Literature DB >> 29222199

Treatment of CD30-Expressing Germ Cell Tumors and Sex Cord Stromal Tumors with Brentuximab Vedotin: Identification and Report of Seven Cases.

Costantine Albany1, Lawrence Einhorn2, Lawrence Garbo3, Thomas Boyd4, Neil Josephson5, Darren R Feldman6.   

Abstract

BACKGROUND: Cytotoxic therapy for relapsed and refractory germ cell tumors or metastatic sex cord stromal tumors is rarely effective and is often accompanied by high adverse event rates. Expression of CD30 has been observed in testicular cancers, and patients with CD30-expressing embryonal carcinomas have worse progression-free survival and overall survival than those with CD30-negative tumors. The objective of this study (NCT01461538) was to characterize the antitumor activity of brentuximab vedotin in patients with CD30-expressing nonlymphomatous malignancies. Enrolled patients included seven patients with relapsed or refractory germ cell tumors or metastatic sex cord stromal tumors described in this case series.
MATERIALS AND METHODS: Forty patients with relapsed or refractory germ cell tumors, metastatic sex cord stromal tumors, or testicular tumors were screened for CD30 expression; 14 patients had tumors that expressed CD30. Seven patients with CD30-expressing testicular cancer were enrolled in the treatment study: five patients with germ cell tumors, one patient with a Leydig cell tumor, and one patient with a Sertoli cell tumor. Patients were treated with brentuximab vedotin at initial doses of 1.8 or 2.4 mg/kg every 3 weeks. Response assessments were performed at cycles 2 and 4 and every 4 cycles thereafter while the patient was receiving treatment.
RESULTS: Two of seven patients achieved an objective response, including one durable complete response and one partial response at a single time point. Both responding patients had germ cell tumors. Treatment with brentuximab vedotin was generally well tolerated.
CONCLUSION: Treatment of relapsed or refractory germ cell tumors with brentuximab vedotin can induce durable responses with a manageable toxicity profile. IMPLICATIONS FOR PRACTICE: This case series of seven patients with relapsed or refractory CD30-expressing germ cell tumors (GCTs) or sex cord stromal tumors demonstrates that brentuximab vedotin has activity against GCTs and is well tolerated in heavily pretreated patients with these aggressive tumor types. One patient achieved a complete response that has been durable for almost 4 years since the discontinuation of treatment with brentuximab vedotin. Therefore, brentuximab vedotin may be a valuable option for physicians who care for this difficult-to-treat patient population. © AlphaMed Press 2017.

Entities:  

Keywords:  CD30 antigen; Clinical trial; Germ cell tumor; Immunoconjugates; Sex cord stromal tumor

Mesh:

Substances:

Year:  2017        PMID: 29222199      PMCID: PMC5905693          DOI: 10.1634/theoncologist.2017-0544

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  29 in total

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3.  Prognostic Factors and Treatment Results After Bleomycin, Etoposide, and Cisplatin in Germ Cell Cancer: A Population-based Study.

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Review 7.  Etiologic factors in testicular germ-cell tumors.

Authors:  Katherine A McGlynn; Michael B Cook
Journal:  Future Oncol       Date:  2009-11       Impact factor: 3.404

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10.  Microtubule-depolymerizing agents used in antibody-drug conjugates induce antitumor immunity by stimulation of dendritic cells.

Authors:  Philipp Müller; Kea Martin; Sebastian Theurich; Jens Schreiner; Spasenija Savic; Grzegorz Terszowski; Didier Lardinois; Viola A Heinzelmann-Schwarz; Max Schlaak; Hans-Michael Kvasnicka; Giulio Spagnoli; Stephan Dirnhofer; Daniel E Speiser; Michael von Bergwelt-Baildon; Alfred Zippelius
Journal:  Cancer Immunol Res       Date:  2014-04-21       Impact factor: 11.151

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  8 in total

Review 1.  Genetics of testicular germ cell tumors.

Authors:  Nirmish Singla; John T Lafin; Rashed A Ghandour; Samuel Kaffenberger; James F Amatruda; Aditya Bagrodia
Journal:  Curr Opin Urol       Date:  2019-07       Impact factor: 2.309

Review 2.  Overcoming Chemotherapy Resistance in Germ Cell Tumors.

Authors:  Zuzana Országhová; Katarina Kalavska; Michal Mego; Michal Chovanec
Journal:  Biomedicines       Date:  2022-04-22

3.  Phase II trial of brentuximab vedotin in relapsed/refractory germ cell tumors.

Authors:  Ryan Ashkar; Darren R Feldman; Nabil Adra; Mohammad Abu Zaid; Samuel A Funt; Sandra K Althouse; Susan M Perkins; Christin I Snow; Kayla M Lazzara; Lina M Sego; David I Quinn; Nasser H Hanna; Lawrence H Einhorn; Costantine Albany
Journal:  Invest New Drugs       Date:  2021-05-24       Impact factor: 3.651

4.  A phase 2, open-label study of brentuximab vedotin in patients with CD30-expressing solid tumors.

Authors:  Jeffrey P Sharman; Jennifer J Wheler; Lawrence Einhorn; Afshin Dowlati; Geoffrey I Shapiro; John Hilton; John M Burke; Tanya Siddiqi; Nancy Whiting; Shadia I Jalal
Journal:  Invest New Drugs       Date:  2019-04-16       Impact factor: 3.850

5.  Promising Immunotherapy in Metastatic Testicular Sex Cord Stromal Tumours After First-Line Chemotherapy.

Authors:  Bingqing Shang; Chuanzhen Cao; Weixing Jiang; Hongzhe Shi; Xingang Bi; Chengxu Cui; Jianzhong Shou; Shan Zheng; Jin Zhang; Aiping Zhou; Changling Li; Jianhui Ma
Journal:  Front Immunol       Date:  2022-01-10       Impact factor: 7.561

6.  Immunotherapies for Pediatric Solid Tumors: A Targeted Update.

Authors:  Ajay Gupta; Timothy P Cripe
Journal:  Paediatr Drugs       Date:  2021-11-25       Impact factor: 3.930

7.  Systemic immune-inflammation index in germ-cell tumours: search for a biological prognostic biomarker.

Authors:  Costantine Albany
Journal:  Br J Cancer       Date:  2018-02-27       Impact factor: 7.640

Review 8.  Molecular Pathways and Targeted Therapies for Malignant Ovarian Germ Cell Tumors and Sex Cord-Stromal Tumors: A Contemporary Review.

Authors:  Asaf Maoz; Koji Matsuo; Marcia A Ciccone; Shinya Matsuzaki; Maximilian Klar; Lynda D Roman; Anil K Sood; David M Gershenson
Journal:  Cancers (Basel)       Date:  2020-05-29       Impact factor: 6.639

  8 in total

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