Marquina Gloria, Manzano Aranzazu, Benavente Celina, Macias Natalia Perez, Rivas Ana, Diaz-Rubio Eduardo, Casado Antonio
Department of Medical Oncology, Hospital Clínico San Carlos, School of Medicine, Complutense University (UCM), IdISSC, Madrid, Spain.
Department of Haemathology, Hospital Clínico San Carlos, School of Medicine, Complutense University (UCM), IdISSC, Madrid, Spain.
Cancer Diagn Progn. 2023 May 3;3(3):302-310. doi: 10.21873/cdp.10216. eCollection 2023 May-Jun.
BACKGROUND/AIM: In patients with advanced platinum-resistant ovarian cancer we prospectively evaluated whether trabectedin could resensitize the tumor cells to platinum rechallenge.
Upon progression to platinum-based chemotherapy, trabectedin was administered as a 3-hour infusion every three weeks and subsequently crossed over to carboplatin/carboplatin-based combinations. The primary endpoints comprised objective response rate (ORR) and time to progression after trabectedin (TTP Trab). Secondary endpoints included ORR following platinum post-trabectedin, the growth modulation index (GMI) assessed as the ratio of successive TTP to platinum, given after (TTP2) and before (TTP1) trabectedin, quality of life (QoL), and ancillary translational studies.
Ten patients with platinum-resistant ovarian cancer from a single institution were treated with trabectedin, one of whom achieved a partial response (PR) reaching the ORR of 10% and six had stable disease (SD) for a disease control rate (DCR) of 70%. After the treatment with platinum post-trabectedin, one patient achieved a PR and two had SD, attaining a rate of resensitization to platinum of 37.5%. The median TTP with trabectedin treatment was 15.0 weeks, while eight patients who received platinum post-trabectedin had the median TTP2 of 19.9 weeks. One patient reached the threshold of GMI >1 (12.5%) as indicator of clinical benefit. QoL of patients was not deteriorated with trabectedin. Predictive biomarkers of response to trabectedin and/or re-exposure to platinum could not be identified.
Although trabectedin did not achieve a wide resensitization to platinum in this heavily pretreated platinum-resistant population, a significant number of patients attained disease control.
背景/目的:在晚期铂耐药卵巢癌患者中,我们前瞻性评估了曲贝替定是否能使肿瘤细胞对再次使用铂类药物产生敏感性。
在铂类化疗进展后,每三周静脉输注曲贝替定3小时,随后交叉使用卡铂/基于卡铂的联合方案。主要终点包括客观缓解率(ORR)和曲贝替定治疗后的无进展生存期(TTP Trab)。次要终点包括曲贝替定治疗后铂类药物治疗的ORR、生长调节指数(GMI),通过曲贝替定治疗后(TTP2)和治疗前(TTP1)连续两次铂类药物治疗的无进展生存期之比进行评估、生活质量(QoL)以及辅助转化研究。
来自单一机构的10例铂耐药卵巢癌患者接受了曲贝替定治疗,其中1例达到部分缓解(PR),ORR为10%,6例病情稳定(SD),疾病控制率(DCR)为70%。曲贝替定治疗后使用铂类药物治疗,1例患者达到PR,2例患者病情稳定,铂类药物再敏化率为37.5%。曲贝替定治疗的中位TTP为15.0周,而8例曲贝替定治疗后接受铂类药物治疗的患者中位TTP2为19.9周。1例患者达到GMI>1的阈值(12.5%),作为临床获益的指标。曲贝替定治疗并未使患者的生活质量恶化。未发现对曲贝替定和/或再次接触铂类药物反应的预测生物标志物。
尽管在这个经过大量预处理的铂耐药人群中,曲贝替定未能使铂类药物广泛再敏化,但仍有相当数量的患者实现了疾病控制。