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Radiation Oncology Journal

2002 (v1, n1) to Present ISSN: 1671-8925

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Nodal tumor response according to the count of peripheral blood lymphocyte subpopulations during preoperative chemoradiotherapy in locally advanced rectal cancer.

Jaesung HEO ; Young Taek OH ; O Kyu NOH ; Mison CHUN ; Jun Eun PARK ; Sung Ran CHO

Radiation Oncology Journal.2016;34(4):305-312. doi:10.3857/roj.2016.01914

PURPOSE: The objective of this prospective study was to evaluate the relationship between the circulating lymphocyte subpopulation counts during preoperative chemoradiotherapy (CRT) and tumor response in locally advanced rectal cancer. MATERIALS AND METHODS: From August 2015 to June 2016, 10 patients treated with preoperative CRT followed by surgery were enrolled. Patients received conventional fractionated radiotherapy (50.4 Gy) with fluorouracil-based chemotherapy. Surgical resection was performed at 4 to 8 weeks after the completion of preoperative CRT. The absolute blood lymphocyte subpopulation was obtained prior to and after 4 weeks of CRT. We analyzed the association between a tumor response and change in the lymphocyte subpopulation during CRT. RESULTS: Among 10 patients, 2 (20%) had evidence of pathologic complete response. In 8 patients with clinically node positive, 4 (50%) had nodal tumor response. All lymphocyte subpopulation counts at 4 weeks after CRT were significantly lower than those observed during pretreatment (p < 0.01). A high decrease in natural killer (NK) cell, count during CRT (baseline cell count − cell count at 4 weeks) was associated with node down staging (p = 0.034). CONCLUSION: Our results suggest that the change of lymphocyte subset to preoperative CRT may be a predictive factor for tumor response in rectal cancer.
Cell Count ; Chemoradiotherapy* ; Drug Therapy ; Humans ; Killer Cells, Natural ; Lymphocyte Subsets* ; Lymphocytes* ; Prospective Studies ; Radiotherapy ; Rectal Neoplasms*

Cell Count ; Chemoradiotherapy* ; Drug Therapy ; Humans ; Killer Cells, Natural ; Lymphocyte Subsets* ; Lymphocytes* ; Prospective Studies ; Radiotherapy ; Rectal Neoplasms*

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Postoperative radiotherapy appeared to improve the disease free survival rate of patients with extrahepatic bile duct cancer at high risk of loco-regional recurrence.

Mi Young KIM ; Jin Hee KIM ; Yonghoon KIM ; Sang Jun BYUN

Radiation Oncology Journal.2016;34(4):297-304. doi:10.3857/roj.2016.01879

PURPOSE: To investigate the outcomes of postoperative radiotherapy (RT), in patients with extrahepatic bile duct (EHBD) cancer by comparing the survival rate between patients undergoing surgery alone or surgery plus postoperative RT, and to identify the prognostic factors affecting survival. MATERIALS AND METHODS: Between 2000 and 2013, 52 patients with EHBD cancer underwent surgical resection. Of these, 33 patients did not receive postoperative RT (group I), and 19 patients did (group II). R1 resection was significantly more frequent in group II. The median radiation dose was 5,040 cGy. RESULTS: The 3-year overall survival (OS) rate for group I and group II was 38% and 56%, respectively (p = 0.274). The 3-year disease free survival (DFS) rate for group I and group II was 20% and 31%, respectively (p = 0.049), and the 3-year loco-regional recurrence free survival (LRFS) rates were 19% and 58%, respectively (p = 0.002). Multivariate analyses showed that postoperative RT and lymphovascular invasion were independent prognostic factors for DFS and LRFS. Overall, 42 patients (80%) experienced treatment failure. Distant metastasis was the predominant pattern of failure in group II. CONCLUSION: Postoperative RT after surgical resection appeared to improve the loco-regional control and DFS rate. More effort is needed to reduce distant metastasis, the major pattern of failure, in patients who receive postoperative RT.
Bile Ducts, Extrahepatic* ; Disease-Free Survival* ; Humans ; Multivariate Analysis ; Neoplasm Metastasis ; Radiotherapy* ; Recurrence* ; Survival Rate ; Treatment Failure

Bile Ducts, Extrahepatic* ; Disease-Free Survival* ; Humans ; Multivariate Analysis ; Neoplasm Metastasis ; Radiotherapy* ; Recurrence* ; Survival Rate ; Treatment Failure

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The impact of radiotherapy on clinical outcomes in parameningeal rhabdomyosarcoma.

