Combination of Olaparib and Radiation Therapy for Triple Negative Breast Cancer: Preliminary Results of the RADIOPARP Phase 1 Trial

被引:36
作者
Loap, Pierre [1 ]
Loirat, Delphine [1 ]
Berger, Frederique [1 ]
Ricci, Francesco [1 ]
Vincent-Salomon, Anne [1 ]
Ezzili, Cyrine [1 ]
Mosseri, Veronique [1 ]
Fourquet, Alain [1 ]
Ezzalfani, Monia [1 ]
Kirova, Youlia [1 ]
机构
[1] Inst Curie, Dept Radiat Oncol, Paris, France
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2021年 / 109卷 / 02期
关键词
PARP INHIBITORS;
D O I
10.1016/j.ijrobp.2020.09.032
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Preclinical studies have evidenced that triple-negative breast cancer (TNBC) cell lines are more sensitive to poly (ADP-ribose) polymerase inhibitors. This provides a strong rationale for developing a new therapeutic approach for TNBC management based on poly (ADP-ribose) polymerase inhibition. The primary goal of the RADIOPARP phase 1 trial was to evaluate the dose-limiting toxicities (DLT) and the maximum tolerated dose of olaparib combined with locoregional radiation therapy. Methods and Materials: RADIOPARP was a single institutional phase 1 trial which evaluated olaparib-radiation therapy combination in patients with inflammatory, locoregionally advanced or metastatic TNBC who received neoadjuvant chemotherapy. Radiation therapy delivered 50 Gy to the breast or to the chest wall. Lymph nodes could be included in target volumes according to local guidelines. The dose-finding toxicity-based study was conducted in sequential and adaptive Bayesian scheme using the time-to-event continual reassessment method, with 4 olaparib dose levels (50 mg, 100 mg, 150 mg, and 200 mg twice per day). Results: Twenty-four patients with Eastern Cooperative Oncology Group Performance Status of 0 or 1 were enrolled from September 2017 to November 2019. Twenty-one patients (87.5%) received the olaparib-radiation therapy combination after breast surgery owing to residual disease after neoadjuvant chemotherapy, and the 3 other patients (12.5%) had unresectable tumors which were refractory to neoadjuvant chemotherapy. All patients received full course combination treatment as follows: 4 patients (pts) at 50 mg twice a day, 8 pts at 100 mg twice a day, 7 pts at 150 mg twice a day, and 5 pts at 200 mg twice a day. No DLT was observed. Conclusions: Olaparib was escalated to the maximum target dose of 200 mg twice a day without DLT. Further follow-up is needed to evaluate the late toxicities. Pending the long-term results of the RADIOPARP trial, we suggest using 200 mg of olaparib twice per day for future trials. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:436 / 440
页数:5
相关论文
共 19 条
  • [1] CAMPBELL AC, 1976, CLIN EXP IMMUNOL, V23, P200
  • [2] Combining PARP Inhibition, Radiation, and Immunotherapy: A Possible Strategy to Improve the Treatment of Cancer?
    Cesaire, Mathieu
    Thariat, Juliette
    Candeias, Serge M.
    Stefan, Dinu
    Saintigny, Yannick
    Chevalier, Francois
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (12)
  • [3] Cardiac toxicity in breast cancer patients: From a fractional point of view to a global assessment
    Chargari, Cyrus
    Kirov, Krassen M.
    Bollet, Marc A.
    Magne, Nicolas
    Vedrine, Lionel
    Cremades, Serge
    Beuzeboc, Philippe
    Fourquet, Alain
    Kirova, Youlia M.
