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Invasive bladder carcinoma: A pilot study of conservative treatment with accelerated radiotherapy and concomitant cisplatin

✍ Scribed by Abderrahim Zouhair; Mahmut Ozsahin; Dominique Schneider; Jean Bauer; Patrice Jichlinski; Arnaud Roth; Pelham Douglas; Raymond Miralbell


Publisher
John Wiley and Sons
Year
2001
Tongue
French
Weight
227 KB
Volume
96
Category
Article
ISSN
0020-7136

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✦ Synopsis


Abstract

From November 1992 to December 1997, 25 patients (inoperable or refusing cystectomy) were included in a prospective study to assess the feasibility, tolerance, and curative potential of accelerated radiotherapy (RT) and concomitant cisplatin. Median age was 74 years (range 49–86). Stage distribution was as follows: 1 T1, 10 T2, 8 T3, and 6 T4. Two patients had clinically positive pelvic nodes. The goal was to deliver a total dose of 40 Gy to the whole pelvis and bladder in 4 weeks using a concomitant boost of 20 Gy to the tumor or to the whole bladder during the third and fourth weeks (total dose 60 Gy), with daily cisplatin (6 mg/m^2^) before RT for patients with creatinine clearance > 50 ml/min. All but one patient completed the RT protocol. Daily cisplatin was sucessfully delivered in 18 patients. One patient presented with grade III ototoxicity. Diarrhea was scored grade III in two and grade IV in two patients. Acute urinary toxicity was scored grade III in one patient. Posttreatment late effects included bladder grade II and grade III in two patients and one patient, respectively; large bowel grade III in one; urethral grade III in one; and femoral head radionecrosis in one. Four‐year overall and disease‐specific survival rates were 23% and 35%, respectively. The latter was 60% for patients with T2 tumors. The 4‐year actuarial locoregional control rate for all patients was 61%. In summary, accelerated RT and concomitant cisplatin is feasible with acceptable tolerance even in relatively old patients. Although outcome was better for patients with low‐stage tumors, local control and survival rates appeared similar to those of standard RT schedules for a similar patient population. Β© 2001 Wiley‐Liss, Inc.


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