Reiko Imai

Dr. Reiko Imai

orcid

Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2016 in International Journal of Radiation Oncology, Biology, Physics
Verified
Journal Article
Closed access
RIReiko Imai
Reiko Imai
TKTadashi Kamada
Tadashi Kamada
NANobuhito Araki
Nobuhito Araki
WSWorking Group for Bone and Soft Tissue Sarcomas
Working Group for Bone and Soft Tissue Sarcomas

22 February 2012 in Cancer
Verified
Journal Article
Open access
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AMAkira Matsunobu
Akira Matsunobu
RIReiko Imai
Reiko Imai
TKTadashi Kamada
Tadashi Kamada
TITakeshi Imaizumi
Takeshi Imaizumi
HTHiroshi Tsuji
Hiroshi Tsuji
FSfor the Working Group for Bone and Soft Tissue Sarcomas
for the Working Group for Bone and Soft Tissue Sarcomas
BACKGROUND: The authors summarized the outcomes of patients with unresectable osteosarcoma of the trunk who received carbon ion radiotherapy (CIRT).METHODS: The authors performed a retrospective analysis of 78 patients who had medically inoperable osteosarcoma of the trunk and received treatment with CIRT between 1996 and 2009. Tumor sites included the pelvis in 61 patients, the spine and paraspinal region in 15 patients, and other sites in 2 patients. The median applied CIRT dose was 70.4 Gray equivalent (GyE) in a total of 16 fixed fractions over 4 weeks.RESULTS: The minimum duration of follow‐up for survivors was 14 months. Forty‐eight patients remained alive. The 5‐year overall survival rate was 33%, and the local control rate was 62%. Thirty‐eight patients who had a clinical target volume 5 years, 8 were able to walk with or without the help of a cane, and 6 were free from pain killers.CONCLUSIONS: CIRT appeared to be a safe and effective modality for the management of unresectable osteosarcoma of the trunk, providing good local control and offering a survival advantage and good long‐term functional results without unacceptable morbidity. Cancer 2012. © 2012 American Cancer Society.

1 August 2010 in International Journal of Radiation Oncology, Biology, Physics
Verified
Journal Article
Closed access
RIReiko Imai
Reiko Imai
TKTadashi Kamada
Tadashi Kamada
HTHiroshi Tsuji
Hiroshi Tsuji
SSShinji Sugawara
Shinji Sugawara
ISItsuko Serizawa
Itsuko Serizawa
WSWorking Group for Bone and Soft Tissue Sarcomas
Working Group for Bone and Soft Tissue Sarcomas

12 August 2013 in Cancer
Verified
Journal Article
Open access
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KMKeiji Matsumoto
Keiji Matsumoto
RIReiko Imai
Reiko Imai
TKTadashi Kamada
Tadashi Kamada
KMKatsuya Maruyama
Katsuya Maruyama
HTHiroshi Tsuji
Hiroshi Tsuji
TSthe Working Group for Bone and Soft Tissue Sarcomas
the Working Group for Bone and Soft Tissue Sarcomas
BACKGROUND: Spinal sarcomas have been one of the most challenging diseases for orthopedic surgeons. The objective of this study was to retrospectively analyze carbon ion radiotherapy (CIRT) treatment results for spinal sarcoma.METHODS: Forty‐seven patients with 48 medically unresectable spinal sarcomas, excluding sacral tumors, received treatment with CIRT between 1996 and 2011. All patients were enrolled in phase 1/2 and phase 2 clinical trials of CIRT for bone and soft tissue sarcoma. The applied dose ranged from 52.8 gray equivalents (GyE) to 70.4 GyE (median, 64.0 GyE) in 16 fixed fractions over 4 weeks.RESULTS: The median patient age was 54 years, and the cohort included 24 men and 23 women. Thirty‐five patients were without prior treatment, and 12 patients had locally recurrent tumors after previous resection. The median follow‐up was 25 months, and the median survival was 44 months (range, 5.2‐148 months). The 5‐year local control, overall survival, and progression free rates were 79%, 52%, and 48%, respectively. None of the 15 patients who had tumors measuring <100 cm3 had a local recurrence. No fatal toxicities occurred during follow‐up. One patient each had a grade 3 late skin reaction and a grade 4 late skin reaction. Vertebral body compression was observed in 7 patients. One patient had a grade 3 late spinal cord reaction. Twenty‐two of the surviving 28 patients who had primary tumors remained ambulatory without supportive devices.CONCLUSIONS: CIRT appears to be both effective and safe for the treatment of patients with unresectable spinal sarcoma. Cancer 2013;119:3496–3503.. © 2013 American Cancer Society.

20 July 2018 in Cancer Medicine
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Journal Article
Open access
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RIReiko Imai
Reiko Imai
TKTadashi Kamada
Tadashi Kamada
NANobuhito Araki
Nobuhito Araki
TSthe Working Group for Carbon Ion Radiotherapy for Bone and Soft Tissue Sarcomas
the Working Group for Carbon Ion Radiotherapy for Bone and Soft Tissue Sarcomas
Carbon ion radiotherapy is known for its high‐precision dose distribution and high biological effectiveness. We evaluated the results of carbon ion radiotherapy in 128 patients with unresectable localized axial soft tissue sarcoma at a single institution. The patients’ median age was 54 years, and the median follow‐up period was 49.4 (range 6.4‐146.4) months. The median tumor volume was 356 cm3. The 5‐year local control, overall survival, and disease‐free survival rates were 65%, 46%, and 39%, respectively. In the univariate analysis, tumor volume, local control, and incidences of metastases were significantly related to overall survival. In the multivariate analysis, tumor volume and local control were significantly related to overall survival. We did not find any factors related to local control. Five patients required surgical intervention because of adverse events in the bones. Carbon ion radiotherapy may be a treatment option for unresectable axial soft tissue sarcoma.

1 May 2018 in Oncotarget
Verified
Journal Article
Open access
OMOsama Mohamad
Osama Mohamad
TSthe Working Group for Bone and Soft Tissue Sarcoma
the Working Group for Bone and Soft Tissue Sarcoma
RIReiko Imai
Reiko Imai
TKTadashi Kamada
Tadashi Kamada
YNYuki Nitta
Yuki Nitta
NANobuhito Araki
Nobuhito Araki
Unresectable pediatric osteosarcoma has poor outcomes with conventional treatments. Twenty-six patients aged 11-20 years (median 16) had inoperable osteosarcoma of the trunk (24 pelvic, 1 mediastinal and 1 paravertebral) without any other lesion at initial examination. There were 22 primary, 1 locally recurrent and 3 metastatic cases. Median CIRT dose was 70.4 Gy RBE (relative biological effectiveness) delivered in 16 fractions. Median follow-up was 32.7 months. Overall survival was 50.0% and 41.7% at 3 and 5 years, respectively. Ten patients survived for more than 5 years (range 5-20.7 years). Local control was 69.9% and 62.9% at 3 and 5 years, respectively and progression-free survival was 34.6% at 3 and 5 years. Only largest tumor diameter correlated with 5-year overall survival and local control. There were 4 grade 3-4 CIRT-related late toxicities, 1 case of bone fracture and no treatment-related mortalities. All patients (except 1) were able to ambulate after CIRT. CIRT was safe and efficacious in the treatment of inoperable pediatric osteosarcoma with improved local control and overall survival compared to conventional treatments. We retrospectively reviewed the records of pediatric and adolescent patients who received carbon ion radiotherapy (CIRT) for inoperable osteosarcoma between 1996 and 2014.