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Anal cancer outcomes in patients treated with intensity modulated versus 3-dimensional chemoradiotherapy [Meeting Abstract]

Cooper, B T; Grew, D; Bitterman, D; Sanfilippo, N; Du, K L
Background: Combined chemoradiotherapy (CRT) has been successful in both tumor eradication and colostomy prevention in patients with squamous-cell carcinoma of the anal canal. Unfortunately, CRT can be toxic with high rates of acute gastrointestinal and skin toxicity. This can necessitate treatment interruptions, prolonging therapy, possibly leading to loss of local control. In RTOG 0529, intensity modulated radiation therapy (IMRT) decreased the rate of treatment interruption compared to historical controls. We aim to compare toxicity and outcomes in patients treated with CRT based on radiation technique. Methods: We retrospectively reviewed 107 consecutive patients, 39 HIV+, 68 HIV-, who underwent definitive CRT for anal cancer at a single institution between 2004 and 2013. Overall survival (OS), colostomy-free survival (CFS), local recurrence-free survival (LRFS) and distant metastasis-free survival (DMFS) were analyzed. Chi-square test was used to compare frequencies and t-test was used to compare means. Kaplan-Meier survival was calculated and differences were evaluated by Log-rank statistic. Results: Median follow-up was 15 months. Radiation technique was IMRT in 60% of patients with the remainder treated with 3-dimensional conformal radiation therapy (3D). Dose to the draining lymph nodes was higher in patients treated with IMRT (mean dose 40 Gy vs. 32 Gy, p < 0.001). Fewer patients had a greater than 10 day treatment break in IMRT cohort than the 3D cohort (21% vs. 43%, p = 0.028). Three-year OS (91% vs. 47%, p < 0.001) and DMFS (88% vs 64%, p= 0.033) were improved in patients treated with IMRT. There was no significant difference in acute GI or skin toxicity. There was no difference in stage, number of chemotherapy cycles and dose reductions, growth factor support, transfusion necessity, hospital admission, LRFS, sphincter function preservation, or CFS. Conclusions: In this cohort, patients treated with IMRT had better OS and DMFS than patients treated with 3D. Higher radiation doses to the draining lymph nodes and fewer prolonged treatment breaks may contribute to improved outcomes in patients treated with IMRT. Further studies are necessary to establish the etiology of this difference in outcomes
EMBASE:71836203
ISSN: 0732-183x
CID: 1561032

Effect of Treatment Time of Day on Radiation Fatigue and Toxicity in Early-Stage Breast Cancer Patients After Breast Conserving Surgery [Meeting Abstract]

Ishaq, O; Valdimarsdottir, H; Cooper, BT; Modrek, A; Redd, W; Formenti, SC
ISI:000373215300134
ISSN: 1879-355x
CID: 2098182

Use of a Flexible Inflatable Multi-Channel Applicator for Vaginal Brachytherapy in the Management of Gynecologic Cancer

Shin, Samuel M; Duckworth, Tamara L; Cooper, Benjamin T; Curtin, John P; Schiff, Peter B; DeWyngaert, J Keith; Lymberis, Stella C
INTRODUCTION: Evaluate use of novel multi-channel applicator (MC) Capri to improve vaginal disease coverage achievable by single-channel applicator (SC) and comparable to Syed plan simulation. MATERIALS AND METHODS: Twenty-eight plans were evaluated from four patients with primary or recurrent gynecologic cancer in the vagina. Each received whole pelvis radiation, followed by three weekly treatments using HDR brachytherapy with a 13-channel MC. Upper vagina was treated to 5 mm depth to 1500 cGy/3 fractions with a simultaneous integrated boost totaling 2100 cGy/3 fractions to tumor. Modeling of SC and Syed plans was performed using MC scans for each patient. Dosimetry for MC and SC plans was evaluated for PTV700 cGy coverage, maximum dose to 2 cm(3) to bladder, rectum, as well as mucosal surface points. Dosimetry for Syed plans was calculated for PTV700 cGy coverage. Patients were followed for treatment response and toxicity. RESULTS: Dosimetric analysis between MC and SC plans demonstrated increased tumor coverage (PTV700 cGy), with decreased rectal, bladder, and contralateral vaginal mucosa dose in favor of MC. These differences were significant (p < 0.05). Comparison of MC and Syed plans demonstrated increased tumor coverage in favor of Syed plans which were not significant (p = 0.71). Patients treated with MC had no cancer recurrence or >/=grade 3 toxicity. CONCLUSION: Use of MC was efficacious and safe, providing superior coverage of tumor volumes
PMCID:4568766
PMID: 26442213
ISSN: 2234-943x
CID: 1793112

