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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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1232687 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 Type+ L/ j" o" B! a: |. {8 ?$ s: _
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
9 k* W* k* E: A+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
: Q; N7 C6 F, L: v  M4 k/ A/ v2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 U  x  X/ |7 c# V$ j4 t3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
  G. F7 W8 C; M$ y# q4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan & ~) s! K9 D* e. w) B( L
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
# |$ X9 J$ `; ^. I) o$ @+ r6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 7 r( v- `* D2 v/ Z4 e# d
7Kinki University School of Medicine, Osaka 589-8511, Japan
2 G: F( z/ K7 G' f8Izumi Municipal Hospital, Osaka 594-0071, Japan % y9 y& U4 J  ?6 E1 ]
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
. W- A* n1 O& u# lCorrespondence 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 - s/ [* d0 R' F! J
AbstractBackground: 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 " A+ Z- G; `7 G: M8 m$ Q

  N0 w1 e( \4 h# HAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
% Y. p! l* ~6 P! Z5 L
" X+ R. S, l: z' @4 _  Z/ rAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
) j2 N; @7 B! O2 u" ~  b' J/ l1 F" I# |1 _# ~
Published online on: Thursday, December 1, 2011 7 P" f3 E) n7 K5 `
9 h/ M' E& _* B6 b9 [2 J2 x
Doi: 10.3892/ol.2011.507
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$ U& K; n+ W- T- aPages: 405-410 2 `+ l- u; y- B9 c
+ s3 B7 R& U9 E
Abstract:: s/ p4 g# N" A5 m4 o. C- I! x' V5 t
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.
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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
; i$ |  C3 T( dF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
6 s/ y- j% S# d- ^, N5 {+ Author Affiliations6 p* L! e  h3 b! \
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ( P8 f, P* z. J3 {# g, D* w9 m
2Department of Thoracic Surgery, Kyoto University, Kyoto ! C) G! @9 L6 h, U& k
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
( L, I8 P% v5 L0 k6 \&#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 ! \' T/ o6 e; Z# ~
Received September 3, 2010.
* @2 Z' J: O# }8 l- |1 W! PRevision received November 11, 2010. 1 E1 u/ d$ K, z& T3 U: M
Accepted November 17, 2010. & {$ a% P  a( U4 m
Abstract
& u4 o& [9 m; a. @) h4 I- JBackground: 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. 8 @7 |" F3 ?1 ~0 U! t
Patients 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.
$ X; U  X: T# K6 a5 s/ [Results: 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. + H1 N5 g0 K: H; C$ X
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 8 a2 w6 x! c! r) C
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。2 N) g5 c% _& j- i
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?' w( @' y% J% z: S- V- l
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
% I- W$ Z- L8 _+ f! ~) U4 i8 Z0 Uhttp://clinicaltrials.gov/ct2/show/NCT01523587' P: x0 c0 J4 A" T$ a% O

# ~. l" k2 z* j4 W: {, Y# T0 nBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
% ?) o  `0 E! T! p6 }8 Ghttp://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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& W! N) T6 {) M! N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 O4 K  X0 _; G. W  B" A- {$ I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 ; g* g! d+ Z+ F8 }8 C, Z0 O& G
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。
; {) H8 H2 j3 ~4 R至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。
2 {$ K4 p% d* @$ j, }' C" g不错。

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