免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Adoptive Cell Transfer of Tumor-Infiltrating Lymphocytes for Metastatic Acral Lentiginous Melanoma.
Adoptive Cell Transfer of Tumor-Infiltrating Lymphocytes for Metastatic Acral Lentiginous Melanoma.
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ACT-TIL 可在转移性肢端黑色素瘤患者中介导客观缓解,并且肢端疾病患者的结局出乎意料地与同期接受治疗的非肢端皮肤黑色素瘤患者相当。需要进一步研究,以理解肢端黑色素瘤中对 ACT-TIL 应答的免疫学基础,并提高 CRs 的发生率。
肢端雀斑样黑色素瘤是源自手掌、足底或甲下皮肤的皮肤黑色素瘤亚型。这些肿瘤的特征是生物学行为侵袭性强、肿瘤突变负荷(TMB)低,以及对免疫检查点阻断敏感性降低。目前尚不清楚TIL(肿瘤浸润淋巴细胞)过继细胞转移(ACT-TIL)对肢端黑色素瘤患者是否有效。
我们分析了1999年至2018年间在单一机构接受ACT-TIL临床试验治疗的442例转移性皮肤黑色素瘤患者的前瞻性收集数据。尽管对治疗结局和基因组数据设盲,我们仍根据诊断时可用的临床病理数据,回顾性地识别出具有肢端亚型的患者。随后,我们评估了肢端黑色素瘤患者的ACT-TIL治疗结局,并将其与同期接受治疗的非肢端黑色素瘤患者进行了比较。
在442例纳入患者中,30例(7%)为肢端黑色素瘤,412例(93%)为非肢端黑色素瘤。各队列在临床特征、方案入组及治疗相关因素方面相似。肢端与非肢端黑色素瘤患者对ACT-TIL的客观缓解率分别为43%和40%(P = .87),其中分别有3%和16%达到完全缓解(CR;P = .07)。中位无进展生存期分别为3.5个月和4.1个月(P = .40),中位总生存期分别为13个月和17个月(P = .79)。肢端黑色素瘤的TMB和紫外线突变特征评分低于非肢端黑色素瘤。
Acral lentiginous melanoma is a subtype of cutaneous melanoma arising from palmar, plantar, or subungual skin. These tumors are characterized by aggressive biology, a low tumor mutational burden (TMB), and diminished sensitivity to immune checkpoint blockade. It is unknown whether adoptive cell transfer of tumor-infiltrating lymphocytes (ACT-TIL) has efficacy in patients with acral melanoma.
We analyzed prospectively collected data from 442 patients with metastatic cutaneous melanoma who were treated on clinical trials of ACT-TIL at a single institution between 1999 and 2018. Although blinded to treatment outcome and genomic data, we retrospectively identified patients who had acral subtype on the basis of clinicopathologic data available at the time of diagnosis. We then evaluated the ACT-TIL treatment outcomes of patients with acral melanoma and compared them with contemporaneously treated patients with nonacral melanoma.
Out of 442 included patients, 30 (7%) had acral melanoma while 412 (93%) had nonacral melanoma. Cohorts had similar clinical characteristics, protocol enrollment, and treatment-related factors. The objective response rate to ACT-TIL in patients with acral and nonacral melanomas was 43% and 40%, respectively ( P = .87), with 3% and 16% having complete responses (CRs; P = .07). Median progression-free survival was 3.5 and 4.1 months ( P = .40) and median overall survival was 13 and 17 months ( P = .79), respectively. Acral melanomas had lower TMB and ultraviolet mutational signature scores than nonacral melanomas.
ACT-TIL can mediate objective responses in patients with metastatic acral melanoma, and outcomes in patients with acral disease were unexpectedly comparable with those of contemporaneously treated patients with nonacral cutaneous melanoma. Further research is necessary to understand the immunologic basis of responses to ACT-TIL in acral melanoma and to increase the frequency of CRs.
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