    [J]. CANCER TREATMENT REVIEWS, 2011, 37 (04) : 321 - 330
  • [4] Sequential designs for phase I clinical trials with late-onset toxicities
    Cheung, YK
    Chappell, R
    [J]. BIOMETRICS, 2000, 56 (04) : 1177 - 1182
  • [5] Homologous recombination DNA repair deficiency and PARP inhibition activity in primary triple negative breast cancer
    Chopra, Neha
    Tovey, Holly
    Pearson, Alex
    Cutts, Ros
    Toms, Christy
    Proszek, Paula
    Hubank, Michael
    Dowsett, Mitch
    Dodson, Andrew
    Daley, Frances
    Kriplani, Divya
    Gevensleben, Heidi
    Davies, Helen Ruth
    Degasperi, Andrea
    Roylance, Rebecca
    Chan, Stephen
    Tutt, Andrew
    Skene, Anthony
    Evans, Abigail
    Bliss, Judith M.
    Nik-Zainal, Serena
    Turner, Nicholas C.
    [J]. NATURE COMMUNICATIONS, 2020, 11 (01)
  • [6] Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis
    Cortazar, Patricia
    Zhang, Lijun
    Untch, Michael
    Mehta, Keyur
    Costantino, Joseph P.
    Wolmark, Norman
    Bonnefoi, Herve
    Cameron, David
    Gianni, Luca
    Valagussa, Pinuccia
    Swain, Sandra M.
    Prowell, Tatiana
    Loibl, Sibylle
    Wickerham, D. Lawrence
    Bogaerts, Jan
    Baselga, Jose
    Perou, Charles
    Blumenthal, Gideon
    Blohmer, Jens
    Mamounas, Eleftherios P.
    Bergh, Jonas
    Semiglazov, Vladimir
    Justice, Robert
    Eidtmann, Holger
    Paik, Soonmyung
    Piccart, Martine
    Sridhara, Rajeshwari
    Fasching, Peter A.
    Slaets, Leen
    Tang, Shenghui
    Gerber, Bernd
    Geyer, Charles E., Jr.
    Pazdur, Richard
    Ditsch, Nina
    Rastogi, Priya
    Eiermann, Wolfgang
    von Minckwitz, Gunter
    [J]. LANCET, 2014, 384 (9938) : 164 - 172
  • [7] Concurrent Veliparib With Chest Wall and Nodal Radiotherapy in Patients With Inflammatory or Locoregionally Recurrent Breast Cancer: The TBCRC 024 Phase I Multicenter Study
    Jagsi, Reshma
    Griffith, Kent A.
    Bellon, Jennifer R.
    Woodward, Wendy A.
    Horton, Janet K.
    Ho, Alice
    Feng, Felix Y.
    Speers, Corey
    Overmoyer, Beth
    Sabel, Michael
    Schott, Anne F.
    Pierce, Lori
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (13) : 1317 - +
  • [8] PARP Inhibitor Drugs in the Treatment of Breast, Ovarian, Prostate and Pancreatic Cancers: An Update of Clinical Trials
    Kamel, Dalia
    Gray, Christopher
    Walia, Jagdeep Singh
    Kumar, Vikaash
    [J]. CURRENT DRUG TARGETS, 2018, 19 (01) : 21 - 37
  • [9] Olaparib protects cardiomyocytes against oxidative stress and improves graft contractility during the early phase after heart transplantation in rats
    Korkmaz-Icoez, Sevil
    Szczesny, Bartosz
    Marcatti, Michela
    Li, Shiliang
    Ruppert, Mihaly
    Lasitschka, Felix
    Loganathan, Sivakkanan
    Szabo, Csaba
    Szabo, Gabor
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2018, 175 (02) : 246 - 261
  • [10] Poly-(ADP-ribose)-polymerase inhibitors as radiosensitizers: a systematic review of pre-clinical and clinical human studies
    Lesueur, Paul
    Chevalier, Francois
    Austry, Jean-Baptiste
    Waissi, Waisse
    Burckel, Helene
    Noel, Georges
    Habrand, Jean-Louis
    Saintigny, Yannick
    Joly, Florence
    [J]. ONCOTARGET, 2017, 8 (40) : 69105 - 69124