Concurrent chemoradiotherapy combined with immunotherapy is superior to traditional concurrent chemoradiotherapy in the treatment of advanced cervical cancer

被引:0
作者
Peng, Hsiu-Huei [1 ,2 ]
Wang, Yi-Lun [2 ]
Lin, Cheng-Tao [1 ,2 ,3 ,4 ]
机构
[1] Chang Gung Mem Hosp, Dept Obstet & Gynecol, Taoyuan, Taiwan
[2] Chang Gung Univ, Coll Med, Linkou Med Ctr, Taoyuan, Taiwan
[3] Chang Gung Mem Hosp, Dept Obstet & Gynecol, Div Gynecol Oncol, Taoyuan, Taiwan
[4] Chang Gung Mem Hosp, Chang Gung Immunol Consortium, Taoyuan, Taiwan
关键词
Cervical cancer; Concurrent chemoradiotherapy; Immunotherapy; STREPTOCOCCAL PREPARATION; CELL-CARCINOMA; OVARIAN-CANCER; OK-432; THERAPY; STAGE; SURVIVAL; OUTCOMES; TRENDS; WOMEN;
D O I
10.12892/ejgo4187.2019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of investigation: In advanced cervical cancer, traditional therapy included concurrent chemoradiotherapy (CCRT), pelvic radiotherapy, and brachytherapy. In the last few years, the development of using of immunotherapy (IMT), targeted therapy, angiogenesis inhibitors, and tyrosine kinase inhibitors encourage us to provide better treatment choices in advanced cervical cancer patients. In this study, the authors propose CCRT combined with immunotherapy (ICRT) as a better treatment option for advanced cervical cancer. Materials and Methods: The authors retrospectively reviewed the medical records of 23 patients with advanced cervical who were treated by CCRT or ICRT between 2000 and 2016 at Chang Gung Memorial Hospital. In CCRT group (total 15 cases), patients were treated with traditional platinum-based chemotherapy and radiotherapy. In ICRT group (total eight cases), patients were treated with CCRT and adjuvant IMT. The authors chose Picibanil (OK-432) plus interleukin-2 (IL-2) for adjuvant IMT. Between CCRT and ICRT groups, they analyzed the difference of age, histological type of cervical cancer, follow-up period, recurrence rate, and diagnosis-to-recurrence period between them. They also analyzed the difference of complete blood cell counts and its differentiating counts after one month of treatment. Results: Within these parameters, the recurrence rate between ICRT and CCRT group showed significant difference (37.5% vs. 86.67%, p = 0.0257). The authors observed that diagnosis-to-recurrence duration was longer in ICRT group than CCRT group (67.32 months vs. 11.92 months, p = 0.1464), although there was no statistical significance found. The laboratory findings one month after treatment showed significant difference in absolute lymphocyte counts (ALC), which showed 1,554.23/mu L vs. 577.38/mu L (mean value, p = 0.0011) in ICRT and CCRT group respectively. Conclusions: This study indicated that CCRT combined with immunotherapy is superior to traditional CCRT in treatment of advanced cervical cancer.
引用
收藏
页码:36 / 39
页数:4
相关论文
共 39 条
  • [1] Cervical Cancer Trends in the United States: A 35-Year Population-Based Analysis
    Adegoke, Olusola
    Kulasingam, Shalini
    Virnig, Beth
    [J]. JOURNAL OF WOMENS HEALTH, 2012, 21 (10) : 1031 - 1037
  • [2] Anti-tumor effect of an intratumoral administration of dendritic cells in combination with TS-1, an oral fluoropyrimidine anti-cancer drug, and OK-432, a streptococcal immunopotentiator - Involvement of Toll-like receptor 4
    Ahmed, SU
    Okamoto, M
    Oshikawa, T
    Tano, T
    Sasai, A
    Kan, S
    Hiroshima, T
    Ohue, H
    Moriya, Y
    Ryoma, Y
    Saito, M
    Sato, M
    [J]. JOURNAL OF IMMUNOTHERAPY, 2004, 27 (06) : 432 - 441
  • [3] Trends in the incidence of cervical cancer and severe precancerous lesions in Denmark, 1997-2012
    Baldur-Felskov, Birgitte
    Munk, Christian
    Nielsen, Thor Schutt Svane
    Dehlendorff, Christian
    Kirschner, Benny
    Junge, Jette
    Kjaer, Susanne K.
