This guidance provides a data-supported approach to diagnosis, staging, treatment and follow up of patients diagnosed with SCLC.
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Recommendation |
Strength of recommendation |
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Diagnosis and Risk Assessment |
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Initial assessment should include smoking history, physical examination, complete blood count, liver enzymes, sodium, potassium, calcium, glucose, LDH and creatinine (pulmonary function tests if localized disease). |
Good practice statement |
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Attention drawn towards potential autoimmune-mediated paraneoplastic symptoms is advised . |
Conditional |
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Combined approach of using the AJCC TNM staging system (9th edition) and the older Veterans Administration (VA) Lung Study Group’s 2-stage classification VA scheme for SCLC staging should be used (appendix 1). |
Good practice statement |
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The effusion should be excluded as a staging element if: 1) multiple cytopathologic examinations of the pleural fluid are negative for cancer; 2) the fluid is not bloody and not an exudate; and 3) clinical judgment concludes that the effusion is not directly related to the cancer. |
Good practice statement |
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Pericardial effusions are classified using the same criteria mentioned above. |
Good practice statement |
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A contrast-enhanced CT of the chest and abdomen is recommended. |
Strong |
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Brain MRI is recommended for all patients. However, contrast enhanced CT is an option when MRI is not available. |
Strong |
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FDG–PET–CT is optional for staging in limited-stage disease, and FDG–PET findings that modify treatment decisions should be pathologically confirmed. |
Conditional |
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FDG–PET–CT is advised to assist in RT volume delineation. |
Conditional |
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In limited-stage disease, additional bone scintigraphy is recommended when no FDG–PET–CT has been carried out. |
Strong |
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In limited-stage disease, a bone marrow aspiration and biopsy are advised in the case of abnormal blood counts suggesting bone marrow involvement only if it changes clinical management. |
Conditional |
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The workup for SCLC should not delay the onset of treatment for >1 week because of the aggressive nature of SCLC. |
Good practice statement |
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Tobacco smoking cessation counseling and intervention should be strongly promoted in patients with SCLC and patients who previously smoked tobacco should be strongly encouraged to remain abstinent. |
Good practice statement |
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Treatment |
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Management of limited-stage disease (i.e. stages I-III SCLC eligible for treatment of curative intent) |
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Surgery should be considered in patients with clinical stages I and II (cT1-2N0) SCLC in the context of a multimodal treatment concept and following a multidisciplinary board decision. |
Strong |
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The aim of surgical treatment should be achieving an R0 resection. |
Strong |
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When considering surgical treatment for SCLC, pathological mediastinal staging should be done. |
Strong |
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Sublobular resection is not recommended for SCLC. |
Conditional |
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After surgical resection, in case of pT1-2N0-1, R0 resection, adjuvant chemotherapy should be given. |
Strong |
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After surgical resection, in case of R1-R2 resection or positive mediastinal lymph nodes (N2), adjuvant chemotherapy should be combined with RT, preferably concurrently. |
Strong |
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The preferred Chemotherapy for patients with limited-stage (stage I-III) SCLC is platinum plus etoposide. |
Strong |
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G-CSF is a treatment option to prevent haematological toxicity. |
Good practice statement |
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Patients with T1-4N0-3M0 tumours and a good PS (0-1) should be treated with concurrent platinum-salt based chemotherapy and thoracic RT. |
Strong |
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The recommended dose fractionation schedule is 66 Gy. in 33 fractions or equivalent doses |
Strong |
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Thoracic RT should be initiated as early as possible, starting on the first or second cycle of Chemotherapy. |
Strong |
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When the patient PS (≥2) or dose to the organs at risk do not allow for the early administration of thoracic RT, it should be postponed until the start of the third cycle of Chemotherapy. |
Strong |
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Sequential CRT is the preferred option for patients who are not candidates for concurrent CRT due to poor PS, comorbidities and/or disease volume. |
Strong |
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In case of response to Chemotherapy, the post-Chemotherapy primary tumour should be included in the radiation field. |
Strong |
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In case of response to Chemotherapy, the pre-Chemotherapy nodal stations should be included in the radiation field. |
Strong |
|
Selective node irradiation is recommended (i.e. involved nodes defined as FDG avid on PET–CT, enlarged on CT and/or biopsy-positive). |
Strong |
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Patients with stage III SCLC with a response after treatment (CRT) and a PS of 0-1 should be offered PCI. |
Strong |
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PCI can be considered in patients with a PS of 2. |
Conditional |
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The role of PCI is not as well defined in patients with stage I-II SCLC or in those >70 years of age or who are frail. In such cases, shared decision making is advised. |
Conditional |
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The recommended PCI regimen is 25 Gy/10 fractions. |
Strong |
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Management of extensive-stage disease (i.e. stage IV or stage III SCLC not eligible for treatment of curative intent) |
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The preferred first-line treatment of extensive-stage SCLC (PS 0-2) is four to six cycles of a platinum plus etoposide |
Strong |
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Cisplatin with irinotecan or topotecan are alternative treatment options. |
Conditional |
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In poor prognosis patients, gemcitabine plus carboplatin is an alternative treatment option. |
Conditional |
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In patients achieving a response after Chemotherapy and a PS of 0-2, RT to the residual primary tumour and lymph nodes (30 Gy/10 fractions) is a treatment option. |
Conditional |
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PCI (20 Gy/5 fractions and 25 Gy/10 fractions) is justified without prior MRI staging or follow-up in patients <75 years of age and a PS of 0-2 who achieved a response after Chemotherapy. |
Strong |
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In patients with extensive-stage SCLC without brain metastases on brain MRI after Chemotherapy and who can be followed-up with regular brain MRI, PCI may be omitted. |
Strong |
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Patients with platinum-refractory SCLC have a poor prognosis and BSC is recommended. |
Conditional |
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Topotecan is recommended for patients with platinum-resistant or -sensitive relapse; CAV , texans, gemcitabine, and oral etoposide are alternative options. |
Strong |
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In patients with platinum-sensitive SCLC, rechallenge with first-line platinum plus etoposide can be considered. |
Strong |