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Table 2 Ongoing trials for unresectable stage III NSCLC patients that may change clinical practice in 5 years

From: Emerging evidence and treatment paradigm of non-small cell lung cancer

Agents

Agent type

Control arm

Status

Chemo-radiotherapy

NCT/Name

Sample size

Primary endpoint

Arm1:TQB2450 + Anlotinib

Arm2: TQB2450

PD-L1 inhibitor

Placebo

Phase III

cCRT/sCRT

NCT04325763

315

PFS

Arm1: Durvalumab + Oleclumab;

Arm2: Durvalumab + Monalizumab

PD-L1 inhibitor;

CD73 inhibitor;

NKG2A inhibitor

Durvalumab + Placebo

Phase III

cCRT

NCT05221840 (PACIFIC-9)

999

PFS

Durvalumab + Domvanalimab

PD-L1 inhibitor;

TIGIT inhibitor

Durvalumab + Placebo

Phase III

cCRT

NCT05211895 (PACIFIC-8)

860

PFS

Durvalumab

PD-L1 inhibitor

Placebo

Phase III

cCRT/sCRT

NCT03706690 (PACIFIC-5)

407

PFS

Durvalumab + cCRT → durvalumab

PD-L1 inhibitor

Placebo

Phase III

cCRT

NCT03519971

(PACIFIC-2)

328

PFS

Arm1: Pembrolizumab + cCRT → pembrolizumab;

Arm2:Pembrolizumab + cCRT → 

pembrolizumab + Olaparib

PD-1 inhibitor;

PARP inhibitor

Durvalumab

Phase III

cCRT

NCT04380636 (KEYLYNK-012)

870

PFS;

OS

Pembrolizumab + vibostolimab + cCRT → pembrolizumab + vibostolimab;

PD-1 inhibitor;

TIGIT inhibitor

Durvalumab

Phase III

cCRT

NCT05298423 (KEYVIBE-006)

784

PFS; OS; PFS + OS (PD-L1 ≥ 1%);

Arm1: Nivolumab + cCRT → 

nivolumab + ipilimumab

Arm2: Nivolumab + cCRT → 

nivolumab

PD-1 inhibitor;

CTLA-4 inhibitor

Durvalumab

Phase III

cCRT

NCT04026412

(CheckMate73L)

888

PFS

Atezolizumab + tiragolumab

PD-L1 inhibitor;

TIGIT inhibitor

Durvalumab

Phase III

cCRT

NCT04513925

(SKYSCRAPER-03)

800

PFS

Osimertinib

EGFR-TKI

Placebo

Phase III

cCRT/sCRT

NCT03521154

(LAURA)

216

PFS

Almonertinib

EGFR-TKI

Placebo

Phase III

cCRT/sCRT

NCT04951635

150

PFS

Arm1: Alectinib

Arm2: Entrectinib

Arm3: Pralsetinib

ALK-TKI;

ROS1-TKI;

RET-TKI

Durvalumab

Phase I-III

cCRT/sCRT

NCT05170204

320

PFS

MRD+:

Durvalumab+

Chemotherapy;

MRD−:

Durvalumab

PD-L1 inhibitor

–

Phase II

cCRT

NCT04585490

48

The change of ctDNA (MRD+) due to the addition of chemotherapy

  1. PFS progression-free survival; cCRT/sCRT concurrent/sequential chemotherapy and radiotherapy; OS overall survival; TKI tyrosine kinase inhibitor; MRD molecular residual disease; ctDNA circulating tumor DNA