Yunseon CHOI ; Do Hoon LIM

Radiation Oncology Journal.2016;34(4):290-296. doi:10.3857/roj.2016.01795

PURPOSE: Radiotherapy (RT) is considered a mainstay of treatment in parameningeal rhabdomyosarcoma (PM-RMS). We aim to determine the treatment outcomes and prognostic factors for PM-RMS patients who treated with RT. In addition, we tried to evaluate the adequate dose and timing of RT. MATERIALS AND METHODS: Twenty-two patients with PM-RMS from 1995 to 2013 were evaluated. Seven patients had intracranial extension (ICE) and 17 patients had skull base bony erosion (SBBE). Five patients showed distant metastases at the time of diagnosis. All patients underwent chemotherapy and RT. The median radiation dose was 50.4 Gy (range, 40.0 to 56.0 Gy). RESULTS: The median follow-up was 28.7 months. Twelve patients (54.5%) experienced failure after treatment; 4 local, 2 regional, and 6 distant failures. The 5-year local control (LC) and overall survival (OS) were 77.7% and 38.5%, respectively. The 5-year OS rate was 50.8% for patients without distant metastases and 0% for patients with metastases (p < 0.001). Radiation dose (<50 Gy vs. ≥50 Gy) did not compromise the LC (p = 0.645). However, LC was affected by ICE (p = 0.031). Delayed administration (>22 weeks) of RT was related to a higher rate of local failure (40.0%). CONCLUSION: RT resulted in a higher rate of local control in PM-RMS. However, it was not extended to survival outcome. A more effective treatment for PM-RMS is warranted.
Diagnosis ; Drug Therapy ; Follow-Up Studies ; Humans ; Ice ; Meninges ; Neoplasm Metastasis ; Radiotherapy* ; Rhabdomyosarcoma* ; Skull Base

Diagnosis ; Drug Therapy ; Follow-Up Studies ; Humans ; Ice ; Meninges ; Neoplasm Metastasis ; Radiotherapy* ; Rhabdomyosarcoma* ; Skull Base

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Early hypopharyngeal cancer treated with different therapeutic approaches: a single-institution cohort analysis.

Nalee KIM ; Jeongshim LEE ; Kyung Hwan KIM ; Jong Won PARK ; Chang Geol LEE ; Ki Chang KEUM

Radiation Oncology Journal.2016;34(4):280-289. doi:10.3857/roj.2016.01711

PURPOSE: Early hypopharyngeal squamous cell carcinoma (HPSCC) is a rarely diagnosed disease, for which the optimal treatment has not been defined yet. We assessed patterns of failure and outcomes in early HPSCC treated with various therapeutic approaches to identify its optimal treatment. MATERIALS AND METHODS: Thirty-six patients with stage I (n = 10) and II (n = 26) treated between January 1992 and March 2014 were reviewed. Patients received definitive radiotherapy (RT) (R group, n = 10), surgery only (S group, n = 19), or postoperative RT (PORT group, n = 7). All patients in both the R and PORT groups received elective bilateral neck irradiation. In the S group, 7 patients had ipsilateral and 8 had bilateral dissection, while 4 patients had no elective dissection. RESULTS: At a median follow-up of 48 months, the 5-year locoregional control (LRC) rate was 65%. Six patients had local failure, 1 regional failure (RF), 3 combined locoregional failures, and 2 distant failures. There was no difference in 5-year LRC among the R, S, and PORT groups (p = 0.17). The presence with a pyriform sinus apex extension was a prognosticator related to LRC (p = 0.01) in the multivariate analysis. Patients with a bilaterally treated neck showed a trend toward a lower RF rate (p = 0.08). CONCLUSION: This study shows that patients with early stage HPSCC involving the pyriform sinus apex might need a tailored approach to improve LRC. Additionally, our study confirms elective neck treatment might have an efficacious role in regional control.
Carcinoma, Squamous Cell ; Cohort Studies* ; Follow-Up Studies ; Humans ; Hypopharyngeal Neoplasms* ; Multivariate Analysis ; Neck ; Pyriform Sinus ; Radiotherapy ; Treatment Failure

Carcinoma, Squamous Cell ; Cohort Studies* ; Follow-Up Studies ; Humans ; Hypopharyngeal Neoplasms* ; Multivariate Analysis ; Neck ; Pyriform Sinus ; Radiotherapy ; Treatment Failure

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Analysis of treatment outcomes for primary tonsillar lymphoma.

