: Gestational choriocarcinoma accounts for 5% of gestational trophoblastic neoplasms. Approximately 50%, 25%, and 25% of gestational choriocarcinoma occur after molar pregnancies, term pregnancies, and other gestational events, respectively. The FIGO scoring system categorizes patients into low (score 0 to 6) and high risk (score 7 or more) choriocarcinoma. Single-agent and multi-agent chemotherapy are used in low- and high-risk patients, respectively. Chemotherapy for localized disease has a goal of eradication of disease without surgery and is associated with favorable prognosis and fertility preservation. Most patients with gestational choriocarcinoma are cured with chemotherapy; however, some (<5.0%) will die as a result of multi-drug resistance, underscoring the need for novel approaches in this group of patients. Although there are limited data due to its rarity, the treatment response with immunotherapy is high, ranging between 50-70%. Novel combinations of immune checkpoint inhibitors with targeted therapies (including VEGFR-2 inhibitors) are under evaluation. PD-L1 inhibitors are considered a potential important opportunity for chemo-resistant patients, and to replace or de-escalate chemotherapy to avoid or minimize chemotherapy toxicity. In this review, the Rare Tumor Working Group and the European Organization for Research and Treatment of Cancer evaluated the current landscape and further perspective in the management of patients diagnosed with gestational choriocarcinoma.
Gestational choriocarcinoma / Bogani, Giorgio; Ray-Coquard, Isabelle; Mutch, David; Vergote, Ignace; Ramirez, Pedro T; Prat, Jaime; Concin, Nicole; Ngoi, Natalie Yan Li; Coleman, Robert L; Enomoto, Takayuki; Takehara, Kazuhiro; Denys, Hannelore; Lorusso, Domenica; Takano, Masashi; Sagae, Satoru; Wimberger, Pauline; Segev, Yakir; Kim, Se Ik; Kim, Jae-Weon; Herrera, Fernanda; Mariani, Andrea; Brooks, Rebecca A; Tan, David; Paolini, Biagio; Chiappa, Valentina; Longo, Mariangela; Raspagliesi, Francesco; Benedetti Panici, Pierluigi; Di Donato, Violante; Caruso, Giuseppe; Colombo, Nicoletta; Pignata, Sandro; Zannoni, Gianfranco; Scambia, Giovanni; Monk, Bradley J. - In: INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER. - ISSN 1525-1438. - 33:10(2023), pp. 1504-1514. [10.1136/ijgc-2023-004704]
Gestational choriocarcinoma
Bogani, Giorgio;Herrera, Fernanda;Benedetti Panici, Pierluigi;Di Donato, Violante;Caruso, Giuseppe;
2023
Abstract
: Gestational choriocarcinoma accounts for 5% of gestational trophoblastic neoplasms. Approximately 50%, 25%, and 25% of gestational choriocarcinoma occur after molar pregnancies, term pregnancies, and other gestational events, respectively. The FIGO scoring system categorizes patients into low (score 0 to 6) and high risk (score 7 or more) choriocarcinoma. Single-agent and multi-agent chemotherapy are used in low- and high-risk patients, respectively. Chemotherapy for localized disease has a goal of eradication of disease without surgery and is associated with favorable prognosis and fertility preservation. Most patients with gestational choriocarcinoma are cured with chemotherapy; however, some (<5.0%) will die as a result of multi-drug resistance, underscoring the need for novel approaches in this group of patients. Although there are limited data due to its rarity, the treatment response with immunotherapy is high, ranging between 50-70%. Novel combinations of immune checkpoint inhibitors with targeted therapies (including VEGFR-2 inhibitors) are under evaluation. PD-L1 inhibitors are considered a potential important opportunity for chemo-resistant patients, and to replace or de-escalate chemotherapy to avoid or minimize chemotherapy toxicity. In this review, the Rare Tumor Working Group and the European Organization for Research and Treatment of Cancer evaluated the current landscape and further perspective in the management of patients diagnosed with gestational choriocarcinoma.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.