Effect of Resident Involvement on Improving Pain Management in a Radiation Oncology Department: A Multidisciplinary Microsystems Approach Focusing on Patient Reported Outcomes [Meeting Abstract]

Cooper, BT; Smith, BE; Oliveri, ML; Brown, J; Cabrera, A; Gumbs, K; Sanfilippo, NJ; Du, KL
ISI:000373215301285
ISSN: 1879-355x
CID: 2097972

Dosimetric Comparison of Proton Therapy, Volumetric Modulated Arc Therapy, and 3-D Conformal Radiation Therapy for the Treatment of Rectal Cancer: An Early Community Experience [Meeting Abstract]

Cooper, BT; Qu, J; Chon, BH; Tsai, HK; Mah, D; Du, KL; DeWyngaert, JK; Yeh, BK
ISI:000373215300448
ISSN: 1879-355x
CID: 2097902

Anal Cancer Outcomes in Patients Treated With Intensity Modulated Compared to 3-Dimensional Radiation Therapy [Meeting Abstract]

Cooper, BT; Bitterman, DS; Grew, D; No, HS; Sanfilippo, NJ; Du, KL
ISI:000373215300421
ISSN: 1879-355x
CID: 2097892

Randomized Trial of Prone Accelerated Whole-Breast Radiation Therapy With a Daily Versus Weekly Boost to the Tumor Bed: Acute Toxicity and Associated Dosimetry [Meeting Abstract]

Cooper, BT; Di Brina, L; Li, X; Fenton-Kerimian, MB; Maisonet, OG; Guth, A; Hitchen, C; Jozsef, G; DeWyngaert, JK; Goldberg, JD; Formenti, SC
ISI:000373215300095
ISSN: 1879-355x
CID: 2097832

Prospective Randomized Trial of Prone Accelerated Intensity Modulated Whole-Breast Radiation Therapy With a Daily Versus Weekly Boost to the Tumor Bed: 3-Year Results [Meeting Abstract]

Cooper, BT; Formenti-Ujlaki, GF; Shin, S; Fenton-Kerimian, MB; Roses, DF; Amber, GA; Jozsef, G; DeWyngaert, J; Formenti, S
ISI:000342331400396
ISSN: 1879-355x
CID: 2409502

Use of Simultaneous Integrated Boost Regimen With Flexible Inflatable Multi-Channel Versus Single Channel and Syed Applicator in the Management of Gynecologic Cancer [Meeting Abstract]

Shin, S; Duckworth, T; Cooper, B; Curtin, JP; Schiff, PB; Lymberis, S; DeWyngaert, JK
ISI:000342331403423
ISSN: 1879-355x
CID: 1314012

Hypofractionated radiation therapy for prostate cancer: biologic and technical considerations

Sanfilippo, Nicholas J; Cooper, Benjamin T
The optimal radiation schedule for the curative treatment of prostate cancer is not known. The dose-response of tumors and normal tissues to fractionated irradiation can be described according to a parameter called the alpha-beta ratio (alpha/beta). In the past several years numerous reports have been published that suggest that the alpha-beta ratio for prostate cancer may be quite low; between 1 and 3. If this hypothesis is true, then a radiation therapy schedule that employs less frequent and larger fractions, termed hypofractionation, may be more efficacious. Multiple randomized trials have been conducted comparing moderate (less than 5 Gy/day) hypofractionated radiation therapy and standard radiation therapy in men with prostate cancer. In the majority of these studies the moderate hypofractionated arm had equivalent efficacy with a similar or improved side effect profile. One area to use caution may be in patients with compromised (IPSS > 12) urinary function at baseline due to an increase in urinary toxicity observed in patients treated with hypofractionated radiation in one study. Extreme hypofractionation (greater than or equal to 5 Gy/day), is currently being compared in a randomized trial. Early prospectively collected data from multiple institutions demonstrates efficacy and toxicity that compares favorably with historical controls. The cost savings from hypofractionation could be profound on a national level and only increases the necessity of testing hypofractionated treatment schedules. Long term data and future trials will help radiation oncologists determine the ideal fractionation scheme based on cost, efficacy, and toxicity.
PMCID:4297324
PMID: 25606574
ISSN: 2330-1910
CID: 1440192