Yun Hee LEE ; Seok Goo CHO ; Seung Eun JUNG ; Sung Hoon KIM ; Joo Hyun O ; Gyeong Sin PARK ; Suk Woo YANG ; In Seok LEE ; Chin Kook RHEE ; Byung Ock CHOI

Radiation Oncology Journal.2016;34(4):273-279. doi:10.3857/roj.2016.01781

PURPOSE: Although each Waldeyer’s ring sub-site is considered an independent prognostic factor, few studies have assessed the prognosis and treatment of tonsillar lymphoma. Treatment outcomes were analyzed in patients with primary tonsillar lymphoma who were treated with chemotherapy and radiotherapy (RT). MATERIALS AND METHODS: Nineteen patients with diffuse large B-cell lymphoma were evaluated, with a median follow-up of 53 months. Age, sex, and histology, amongst other factors, were reviewed. Progression-free survival (PFS) and overall survival (OS) rates were analyzed. RESULTS: Most patients had Ann Arbor stage I-II (94.7%), IPI score of 0 (89.5%), and complete remission after chemotherapy (89.5%). The 5-year PFS and OS rates were 74.6% and 80%, respectively. In univariate analysis, the rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) regimen resulted in a better PFS than the cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) regimen (88.9% vs. 50.0%; p = 0.053). RT dose was related to the survival outcome (p = 0.010 for PFS, p = 0.044 for OS). Patients were classified into the CHOP + RT (>40 Gy) group and R-CHOP + RT (≤40 Gy) group. The 5-year PFS rates were 50% in the CHOP + RT group, and 100 % in the R-CHOP + RT group (p = 0.018). The 5-year OS rates were 66.7% and 100%, respectively (p = 0.087). CONCLUSION: Primary tonsillar lymphoma patients typically have favorable outcomes. Chemotherapy (R-CHOP) combined with relatively lower dose consolidative RT may be safe and effective for primary tonsillar lymphoma.
Cyclophosphamide ; Disease-Free Survival ; Doxorubicin ; Drug Therapy ; Follow-Up Studies ; Humans ; Lymphoma* ; Lymphoma, B-Cell ; Lymphoma, Non-Hodgkin ; Palatine Tonsil ; Prednisone ; Prognosis ; Radiotherapy ; Rituximab ; Vincristine

Cyclophosphamide ; Disease-Free Survival ; Doxorubicin ; Drug Therapy ; Follow-Up Studies ; Humans ; Lymphoma* ; Lymphoma, B-Cell ; Lymphoma, Non-Hodgkin ; Palatine Tonsil ; Prednisone ; Prognosis ; Radiotherapy ; Rituximab ; Vincristine

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Treatment outcomes after adjuvant radiotherapy following surgery for patients with stage I endometrial cancer.

Jiyoung KIM ; Kyung Ja LEE ; Kyung Ran PARK ; Boram HA ; Yi Jun KIM ; Wonguen JUNG ; Rena LEE ; Seung Cheol KIM ; Hye Sung MOON ; Woong JU ; Yun Hwan KIM ; Jihae LEE

Radiation Oncology Journal.2016;34(4):265-272. doi:10.3857/roj.2016.01648

PURPOSE: The purpose of this study is to evaluate the treatment outcomes of adjuvant radiotherapy using vaginal brachytherapy (VB) with a lower dose per fraction and/or external beam radiotherapy (EBRT) following surgery for patients with stage I endometrial carcinoma. MATERIALS AND METHODS: The subjects were 43 patients with the International Federation of Gynecology and Obstetrics (FIGO) stage I endometrial cancer who underwent adjuvant radiotherapy following surgery between March 2000 and April 2014. Of these, 25 received postoperative VB alone, while 18 received postoperative EBRT to the whole pelvis; 3 of these were treated with EBRT plus VB. The median EBRT dose was 50.0 Gy (45.0–50.4 Gy) and the VB dose was 24 Gy in 6 fractions. Tumor dose was prescribed at a depth of 5 mm from the cylinder surface and delivered twice per week. RESULTS: The median follow-up period for all patients was 57 months (range, 9 to 188 months). Five-year disease-free survival (DFS) and overall survival (OS) for all patients were 92.5% and 95.3%, respectively. Adjuvant radiotherapy was performed according to risk factors and stage IB, grade 3 and lymphovascular invasion were observed more frequently in the EBRT group. Five-year DFS for EBRT and VB alone were 88.1% and 96.0%, respectively (p = 0.42), and 5-year OS for EBRT and VB alone were 94.4% and 96%, respectively (p = 0.38). There was no locoregional recurrence in any patient. Two patients who received EBRT and 1 patient who received VB alone developed distant metastatic disease. Two patients who received EBRT had severe complications, one each of grade 3 gastrointestinal complication and pelvic bone insufficiency fracture. CONCLUSION: Adjuvant radiotherapy achieved high DFS and OS with acceptable toxicity in stage I endometrial cancer. VB (with a lower dose per fraction) may be a viable option for selected patients with early-stage endometrial cancer following surgery.
Brachytherapy ; Disease-Free Survival ; Endometrial Neoplasms* ; Female ; Follow-Up Studies ; Fractures, Stress ; Gynecology ; Humans ; Obstetrics ; Pelvic Bones ; Pelvis ; Radiotherapy ; Radiotherapy, Adjuvant* ; Radiotherapy, Conformal ; Recurrence ; Risk Factors

