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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1127698 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type2 {, G1 r4 x, n8 L& U1 A! Y0 j
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ( V$ N7 Q" @7 j& S  Y7 W7 Z. R
+ Author Affiliations
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" b5 E% \6 I! B2 X) H) |6 q3 T7 a/ [1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
2 N9 n, r- H* y8 f1 Y/ f2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
' s  A! x4 F0 a3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 1 A. Z+ N  ^1 D5 j( ?  u
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 1 J1 h3 N4 v' _4 Z$ C
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
. J3 X( n1 N( m+ ^1 b' N: P5 ~6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan % i& n) O) B4 k9 q. X, ?, Q
7Kinki University School of Medicine, Osaka 589-8511, Japan * X' r2 w8 N) @* N; ?9 f. C  r. U
8Izumi Municipal Hospital, Osaka 594-0071, Japan
* _9 {* f# m5 L9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
8 A* w, e& v  W8 w1 F  w6 w# KCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
8 ?5 u. i4 B! y; VAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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4 H1 k* e4 g" rAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 5 E0 x* J6 q; O: ~6 S" d) A; x; ?( C: n' x

& E# a5 P7 L' m4 d0 |( `/ b, IAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ; F2 w) E; K( Y$ y) E

8 P$ n: c8 m! U: t6 xPublished online on: Thursday, December 1, 2011
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+ J& {0 Q4 B  [2 Z8 L. Z$ r* YDoi: 10.3892/ol.2011.507   D- q9 G! ]$ d- Z* ~  [
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Pages: 405-410 : t$ I1 {( r6 `1 t# l
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Abstract:1 G" P: F9 ]+ j6 s
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.. ]+ n7 j0 ~: D. l4 P. R$ _% _

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
: b* E* b: Y9 R& W- S4 [F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 + V7 W, G* t- R/ A
+ Author Affiliations
  l8 G. v$ ]8 W. @5 D8 O7 I" p! j1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ; @% \; k/ M) c8 e
2Department of Thoracic Surgery, Kyoto University, Kyoto 6 b$ s! A5 Y  _) X2 R3 c8 r; J
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan $ x) _. [; j/ X6 T+ J- O% E
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
7 N2 h+ N& K) Z% E& c- D( gReceived September 3, 2010. 9 v; E! Z* [5 ?2 h3 F6 k
Revision received November 11, 2010. ; ?2 G' Z8 U: V+ A" G7 Y3 w# C
Accepted November 17, 2010. / z3 j4 o% ^1 q$ D# y
Abstract# W) E/ f1 b4 l+ @- ?
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
2 U& o* P0 a2 ^* ~: P; s/ B' Q  vPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
; V" q- c+ d$ _$ xResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
2 v7 `$ X5 s0 O% H$ KConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ! [0 Y3 [- L1 S( X5 w% W
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
, S0 y4 g/ Z6 ]3 I9 U今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?2 I+ n" V+ k7 c7 |8 d3 u
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
: W: N4 x1 k* X" ~http://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC; z8 [, {4 |, {- Y4 M+ D2 D
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。4 `# n! V6 g9 _. i1 a3 h1 p
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 : `# S3 n4 m+ E" P; j
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
) L! \8 S- ^& K$ `/ s( _& ^0 Z至今为止,未出 ...

' B8 n4 e$ E* V8 J! X! ^3 n没有副作用是第一追求,效果显著是第二追求。  A7 \$ x  y0 B1 ^
不错。

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