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DOI 10.1016/j.ijrobp.2024.09.040

Медицинская библиотека · International journal of radiation oncology, biology, physics · 2024

Bladder Adjuvant Radiation Therapy (BART): Acute and Late Toxicity From a Phase III Multicenter Randomized Controlled Trial.

Murthy Vedang, Maitre Priyamvada, Bakshi Ganesh, Pal Mahendra, Singh Maneesh, Sharma Rakesh, Gudipudi Duleep, Pujari Lincoln, Pandey Himanshu, Bandekar Bhavesh, Joseph Deepa, Krishnatry Rahul, Phurailatpam Reena, Kannan Sadhana, Arora Amandeep, Misra Ankit, Joshi Amit, Noronha Vanita, Prabhash Kumar, Menon Santosh, Prakash Gagan

СтатьяКлиническое исследование III фазыРандомизированное исследованиеМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

PURPOSE: To report toxicity from the multicenter phase III randomized trial of Bladder Adjuvant Radiation Therapy (BART) after radical cystectomy and chemotherapy in high-risk muscle-invasive bladder cancer (MIBC).

METHODS AND MATERIALS: Patients with nonmetastatic urothelial MIBC with ≥1 high-risk feature after radical cystectomy- pT3-4, pN1-3, nodal yield <10, positive margin, or ≥cT3 downstaged with neoadjuvant chemotherapy- were randomized 1:1 to observation (Obs) or adjuvant radiation therapy (RT) at 4 centers, stratified by pN stage (N0, N+) and chemotherapy (neoadjuvant, adjuvant, none). Stoma-sparing image guided intensity modulated RT 50.4 Gy in 28# was prescribed to the cystectomy bed and pelvic nodes. Acute toxicity (≤3 months of RT/randomization) and late toxicity were assessed per protocol using Common Terminology Criteria for Adverse Event v5.0. Patients progressing within 3 or 6 months of randomization were excluded from acute or late toxicity analysis, respectively.

RESULTS

The BART trial enrolled 153 patients (Obs = 76, RT = 77). About half (49%) had pN+. Nearly 90% received chemotherapy (70% neoadjuvant; most commonly gemcitabine plus cisplatin). In the RT arm, 63/77 completed RT per protocol with no toxicity-related RT termination. Of the 134 patients analyzable for acute toxicity, no difference was observed in grade 3 (Obs 4.2% vs RT 1.6%, P = .34). Grade 2 effects were higher with RT (17.5% vs 1.1%, P < .001), mainly diarrhea/enteritis or proctitis. Late toxicity was analyzable for 104 patients (Obs = 57, RT = 47) with a median follow-up of 27 months. Grades 3 to 4 toxicity were about 10% (Obs 10.5% vs RT 8.4%, P = .62), and cumulative late grade 2+ toxicity was similar in both groups (17.5% vs 23.3%, P = .27).

CONCLUSIONS

In the largest trial of adjuvant RT for high-risk urothelial MIBC, severe acute and late toxicity were low and similar with obervation or radiation therapy. The oncological outcomes are awaited.

Для цитирования: Murthy Vedang, Maitre Priyamvada, Bakshi Ganesh, Pal Mahendra, Singh Maneesh, Sharma Rakesh, Gudipudi Duleep, Pujari Lincoln, Pandey Himanshu, Bandekar Bhavesh, Joseph Deepa, Krishnatry Rahul, Phurailatpam Reena, Kannan Sadhana, Arora Amandeep, Misra Ankit, Joshi Amit, Noronha Vanita, Prabhash Kumar, Menon Santosh, Prakash Gagan. Bladder Adjuvant Radiation Therapy (BART): Acute and Late Toxicity From a Phase III Multicenter Randomized Controlled Trial.. International journal of radiation oncology, biology, physics. 2024. DOI: 10.1016/j.ijrobp.2024.09.040.

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