free (DFS) and overall survival (OS); to determine whether the dose density of the agents improves DFS and OS; and to compare toxicities. Patients and Methods: A total of 2,005 female patients were randomly assigned to receive one of the following regimens: (I) sequential A × 4 (doses) → T × 4 → C × 4 with doses every 3 weeks, (II) sequential A × 4 → T × 4 → C × 4 every 2 weeks with filgrastim, (III) concurrent AC × 4 → T × 4 every 3 weeks, or (IV) concurrent AC × 4 → T × 4 every 2 weeks with filgrastim. Results: A protocol-specified analysis was performed at a median follow-up of 36 months: 315 patients had experienced relapse or died, compared with 515 expected treatment failures. Dose-dense treatment improved the primary end point, DFS (risk ratio [RR] = 0.74; P = .010), and OS (RR = 0.69; P = .013). Four-year DFS was 82% for the dose-dense regimens and 75% for the others. There was no difference in either DFS or OS between the concurrent and sequential schedules. There was no interaction between density and sequence. Severe neutropenia was less frequent in patients who received the dose-dense regimens. Conclusion: Dose density improves clinical outcomes significantly, despite the lower than expected number of events at this time. Sequential chemotherapy is as effective as concurrent chemotherapy.


2008 ◽  
Vol 118 (4) ◽  
pp. 646-649 ◽  
Author(s):  
Takashi Matsuzuka ◽  
Makoto Kano ◽  
Hiroshi Ogawa ◽  
Tomohiro Miura ◽  
Yasuhiro Tada ◽  
...  

Author(s):  
Karvita B. Ahluwalia ◽  
Nidhi Sharma

It is common knowledge that apparently similar tumors often show different responses to therapy. This experience has generated the idea that histologically similar tumors could have biologically distinct behaviour. The development of effective therapy therefore, has the explicit challenge of understanding biological behaviour of a tumor. The question is which parameters in a tumor could relate to its biological behaviour ? It is now recognised that the development of malignancy requires an alteration in the program of terminal differentiation in addition to aberrant growth control. In this study therefore, ultrastructural markers that relate to defective terminal differentiation and possibly invasive potential of cells have been identified in human oral leukoplakias, erythroleukoplakias and squamous cell carcinomas of the tongue.


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