    [J]. CANCER CAUSES & CONTROL, 2015, 26 (08) : 1105 - 1116
  • [4] Posttherapy surveillance of women with cervical cancer: An outcomes analysis
    Bodurka-Bevers, D
    Morris, M
    Eifel, PJ
    Levenback, C
    Bevers, MW
    Lucas, KR
    Wharton, JT
    [J]. GYNECOLOGIC ONCOLOGY, 2000, 78 (02) : 187 - 193
  • [5] EphA3 as a target for antibody immunotherapy in acute lymphoblastic leukemia
    Charmsaz, S.
    Al-Ejeh, F.
    Yeadon, T. M.
    Miller, K. J.
    Smith, F. M.
    Stringer, B. W.
    Moore, A. S.
    Lee, F-T
    Cooper, L. T.
    Stylianou, C.
    Yarranton, G. T.
    Woronicz, J.
    Scott, A. M.
    Lackmann, M.
    Boyd, A. W.
    [J]. LEUKEMIA, 2017, 31 (08) : 1779 - 1787
  • [6] Immunomodulatory therapy in refractory/recurrent ovarian cancer
    Chen, Chao-Yu
    Lai, Chyong-Huey
    Yang, Lan-Yan
    Tang, Yun-Hsin
    Chou, Hung-Hsueh
    Chang, Chee-Jen
    Lin, Cheng-Tao
    [J]. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2015, 54 (02): : 143 - 149
  • [7] Impact of Sequencing Targeted Therapies With High-dose Interleukin-2 Immunotherapy: An Analysis of Outcome and Survival of Patients With Metastatic Renal Cell Carcinoma From an On-going Observational IL-2 Clinical Trial: PROCLAIMSM
    Clark, Joseph I.
    Wong, Michael K. K.
    Kaufman, Howard L.
    Daniels, Gregory A.
    Morse, Michael A.
    McDermott, David F.
    Agarwala, Sanjiv S.
    Lewis, Lionel D.
    Stewart, John H.
    Vaishampayan, Ulka
    Curti, Brendan
    Gonzalez, Rene
    Lutzky, Jose
    Rudraptna, Venkatesh
    Cranmer, Lee D.
    Jeter, Joanne M.
    Hauke, Ralph J.
    Miletello, Gerald
    Milhem, Mohammed M.
    Amin, Asim
    Richart, John M.
    Fishman, Mayer
    Hallmeyer, Sigrun
    Patel, Sapna P.
    Van Veldhuizen, Peter
    Agarwa, Neeraj
    Taback, Bret
    Treisman, Jonathan S.
    Ernstoff, Marc S.
    Perritt, Jessica C.
    Hua, Hong
    Rao, Tharak B.
    Dutcher, Janice P.
    Aung, Sandra
    [J]. CLINICAL GENITOURINARY CANCER, 2017, 15 (01) : 31 - 41
  • [8] Biological modelling of the radiation dose escalation effect of regional hyperthermia in cervical cancer
    Crezee, J.
    van Leeuwen, C. M.
    Oei, A. L.
    van Heerden, L. E.
    Bel, A.
    Stalpers, L. J. A.
    Ghadjar, P.
    Franken, N. A. P.
    Kok, H. P.
    [J]. RADIATION ONCOLOGY, 2016, 11
  • [9] Successful treatment of a primary uterine B-cell lymphoma with rituximab-CHOP immunochemotherapy
    Egyed, M.
    Kollar, B.
    Prievara, F. T.
    Viski, A.
    Bajzik, G.
    Pajor, L.
    Torday, L.
    [J]. HAEMATOLOGICA, 2007, 92 (02) : 26 - 27
  • [10] Follow-up for women after treatment for cervical cancer: A systematic review
    Elit, Laurie
    Fyles, Anthony W.
    Devries, Michaela C.
    Oliver, Thomas K.
    Fung-Kee-Fung, Michael
    [J]. GYNECOLOGIC ONCOLOGY, 2009, 114 (03) : 528 - 535