Bintrafusp Alfa for Recurrent or Metastatic Cervical Cancer After Platinum Failure

Author:

Birrer Michael1,Li Guiling2,Yunokawa Mayu3,Lee Jung-Yun4,Kim Byoung Gie5,Oppermann Christina Pimentel6,Zhou Qi7,Nishio Shin8,Okamoto Aikou9,Wu Xiaohua10,Mileshkin Linda11,Oaknin Ana12,Ray-Coquard Isabelle13,Hasegawa Kosei14,Jehl Genevieve15,Vugmeyster Yulia16,Zhang Sen1617,Bajars Marcis15,Yonemori Kan18

Affiliation:

1. University of Arkansas Medical Sciences, Little Rock

2. Union Hospital Tongji Medical College Huazhong University of Science and Technology, Wuhan, Hubei, China

3. Cancer Institute Hospital of JFCR, Tokyo, Japan

4. Severance Hospital, Yonsei University Health System, Seoul, Republic of Korea

5. Samsung Medical Center, Seoul, Republic of Korea

6. Hospital Mãe de Deus, Porto Alegre, Brazil

7. Chongqing University Cancer Hospital, Chongqing, China

8. Kurume University School of Medicine, Fukuoka, Japan

9. Jikei University Hospital, Tokyo, Japan

10. Fudan University Shanghai Cancer Center, Shanghai, China

11. Peter MacCallum Cancer Centre, Melbourne, Australia

12. Gynaecologic Cancer Programme Vall d’Hebron Institute of Oncology (VHIO), Hospital Universitari Vall d’Hebron, Vall d’Hebron Barcelona Hospital Campus, Barcelona, Spain

13. Centre Léon Bérard, University Claude Bernard Lyon 1, Lyon, France

14. Saitama Medical University International Medical Center, Saitama, Japan

15. the healthcare business of Merck KGaA, Darmstadt, Germany

16. EMD Serono, Billerica, Massachusetts

17. Now with Theseus Pharmaceuticals, Cambridge, Massachusetts

18. National Cancer Center Hospital, Tokyo, Japan

Abstract

ImportanceCervical cancer is a common and lethal cancer worldwide. Bintrafusp alfa is a first-in-class bifunctional fusion protein composed of the extracellular domain of the human transforming growth factor β receptor II (or transforming growth factor β trap) fused via a flexible linker to the C-terminus of each heavy chain of an immunoglobulin G1 antibody blocking programmed cell death 1 ligand 1.ObjectiveTo evaluate the safety and response rates of bintrafusp alfa in patients with recurrent or metastatic cervical cancer.Design, Setting, and ParticipantsThis phase 2 nonrandomized controlled trial evaluated bintrafusp alfa monotherapy in patients with recurrent or metastatic cervical cancer with disease progression during or after platinum-based chemotherapy. Data were collected from March 2020 to February 2022.InterventionPatients received bintrafusp alfa, 1200 mg, intravenously once every 2 weeks.Main Outcomes and MeasuresThe primary end point was confirmed objective response rate per Response Evaluation Criteria in Solid Tumors version 1.1 by an independent review committee.ResultsAt data cutoff, 146 of 203 screened patients received 1 or more doses of bintrafusp alfa; of these, the median (range) age was 53 (24-79) years. The study met its primary end point of a 95% CI above the objective response rate benchmark of 15%, with a confirmed objective response rate of 21.9% (95% CI, 15.5-29.5) per the independent review committee. Of these patients, 19 (59.4%) had a durable response of 6 months or more. At data cutoff, responses were ongoing in 13 of 32 responders (40.6%). The most common treatment-related adverse events were anemia (25 [17.1%]), rash (21 [14.4%]), hypothyroidism (15 [10.3%]), and pruritus (15 [10.3%]). Any-cause adverse events of special interest included anemia (82[56.2%]), bleeding events (81 [55.5%]), and immune-related adverse events (49 [33.6%]).Conclusions and RelevanceThis phase 2 nonrandomized controlled trial of bintrafusp alfa met its primary end point, which may support the potential of a bispecific therapy targeting transforming growth factor β and programmed cell death 1 ligand 1 in patients with recurrent or metastatic cervical cancer.Trial RegistrationClinicalTrials.gov Identifier: NCT04246489

Publisher

American Medical Association (AMA)

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