Brachytherapy ; Disease-Free Survival ; Endometrial Neoplasms* ; Female ; Follow-Up Studies ; Fractures, Stress ; Gynecology ; Humans ; Obstetrics ; Pelvic Bones ; Pelvis ; Radiotherapy ; Radiotherapy, Adjuvant* ; Radiotherapy, Conformal ; Recurrence ; Risk Factors

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Hypofractionated stereotactic body radiotherapy in low- and intermediate-risk prostate carcinoma.

Hun Jung KIM ; Jeong Hoon PHAK ; Woo Chul KIM

Radiation Oncology Journal.2016;34(4):260-264. doi:10.3857/roj.2015.01571

PURPOSE: Stereotactic body radiotherapy (SBRT) takes advantage of low α/β ratio of prostate cancer to deliver a large dose in few fractions. We examined clinical outcomes of SBRT using CyberKnife for the treatment of low- and intermediate-risk prostate cancer. MATERIALS AND METHODS: This study was based on a retrospective analysis of the 33 patients treated with SBRT using CyberKnife for localized prostate cancer (27.3% in low-risk and 72.7% in intermediate-risk). Total dose of 36.25 Gy in 5 fractions of 7.25 Gy were administered. The acute and late toxicities were recorded using the Radiation Therapy Oncology Group scale. Prostate-specific antigen (PSA) response was monitored. RESULTS: Thirty-three patients with a median 51 months (range, 6 to 71 months) follow-up were analyzed. There was no biochemical failure. Median PSA nadir was 0.27 ng/mL at median 33 months and PSA bounce occurred in 30.3% (n = 10) of patients at median at median 10.5 months after SBRT. No grade 3 acute toxicity was noted. The 18.2% of the patients had acute grade 2 genitourinary (GU) toxicities and 21.2% had acute grade 2 gastrointestinal (GI) toxicities. After follow-up of 2 months, most complications had returned to baseline. There was no grade 3 late GU and GI toxicity. CONCLUSION: Our experience with SBRT using CyberKnife in low- and intermediate-risk prostate cancer demonstrates favorable efficacy and toxicity. Further studies with more patients and longer follow-up duration are required.
Follow-Up Studies ; Humans ; Prostate* ; Prostate-Specific Antigen ; Prostatic Neoplasms ; Radiosurgery* ; Radiotherapy ; Retrospective Studies

Follow-Up Studies ; Humans ; Prostate* ; Prostate-Specific Antigen ; Prostatic Neoplasms ; Radiosurgery* ; Radiotherapy ; Retrospective Studies

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Radiotherapy and immune checkpoint blockades: a snapshot in 2016.

Taeryool KOO ; In Ah KIM

Radiation Oncology Journal.2016;34(4):250-259. doi:10.3857/roj.2016.02033

Immune checkpoint blockades including monoclonal antibodies (mAbs) of cytotoxic T-lymphocyte antigen-4 (CTLA-4), programmed death-1 (PD-1), and programmed death-ligand 1 (PD-L1) have been emerged as a promising anticancer therapy. Several immune checkpoint blockades have been approved by US Food and Drug Administration (FDA), and have shown notable success in clinical trials for patients with advanced melanoma and non-small cell lung cancer. Radiotherapy is a promising combination partner of immune checkpoint blockades due to its potent pro-immune effect. This review will cover the current issue and the future perspectives for combined with radiotherapy and immune checkpoint blockades based upon the available preclinical and clinical data.
Antibodies, Monoclonal ; Carcinoma, Non-Small-Cell Lung ; Humans ; Melanoma ; Programmed Cell Death 1 Receptor ; Radiotherapy* ; T-Lymphocytes, Cytotoxic ; United States Food and Drug Administration

Antibodies, Monoclonal ; Carcinoma, Non-Small-Cell Lung ; Humans ; Melanoma ; Programmed Cell Death 1 Receptor ; Radiotherapy* ; T-Lymphocytes, Cytotoxic ; United States Food and Drug Administration

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Tumor hypoxia and reoxygenation: the yin and yang for radiotherapy.

