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OncoMatch/Clinical Trials/NCT06217757

Safety and Tolerability of LDRT+Sugemalimab+Chemotherapy+Olaparib for First-Line Treatment of SLFN-11 Positive ES-SCLC

Is NCT06217757 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including Etoposide and Cisplatin for lung cancer.

Phase 1/2RecruitingSichuan UniversityNCT06217757Data as of May 2026

Treatment: Etoposide · Cisplatin · Sugemalimab · OlaparibThe purpose of this study was to evaluate the safety and efficacy of low-dose radiotherapy (LDRT) combined with sugemalimab, olaparib, chemotherapy in the first-line treatment of SLFN-11 positive extensive stage small cell lung cancer.

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Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: SLFN11 positive (positive)

Disease stage

Required: Stage IV

Metastatic disease required

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: immune checkpoint inhibitor

Exception: therapeutic anti-tumor vaccines

No previous treatment with immune checkpoint inhibitors and PARP inhibitors, including but not limited to other anti-PD-1, anti-PD-L1 and anti-programmed cell death ligand 2 (anti-PD-L2) antibodies, with the exception of therapeutic anti-tumor vaccines

Cannot have received: PARP inhibitor

No previous treatment with ... PARP inhibitors

Cannot have received: chemotherapy

No prior chemotherapy or radiation therapy to the chest lesion

Cannot have received: radiation therapy

Exception: external chest radiotherapy for palliative purposes (e.g., bone metastases) is allowed, but must be completed prior to the first administration of study drug

No prior chemotherapy or radiation therapy to the chest lesion. History of thoracic radiotherapy or plan to receive intensive thoracic radiotherapy prior to systemic therapy. External chest radiotherapy for palliative purposes (e.g., bone metastases) is allowed, but must be completed prior to the first administration of study drug

Cannot have received: systemic antitumor therapy

Prior systemic antitumor therapy (chemotherapy, targeted agents such as PARP inhibitors) or immune checkpoint inhibitors for SCLC

Cannot have received: allogeneic stem cell transplant

Previous allogeneic stem cell or solid organ transplantation

Lab requirements

Blood counts

adequate organ and bone marrow functional reserve

Kidney function

adequate organ and bone marrow functional reserve and normal major organ function

Liver function

adequate organ and bone marrow functional reserve and normal major organ function

Have adequate organ and bone marrow functional reserve and normal major organ function. Inadequate bone marrow function and vital organ function reserve [excluded]

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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