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Debulking Chemotherapy Can Overcome Primary Resistance to Teclistamab in Relapsed Refractory Multiple Myeloma.

1/5 보강
Blood cancer discovery 2026
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
19 patients; 79% then responded to teclistamab, including 100% who no longer had Hi-MM.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
In conclusion, simple clinical parameters correlate with response to teclistamab, while debulking chemotherapy can overcome Hi-MM and successfully bridge patients to teclistamab or salvage non-responders.

Sharma R, Pelland AA, Lajkosz K, Masih-Khan E, Vohra HS, Bhella S, Chen CI, Kukreti V, Stewart AK, Trudel S, Yang C, Reece DE, Venner C, Lancman G

📝 환자 설명용 한 줄

Bispecific antibodies have revolutionized the treatment of multiple myeloma (MM), however primary treatment failure occurs in 30-40% of patients.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 표본수 (n) 90
  • p-value p<0.001

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BibTeX ↓ RIS ↓
APA Sharma R, Pelland AA, et al. (2026). Debulking Chemotherapy Can Overcome Primary Resistance to Teclistamab in Relapsed Refractory Multiple Myeloma.. Blood cancer discovery. https://doi.org/10.1158/2643-3230.BCD-25-0372
MLA Sharma R, et al.. "Debulking Chemotherapy Can Overcome Primary Resistance to Teclistamab in Relapsed Refractory Multiple Myeloma.." Blood cancer discovery, 2026.
PMID 41810881

Abstract

Bispecific antibodies have revolutionized the treatment of multiple myeloma (MM), however primary treatment failure occurs in 30-40% of patients. In this study, we analyzed correlates of response to teclistamab and strategies to overcome primary resistance. Across two independent cohorts (n=90), we developed Hi-MM, defined by extramedullary disease, plasma cell leukemia, bone marrow plasmacytosis ≥50%, or transfusion within 30 days, as a composite correlate of non-response. Patients without Hi-MM had ORR of 84-96% (vs 20-40% with Hi-MM), and significantly superior progression-free (p<0.001) and overall survival (p<0.001). Debulking chemotherapy was utilized in 19 patients; 79% then responded to teclistamab, including 100% who no longer had Hi-MM. All four patients who were primary refractory to a BCMA bispecific immediately prior to debulking then achieved deep responses to teclistamab. In conclusion, simple clinical parameters correlate with response to teclistamab, while debulking chemotherapy can overcome Hi-MM and successfully bridge patients to teclistamab or salvage non-responders.

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