Beom Ju HONG ; Jeongwoo KIM ; Hoibin JEONG ; Seoyeon BOK ; Young Eun KIM ; G One AHN

Radiation Oncology Journal.2016;34(4):239-249. doi:10.3857/roj.2016.02012

Tumor hypoxia, a common feature occurring in nearly all human solid tumors is a major contributing factor for failures of anticancer therapies. Because ionizing radiation depends heavily on the presence of molecular oxygen to produce cytotoxic effect, the negative impact of tumor hypoxia had long been recognized. In this review, we will highlight some of the past attempts to overcome tumor hypoxia including hypoxic radiosensitizers and hypoxia-selective cytotoxin. Although they were (still are) a very clever idea, they lacked clinical efficacy largely because of ‘reoxygenation’ phenomenon occurring in the conventional low dose hyperfractionation radiotherapy prevented proper activation of these compounds. Recent meta-analysis and imaging studies do however indicate that there may be a significant clinical benefit in lowering the locoregional failures by using these compounds. Latest technological advancement in radiotherapy has allowed to deliver high doses of radiation conformally to the tumor volume. Although this technology has brought superb clinical responses for many types of cancer, recent modeling studies have predicted that tumor hypoxia is even more serious because ‘reoxygenation’ is low thereby leaving a large portion of hypoxic tumor cells behind. Wouldn’t it be then reasonable to combine hypoxic radiosensitizers and/or hypoxia-selective cytotoxin with the latest radiotherapy? We will provide some preclinical and clinical evidence to support this idea hoping to revamp an enthusiasm for hypoxic radiosensitizers or hypoxia-selective cytotoxins as an adjunct therapy for radiotherapy.
Anoxia* ; Cytotoxins ; Hope ; Humans ; Oxygen ; Radiation, Ionizing ; Radiotherapy* ; Treatment Outcome ; Tumor Burden

Anoxia* ; Cytotoxins ; Hope ; Humans ; Oxygen ; Radiation, Ionizing ; Radiotherapy* ; Treatment Outcome ; Tumor Burden

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Organ preservation with neoadjuvant chemoradiation in patients with orbit invasive sinonasal cancer otherwise requiring exenteration.

Mark J AMSBAUGH ; Mehran YUSUF ; Craig SILVERMAN ; Jeffrey BUMPOUS ; Cesar A PEREZ ; Keven POTTS ; Paul TENNANT ; Rebecca REDMAN ; Neal DUNLAP

Radiation Oncology Journal.2016;34(3):209-215. doi:10.3857/roj.2016.01739

PURPOSE: We sought to determine if organ preservation (OP) with neoadjuvant chemoradiation (CRT) was feasible in patients with sinonasal cancer determined to require exenteration. MATERIALS AND METHODS: Twenty patients were determined to require exenteration for definitive treatment from 2005 to 2014. Fourteen patients underwent OP and 6 patients received exenteration with adjuvant CRT. Exenteration free survival (EFS), locoregional control (LRC), progression-free survival (PFS), and overall survival (OS) were estimated. RESULTS: Five patients (36%) receiving OP had complete disease response at time of surgery. With a median follow-up of 18.8 months, EFS was 62% at 2 years for patients undergoing OP. At 2 years, there were no significant differences in LRC, PFS or OS (all all p > 0.050) between the groups. Less grade 3 or greater toxicity was seen in patients undergoing OP (p = 0.003). Visual function was preserved in all patients undergoing OP. CONCLUSION: For patients with sinonasal cancer, OP may avoid exenteration, offering similar disease control and improved toxicity.
Disease-Free Survival ; Follow-Up Studies ; Humans ; Orbit* ; Organ Preservation*

Disease-Free Survival ; Follow-Up Studies ; Humans ; Orbit* ; Organ Preservation*

Country

Republic of Korea

Publisher

ElectronicLinks

Editor-in-chief

E-mail

Abbreviation

Radiation Oncology Journal

Vernacular Journal Title

ISSN

2234-1900

EISSN

Year Approved

2007

Current Indexing Status

Currently Indexed

Start Year

Description

Previous Title

The Journal of the Korean Society for Therapeutic Radiology and Oncology
Journal of the Korean Society for Therapeutic Radiology

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