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March 30, 2026International Journal of Lung Cancer0 citationsOpen Access

Clinical course of tarlatamab as third-line therapy for small-cell lung cancer on haemodialysis: a case report

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NTNozomu TsurumakiYKYusaku KusabaHHHiroto Hatano

Key Points

  • To assess the efficacy and safety of tarlatamab as third-line therapy in a dialysis patient with small-cell lung cancer.
  • Described a case involving a 76-year-old man with ES-SCLC and chronic kidney disease on dialysis.
  • Administered four cycles of carboplatin/etoposide/atezolizumab, followed by amrubicin.
  • Conducted whole-brain and stereotactic radiotherapies prior to tarlatamab treatment.
  • Monitored for side effects including immune effector cell-associated neurotoxicity syndrome.
  • Upon starting tarlatamab, the patient experienced a 31% reduction in target lesions.
  • Treatment was halted due to performance status decline and complications like aspiration pneumonia.
  • Survival time was approximately 17.5 months from SCLC diagnosis, and 2.3 months after initiating tarlatamab.

Abstract

Tarlatamab, a DLL3-directed, CD3-engaging bispecific T-cell engager, has demonstrated efficacy in extensive-stage small cell lung cancer (ES-SCLC) after platinum-based chemotherapy; however, evidence for its efficacy in patients with renal dysfunction requiring dialysis remains scarce. We describe the case of a 76-year-old man with chronic kidney disease on maintenance haemodialysis and ES-SCLC (cT4N3M1c with malignant pleural effusion and adrenal and brain metastases; stage IVB) receiving four carboplatin/etoposide/atezolizumab cycles, followed by 11 amrubicin cycles. During treatment, whole-brain radiotherapy (30 Gy/10 fractions) and stereotactic radiotherapy to the right frontal brain metastasis (35 Gy/10 fractions) were performed. Upon subsequent mediastinal and right adrenal progression, third-line tarlatamab treatment was initiated. On day 12 after treatment initiation, immune effector cell–associated neurotoxicity syndrome grade 3 was diagnosed, and dexamethasone treatment was started. The patient’s course was complicated by aspiration pneumonia with acute respiratory failure. Follow-up computed tomography demonstrated 31% reduction in the target lesions. However, treatment was discontinued because of performance status decline, and he was transitioned to best supportive care. The survival time was approximately 17.5 months from the initial diagnosis of SCLC and 2.3 months from the initiation of tarlatamab therapy. Although radiologic evaluation demonstrated shrinkage of the target lesions, continuation of tarlatamab was not feasible in this case because of performance status deterioration associated with ICANS and pneumonia. Given the limited evidence regarding the safety of tarlatamab in dialysis patients, its use in this population requires careful consideration and close monitoring.

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Cite This Study

Tsurumaki et al. (2026) studied this question.

synapsesocial.com/papers/69c9c5c5f8fdd13afe0bdb3chttps://doi.org/10.1016/j.ijlcan.2026.100022
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