Using adaptive magnetic resonance image‐guided radiation therapy for treatment of inoperable pancreatic cancer

Cancer Medicine - Tập 8 Số 5 - Trang 2123-2132 - 2019
Soumon Rudra1, Naomi Jiang2, Stephen A. Rosenberg3, Jeffrey R. Olsen1, Michael Roach1, Leping Wan1, Lorraine Portelance4, Eric A. Mellon4, A. Bruynzeel5, Frank J. Lagerwaard5, M. Bassetti3, Parag J. Parikh1, Percy P. Lee2
1Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri
2Department of Radiation Oncology, David Geffen School of Medicine at UCLA, Los Angeles, California
3Department of Human Oncology, University of Wisconsin School of Medicine and Public Health, Carbone Cancer Center, Madison, Wisconsin
4Department of Radiation Oncology, Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida
5Department of Radiation Oncology, VU University Medical Center, Amsterdam, Netherlands

Tóm tắt

AbstractBackground

Adaptive magnetic resonance imaging‐guided radiation therapy (MRgRT) can escalate dose to tumors while minimizing dose to normal tissue. We evaluated outcomes of inoperable pancreatic cancer patients treated using MRgRT with and without dose escalation.

Methods

We reviewed 44 patients with inoperable pancreatic cancer treated with MRgRT. Treatments included conventional fractionation, hypofractionation, and stereotactic body radiation therapy. Patients were stratified into high‐dose (biologically effective dose [BED10] >70) and standard‐dose groups (BED10 ≤70). Overall survival (OS), freedom from local failure (FFLF) and freedom from distant failure (FFDF) were evaluated using Kaplan‐Meier method. Cox regression was performed to identify predictors of OS. Acute gastrointestinal (GI) toxicity was assessed for 6 weeks after completion of RT.

Results

Median follow‐up was 17 months. High‐dose patients (n = 24, 55%) had statistically significant improvement in 2‐year OS (49% vs 30%, P = 0.03) and trended towards significance for 2‐year FFLF (77% vs 57%, P = 0.15) compared to standard‐dose patients (n = 20, 45%). FFDF at 18 months in high‐dose vs standard‐dose groups was 24% vs 48%, respectively (P = 0.92). High‐dose radiation (HR: 0.44; 95% confidence interval [CI]: 0.21‐0.94; P = 0.03) and duration of induction chemotherapy (HR: 0.84; 95% CI: 0.72‐0.98; P = 0.03) were significantly correlated with OS on univariate analysis but neither factor was independently predictive on multivariate analysis. Grade 3+ GI toxicity occurred in three patients in the standard‐dose group and did not occur in the high‐dose group.

Conclusions

Patients treated with dose‐escalated MRgRT demonstrated improved OS. Prospective evaluation of high‐dose RT regimens with standardized treatment parameters in inoperable pancreatic cancer patients is warranted.

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