Clinical management and outcomes associated with etoposide, doxorubicin, and cisplatin plus mitotane treatment in metastatic adrenocortical carcinoma: a single institute experience

被引:10
作者
Uchihara, Masaki [1 ,2 ]
Tanioka, Maki [1 ]
Kojima, Yuki [1 ]
Nishikawa, Tadaaki [1 ]
Sudo, Kazuki [1 ]
Shimoi, Tatsunori [1 ]
Noguchi, Emi [1 ]
Maeshima, Akiko Miyagi [3 ]
Yonemori, Kan [1 ]
机构
[1] Natl Canc Ctr, Dept Med Oncol, Chuo Ku, Tsukiji 5-1-1, Tokyo 1040045, Japan
[2] Natl Ctr Global Hlth & Med, Dept Diabet Endocrinol & Metab, Toyama 1-21-1, Shinjuku Ku City, Tokyo 1628655, Japan
[3] Natl Canc Ctr, Dept Diagnost Pathol, Chuo Ku, Tsukiji 5-1-1, Tokyo 1040045, Japan
关键词
Adrenocortical carcinoma; EDP; Mitotane; Adrenal insufficiency; Hypercortisolism; SURVIVAL; CHEMOTHERAPY; THERAPY;
D O I
10.1007/s10147-021-02021-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Adrenocortical carcinoma (ACC) is a rare and aggressive disease that is often diagnosed at an advanced stage. There is no standard treatment for metastatic ACC; EDP-M (etoposide, doxorubicin, and cisplatin plus mitotane) is one treatment option. A randomized controlled trial (FIRM-ACT) evaluating the efficacy of EDP-M showed progression-free survival (PFS) was 5.0 months, overall survival (OS) was 14.8 months, the response rate was 19%, and adrenal insufficiency occurred in 3.4% of patients. However, the efficacy and safety of this regimen in Asia are not fully reported. Methods We retrospectively analyzed 43 patients diagnosed with metastatic ACC at the National Cancer Center Hospital between 1997 and 2020. We evaluated PFS, OS, and response in 17 patients who received EDP-M as first-line therapy. Results The median age at treatment initiation was 45 years (range 18-74). Eight patients (47%) had autonomous hormone production, including six patients with hypercortisolism. The best response of partial response and stable disease was seen in two (12%) and ten (59%) patients, respectively. The median PFS was 6.2 months [95% confidence interval (CI): 4.3-10.0]. The median OS was 15.4 months (95% CI 11.6-not reached). Three patients received only one cycle due to adverse effects associated with hypercortisolism. Grade 3/4 adverse events associated with adrenal insufficiency occurred in three (17%) cases, resulting in EDP-M discontinuation. Conclusions The EDP-M regimen had similar PFS to that observed in FIRM-ACT. Adrenal insufficiency was more frequent in the current study, but this could be managed with supportive endocrinological care such as cortisol replacement.
引用
收藏
页码:2275 / 2281
页数:7
相关论文
共 30 条
  • [1] Baudin E, 2001, CANCER, V92, P1385, DOI 10.1002/1097-0142(20010915)92:6<1385::AID-CNCR1461>3.0.CO
  • [2] 2-2
  • [3] Prognostic Role of Overt Hypercortisolism in Completely Operated Patients with Adrenocortical Cancer
    Berruti, Alfredo
    Fassnacht, Martin
    Haak, Harm
    Else, Tobias
    Baudin, Eric
    Sperone, Paola
    Kroiss, Matthias
    Kerkhofs, Thomas
    Williams, Andrew R.
    Ardito, Arianna
    Leboulleux, Sophie
    Volante, Marco
    Deutschbein, Timo
    Feelders, Richards
    Ronchi, Cristina
    Grisanti, Salvatore
    Gelderblom, Hans
    Porpiglia, Francesco
    Papotti, Mauro
    Hammer, Gary D.
    Allolio, Bruno
    Terzolo, Massimo
    [J]. EUROPEAN UROLOGY, 2014, 65 (04) : 832 - 838
  • [4] Phase II study of weekly paclitaxel and sorafenib as second/third-line therapy in patients with adrenocortical carcinoma
    Berruti, Alfredo
    Sperone, Paola
    Ferrero, Anna
    Germano, Antonina
    Ardito, Arianna
    Priola, Adriano Massimiliano
    De Francia, Silvia
    Volante, Marco
    Daffara, Fulvia
    Generali, Daniele
    Leboulleux, Sophie
    Perotti, Paola
    Baudin, Eric
    Papotti, Mauro
    Terzolo, Massimo
    [J]. EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2012, 166 (03) : 451 - 458
  • [5] Adding metyrapone to chemotherapy plus mitotane for Cushing's syndrome due to advanced adrenocortical carcinoma
    Claps, Melanie
    Cerri, Sara
    Grisanti, Salvatore
    Lazzari, Barbara
    Ferrari, Vittorio
    Roca, Elisa
    Perotti, Paola
    Terzolo, Massimo
    Sigala, Sandra
    Berruti, Alfredo
    [J]. ENDOCRINE, 2018, 61 (01) : 169 - 172
  • [6] COSENTINI D, 2018, ENDOCR CONNECT
  • [7] Prospective evaluation of mitotane toxicity in adrenocortical cancer patients treated adjuvantly
    Daffara, Fulvia
    De Francia, Silvia
    Reimondo, Giuseppe
    Zaggia, Barbara
    Aroasio, Emiliano
    Porpiglia, Francesco
    Volante, Marco
    Termine, Angela
    Di Carlo, Francesco
    Dogliotti, Luigi
    Angeli, Alberto
    Berruti, Alfredo
    Terzolo, Massimo
    [J]. ENDOCRINE-RELATED CANCER, 2008, 15 (04) : 1043 - 1053
  • [8] New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1)
    Eisenhauer, E. A.
    Therasse, P.
    Bogaerts, J.
    Schwartz, L. H.
    Sargent, D.
    Ford, R.
    Dancey, J.
    Arbuck, S.
    Gwyther, S.
    Mooney, M.
    Rubinstein, L.
    Shankar, L.
    Dodd, L.
    Kaplan, R.
    Lacombe, D.
    Verweij, J.
    [J]. EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) : 228 - 247
  • [9] European Society of Endocrinology Clinical Practice Guidelines on the management of adrenocortical carcinoma in adults, in collaboration with the European Network for the Study of Adrenal Tumors
    Fassnacht, Martin
    Dekkers, Olaf M.
    Else, Tobias
    Gaudin, Eric
    Berruti, Alfredo
    de Krijger, Ronald R.
    Haak, Harm R.
    Mihail, Radu
    Assie, Guillaume
    Terzolo, Massimo
    [J]. EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2018, 179 (04) : G1 - G46
  • [10] Linsitinib (OSI-906) versus placebo for patients with locally advanced or metastatic adrenocortical carcinoma: a double-blind, randomised, phase 3 study
    Fassnacht, Martin
    Berruti, Alfredo
    Baudin, Eric
    Demeure, Michael J.
    Gilbert, Jill
    Haak, Harm
    Kroiss, Matthias
    Quinn, David I.
    Hesseltine, Elizabeth
    Ronchi, Cristina L.
    Terzolo, Massimo
    Choueiri, Toni K.
    Poondru, Srinivasu
    Fleege, Tanya
    Rorig, Ramona
    Chen, Jihong
    Stephens, Andrew W.
    Worden, Francis
    Hammer, Gary D.
    [J]. LANCET ONCOLOGY, 2015, 16 (04) : 426 - 435